Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog. - Wikidata - awgldk - TriplyDB

Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog.

Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog.

http://www.wikidata.org/entity/Q24537423

about

Equine Multiple Congenital Ocular Anomalies maps to a 4.9 megabase interval on horse chromosome 6 A missense mutation in PMEL17 is associated with the Silver coat color in the horse Congenital sensorineural deafness in dalmatian dogs associated with quantitative trait loci Canine behavioral genetics: pointing out the phenotypes and herding up the genes Melanosomes--dark organelles enlighten endosomal membrane transport The Genetics of Deafness in Domestic Animals The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes Inactivation of Pmel alters melanosome shape but has only a subtle effect on visible pigmentation The dynamic proliferation of CanSINEs mirrors the complex evolution of Feliforms Man's best friend becomes biology's best in show: genome analyses in the domestic dog The IGF1 small dog haplotype is derived from Middle Eastern grey wolves Collie eye anomaly in Hokkaido dogs: case study Feline deafness.Development and use of DNA archives at veterinary teaching hospitals to investigate the genetic basis of disease in dogs Equine multiple congenital ocular anomalies and silver coat colour result from the pleiotropic effects of mutant PMEL.Genetic effects on coat colour in cattle: dilution of eumelanin and phaeomelanin pigments in an F2-Backcross Charolais x Holstein population.Multiple splice variants within the bovine silver homologue (SILV) gene affecting coat color in cattle indicate a function additional to fibril formation in melanophores.Canine morphology: hunting for genes and tracking mutations Regulatory activities of transposable elements: from conflicts to benefits.Insights into morphology and disease from the dog genome project.RsaI repetitive DNA in Buffalo Bubalus bubalis representing retrotransposons, conserved in bovids, are part of the functional genes.Two SNPs in the SILV gene are associated with silver coat colour in ponies.Mutations in or near the transmembrane domain alter PMEL amyloid formation from functional to pathogenic Evolutionary genomics of dog domestication.Interaction of MC1R and PMEL alleles on solid coat colors in Highland cattle.Teaching an old dog new tricks: SINEs of canine genomic diversity.Endogenous retrovirus insertion in the KIT oncogene determines white and white spotting in domestic cats Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide.A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats.Transmissible [corrected] dog cancer genome reveals the origin and history of an ancient cell lineage.Dual loss of ER export and endocytic signals with altered melanosome morphology in the silver mutation of Pmel17 An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers Carnivore-specific SINEs (Can-SINEs): distribution, evolution, and genomic impact.Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome in PMEL17 (Silver) mutant ponies: five cases.Mapping of the domestic cat "SILVER" coat color locus identifies a unique genomic location for silver in mammals.Breed relationships facilitate fine-mapping studies: a 7.8-kb deletion cosegregates with Collie eye anomaly across multiple dog breeds.Genome sequence, population history, and pelage genetics of the endangered African wild dog (Lycaon pictus).Beyond the MHC: A canine model of dermatomyositis shows a complex pattern of genetic risk involving novel loci.The Kringle-like Domain Facilitates Post-endoplasmic Reticulum Changes to Premelanosome Protein (PMEL) Oligomerization and Disulfide Bond Configuration and Promotes Amyloid Formation.Pharmacological BACE1 and BACE2 inhibition induces hair depigmentation by inhibiting PMEL17 processing in mice.

P2860

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P2860

Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog.

http://www.wikidata.org/entity/Q24537423

description

2006 nî lūn-bûn

@nan

2006 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հունվարին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

@zh-hant

2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog

@nl

Retrotransposon insertion in S ...... atterning of the domestic dog.

@ast

Retrotransposon insertion in S ...... atterning of the domestic dog.

@en

type

label

Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog

@nl

Retrotransposon insertion in S ...... atterning of the domestic dog.

@ast

Retrotransposon insertion in S ...... atterning of the domestic dog.

@en

prefLabel

Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog

@nl

Retrotransposon insertion in S ...... atterning of the domestic dog.

@ast

Retrotransposon insertion in S ...... atterning of the domestic dog.

@en

P1433

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Q24537423-3A418D98-1523-48A8-874F-3877FA3EFF34

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P356

PNAS.0506940103

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Retrotransposon insertion in S ...... atterning of the domestic dog.

@en

P2093

Christine A Rees

http://www.w3.org/2001/XMLSchema#string

Jacquelyn M Wahl

http://www.w3.org/2001/XMLSchema#string

Keith E Murphy

http://www.w3.org/2001/XMLSchema#string

Leigh Anne Clark

http://www.w3.org/2001/XMLSchema#string

P2860

Pmel17 initiates premelanosome morphogenesis within multivesicular bodies

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12

The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

Genomic organization and sequence of D12S53E (Pmel 17), the human homologue of the mouse silver (si) locus

Polymerization of 5,6-dihydroxyindole-2-carboxylic acid to melanin by the pmel 17/silver locus protein

P304

1376-1381

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scholarly article

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10.1073/PNAS.0506940103

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P433

5

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103

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2006-01-09T00:00:00Z

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7365182

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16407134

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retrotransposon

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1360527

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