Highly effective SNP-based association mapping and management of recessive defects in livestock. - Wikidata - awgldk - TriplyDB

Highly effective SNP-based association mapping and management of recessive defects in livestock.

Highly effective SNP-based association mapping and management of recessive defects in livestock.

http://www.wikidata.org/entity/Q34762263

about

Balancing selection of a frame-shift mutation in the MRC2 gene accounts for the outbreak of the Crooked Tail Syndrome in Belgian Blue Cattle Pedigree analysis of Czech Holstein calves with schistosoma reflexum CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs Dystonia and Paroxysmal Dyskinesias: Under-Recognized Movement Disorders in Domestic Animals? A Comparison with Human Dystonia/Paroxysmal Dyskinesias.A reverse genetic approach identifies an ancestral frameshift mutation in RP1 causing recessive progressive retinal degeneration in European cattle breeds Bovine polledness--an autosomal dominant trait with allelic heterogeneity A MusD retrotransposon insertion in the mouse Slc6a5 gene causes alterations in neuromuscular junction maturation and behavioral phenotypes Non-synonymous FGD3 Variant as Positional Candidate for Disproportional Tall Stature Accounting for a Carcass Weight QTL (CW-3) and Skeletal Dysplasia in Japanese Black Cattle A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle.KDM2B is implicated in bovine lethal multi-organic developmental dysplasia Using regulatory and epistatic networks to extend the findings of a genome scan: identifying the gene drivers of pigmentation in merino sheep An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle Overview on the Role of Advance Genomics in Conservation Biology of Endangered Species Genomics advances the study of inbreeding depression in the wild RNA-seq analysis of single bovine blastocysts Genome wide signatures of positive selection: the comparison of independent samples and the identification of regions associated to traits Detection of haplotypes associated with prenatal death in dairy cattle and identification of deleterious mutations in GART, SHBG and SLC37A2 Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene.Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.Defective glycinergic synaptic transmission in zebrafish motility mutants.Analysis of a zebrafish behavioral mutant reveals a dominant mutation in atp2a1/SERCA1.A novel syndrome of lethal familial hyperekplexia associated with brain malformation.Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations C-Nap1 mutation affects centriole cohesion and is associated with a Seckel-like syndrome in cattle.Mapping QTL influencing gastrointestinal nematode burden in Dutch Holstein-Friesian dairy cattle A genome wide survey of SNP variation reveals the genetic structure of sheep breeds Whole-genome SNP association in the horse: identification of a deletion in myosin Va responsible for Lavender Foal Syndrome.A hidden markov model combining linkage and linkage disequilibrium information for haplotype reconstruction and quantitative trait locus fine mapping Performance of single nucleotide polymorphisms versus haplotypes for genome-wide association analysis in barley.Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene.Genome-wide association study identifies candidate genes for piglet splay leg syndrome in different populations.Use of haplotypes to identify regions harbouring lethal recessive variants in pigs.A novel nonsense mutation in the DMP1 gene identified by a genome-wide association study is responsible for inherited rickets in Corriedale sheep.A nonsense mutation in PLD4 is associated with a zinc deficiency-like syndrome in Fleckvieh cattle.Association mapping of quantitative disease resistance in a natural population of loblolly pine (Pinus taeda L.).New phenotypes for new breeding goals in dairy cattle.A splice site variant in the bovine RNF11 gene compromises growth and regulation of the inflammatory response.Bovine mastitis: frontiers in immunogenetics Glycine transporters as novel therapeutic targets in schizophrenia, alcohol dependence and pain.A deletion in the bovine FANCI gene compromises fertility by causing fetal death and brachyspina.

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Highly effective SNP-based association mapping and management of recessive defects in livestock.

http://www.wikidata.org/entity/Q34762263

description

2008 nî lūn-bûn

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2008 թուականի Մարտին հրատարակուած գիտական յօդուած

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2008 թվականի մարտին հրատարակված գիտական հոդված

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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name

Highly effective SNP-based ass ...... ecessive defects in livestock.

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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type

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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Nature Genetics

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Highly effective SNP-based ass ...... ecessive defects in livestock.

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Brian R Pearce

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Corinne Fasquelle

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Daniel Desmecht

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Eloisa Carta

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Frédéric Rollin

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Haisheng Nie

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Jean-Claude Frennet

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Jorgen S Agerholm

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Kirsten Harvey

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Latifa Karim

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449-454

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scholarly article

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10.1038/NG.96

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4

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40

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Merete Fredholm

Carole Charlier

Claus B Jørgensen

Robert J. Harvey

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2008-03-16T00:00:00Z

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5507318

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18344998

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