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		    <titleInfo>
				<title>Assessment of the serum zinc, copper, β-carotene and vitamin A and hoof zinc and copper status in different locomotion scores of dairy cattle</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Sadeghi-nasab</namePart>
				<affiliation>Department of Clinical Sciences, Faculty of Para-veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">S. M.</namePart>
				<namePart type="given">Zolhavarieh</namePart>
				<affiliation>Department of Clinical Sciences, Faculty of Para-veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">H.</namePart>
				<namePart type="given">Aliarabi</namePart>
				<affiliation>Department of Animal Science, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">B.</namePart>
				<namePart type="given">Dadmehr</namePart>
				<affiliation>Department of Basic Sciences, Applied Science Education Center of Farab Amarlou, Jirandeh, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Bahari</namePart>
				<affiliation>Department of Clinical Sciences, Faculty of Para-veterinary Science, Bu-Ali Sina University, Hamedan, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">P.</namePart>
				<namePart type="given">Zamani</namePart>
				<affiliation>Department of Animal Science, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">Z.</namePart>
				<namePart type="given">Baradaran-seyed</namePart>
				<affiliation>Graduated from Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">H.</namePart>
				<namePart type="given">Sharifi</namePart>
				<affiliation>Department of Food
Hygiene, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">Z.</namePart>
				<namePart type="given">Bakhtiari</namePart>
				<affiliation>Department of Animal Science, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">F.</namePart>
				<namePart type="given">Abolghazi</namePart>
				<affiliation>Graduated from Faculty of Chemistry, Bu-Ali Sina University, Hamedan, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Serum level of zinc, copper, β-carotene, vitamin A, and concentrations of Zn and Cu in hoof of 97multiparous Holstein dairy cows with different locomotion scores (LSs) were evaluated. Simultaneously, Znand Cu concentrations of close up, fresh and high yielding cattle rations were 77, 94, 75 and 31, 28, 22 ppm, respectively. Based on LSs, despite normal serum copper levels in all three groups, with increasing degree of lameness serum and hoof Cu concentrations of the severe lame group were significantly lower than healthy and moderate lame groups (P=0.0178) and (P=0.0002), respectively. Serum β-carotene and vitamin A level of the three groups were sub-optimal. Significant negative correlations were observed between LSs with serum vitamin A level (r=-0.246, P=0.0145), LSs with hoof Cu concentration (r=-0.323, P=0.0150) and serum Zn concentration and Cu (r=-0.281, P=0.032). The results suggest that the deterioration of hoof tissue may be associated with reduced copper hoof content. Our findings demonstrated that lame group was at risk of subclinical vitamin A deficiency, which could be established from the healthy stages. Possibly, excess consumption of Zn could conflict with Cu absorption and utilization. Furthermore, vitamin A supplementation may have assisted in reduction of lameness in experimental animals. In conclusion, the serum and hoof concentrations and dietary intake of copper, zinc and vitamin A can have an impact on degrees of lameness and their interactions should be considered.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>277</start>
					<end>282</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1823_968f84f3f5fbca5759c672b3d87cc7be.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1823</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Effect of dietary γ-aminobutyric acid on performance parameters and some plasma metabolites in Cherry Valley ducks under high ambient temperature</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">S.</namePart>
				<namePart type="given">Zhigang</namePart>
				<affiliation>Department of Animal Science, College of Animal Science and Technology, Shandong Agricultural
University, Taian, Shandong, 271018, China</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Sheikhahmadi</namePart>
				<affiliation>Department of Animal Science, Faculty of Agriculture,
University of Kurdistan, Sanandaj, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">Z.</namePart>
				<namePart type="given">Li</namePart>
				<affiliation>MSc Student in Animal Science, Department of Animal Science, College of Animal Science and Technology, Shandong Agricultural University, Taian, Shandong, 271018,
China</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Gamma aminobutyric acid (GABA) is one of the inhibitory neurotransmitters that may have the ability torelieve the intensity of stress. Heat stress remains a major threat for duck production in summer in most areas of China. The current study was conducted to investigate the effect of dietary GABA on performanceparameters and plasma metabolites of heat exposed ducks. Two thousand Cherry Valley ducks (19 d) wererandomly divided into two groups, each group with five replicates. One group was fed basal diet and theother fed basal diet with 100 mg/kg GABA for 42 days. The ambient temperature from day 19 to 42 was 29.7 ± 3.5°C. Growth performance and rectal temperature were determined on days 19, 32 and 42. Plasmasamples were collected at day 42. The results showed that dietary GABA had no significant effect on ducks’rectal temperature but decreased the feed intake (P&lt;0.05). No differences were observed on survival rate,body weight, and dressing percentage. Gamma aminobutyric acid decreased feed conversion ratios (P&lt;0.05)and plasma glucose concentration (P&lt;0.05). However, GABA increased plasma concentrations of triglycerideand free fatty acids (P&lt;0.05). No differences of GABA concentrations were found in the blood, heart, liver,and kidney between the two groups, but was increased in the brain of GABA group (P&lt;0.05). These findingssuggest that 100 mg/kg dietary GABA decreased feed intake and increased fat mobilization in ducks exposed to high ambient temperature, which might attenuate the adverse effects of heat stress on duck production.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>283</start>
					<end>290</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1824_94762362d1df648ad9411a91bdaa7e5f.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1824</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Prevalence of different aggression types and assessment of related determinants in a population of Iranian domestic dogs</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Abbaszadeh Hasiri</namePart>
				<affiliation>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">O. A.</namePart>
				<namePart type="given">Nekouei Jahromi</namePart>
				<affiliation>Centre for Veterinary Epidemiological Research, Department of Health Management, Atlantic Veterinary College,
University of Prince Edward Island, Prince Edward Island, Canada</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Shojaee Tabrizi</namePart>
				<affiliation>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Prevalence of different aggression types and some related risk indicators were studied in 434 dogspresented to the School of Veterinary Medicine at Shiraz University over a one-year period (From March2010 to June 2011). After taking case histories and examining all dogs, related questionnaires werecompleted for each dog and the nine classical types of aggression were evaluated. 25.3% of all cases hadbitten at least one person or animal during their life. The most frequent aggression type was conflict(dominance) aggression (36.6%) followed by fear (20.9%) and protectiveness (20.9%) aggression,intraspecific (7.8%), medical (3.9%), redirected (2.6%), pain (2.6%), maternal (2.6%) and predationaggression (1.9%). Sex, age and indoor/outdoor keeping had a significant effect on conflict aggression. Males (P&lt;0.001), more than 2 years of age (P=0.001) and outdoor dogs (P=0.02) revealed significantly higher levels of conflict aggression. The majority of the cases did not understand obedience orders of the owners and needed more training to obey properly. Raising the level of socialization of the pet and owner’s knowledge about training principles may reduce these behavioral problems in Iran.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>291</start>
					<end>298</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1825_eddbe911806e232d828d70d0584a9602.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1825</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Effect of follicular size on in vitro maturation, fertilization and culture of sheep embryos</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">A. R.</namePart>
				<namePart type="given">Wani</namePart>
				<affiliation>MVSc Student in Animal Reproduction, Department of Animal Reproduction,
Gynaecology and Obstetrics, Faculty of Veterinary Sciences and Animal Husbandry Sher-e-Kashmir, University of Agricultural Sciences and Technology of Kashmir,  India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">M. Z.</namePart>
				<namePart type="given">Khan</namePart>
				<affiliation>Department of Animal Reproduction, Gynaecology and Obstetrics, Faculty of Veterinary Sciences
and Animal Husbandry, Sher-e-Kashmir, University of Agricultural Sciences and Technology of Kashmir,
Srinagar, Jammu and Kashmir, 190 006, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">K. A.</namePart>
				<namePart type="given">Sofi</namePart>
				<affiliation>Department of Animal Reproduction, Gynaecology and Obstetrics, Faculty of Veterinary Sciences
and Animal Husbandry, Sher-e-Kashmir, University of Agricultural Sciences and Technology of Kashmir,
Srinagar, Jammu and Kashmir, 190 006, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A. A.</namePart>
				<namePart type="given">Malik</namePart>
				<affiliation>Department of Animal Reproduction, Gynaecology and Obstetrics, Faculty of Veterinary Sciences
and Animal Husbandry, Sher-e-Kashmir, University of Agricultural Sciences and Technology of Kashmir,
Srinagar, Jammu and Kashmir, 190 006, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">F. A.</namePart>
				<namePart type="given">Lone</namePart>
				<affiliation>Department of Animal Reproduction, Gynaecology and Obstetrics, Faculty of Veterinary Sciences
and Animal Husbandry, Sher-e-Kashmir, University of Agricultural Sciences and Technology of Kashmir,
Srinagar, Jammu and Kashmir, 190 006, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">F. A.</namePart>
				<namePart type="given">Bhat</namePart>
				<affiliation>MVSc Student in Animal Reproduction, Department of Animal Reproduction,
Gynaecology and Obstetrics, Faculty of Veterinary Sciences and Animal Husbandry Sher-e-Kashmir, University of Agricultural Sciences and Technology of Kashmir, 
India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>A study was conducted to investigate the effect of follicular size (small, &lt;2 mm diameter and large, ≥2mm) on in vitro maturation, fertilization and culture of ovine oocytes. The ovaries (n=80) were collectedfrom abattoirs in Srinagar city, India and transported in normal saline solution containing 50 μg gentamicinsulphate per ml in a thermos flask. The oocytes were collected by puncture technique and good and fairquality oocytes obtained were subjected to maturation in TCM-199 supplemented with epidermal growthfactor (EGF) for 24 h under 5% CO2 and humidified atmosphere at 38.5°C. The matured oocytes were thensubsequently subjected to fertilization and culturing was done for six days. The results revealed that thematuration rate of large follicle oocytes (85.20%) was higher than small follicle oocytes (52.44%, P=0.002).In vitro fertilization rates for small and large follicle oocytes were not significantly different (79.54 and76.65%, respectively). However, cleavage and morula rates were higher in large follicle oocytes (58.69 and34.13%) than small follicle oocytes (38.63 and 19.32%, respectively, P&lt;0.05). In conclusion, there is higherdevelopmental competence of oocytes from the large follicles than small follicles and the pre-maturation ofoocyte occurring during follicular growth is essential for subsequent embryonic development in sheep.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>299</start>
					<end>304</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1826_38c88bc2cdd28153ecd145c4b2823eab.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1826</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>The effect of seminal plasma on the quality of coated ram frozen-thawed spermatozoa</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Roostaei-Ali Mehr</namePart>
				<affiliation>Department of Animal Science, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">F.</namePart>
				<namePart type="given">Sharafi</namePart>
				<affiliation>Graduated from Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Two experiments were designed to examine the effects of crude seminal plasma (CSP) exposure ofejaculated and epididymal spermatozoa before freezing. Experiment 1, two consecutive ejaculates werecollected (n=4) within 5 min, the second one was carried out in a tube containing Fiser extender (coatedspermatozoa); by centrifugation, seminal plasma was removed from coated ejaculates. The pellets were split into three parts and 0, 50 and 100% CSP (v/v) was added and they were frozen. Samples were thawed and incubated at 37°C for 6 h. The highest progressive motility (10.41%) and the highest hypo-osmotic responses (12.62%) were found for the coated spermatozoa without CSP at 6 (P&lt;0.05). The maximum viability was found for coated spermatozoa without CSP at 0 (29.4%) and 6 (17%, P&lt;0.05). Experiment 2, epididymal spermatozoa were recovered (n=6), pooled and split into three fractions and 0, 50 and 100% CSP and the diluents were added, after that they were frozen. Thawed epididymal spermatozoa were incubated at 37°C for 6 h. The highest (33.3%) and lowest (25%) progressive motility were found for the epididymal spermatozoa without CSP and the epididymal spermatozoa with 100% CSP at 0, respectively (P&lt;0.05). The highest (19.37%) and the lowest (9.38%) viability were related to the epididymal spermatozoa with 0 and 100% CSP at 6, respectively (P&lt;0.05). Under the conditions of the current study, the addition of CSP to the ram epididymal and coated spermatozoa strengthened the detrimental effect of the freezing procedure.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>305</start>
					<end>312</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1827_839bc1d79d0b4ae205573112a03f1db2.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1827</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>The prenatal development in swamp buffalo (Bubalus carabanensis)</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">N.</namePart>
				<namePart type="given">Van Hanh</namePart>
				<affiliation>Laboratory of Embryo Biotechnology, Institute of Biotechnology, Vietnam Academy of Science and
Technology, 18 Hoang Quoc Viet, Hanoi, Vietnam</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">N. M.</namePart>
				<namePart type="given">Sousa</namePart>
				<affiliation>Department of Physiology of Animal Reproduction,
Faculty of Veterinary Medicine, University of Liege, B-4000 Sart-Tilman, Liege, Belgium</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">J. F.</namePart>
				<namePart type="given">Beckers</namePart>
				<affiliation>Department of Physiology of Animal Reproduction,
Faculty of Veterinary Medicine, University of Liege, B-4000 Sart-Tilman, Liege, Belgium</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">X. N.</namePart>
				<namePart type="given">Bui</namePart>
				<affiliation>Laboratory of Embryo Biotechnology, Institute of Biotechnology, Vietnam Academy of Science and
Technology, 18 Hoang Quoc Viet, Hanoi, Vietnam</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>There are morphological and reproductive physiological differences between swamp buffalo (Bubaluscarabanensis) and river buffalo (Bubalus bubalis). The development of fetus weight and fetus biometry wasreported in river buffalo and other animals but not in swamp buffalo. The aim of this study was to describethe inherent variability in fetus related measurements during swamp buffalo pregnancy. The data is based on measurements of 267 fetuses and 5 new born claves from swamp buffalo. The results show that a significant linear correlation exists between estimated age of fetuses and parameters of fetus sizes. There were correlations between crown-rump length (CRL) and other fetal parameters, as well as between fetus weight and its parameters. In conclusion, our data indicated that the feasibility and value of fetal measures in swamp buffaloes being used for the evaluation of fetal development.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>313</start>
					<end>319</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1828_35e6462b90a4d5647cb4b34cde95f93b.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1828</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Histochemical study of river buffalo’s uterine endometrium in follicular and luteal phases</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">R.</namePart>
				<namePart type="given">Shahrooz</namePart>
				<affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Razi</namePart>
				<affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Babai</namePart>
				<affiliation>Graduated from Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>This study was conducted to evaluate histochemical alterations of river buffalo’s uterine wall acid andalkaline phosphatases (ALP and ACP), lipase and carbohydrate ratio during follicular and luteal phases.Forty apparently healthy and non pregnant river buffalos were considered for removal of the uterus aftersacrifice in slaughterhouse. All dissected uteri were divided into two luteal (by observing corpus luteum onthe ovary) and follicular phase (by identifying growing follicles) specimens. In order to prepare frozensection slides, the fresh samples of uterus were transferred into chilled normal saline and cut with cryostat.ALP, ACP, lipase and periodic acid-schiff (PAS) staining techniques (paraffin sections) were conducted.Endometrial epithelium, glandular cells, vascular endothelium and macrophages in luteal phase showedpositive reaction to both phosphatases. Comparing the luteal and follicular phases showed that, the mentioned cells presented significantly higher reaction to both phosphatases in luteal stage. The number of endometrial macrophages increased in luteal phase. The cytoplasmic carbohydrate ratio of endometrial epithelium and glands were significantly higher in follicular phase. Reactions to PAS staining revealed that, the glandular cells showed remarkably denser PAS stained cytoplasm in comparison to epithelial and endothelial cells. In luteal phase, uterus represented higher lipase ratio in comparison to follicular phase. In conclusion, similar to other bovine and buffalo species, in river buffalos the histochemical alterations in endometrial phosphatases, carbohydrates (mainly glycogen) and lipase depend on cyclic hormonal changes.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>320</start>
					<end>326</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1829_d5493cb9dc93a2b5c16402469af00cc3.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1829</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Leptin receptor mRNA expression in Taleshi ram gonads</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Roostaei-Ali Mehr</namePart>
				<affiliation>Department of Animal Science, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">R.</namePart>
				<namePart type="given">Rajabi-Toustani</namePart>
				<affiliation>Graduated from Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">R.</namePart>
				<namePart type="given">Motamedi-Mojdehi</namePart>
				<affiliation>Graduated from Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Leptin is secreted mainly by fat, which is involved in energy metabolism and reproduction. Leptin and itsreceptor (Ob-R) have been detected in human spermatozoa and testis, thus it can be concluded leptin involves in male physiology. The goal of this study was determination of the presence of leptin receptor mRNA in the ram testis, epididymis and spermatozoa by reverse transcription polymerase chain reaction (RT-PCR). Ejaculated spermatozoa from ten fertile Taleshi ram were collected by means of an artificial vagina. Testes, placental cotyledons and adrenal glands were obtained from abattoir. Placental cotyledons and adrenal glands were used as the positive control. Epididymal spermatozoa recovery was performed from epididymis. To purify spermatozoa, motile sperm were isolated by the swim-up procedure. Total RNA was isolated from epididymal spermatozoa, ejaculated spermatozoa, adrenal gland and placental cotyledon and then they were purified. The mRNA for the long form (Ob-Rb) and the short form (Ob-Ra) of leptin receptor was detected in testis. RT-PCR analysis of total RNA from epididymal spermatozoa and ejaculated spermatozoa revealed the presence of leptin mRNA in these cells. The mRNA for Ob-Rb was observed in epididymis and epididymal spermatozoa, but the Ob-Ra mRNA was absent. The presence of Ob-Ra mRNA was found in ejaculated spermatozoa, whereas Ob-Rb mRNA did not exist. It can be concluded that the mRNA for leptin receptor is present in ram gonads and spermatozoa.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>327</start>
					<end>333</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1830_7ca0acec4dd89eef6a2cf6a03e635e55.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1830</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Survey of accessory gene regulator (agr) groups and TSST-1 encoding gene (tst) in Staphylococcus aureus isolated from ewes with mastitis in the northwest of Iran</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">H.</namePart>
				<namePart type="given">Dastmalchi Saei</namePart>
				<affiliation>Department of Microbiology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">S.</namePart>
				<namePart type="given">Aghdasi</namePart>
				<affiliation>Graduated from Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">H.</namePart>
				<namePart type="given">Mohammad-Zadeh</namePart>
				<affiliation>Graduated from Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Accessory gene regulator (agr locus) is a global regulator of many virulence gene expressions inStaphylococcus aureus. Four interference classes related to genetic polymorphisms in the agr locus have sofar been described. In the present study, the agr locus specificity groups were studied within a total of 43 S.aureus isolates which were isolated from ewes with mastitis in three regions in the Northwest of Iran. Inaddition, the isolates were examined for the presence of TSST-1 (toxic shock syndrome toxin-1) encodinggene (tst) using PCR. Identification of agr groups, using agr group-specific multiplex PCR, classified themajority of isolates into group I (51.16%) and to a lesser extent into agr group IV (44.19%). Only one isolate (2.23%) for each of the agr groups II and III was found. This study also indicated that 44.19% of isolates (n=19) possessed the tst gene and that 94.74% (n=18) belonged to agr group I. According to the results, certain agr groups comprised the great majority of sheep mastitis associated S. aureus isolates. Moreover, the high proportion of S. aureus isolates was tst positive, indicating an issue requiring consideration as it is relevant to food hygiene. The results also showed a variation in distribution of the tst gene among the different agr groups.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>334</start>
					<end>340</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1831_59f80266236ca4fea40172b6421b530e.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1831</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Effects of co-administration of ghrelin agonist (GHRP-2) and GH on TNF-α, IL-6 and iNOS gene expression induced by LPS in the mouse brain</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Zendehdel</namePart>
				<affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">P.</namePart>
				<namePart type="given">Allahdini</namePart>
				<affiliation>Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">E.</namePart>
				<namePart type="given">Safarpour</namePart>
				<affiliation>Department of Biology, Qom Branch, Islamic Azad University, Qom, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">Z.</namePart>
				<namePart type="given">Abrehdari</namePart>
				<affiliation>Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Pourrahimi</namePart>
				<affiliation>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">R.</namePart>
				<namePart type="given">Mazaheri Nezhad Fard</namePart>
				<affiliation>Rastegar Reference Laboratory, Faculty of
Veterinary Medicine, University of Tehran, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>The aim of this study was to examine the anti-inflammatory effects of co-administration of growthhormone-releasing peptide-2 (GHRP-2) and growth hormone (GH) on tumor necrosis factor-α (TNF-α),interleukin-6 (IL-6) and inducible nitric oxide synthase (iNOS) gene expression induced by LPS in the mousebrain. Thirty-five male NMRI mice (25±5 g) were injected through the mouse tail vein with saline, GHRP-2(100 μg/kg), GH (25 μg/kg) or GHRP-2 + GH, 30 min before the intraperitoneal injection of LPS (5 mg/kg).Then, inflammation was induced by the intraperitoneal injection of LPS. The control animals received sterilesaline in the first and second injections. Changes in the expression level of TNF-α, IL-6 and iNOS geneswere studied in the mouse brain by a semi quantitative RT-PCR method. The results of this study showedthat GHRP-2 or GH significantly decreased the expression of TNF-α and IL-6 genes in brain 2 h after theinjection of LPS. Co-administration of GHRP-2 and GH markedly reduced the expression of TNF-α and IL-6genes. LPS had no effect on the expression of iNOS gene in brain. The data suggest that co-administration of GHRP-2 and GH has a protective effect in brain inflammation induced by LPS through inhibition of TNF-αand IL-6.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>341</start>
					<end>344</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1832_6d039faf72a6976609582c84cea08dc5.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1832</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Comparison of microscopy and blood-PCR for the diagnosis of clinical Johne’s disease in domestic ruminants</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">S. V.</namePart>
				<namePart type="given">Singh</namePart>
				<affiliation>Microbiology Laboratory, Animal Health Division, Central Institute for Research on Goats, Makhdoom, PO-Farah, Pin-281122, District Mathura, Uttar Pradesh, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">P. K.</namePart>
				<namePart type="given">Singh</namePart>
				<affiliation>National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Tajganj, Agra-282 001, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">S.</namePart>
				<namePart type="given">Gupta</namePart>
				<affiliation>Microbiology Laboratory, Animal Health Division, Central Institute for Research on Goats, Makhdoom, PO-Farah, Pin-281122, District Mathura, Uttar Pradesh, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">K. K.</namePart>
				<namePart type="given">Chaubey</namePart>
				<affiliation>Microbiology Laboratory, Animal Health Division, Central Institute for Research on Goats, Makhdoom, PO-Farah, Pin-281122, District Mathura, Uttar Pradesh, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">B.</namePart>
				<namePart type="given">Singh</namePart>
				<affiliation>Microbiology Laboratory, Animal Health Division, Central Institute for Research on Goats, Makhdoom, PO-Farah, Pin-281122, District Mathura, Uttar Pradesh, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Kumar</namePart>
				<affiliation>Microbiology Laboratory, Animal Health Division, Central Institute for Research on Goats, Makhdoom, PO-Farah, Pin-281122, District Mathura, Uttar Pradesh, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A. V.</namePart>
				<namePart type="given">Singh</namePart>
				<affiliation>National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Tajganj, Agra-282 001, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">N.</namePart>
				<namePart type="given">Kumar</namePart>
				<affiliation>Microbiology Laboratory, Animal Health Division, Central Institute for Research on Goats, Makhdoom, PO-Farah, Pin-281122, District Mathura, Uttar Pradesh, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Microscopy as “field based test” was compared with IS900 blood PCR for the diagnosis and estimationof prevalence of Mycobacterium avium subspecies paratuberculosis (MAP) in domestic livestock withclinical Johne’s disease (JD). Of 252 animals screened, 39.3 and 13.1% were positive by faecal microscopyand blood PCR, respectively. Proportional agreement between “microscopy” and blood PCR was substantial.1262 faecal samples from animals suspected of clinical JD were screened by microscopy in 2009-2010 and41.3% were positive. Prevalence of MAP was highest in cattle (61.8%), followed by goats (41.3%), sheep(33.4%) and buffaloes (15.7%). Faecal microscopy was cost effective, easy to adopt and repeatable for thescreening of domestic ruminant population against MAP infection.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>345</start>
					<end>349</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1833_d43044a2bd892c904f91ef1040a56ace.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1833</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Development of a recombinant protein-based dot-blot hybridization assay for the detection of antibody to chicken infectious bronchitis virus</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">H.</namePart>
				<namePart type="given">Akrami</namePart>
				<affiliation>Department of Biology, Faculty of Science, Razi University, Kermanshah, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Hedayati</namePart>
				<affiliation>Iranian Veterinary
Organization, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Farshian</namePart>
				<affiliation>Iranian Veterinary
Organization, Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">G.</namePart>
				<namePart type="given">Haqshenas</namePart>
				<affiliation>National Research Center for Genetic Engineering and Biotechnology (NRCGEB), Tehran, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Nucleocapsid (N) protein of infectious bronchitis virus (IBV), one of the viral structural proteins, inducesstrong antibody response in natural infection. In this study, a simple, recombinant N protein-based dot-blottest was developed to serologically examine chicken serum samples for the presence of IBV antibody.Initially, 72 serum samples were tested for the presence of IBV antibody using a commercial enzyme linkedimmunosorbent assay (ELISA) kit. Forty six IBV positive serum samples (group A) produced strong signalsin the dot-blot assay. Seven negative serum samples (group B) produced weak but specific signals using thedot-blot assay in conjunction with Western blot analysis. The remaining 19 samples (group C) from IBVnegative specific pathogen free (SPF) chickens did not produce visible signals using the dot-blot assay. Inconclusion, the above results suggest that the dot-blot assay is a reliable, sensitive, and specific test forserological detection of IBV positive chickens.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>350</start>
					<end>353</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1834_d2cc9e56e446e2bb4439ec09443a447d.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1834</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Cloning and sequence analysis of VP1, VP2 and VP3 genes of Indian chicken anemia virus</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">C.</namePart>
				<namePart type="given">Hiremath</namePart>
				<affiliation>MVSc in Veterinary Microbiology, Department of Veterinary Microbiology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University, Anand 388001, Gujarat, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">M. K.</namePart>
				<namePart type="given">Jhala</namePart>
				<affiliation>Department of
Veterinary Microbiology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University, Anand 388001, Gujarat, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">B. B.</namePart>
				<namePart type="given">Bhanderi</namePart>
				<affiliation>Department of
Veterinary Microbiology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University, Anand 388001, Gujarat, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">C. G.</namePart>
				<namePart type="given">Joshi</namePart>
				<affiliation>Department of Animal Biotechnology, College of Veterinary Science and Animal Husbandry, Anand Agricultural University, Anand 388001, Gujarat, India</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>Chicken anemia virus was detected by PCR in tissue samples collected from poultry flocks in Gujarat,India. The VP1, VP2 and VP3 gene sequences of CAV from Anand, Gujarat were obtained after cloning thePCR products in pDrive cloning vector. Nucleotide sequence alignment with other CAV sequencesdemonstrated overall identity of 95-98.8%, 98.8-99.8% and 98.8-100% for VP1, VP2 and VP3 regions,respectively. Deduced amino acid sequences revealed 91.7-99.7%, 99-100% and 97.3-100% homologies forVP1, VP2 and VP3 proteins, respectively, indicating high level of genome conservation. Further, placementof critical nucleotides and amino acids at particular positions indicated that Anand CAV is possibly of morepathogenic potential. The CAV isolates were phylogenetically grouped together independent of theirgeographic origin.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>354</start>
					<end>357</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1835_2ba7adeb2b2b8af37555743398ae9d2d.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1835</identifier>
			</mods>
		<mods version="3.5">
		    <titleInfo>
				<title>Gastroesophageal intussusception in a domestic short-hair cat</title>
			</titleInfo>
				<name type="personal">
				<namePart type="family">M.</namePart>
				<namePart type="given">Abbaszadeh Hasiri</namePart>
				<affiliation>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">A.</namePart>
				<namePart type="given">Shojaee Tabrizi</namePart>
				<affiliation>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
				<name type="personal">
				<namePart type="family">M. S.</namePart>
				<namePart type="given">Ahrari Khafi</namePart>
				<affiliation>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</affiliation>
				<role>
				<roleTerm type="text" authority="marcrelator">author</roleTerm>
				</role>
			</name>
			<typeOfResource>text</typeOfResource>
			<genre>article</genre>
			<originInfo>
				<dateIssued keyDate="yes" encoding="w3cdtf">2013</dateIssued>
			</originInfo>
			<language>
				<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
			</language>
			<abstract>A 4-month-old, intact male domestic short-hair cat was presented to Veterinary Hospital with an acuteonset of regurgitation and respiratory distress. Thoracic and abdominal radiographs identified a massconsisted of a heterogeneous mixture of soft tissue and gas densities between heart and craniodorsal part of the diaphragm that was shifted to the left. The stomach could not be seen clearly. Radiographic signssuggested a tentative diagnosis of gastroesophageal intussusception (GEI). Esophagoscopy revealed gastricmucosa in the lumen of the esophagus, and a diagnosis of GEI was made. The GEI was manually reduced by use of insertion tube of scope. Ten days later, the case was euthanized because of GEI recurrence andaspiration pneumonia. Gastroesophageal intussusception is a rare condition in cats. This case report showsthat gastropexy along with manual reduction of GEI is essential for prevention of recurrence and reduction ofmortality.</abstract>
			<relatedItem type="host">
			<titleInfo>
				<title>مجله تحقیقات دامپزشکی ایران</title>
			</titleInfo>
			<originInfo>
				<publisher>معاونت پژوهشی‌ دانشگاه شیراز</publisher>
			</originInfo>
			<identifier type="issn">1728-1997</identifier>
			<part>
				<detail type="volume">
					<number>14</number>
					<caption>v.</caption>
				</detail>
				<detail type="issue">
				<number>4</number>
				<caption>no.</caption>
				</detail>
				<text type="year">2013</text>
				<extent unit="pages">
					<start>358</start>
					<end>361</end>
				</extent>
			</part>
			</relatedItem>
			<identifier type="uri">https://ijvr.shirazu.ac.ir/article_1836_289ecf9c9fdef2d82687ed10734a37a3.pdf</identifier>
			<identifier type="doi">dx.doi.org/10.22099/ijvr.2013.1836</identifier>
			</mods>
		</modsCollection>