In Silico Analysis of Missense Mutations in LPAR6 Reveals Abnormal Phospholipid Signaling Pathway Leading to Hypotrichosis

EGFR-Ras-Raf Signaling in Epidermal Stem Cells: Roles in Hair Follicle Development, Regeneration, Tissue Remodeling and Epidermal Cancers

(2013) Eszter Doma et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Identification of Potential Plk1 Targets in a Cell-Cycle Specific Proteome through Structural Dynamics of Kinase and Polo Box-Mediated Interactions

(2013) Nousheen Bibi et al.   PLoS One

A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis

(2012) Atsushi Fujimoto et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan

(2011) S. Khan et al.   CLINICAL AND EXPERIMENTAL DERMATOLOGY

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

(2011) Asuka Inoue et al.   EMBO JOURNAL

Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm

(2011) Regina C. Betz et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture

(2010) Yutaka Shimomura et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes

(2010) Sulman Basit et al.   HUMAN GENETICS

Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3

(2010) Gul Naz et al.   HUMAN GENETICS

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families

(2010) Naveed Wasif et al.   HUMAN GENETICS

Mutations in theP2RY5gene underlie autosomal recessive hypotrichosis in 13 Pakistani families

(2009) M. Tariq et al.   BRITISH JOURNAL OF DERMATOLOGY

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

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

AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility

(2009) Garrett M. Morris et al.   JOURNAL OF COMPUTATIONAL 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

In Vitro Analysis of LIPH Mutations Causing Hypotrichosis Simplex: Evidence Confirming the Role of Lipase H and Lysophosphatidic Acid in Hair Growth

(2009) Sandra M. Pasternack et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

A novel deletion mutation in P2RY5/LPA6 gene cause autosomal recessive woolly hair with hypotrichosis

(2009) L Horev et al.   JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

MPEx: A tool for exploring membrane proteins

(2009) Craig Snider et al.   PROTEIN SCIENCE

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

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