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Research 91–120 of 111
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Hair shaft disorders in children – An update
- 196 The endocannabinoid tone regulates human sebocyte biology
- Dermatoscopy of hair shaft disorders
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Trichoscopy in Hair Shaft Disorders
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Peer Review #2 of "Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis (v0.1)"
- Hair Loss in Children
- Group IID, IIE, IIF and III secreted phospholipase A2s
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Minoxidil
- Adverse Reactions to Biologic Medications Used in Allergy and Immunology Diseases
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Biology and Genetics of Hair
- 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
- Molecular Genetics of Alopecias
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Current Genetics in Hair Diseases
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report