(Q34754724)

4 August 2017

Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair (English)

1 reference

G protein-coupled receptor

4 August 2017

0 references

1 reference

Yutaka Shimomura

1

1 reference

4 August 2017

Muhammad Wajid

2

1 reference

4 August 2017

Yoshiyuki Ishii

3

1 reference

4 August 2017

Lawrence Shapiro

4

1 reference

4 August 2017

Lynn Petukhova

5

1 reference

4 August 2017

Derek Gordon

6

1 reference

4 August 2017

Angela M Christiano

7

1 reference

4 August 2017

language of work or name

English

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publication date

24 February 2008

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4 August 2017

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4 August 2017

40

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4 August 2017

3

1 reference

4 August 2017

335-339

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https://scigraph.springernature.com/pub.10.1038/ng.100

4 August 2017

0 references

cites work

Quantitative hair form variation in seven populations

1 reference

21 January 2018

Hair shape of curly hair

1 reference

Unraveling the molecular mechanisms of hair and nail genodermatoses

21 January 2018

1 reference

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

21 January 2018

1 reference

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

21 January 2018

1 reference

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

21 January 2018

1 reference

Characterization of vasopressin V2 receptor mutants in nephrogenic diabetes insipidus in a polarized cell model

21 January 2018

1 reference

Purinergic receptors are part of a functional signaling system for proliferation and differentiation of human epidermal keratinocytes

21 January 2018

1 reference

Hair follicle-specific keratins and their diseases

21 January 2018

1 reference

Nested genes in the human genome

21 January 2018

1 reference

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

21 January 2018

1 reference

Molecular characterization of the retinoblastoma susceptibility gene

21 January 2018

1 reference

Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia

21 January 2018

1 reference

Intron 17 of the human retinoblastoma susceptibility gene encodes an actively transcribed G protein-coupled receptor gene

21 January 2018

1 reference

Identification of 6H1 as a P2Y purinoceptor: P2Y5.

21 January 2018

1 reference

The 6H1 orphan receptor, claimed to be the p2y5 receptor, does not mediate nucleotide-promoted second messenger responses

21 January 2018

1 reference

Identification of p2y9/GPR23 as a Novel G Protein-coupled Receptor for Lysophosphatidic Acid, Structurally Distant from the Edg Family

21 January 2018

1 reference

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

21 January 2018

1 reference

A novel phosphatidic acid-selective phospholipase A1 that produces lysophosphatidic acid

21 January 2018

1 reference

Common Variants in RB1 Gene and Risk of Invasive Ovarian Cancer

21 January 2018

1 reference

Human hair shape is programmed from the bulb

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Hereditary woolly hair and keratosis pilaris

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.100

1 reference

Dimensions Publication ID

4 August 2017

0 references

1 reference