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Research 31–60 of 33
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Current Genetics in Hair Diseases
- Study on the Efficacy and Potential Mechanism of Topical Shen Bai Hair Growing Decoction against Androgenetic Alopecia Based on Ultrahigh Performance Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry and RNA-seq
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- Molecular Genetics of Alopecias
- Effects of a gintonin-enriched fraction on hair growth: an in vitro and in vivo study
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Biology and Genetics of Hair
- Hair growth promoting effects of adipose tissue-derived stem cells
- Congenital hair loss disorders: Rare, but not too rare
- Genetics of Structural Hair Disorders
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- 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
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Trichoscopy in Hair Shaft Disorders
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Novel lysophosphoplipid receptors: their structure and function
- Lysophosphatidic acid and signaling in sensory neurons
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Lysophospholipid Mediators in Health and Disease
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways