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Research 30 of 53
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Lysophospholipid Mediators in Health and Disease
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Novel lysophosphoplipid receptors: their structure and function
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- 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
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Woolly Antics between the Sheaths
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Biology and Genetics of Hair
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- “Cold” X5 Hairlaser™ used to treat male androgenic alopecia and hair growth: an uncontrolled pilot study
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Inherited Disorders of the Hair
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Genetics of Structural Hair Disorders
- 15. Hair and Nails