(Q46753750)

24 December 2017

title

Interactions of the vitamin D receptor with the corepressor hairless: analysis of hairless mutants in atrichia with papular lesions (English)

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24 December 2017

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Jining Wang

1

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24 December 2017

Peter J Malloy

series ordinal

2

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24 December 2017

David Feldman

series ordinal

3

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24 December 2017

language of work or name

English

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publication date

3 July 2007

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24 December 2017

Journal of Biological Chemistry

published in

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24 December 2017

volume

282

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24 December 2017

issue

35

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24 December 2017

page(s)

25231-25239

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24 December 2017

Structure and expression of the hairless gene of mice

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor

21 January 2018

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The thyroid hormone-regulated corepressor hairless associates with histone deacetylases in neonatal rat brain

21 January 2018

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Physical and functional interaction between the vitamin D receptor and hairless corepressor, two proteins required for hair cycling

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M702939200

Hairless suppresses vitamin D receptor transactivation in human keratinocytes

21 January 2018

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Alopecia universalis associated with a mutation in the human hairless gene

21 January 2018

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A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers

21 January 2018

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Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia

21 January 2018

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A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichias

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Atrichia with papular lesions resulting from compound heterozygous mutations in the hairless gene: A lesson for differential diagnosis of alopecia universalis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia

21 January 2018

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Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Identification of mutations in the human hairless gene in two new families with congenital atrichia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

The co-repressor hairless has a role in epithelial cell differentiation in the skin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

The vitamin D receptor and the syndrome of hereditary 1,25-dihydroxyvitamin D-resistant rickets

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Targeted expression of human vitamin d receptor in the skin promotes the initiation of the postnatal hair follicle cycle and rescues the alopecia in vitamin D receptor null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Ligand-independent actions of the vitamin D receptor maintain hair follicle homeostasis

21 January 2018

1 reference

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Hairless triggers reactivation of hair growth by promoting Wnt signaling

21 January 2018

1 reference

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Development and progression of alopecia in the vitamin D receptor null mouse

21 January 2018

1 reference

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A novel missense mutation in the mouse hairless gene causes irreversible hair loss: genetic and molecular analyses of Hr m1Enu

21 January 2018

1 reference

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A unique insertion/substitution in helix H1 of the vitamin D receptor ligand binding domain in a patient with hereditary 1,25-dihydroxyvitamin D-resistant rickets

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

A novel inborn error in the ligand-binding domain of the vitamin D receptor causes hereditary vitamin D-resistant rickets

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Novel mechanism of nuclear receptor corepressor interaction dictated by activation function 2 helix determinants

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M702939200

Hairless and Wnt signaling: allies in epithelial stem cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Repression of transcription by TSGA/Jmjd1a, a novel interaction partner of the ETS protein ER71.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Methylation: lost in hydroxylation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Histone demethylation by a family of JmjC domain-containing proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

JHDM2A, a JmjC-containing H3K9 demethylase, facilitates transcription activation by androgen receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Nuclear receptor repression mediated by a complex containing SMRT, mSin3A, and histone deacetylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Identification of mammalian Sds3 as an integral component of the Sin3/histone deacetylase corepressor complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

The role of corepressors in transcriptional regulation by nuclear hormone receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Histone deacetylases (HDACs): characterization of the classical HDAC family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

The N-CoR/histone deacetylase 3 complex is required for repression by thyroid hormone receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

JmjC: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2β

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702939200

21 January 2018

Identifiers

DOI

10.1074/JBC.M702939200

1 reference

24 December 2017

1 reference

24 December 2017