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Article

[Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndrome].

Annales de dermatologie et de venereologie - 1 Nov 2008

Dereure O

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Share to LPA gene
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Share to Hypotrichosis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Receptors, Purinergic P2

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Source

Identifiers

PMID: 19061667
DOI: 10.1016/j.annder.2008.09.001

Genes

LPA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndrome].PMID 19061667Read ↗

A novel deletion mutation in P2RY5/LPA(6) gene cause autosomal recessive woolly hair with hypotrichosis.Semantic proximity Read ↗

Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair.Semantic proximity Read ↗

Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hairSemantic proximity Read ↗

Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.Semantic proximity Read ↗

In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis.Semantic proximity Read ↗

Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.Semantic proximity Read ↗

The β9 loop domain of PA-PLA1α has a crucial role in autosomal recessive woolly hair/hypotrichosis.Semantic proximity Read ↗

[The role in harlequin ichthyosis of mutations in lipid transporter ABCA12].Semantic proximity Read ↗

Cell-trafficking impairment in disease-associated LPA6 missense mutants and a potential pharmacoperone therapy for autosomal recessive woolly hair/hypotrichosis.Semantic proximity Read ↗

Analysis of unique mutations in the LPAR6 gene identified in a Japanese family with autosomal recessive woolly hair/hypotrichosis: Establishment of a useful assay system for LPA6.Semantic proximity Read ↗

[Progressive familial hyperpigmentation is associated with mutations activating the KIT receptor ligand].Semantic proximity Read ↗

A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.Semantic proximity Read ↗

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