Factor XI Deficiency (FXID) is caused by imperfect insertion of poly adenine which is resulted in introduction of premature stop codon in FXI gene. Substitution of guanine into thymine in SLC35A3 gene caused Complex Vertebral Malformation (CVM). The research was aimed to detect the presence or absence of a genetic defect mainly CVM using SLC35A3 gene and FXID using FXI gene in Indonesian Bali cattle. The presence of this genetic defect may have a significant economic impact on the breeding program. The research of genetic defect was done mostly in dairy cattle, but there was no report for screening of genetic defect in Bali cattle. In this study, 303 fresh blood samples and 22 semen samples which were collected from Indonesian Bali cattle ...
Pleomorphic adenoma gene 1 (PLAG1) is a zinc finger transcription factor gene located on bovine chro...
Complex vertebral malformation (CVM) is an inherited, autosomal recessive disorder of Holstein cattl...
Complex vertebral malformation (CVM) is an autosomal recessive genetic syndrome present i...
Factor XI Deficiency (FXID) is caused by imperfect insertion of poly adenine which is resulted in in...
In this study 170 Holstein cows reared in the Bursa Region of Turkey were screened in order to detec...
We investigated the occurrence of Factor XI (FXI) deficiency syndrome in the following Indian dairy ...
Abstract Background Bovine leukocyte adhesion deficiency (BLAD), deficiency of uridine monophosphate...
The infertility problem named Repeat Breeder Syndrome is an important issue in cattle breeding. Besi...
The aim of this study was to compare the prevalence of factor XI deficiency (FXID) carriers and pote...
Not AvailableComplex vertebral malformation (CVM) has considerable economic impact on dairy cattle b...
In the framework of this thesis was performed genotyping of 46 specimens of the breed Czech red catt...
138-140In the present investigation, screening of genetic disorders, viz., Bovine leukocyte adhesion...
This research aimed to evaluate the prevalence of the most common lethal diseases in the Lithuanian ...
The aim of this study was to identify the deficiency of uridine monophosphate synthase (DUMPS) and t...
Dexter cattle are a small breed of cattle originating in Ireland that have been bred in Australia fo...
Pleomorphic adenoma gene 1 (PLAG1) is a zinc finger transcription factor gene located on bovine chro...
Complex vertebral malformation (CVM) is an inherited, autosomal recessive disorder of Holstein cattl...
Complex vertebral malformation (CVM) is an autosomal recessive genetic syndrome present i...
Factor XI Deficiency (FXID) is caused by imperfect insertion of poly adenine which is resulted in in...
In this study 170 Holstein cows reared in the Bursa Region of Turkey were screened in order to detec...
We investigated the occurrence of Factor XI (FXI) deficiency syndrome in the following Indian dairy ...
Abstract Background Bovine leukocyte adhesion deficiency (BLAD), deficiency of uridine monophosphate...
The infertility problem named Repeat Breeder Syndrome is an important issue in cattle breeding. Besi...
The aim of this study was to compare the prevalence of factor XI deficiency (FXID) carriers and pote...
Not AvailableComplex vertebral malformation (CVM) has considerable economic impact on dairy cattle b...
In the framework of this thesis was performed genotyping of 46 specimens of the breed Czech red catt...
138-140In the present investigation, screening of genetic disorders, viz., Bovine leukocyte adhesion...
This research aimed to evaluate the prevalence of the most common lethal diseases in the Lithuanian ...
The aim of this study was to identify the deficiency of uridine monophosphate synthase (DUMPS) and t...
Dexter cattle are a small breed of cattle originating in Ireland that have been bred in Australia fo...
Pleomorphic adenoma gene 1 (PLAG1) is a zinc finger transcription factor gene located on bovine chro...
Complex vertebral malformation (CVM) is an inherited, autosomal recessive disorder of Holstein cattl...
Complex vertebral malformation (CVM) is an autosomal recessive genetic syndrome present i...