A single-base change in the tyrosine kinase II domain of ovine FGFR3 causes hereditary chondrodysplasia in sheep.
about
Balancing selection of a frame-shift mutation in the MRC2 gene accounts for the outbreak of the Crooked Tail Syndrome in Belgian Blue CattleGenetic architecture of body size in mammalsA novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndromeTranscriptome Analysis in Domesticated Species: Challenges and StrategiesFibroblast growth factor signaling in skeletal development and diseaseA 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 livestockDeletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattleSixteen years and counting: the current understanding of fibroblast growth factor receptor 3 (FGFR3) signaling in skeletal dysplasiasMeclozine facilitates proliferation and differentiation of chondrocytes by attenuating abnormally activated FGFR3 signaling in achondroplasiaCanine fibroblast growth factor receptor 3 sequence is conserved across dogs of divergent skeletal size.Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene.Selective sweep mapping of genes with large phenotypic effects.The Fibroblast Growth Factor signaling pathwayWhole-genome sequencing reveals a potential causal mutation for dwarfism in the Miniature Shetland pony.A critical analysis of disease-associated DNA polymorphisms in the genes of cattle, goat, sheep, and pig.FGF signaling in the osteoprogenitor lineage non-autonomously regulates postnatal chondrocyte proliferation and skeletal growth.Approach to Investigating Congenital Skeletal Abnormalities in Livestock.A case presentation of spider lamb syndrome in a Kermanian breed lambGenetic diversity analyses reveal first insights into breed-specific selection signatures within Swiss goat breeds.Achondroplasia: Development, pathogenesis, and therapy.Fibroblast growth factor receptor 3 effects on proliferation and telomerase activity in sheep growth plate chondrocytesIn a shake of a lamb's tail: using genomics to unravel a cause of chondrodysplasia in Texel sheep.A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactyly.
P2860
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P2860
A single-base change in the tyrosine kinase II domain of ovine FGFR3 causes hereditary chondrodysplasia in sheep.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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name
A single-base change in the ty ...... ary chondrodysplasia in sheep.
@en
A single-base change in the ty ...... ary chondrodysplasia in sheep.
@nl
type
label
A single-base change in the ty ...... ary chondrodysplasia in sheep.
@en
A single-base change in the ty ...... ary chondrodysplasia in sheep.
@nl
prefLabel
A single-base change in the ty ...... ary chondrodysplasia in sheep.
@en
A single-base change in the ty ...... ary chondrodysplasia in sheep.
@nl
P2093
P2860
P1433
P1476
A single-base change in the ty ...... ary chondrodysplasia in sheep.
@en
P2093
P2860
P356
10.1111/J.1365-2052.2005.01398.X
P577
2006-02-01T00:00:00Z