(Q24306390)

GOA release 2020-03-11

hair cycle

1 reference

GOA release 2020-03-11

author

Hans Christian Hennies

4

object named as

Hans Christian Hennies

Hans Christian

Hennies

1 reference

19 October 2023

Utz Fischer

15

Utz

Fischer

1 reference

19 October 2023

Markus M Nöthen

14

Markus M

Nöthen

1 reference

19 October 2023

Maurice van Steensel

8

Maurice

van Steensel

1 reference

19 October 2023

Sandra M Pasternack

1

Sandra M

Pasternack

1 reference

19 October 2023

Melanie Refke

2

Melanie

Refke

1 reference

19 October 2023

Elham Paknia

3

Elham

Paknia

1 reference

19 October 2023

Thomas Franz

5

Thomas

Franz

1 reference

19 October 2023

Niklas Schäfer

6

Niklas

Schäfer

1 reference

19 October 2023

Alan Fryer

7

Alan

Fryer

1 reference

19 October 2023

Elizabeth Sweeney

9

Elizabeth

Sweeney

1 reference

19 October 2023

Miquel Just

10

Miquel

Just

1 reference

19 October 2023

Clemens Grimm

11

Clemens

Grimm

1 reference

19 October 2023

Roland Kruse

12

Roland

Kruse

1 reference

19 October 2023

Carlos Ferrándiz

13

Carlos

Ferrándiz

1 reference

19 October 2023

Regina C Betz

16

Regina C

American Journal of Human Genetics

Betz

1 reference

19 October 2023

language of work or name

English

0 references

publication date

10 January 2013

0 references

published in

0 references

volume

92

0 references

page(s)

81-7

0 references

issue

1

0 references

cites work

APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

snRNP Sm proteins share two evolutionarily conserved sequence motifs which are involved in Sm protein-protein interactions

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Strategies for multilocus linkage analysis in humans

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Pushing the limits of the scanning mechanism for initiation of translation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Translation initiation at non-AUG triplets in mammalian cells

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Assignment of the gene for the small nuclear ribonucleoprotein E (SNRPE) to human chromosome 1q25-q43

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

ENU mutagenesis in mice identifies candidate genes for hypogonadism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Systemic splicing factor deficiency causes tissue-specific defects: a zebrafish model for retinitis pigmentosa.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Hereditary hypotrichosis simplex

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3542472

Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23246290

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.AJHG.2012.10.022