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Research 151–180 of 1000+
- Testosterone stimulates proliferation and inhibits interleukin‐6 production of normal and hereditary gingival fibromatosis fibroblasts
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Multiple, hereditary dome-shaped papules and acrochordons. Birt-Hogg-Dube syndrome
- Editorial: Vitamin D 1α-Hydroxylase Knockout Mice as a Hereditary Rickets Animal Model
- Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Hair Loss, Insulin Resistance, and Heredity in Middle-aged Women. a Population-based Study
- The human keratins: biology and pathology
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Keratins of the Human Hair Follicle
- Genetic Basis of Male Pattern Baldness
- Genetic Disorders and Defects in Vitamin D Action
- Hair follicle group and skin follicle population of Australian Merino sheep
- The role of vitamin D receptor mutations in the development of alopecia
- ANALYSIS OF THE RELATION BETWEEN ALOPECIA AND RESISTANCE TO 1,25‐DIHYDROXYVITAMIN D
- Reversal of Baldness in Patient Receiving Minoxidil for Hypertension
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Central hair loss in African American women: Incidence and potential risk factors
- Skin diseases in the alpaca (<i>Vicugna pacos</i>): a literature review and retrospective analysis of 68 cases (Cornell University 1997–2006)
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Role of insulin resistance and diet in acne
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- hKAP1.6 and hKAP1.7, Two Novel Human High Sulfur Keratin-Associated Proteins are Expressed in the Hair Follicle Cortex
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Genetics of Structural Hair Disorders
- Characterization of Human Keratin-Associated Protein 1 Family Members
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Androgenetic alopecia in adolescents.
- AN UPDATE OF HAIR SHAFT DISORDERS