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Research 541–570 of 1000+
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Demographic Characteristics and Association of Serum Vitamin B12, Ferritin and Thyroid Function with Premature Canities in Indian Patients from an Urban Skin Clinic of North India: A Retrospective Analysis of 71 Cases.
- Dynamic Trichoscopy
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Androgenic alopecia: an entity to consider in adolescence
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Animal models of human skin disease
- Electrophoretic analysis of human hair keratins
- New idea for hair transplantation to preserve more donor hair follicles
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Clinical characteristics and factors associated with different BASP subtypes of androgenetic alopecia
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- An Unusual Compulsive Behavior Related to Scalp Psoriasis and Hair Follicle Anxiety in Young Men
- The Role of Moracin M in Promoting Hair Growth: Insights into Mechanisms of WNT/β- Catenin Pathway Activation and Angiogenesis Enhancement in Human Dermal Papilla Cells
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Role of anti-miasmatic remedy in case of alopecia areata
- [Monilethrix is a hereditary hair shaft disorder].
- Allergen of the Month—Witch Hazel
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- FGF5 is a crucial regulator of hair length in humans
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type