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Research 331–360 of 1000+
- Alopecia and its medical management
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Female pattern hair loss
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- Nonclassic congenital adrenal hyperplasia
- Congenital adrenal hyperplasia
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Biology of Human Hair: Know Your Hair to Control It
- Becker nevus of the face with asymmetrical growth of beard hair
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Keratins: the hair shaft's backbone revealed
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Alopesi Tedavisinde Kullanılan İlaç Tedavileri ve Yeni Yaklaşımlar
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2