Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex (Q34171304)

31 July 2017

Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex (English)

1 reference

31 July 2017

Cheng Zhou

1

1 reference

31 July 2017

Dongjie Zang

2

1 reference

31 July 2017

Yan Jin

3

1 reference

31 July 2017

Huafeng Wu

4

1 reference

31 July 2017

Zhengyi Liu

5

1 reference

31 July 2017

Juan Du

6

1 reference

31 July 2017

Jianzhong Zhang

7

1 reference

31 July 2017

26 April 2011

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31 July 2017

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31 July 2017

32

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31 July 2017

710-714

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31 July 2017

7

1 reference

Alopecia universalis associated with a mutation in the human hairless gene

31 July 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

Direct selection of human genomic loci by microarray hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

When ribosomes go bad: diseases of ribosome biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

The YH database: the first Asian diploid genome database

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

SOAP2: an improved ultrafast tool for short read alignment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

Ribosomopathies: human disorders of ribosome dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

How common are extraribosomal functions of ribosomal proteins?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

Transcription by moonlight: structural basis of an extraribosomal activity of ribosomal protein S10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

In situ expression of ribosomal protein L21 in developing tooth germ of the mouse lower first molar.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12 approximately 12.3 in a Chinese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

A novel U2HR non-synonymous mutation in a Chinese patient with Marie Unna Hereditary Hypotrichosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

inferred from DOI database lookup

7 January 2021

based on heuristic

Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

inferred from DOI database lookup

7 January 2021

based on heuristic

A new clinical variant of hereditary localized alopecia: report of a Chinese family mapped to chromosome 2p25.1-2p23.2.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21503

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/HUMU.21503

1 reference

31 July 2017

1 reference