A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.
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Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowthCopy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasiaDifferentiating inbred mouse strains from each other and those with single gene mutations using hair proteomicsTrps1 and its target gene Sox9 regulate epithelial proliferation in the developing hair follicle and are associated with hypertrichosisA whole genome Bayesian scan for adaptive genetic divergence in West African cattle.Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalitiesAssociation of TRPS1 gene with different EMT markers in ERα-positive and ERα-negative breast cancer.Dual role of the Trps1 transcription factor in dentin mineralization.The genetics of human skin disease.Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis.X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis.Congenital Generalized Hypertrichosis, Gingival Hyperplasia, a Coarse Facies with Constriction Bands: A Rare AssociationTranscriptional repression of the Dspp gene leads to dentinogenesis imperfecta phenotype in Col1a1-Trps1 transgenic mice.Copy number variations on chromosome 4q26-27 are associated with Cantu syndromeAmbras Syndrome with Gingival Hyperplasia: A Rare Entity.To grow or not to grow: hair morphogenesis and human genetic hair disordersCo-segregation of trichorhinophalangeal syndrome with a t(8;13)(q23.3;q21.31) familial translocation that appears to increase TRPS1 gene expression.[Genetic hair diseases. An update].Recent progress on the identity and characterization of factors that shape gene organization during eukaryotic evolution.Fate mapping of Trps1 daughter cells during cardiac development using novel Trps1-Cre mice.
P2860
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P2860
A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
A position effect on TRPS1 is ...... d the Koala phenotype in mice.
@en
type
label
A position effect on TRPS1 is ...... d the Koala phenotype in mice.
@en
prefLabel
A position effect on TRPS1 is ...... d the Koala phenotype in mice.
@en
P2093
P2860
P356
P1476
A position effect on TRPS1 is ...... d the Koala phenotype in mice.
@en
P2093
Angela M Christiano
Dorothy Warburton
Friedrich A M Baumeister
John P Sundberg
Katherine A Fantauzzo
Marija Tadin-Strapps
Sarah E Mentzer
P2860
P304
P356
10.1093/HMG/DDN247
P577
2008-08-19T00:00:00Z