نتایج جستجو برای: iranian holstein

تعداد نتایج: 50304  

Bovine spongiform encephalopathy (BSE) is a fatal infectious neurodegenerative disease in cattle, characterized by the accumulation of an abnormal, proteaseresistant prion protein (PrPSc) in the brain. BSE is similar to scrapie in sheep and goats and Creuzfeldt-Jakob disease in humans. Susceptibility in cattle hasbeen shown to be under the influence of two polymorphic locations, which are...

Fibroblast growth factor 2 (FGF2) serves in the uterine endometrium during estrous presenting in the bovine mammary gland which is responsible to express interferon-T (IFNT), and is an important agent to encourage the continuation of pregnancy in the ruminants. Significant associations have been found between genes affected by IFNT and genes that are responsible for milk production traits. Seme...

2017
T. C. Shende P. S. Kulkarni P. C. Pawar

The world is going through the debate on hazardous effects of consumption of A1 milk on human health by producing of hazardous chemical compound like beta casomorphin-7 and how this is not the case with A2. The aim of the present study was to genotype the existing population of crossbred Holstein-Friesian (HF) cattle for polymorphism in â-Casein gene (CSN2) using PCR-RFLP technique. Total of 47...

2004
B. J. Heins L. B. Hansen

First-parity Holstein (H), Normande-Holstein (NxH) crossbred, Montbeliarde-Holstein (MxH) crossbred and Scandinavian-Holstein (SxH) crossbred cows calving from June 2001 to December 2003 were compared for dystocia and stillbirths from seven California herds. Dystocia scores ranging from 1 (no assistance) to 5 (hard pull) and stillbirths (1 for alive and 0 for dead) were recorded for 1695 Holste...

M. Hosseinpour Mashhadi, M. Mahmoudi M. Rastin M.R. Nassiri N. Tabasi N.E.J. Kashan R. Vaez Torshizi S.E. Nooraee

Quantitative traits locus for milk production traits has been described on centromeric end of bovine chromosome 14. Reports name the acyl coA: diacylglycerol acyltransferase (DGAT1) gene as a potential candidate gene with dinucleotide substitution (AA to GC) in exon VIII which causes the change of lysine to alanine in amino acid (K232A).The aim of the present study was to estimate the frequency...

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