Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family
about
Linkage mapping of the porcine hairless gene (HR ) to chromosome 14Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosisThe effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosisAnalysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle.Mutations in the hairless gene underlie APL in three families of Pakistani originAutosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 geneMolecular basis of autosomal recessive diseases among the Palestinian Arabs.The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.The role of the hairless (hr) gene in the regulation of hair follicle catagen transformation.Nonsense mutations in the hairless gene underlie APL in five families of Pakistani origin.Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutationAlopecia: possible causes and treatments, particularly in captive nonhuman primatesModulation of vitamin d receptor activity by the corepressor hairless: differential effects of hairless isoforms.Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes.Hairless and the polyamine putrescine form a negative regulatory loop in the epidermisThyroid hormone action on skin.Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis.The hairless promoter is differentially regulated by thyroid hormone in keratinocytes and neuroblastoma cells.A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents.Detection of a novel missense mutations in atrichia with papular lesions.Interactions of the vitamin D receptor with the corepressor hairless: analysis of hairless mutants in atrichia with papular lesions.Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesions.Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesions.Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA.
P2860
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P2860
Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family
description
1999 nî lūn-bûn
@nan
1999 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մարտին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Genomic organization of the hu ...... in an Arab Palestinian family
@ast
Genomic organization of the hu ...... in an Arab Palestinian family
@en
Genomic organization of the hu ...... in an Arab Palestinian family
@nl
type
label
Genomic organization of the hu ...... in an Arab Palestinian family
@ast
Genomic organization of the hu ...... in an Arab Palestinian family
@en
Genomic organization of the hu ...... in an Arab Palestinian family
@nl
prefLabel
Genomic organization of the hu ...... in an Arab Palestinian family
@ast
Genomic organization of the hu ...... in an Arab Palestinian family
@en
Genomic organization of the hu ...... in an Arab Palestinian family
@nl
P2093
P356
P1433
P1476
Genomic organization of the hu ...... in an Arab Palestinian family
@en
P2093
Abdallah HM
Christiano AM
Faiyaz ul Haque M
Zlotogorski A
P304
P356
10.1006/GENO.1998.5699
P407
P577
1999-03-01T00:00:00Z