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Research 31–60 of 1000+
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Genetic Basis of Alopecia Areata
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Ptosis in childhood
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Adenolipoma—Eccrine and Apocrine Variants With Evidence for a Hamartomatous Process
- The Genetic Architecture of Alopecia Areata
- No difference in the proteome of racially and geometrically classified scalp hair sample from a South African cohort: Preliminary findings
- The Molecular Biology of the Vitamin D Receptor
- The relationship between keratin 18 and epithelial-derived tumors: as a diagnostic marker, prognostic marker, and its role in tumorigenesis
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- TONGUE, RED
- Microarray analysis of androgenetic and senescent alopecia: Comparison of gene expression shows two distinct profiles
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Molecular Genetics of Human Hair Diseases
- Polycystic ovary syndrome
- Genetic Control/Involvement in Hair Fiber Traits
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Keratin expression by corneal and limbal stem cells during development
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Estrogens
- The organization of the keratin I and II gene clusters in placental mammals and marsupials show a striking similarity
- Targeting of Smoothened for therapeutic gain