Homozygosity mapping approach identifies a missense mutation in equine cyclophilin B (PPIB) associated with HERDA in the American Quarter Horse
about
Lack of cyclophilin B in osteogenesis imperfecta with normal collagen foldingProlyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complexVeterinary Pathology - A Path Forward with New Directions and OpportunitiesCrystal structures of wild-type and mutated cyclophilin B that causes hyperelastosis cutis in the American quarter horseSevere osteogenesis imperfecta in cyclophilin B-deficient miceWhole genome sequence and analysis of the Marwari horse breed and its genetic originNext generation sequencing gives an insight into the characteristics of highly selected breeds versus non-breed horses in the course of domestication.Applied equine genetics.Whole-genome SNP association in the horse: identification of a deletion in myosin Va responsible for Lavender Foal Syndrome.Whole-genome sequencing and genetic variant analysis of a Quarter Horse mareMutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes.Equine clinical genomics: A clinician's primer.Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl Hydroxylation.Ancient genomic changes associated with domestication of the horse.Harnessing the genetic toolbox for the benefit of the racing Thoroughbred.RNA sequencing as a powerful tool in searching for genes influencing health and performance traits of horses.Cutaneous asthenia (Ehlers-Danlos-like syndrome) of Burmese cats.Genetic testing in veterinary dermatology.Tensile properties in collagen-rich tissues of Quarter Horses with hereditary equine regional dermal asthenia (HERDA).Targeted analysis of four breeds narrows equine Multiple Congenital Ocular Anomalies locus to 208 kilobases.Mutation in cyclophilin B that causes hyperelastosis cutis in American Quarter Horse does not affect peptidylprolyl cis-trans isomerase activity but shows altered cyclophilin B-protein interactions and affects collagen foldingPrevalence of the mutation in cyclophilin B (PPIB), a causal candidate gene for HERDA, among Quarter Horses in France.Increased susceptibility of skin from HERDA (Hereditary Equine Regional Dermal Asthenia)-affected horses to bacterial collagenase degradation: a potential contributing factor to the clinical signs of HERDA.
P2860
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P2860
Homozygosity mapping approach identifies a missense mutation in equine cyclophilin B (PPIB) associated with HERDA in the American Quarter Horse
description
2007 nî lūn-bûn
@nan
2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Homozygosity mapping approach ...... in the American Quarter Horse
@ast
Homozygosity mapping approach ...... in the American Quarter Horse
@en
Homozygosity mapping approach ...... in the American Quarter Horse
@nl
type
label
Homozygosity mapping approach ...... in the American Quarter Horse
@ast
Homozygosity mapping approach ...... in the American Quarter Horse
@en
Homozygosity mapping approach ...... in the American Quarter Horse
@nl
prefLabel
Homozygosity mapping approach ...... in the American Quarter Horse
@ast
Homozygosity mapping approach ...... in the American Quarter Horse
@en
Homozygosity mapping approach ...... in the American Quarter Horse
@nl
P2093
P3181
P1433
P1476
Homozygosity mapping approach ...... in the American Quarter Horse
@en
P2093
Danika L Bannasch
Robert C Tryon
Stephen D White
P304
P3181
P356
10.1016/J.YGENO.2007.03.009
P407
P577
2007-07-01T00:00:00Z