Complex Leopard non-associated congenital night blindness in Mangalarga Marchador foals
نویسندگان
چکیده
منابع مشابه
Heart rate variability in Mangalarga Marchador horses after physical exercise
The aim of this study was to evaluate the influence of physical exercise (marcha gait) on heart rate variability indices in Mangalarga Marchador horses. Twenty-five animals, fourteen females and eleven males, aged 6.4 ± 2.7 years and with a mean weight of 428.3 ± 24.7 kg, were used. Electrocardiograms were recorded at two different time points: rest and immediately after exercise (40 min of aer...
متن کاملGenetic diversity and population structure in Brazilian Mangalarga Marchador horses.
One hundred and fifteen unrelated Mangalarga Marchador horses were sampled from three geographically distinct regions of Minas Gerais State, Brazil (South, Southeast, and Northeast) and tested for 10 microsatellite loci. Genetic diversity and population structure parameters were estimated with ARLEQUIN 3.0, CERVUS 2.0, POPGENE 1.31, GENEPOP on the web, STRUCTURE 2.0, and SPAGEDI 1.2 software pa...
متن کاملCongenital Stationary Night Blindness Panel
Test code: OP1201 The Blueprint Genetics Congenital Stationary Night Blindness Panel is a 17 gene test for genetic diagnostics of patients with clinical suspicion of congenital stationary night blindness. The panel covers genes associated with autosomal recessive, autosomal dominant and X-linked forms of congenital stationary night blindness (CSNB). The clinical utility of this diagnostic panel...
متن کاملTwenty-five thousand years of fluctuating selection on leopard complex spotting and congenital night blindness in horses.
Leopard complex spotting is inherited by the incompletely dominant locus, LP, which also causes congenital stationary night blindness in homozygous horses. We investigated an associated single nucleotide polymorphism in the TRPM1 gene in 96 archaeological bones from 31 localities from Late Pleistocene (approx. 17 000 YBP) to medieval times. The first genetic evidence of LP spotting in Europe da...
متن کاملCongenital Stationary Night Blindness Panel
Test code: OP1201 The Blueprint Genetics Congenital Stationary Night Blindness Panel is a 17 gene test for genetic diagnostics of patients with clinical suspicion of congenital stationary night blindness. The panel covers genes associated with autosomal recessive, autosomal dominant and X-linked forms of congenital stationary night blindness (CSNB). The clinical utility of this diagnostic panel...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Brazilian Journal of Veterinary Medicine
سال: 2020
ISSN: 2527-2179,0100-2430
DOI: 10.29374/2527-2179.bjvm106220