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Research 181–210 of 1000+
- 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
- Experiences with Parieto-Occipital Flaps in Hair Transplantation
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema
- Congenital atrichia and hypotrichosis
- Algorithm of Hair Restoration Surgery in Children
- Focal and Generalized Alopecia
- The role of vasoactive peptides in skin homeostasis—focus on adiponectin and the kallikrein-kinin system
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Nutritive Beeinflussung des Haarwachstums
- Androgenetic Alopecia: Stress of Discovery
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)