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Research 301–330 of 1000+
- Dysregulated behaviour of hair follicle stem cells triggers alopecia and provides potential therapeutic targets
- MiR-199a-3p Regulates the PTPRF/β-Catenin Axis in Hair Follicle Development: Insights into the Pathogenic Mechanism of Alopecia Areata
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Alopecia areata: a review of disease pathogenesis
- Keratin gene mutations in disorders of human skin and its appendages
- Genetic Disorders and Defects in Vitamin D Action
- Biology and Genetics of Hair
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Next generation human skin constructs as advanced tools for drug development
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Generalized Hair-Follicle Hamartoma
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Molecular Genetic and Endocrine Mechanisms of Hair Growth
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Calcitonin gene‐related peptide (CGRP) may award relative protection from interferon‐γ‐induced collapse of human hair follicle immune privilege
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Alopecia Universalis Successfully Treated With Adalimumab
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Alopecia Areata. Current situation and perspectives
- Identifying genes associated with the development of human polycystic ovary syndrome
- The ITGB6 gene: its role in experimental and clinical biology
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Influence of <i>FHIT</i> on benzo[ <i>a</i> ]pyrene-induced tumors and alopecia in mice: Chemoprevention by budesonide and <i>N</i> -acetylcysteine
- The Genetics of Human Skin Disease