(Q42608120)

3 November 2017

title

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis (English)

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Erratum: Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

3 November 2017

corrigendum / erratum

1 reference

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/NG0609-762B

author

Markus M Nöthen

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3 November 2017

25

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28

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29

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38

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3 November 2017

Alessandro Terrinoni

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Sven Cichon

object named as

Sven Cichon

12

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Marcel Huber

object named as

Marcel Huber

19

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Regina Christine Betz

13

object named as

Regina C Betz

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3 November 2017

11

Roland Kruse

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3 November 2017

10

Xue-Jun Zhang

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3 November 2017

1

Yaran Wen

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3 November 2017

16

Michel van Geel

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3 November 2017

17

Peter M Steijlen

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3 November 2017

32

Dandan Shang

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3 November 2017

20

Giles S Dunnill

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3 November 2017

27

Yves de Prost

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3 November 2017

Yang Liu

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3 November 2017

Yiming Xu

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3 November 2017

Yiwei Zhao

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3 November 2017

Rui Hua

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3 November 2017

Kaibo Wang

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3 November 2017

Miao Sun

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3 November 2017

Yuanhong Li

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3 November 2017

Sen Yang

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3 November 2017

Maurice A M van Steensel

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3 November 2017

Daniel Hohl

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3 November 2017

Cameron Kennedy

21

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3 November 2017

Andrew Messenger

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3 November 2017

Colin S Munro

23

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3 November 2017

Christine Bodemer

26

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3 November 2017

Rod Sinclair

30

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3 November 2017

Jack Green

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3 November 2017

Qing Liu

33

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3 November 2017

Yang Luo

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3 November 2017

Li Jiang

35

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3 November 2017

Hong-Duo Chen

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3 November 2017

Wilson H-Y Lo

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3 November 2017

Chun-Di He

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3 November 2017

Xue Zhang

40

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3 November 2017

language of work or name

English

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publication date

4 January 2009

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3 November 2017

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3 November 2017

volume

41

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3 November 2017

issue

2

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3 November 2017

page(s)

228-233

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https://scigraph.springernature.com/pub.10.1038/ng.276

3 November 2017

exact match

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cites work

The biology of hair follicles

1 reference

Epithelial stem cells: a folliculocentric view

21 January 2018

1 reference

Stem cells in the skin: waste not, Wnt not.

21 January 2018

1 reference

beta-Catenin controls hair follicle morphogenesis and stem cell differentiation in the skin

21 January 2018

1 reference

WNT signals are required for the initiation of hair follicle development

21 January 2018

1 reference

Transient activation of beta -catenin signaling in cutaneous keratinocytes is sufficient to trigger the active growth phase of the hair cycle in mice.

21 January 2018

1 reference

Wnt-dependent de novo hair follicle regeneration in adult mouse skin after wounding

21 January 2018

1 reference

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

21 January 2018

1 reference

Hairless triggers reactivation of hair growth by promoting Wnt signaling

21 January 2018

1 reference

Hairless and Wnt signaling: allies in epithelial stem cell differentiation

21 January 2018

1 reference

Alopecia universalis associated with a mutation in the human hairless gene

21 January 2018

1 reference

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

21 January 2018

1 reference

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

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing

21 January 2018

1 reference

Translation matters: protein synthesis defects in inherited disease

21 January 2018

1 reference

An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.

21 January 2018

1 reference

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma

21 January 2018

1 reference

Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cycling

21 January 2018

1 reference

uAUG and uORFs in human and rodent 5'untranslated mRNAs

21 January 2018

1 reference

Evolutionary conservation suggests a regulatory function of AUG triplets in 5'-UTRs of eukaryotic genes

21 January 2018

1 reference

A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family

21 January 2018

1 reference

Downstream control of upstream open reading frames

21 January 2018

1 reference

Identification of a Novel Locus for Marie Unna Hereditary Hypotrichosis to a 17.5 cM Interval at 1p21.1–1q21.3

21 January 2018

1 reference

12 December 2020

Marie Unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless

1 reference

12 December 2020

Translational pathophysiology: a novel molecular mechanism of human disease

1 reference

12 December 2020

Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.

1 reference

12 December 2020

Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis

1 reference

12 December 2020

Controls of hair follicle cycling

1 reference

12 December 2020

Guess what! Hypotrichosis congenita of Marie Unna: comment

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.276

1 reference

Dimensions Publication ID

3 November 2017

1040875041

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