Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndrome;Implication du récepteur P2Y5 et de son ligand LPA dans l'hypotrichose simplex et le syndrome des cheveux laineux autosomique récessif

Annales de Dermatologie et de Venereologie

Volumn 135, Issue 11, 2008, Pages 794-795

  Dereure, O ^a  

^a HÔPITAL SAINT ELOI   (France)

Author keywords

[No Author keywords available]

Indexed keywords

PURINERGIC P2Y RECEPTOR; PURINERGIC P2Y5 RECEPTOR; UNCLASSIFIED DRUG; LPAR4 PROTEIN, HUMAN; LYSOPHOSPHATIDIC ACID; LYSOPHOSPHOLIPID; PURINERGIC P2 RECEPTOR;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 13Q; GENE MUTATION; HAPLOTYPE; HOMOZYGOSITY; HUMAN; HYPOTRICHOSIS; WOOLLY HAIR SYNDROME; GENETICS; HAIR DISEASE; MUTATION; PATHOPHYSIOLOGY; PHYSIOLOGY; RECESSIVE GENE; SYNDROME;

GENES, RECESSIVE; HAIR DISEASES; HYPOTRICHOSIS; LYSOPHOSPHOLIPIDS; MUTATION; RECEPTORS, PURINERGIC P2; SYNDROME;

EID: 58849083717     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.annder.2008.09.001     Document Type: Article

References (2)

1. Shimomura Y., Wajid M., Ishii Y., Shapiro L., Petukhova L., Gordon D., et al. Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair. Nat Genet 40 (2008) 335-339
2. Sandra M., Pasternack, Ivar von Kügelgen, Khalid Al Aboud, Young-Ae Lee, Franz Rüschendorf, et al. G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. Nat Genet 40 (2008) 329-334