Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6

A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2)

(2009) M Jelani et al.   CLINICAL GENETICS

Roles of lysophosphatidic acid in cardiovascular physiology and disease

(2008) S SMYTH   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS

Two pathways for lysophosphatidic acid production

(2008) J AOKI   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS

Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in theP2RY5gene

(2008) Yutaka Shimomura et al.   EXPERIMENTAL DERMATOLOGY

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

(2008) Lynn Petukhova et al.   GENOMICS

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

(2008) Zahid Azeem et al.   HUMAN GENETICS

Lysophospholipid signaling in the function and pathology of the reproductive system

(2008) X. Ye   HUMAN REPRODUCTION UPDATE

Mutations in the Lipase H Gene Underlie Autosomal Recessive Woolly Hair/Hypotrichosis

(2008) Yutaka Shimomura et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

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

(2008) Sandra M Pasternack et al.   NATURE GENETICS

Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair

(2008) Yutaka Shimomura et al.   NATURE GENETICS