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Research 91–120 of 1000+
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- A missense mutation in Lama3 causes androgen alopecia
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- THE PATHOGENESIS OF ALOPECIA AREATA
- What causes hidradenitis suppurativa ?—15 years after
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Coronavirus Infection and Cholesterol Metabolism
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Alopecia in Epidermolysis Bullosa
- The dermatological consequences of obesity
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- Clonal analysis of stem cells in differentiation and disease
- Null Mutation of 5α-Reductase Type I Gene Alters Ethanol Consumption Patterns in a Sex-Dependent Manner
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Molecular Genetics of Alopecias
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Expression of lipid-protein gene PLP2 in Liaoning cashmere goat
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish