We investigated the occurrence of Factor XI (FXI) deficiency syndrome in the following Indian dairy animals: Bos taurus Holstein-Friesian and Jersey cattle, Bos indicus Indian cattle breeds, B. taurus x B. indicus crossbreds and the river buffalo Bubalus bubalis. Factor XI deficiency is an autosomal recessive bleeding disorder known to affect Hol-stein cattle worldwide. A total of 1001 dairy animals, mainly bulls, were genotyped to detect the mutation within exon 12 of the gene encoding for factor XI. Two Holstein bulls were detected as heterozygous (carrier) for FXI deficiency, giving a carrier frequency of 0.6 % in Indian Holstein cattle. None of the other cattle or buffalo breeds was found to be a carrier for FXI. Sequence comparison bet...
Hereditary factor XI (FXI) deficiency is a mild bleeding disorder, rare in the general population bu...
ABSTRACT: Albinism is a genetic disease characterized by deficient melanin production making affecte...
Congenital Factor XI (FXI) deficiency shows a high variability in clinical phenotype. To date, many ...
In this study 170 Holstein cows reared in the Bursa Region of Turkey were screened in order to detec...
Factor XI Deficiency (FXID) is caused by imperfect insertion of poly adenine which is resulted in in...
138-140In the present investigation, screening of genetic disorders, viz., Bovine leukocyte adhesion...
The aim of this study was to compare the prevalence of factor XI deficiency (FXID) carriers and pote...
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...
In the framework of this thesis was performed genotyping of 46 specimens of the breed Czech red catt...
Factor XI (FXI)-deficiency is a rare coagulation disorder inherited as an autosomal recessive trait,...
ABSTRACT: Glycogen storage disease type II (GSD-II) and congenital myasthenic syndrome (CMS) are imp...
Çakır, Volkan (Arel Author), Berber, Ergül (Arel Author)Background. Factor XI (FXI) deficiency is an...
Factor XI deficiency is a rare bleeding diathesis found predominantly in Ashkenazi Jewish kindreds. ...
Factor XI (FXI) deficiency is an autosomal bleeding disorder, usually posttrauma or postsurgery, cha...
Hereditary factor XI (FXI) deficiency is a mild bleeding disorder, rare in the general population bu...
ABSTRACT: Albinism is a genetic disease characterized by deficient melanin production making affecte...
Congenital Factor XI (FXI) deficiency shows a high variability in clinical phenotype. To date, many ...
In this study 170 Holstein cows reared in the Bursa Region of Turkey were screened in order to detec...
Factor XI Deficiency (FXID) is caused by imperfect insertion of poly adenine which is resulted in in...
138-140In the present investigation, screening of genetic disorders, viz., Bovine leukocyte adhesion...
The aim of this study was to compare the prevalence of factor XI deficiency (FXID) carriers and pote...
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...
In the framework of this thesis was performed genotyping of 46 specimens of the breed Czech red catt...
Factor XI (FXI)-deficiency is a rare coagulation disorder inherited as an autosomal recessive trait,...
ABSTRACT: Glycogen storage disease type II (GSD-II) and congenital myasthenic syndrome (CMS) are imp...
Çakır, Volkan (Arel Author), Berber, Ergül (Arel Author)Background. Factor XI (FXI) deficiency is an...
Factor XI deficiency is a rare bleeding diathesis found predominantly in Ashkenazi Jewish kindreds. ...
Factor XI (FXI) deficiency is an autosomal bleeding disorder, usually posttrauma or postsurgery, cha...
Hereditary factor XI (FXI) deficiency is a mild bleeding disorder, rare in the general population bu...
ABSTRACT: Albinism is a genetic disease characterized by deficient melanin production making affecte...
Congenital Factor XI (FXI) deficiency shows a high variability in clinical phenotype. To date, many ...