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Research 121–150 of 1000+
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Current Genetics in Hair Diseases
- Effects of Hormones and Endocrine Disorders on Hair Growth
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Emerging biomedical engineering strategies for hair follicle regeneration
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Congenital hypotrichosis due to short anagen
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Hair loss in infancy and childhood
- Hereditary, Congenital, and Acquired Alopecias
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Loose anagen hair syndrome
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Adequate Nutrition and Premature Hair Graying: A Review of Literature
- Hair Care and Cosmetics
- Hair in health and disease: an introduction
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987