Identification of a nonsense mutation in CWC15 associated with decreased reproductive efficiency in Jersey cattle
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Use of Genomic Tools to Improve Cattle Health in the Context of Infectious DiseasesA reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breedsBovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3A 660-Kb deletion with antagonistic effects on fertility and milk production segregates at high frequency in Nordic Red cattle: additional evidence for the common occurrence of balancing selection in livestockA nonsense mutation in TMEM95 encoding a nondescript transmembrane protein causes idiopathic male subfertility in cattleInvited review: overview of new traits and phenotyping strategies in dairy cattle with a focus on functional traitsGenomic Footprints in Selected and Unselected Beef Cattle Breeds in Korea.Screening of whole genome sequences identified high-impact variants for stallion fertility.A single nucleotide polymorphism in COQ9 affects mitochondrial and ovarian function and fertility in Holstein cows†.Detection of haplotypes associated with prenatal death in dairy cattle and identification of deleterious mutations in GART, SHBG and SLC37A2Design and development of exome capture sequencing for the domestic pig (Sus scrofa).Use of haplotypes to identify regions harbouring lethal recessive variants in pigs.Predicting haplotype carriers from SNP genotypes in Bos taurus through linear discriminant analysisHomozygous haplotype deficiency reveals deleterious mutations compromising reproductive and rearing success in cattle.Genomic analysis for managing small and endangered populations: a case study in Tyrol Grey cattleThe Relationship between Runs of Homozygosity and Inbreeding in Jersey Cattle under SelectionGenome-Wide Study of Structural Variants in Bovine Holstein, Montbéliarde and Normande Dairy Breeds.Inbreeding and purging at the genomic Level: the Chillingham cattle reveal extensive, non-random SNP heterozygosity.Use of SNP genotypes to identify carriers of harmful recessive mutations in cattle populations.A simple strategy for managing many recessive disorders in a dairy cattle breeding programNGS-based reverse genetic screen for common embryonic lethal mutations compromising fertility in livestock.Candidate lethal haplotypes and causal mutations in Angus cattle.Limited representation of OMIA causative mutations for cattle in SNP databases.Screening for JH1 genetic defect carriers in Jersey cattle by a polymerase chain reaction and restriction fragment length polymorphism assay.The Effect of Sperm Morphology and Sire Fertility on Calving Rate of Finnish Ayrshire AI Bulls.
P2860
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P2860
Identification of a nonsense mutation in CWC15 associated with decreased reproductive efficiency in Jersey cattle
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@ast
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@en
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@nl
type
label
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@ast
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@en
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@nl
prefLabel
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@ast
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@en
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@nl
P2093
P2860
P50
P1433
P1476
Identification of a nonsense m ...... ve efficiency in Jersey cattle
@en
P2093
Daniel J Null
Matthew C McClure
Paul M VanRaden
Tad S Sonstegard
P2860
P304
P356
10.1371/JOURNAL.PONE.0054872
P407
P577
2013-01-22T00:00:00Z