Novel mutations in the lipase H gene lead to secretion defects of LIPH in Chinese patients with autosomal recessive woolly hair/hypotrichosis (ARWH/HT)

Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta

(2015) F. Seymen et al.   JOURNAL OF DENTAL RESEARCH

A homozygous missense variant in type I keratinKRT25causes autosomal recessive woolly hair

(2015) Muhammad Ansar et al.   JOURNAL OF MEDICAL GENETICS

Evidence for genetic heterogeneity in Carvajal syndrome

(2012) Nancy Nehme et al.   CELL AND TISSUE RESEARCH

The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis

(2012) Satoru Shinkuma et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

LPA-producing enzyme PA-PLA1α regulates hair follicle development by modulating EGFR signalling

(2011) Asuka Inoue et al.   EMBO JOURNAL

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

(2009) Keisuke Yanagida et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis

(2009) Yutaka Shimomura et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair

(2009) Liran Horev et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

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