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Research 30 of 94
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Lysophospholipid Mediators in Health and Disease
- Woolly Antics between the Sheaths
- Genetics of Alopecia
- Gene that causes woolly hair revealed
- Gingerol ameliorates chronic graft-versus-host disease by regulating treg/Th17 transdifferenciation
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Hair growth promoting effects of adipose tissue-derived stem cells
- Molecular Genetics of Alopecias
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Biology and Genetics of Hair
- Non-Edg family LPA receptors: the cutting edge of LPA research
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Trichoscopy in Hair Shaft Disorders
- The hair follicle enigma
- Genetics of Structural Hair Disorders
- “Cold” X5 Hairlaser™ used to treat male androgenic alopecia and hair growth: an uncontrolled pilot study
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Effects of a gintonin-enriched fraction on hair growth: an in vitro and in vivo study
- Inherited Disorders of the Hair
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2