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Research 211–240 of 1000+
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Morphological Approach to Hair Disorders
- Macrophage-Stimulating Protein Promotes Hair Growth Ex Vivo and Induces Anagen from Telogen Stage Hair Follicles In Vivo
- Main Plenary Sessions: Summaries of Papers
- Abstracts
- Lentiginosis within plaques of linear atrophoderma of Moulin: a twin-spotting phenomenon?
- Anti-androgen therapy in dermatology: a review
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Transport of Biotin in Human Keratinocytes
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Edar Signaling in the Control of Hair Follicle Development
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Targeted Overexpression of the Angiogenesis Inhibitor Thrombospondin-1 in the Epidermis of Transgenic Mice Prevents Ultraviolet-B-Induced Angiogenesis and Cutaneous Photo-Damage
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- 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
- The ITGB6 gene: its role in experimental and clinical biology
- Significance of the polyglutamine tract polymorphism in the androgen receptor
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Factors associated with early-onset androgenetic alopecia: A scoping review
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT