Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans - Wikidata - wikimedia - TriplyDB

Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans

Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans

http://www.wikidata.org/entity/Q24685715

about

Canine population structure: assessment and impact of intra-breed stratification on SNP-based association studies The Finnish lapphund retinal atrophy locus maps to the centromeric region of CFA9 An integrated 4249 marker FISH/RH map of the canine genome Transcriptome Analysis in Domesticated Species: Challenges and Strategies Origin, genetic diversity, and genome structure of the domestic dog Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies Man's best friend becomes biology's best in show: genome analyses in the domestic dog Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans.From caveman companion to medical innovator: genomic insights into the origin and evolution of domestic dogs.Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa.Leading the way: canine models of genomics and disease Bone disorders in the dog: a review of modern genetic strategies to find the underlying causes.Insights into morphology and disease from the dog genome project.Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa COL9A2 and COL9A3 mutations in canine autosomal recessive oculoskeletal dysplasia.Franklin H. Epstein Lecture. Both ends of the leash--the human links to good dogs with bad genes.The genetics of eye disorders in the dog A second-generation genetic linkage map of the domestic dog, Canis familiaris.Canine inherited retinal degenerations: update on molecular genetic research and its clinical application.Genetic mapping of a naturally occurring hereditary renal cancer syndrome in dogs DNA testing and domestic dogs Dog star rising: the canine genetic system.Understanding hereditary diseases using the dog and human as companion model systems.Advances in the molecular understanding of canine retinal diseases.Finding cardiovascular disease genes in the dog.Single-nucleotide-polymorphism-based association mapping of dog stereotypes Identification of a novel mutation in the PRCD gene causing autosomal recessive retinitis pigmentosa in a Turkish family.Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3.Comparative genomic mapping of uncharacterized canine retinal ESTs to identify novel candidate genes for hereditary retinal disorders.Whole-genome sequence, SNP chips and pedigree structure: building demographic profiles in domestic dog breeds to optimize genetic-trait mapping Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod-cone degeneration interval and identifies ancestral disease-transmitting chromosome.Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes.PCR multiplexed microsatellite panels to expedite canine genetic disease linkage analysis.The genetics of inherited retinal disorders in dogs: implications for diagnosis and management

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Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans

http://www.wikidata.org/entity/Q24685715

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1998 nî lūn-bûn

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1998 թուականի Մարտին հրատարակուած գիտական յօդուած

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1998 թվականի մարտին հրատարակված գիտական հոդված

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Linkage analysis and comparati ...... is pigmentosa (RP17) in humans

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Linkage analysis and comparati ...... is pigmentosa (RP17) in humans

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Linkage analysis and comparati ...... is pigmentosa (RP17) in humans

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Linkage analysis and comparati ...... is pigmentosa (RP17) in humans

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Linkage analysis and comparati ...... is pigmentosa (RP17) in humans

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A A Langston

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C S Mellersh

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P2860

Structure and characterization of the human tissue inhibitor of metalloproteinases-2 gene

Retinitis pigmentosa locus on 17q (RP17): fine localization to 17q22 and exclusion of the PDEG and TIMP2 genes

Linkage of early-onset familial breast cancer to chromosome 17q21

Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa

An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q

Shared synteny of human chromosome 17 loci in Canids

Human embryonic/atrial myosin alkali light chain gene: characterization, sequence, and chromosomal location

Easy calculations of lod scores and genetic risks on small computers

Construction of small-insert genomic DNA libraries highly enriched for microsatellite repeat sequences.

Comparative maps: adding pieces to the mammalian jigsaw puzzle.

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