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Research 211–240 of 727
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- Menopause - Andropause - Anti-Aging 2008, 11.-13. Dezember 2008, Wien - Abstracts
- The investigation of the efficacy and safety of stromal vascular fraction in the treatment of nanofat-treated acne scar: a randomized blinded controlled clinical trial
- The potential impact of melanosomal pH and metabolism on melanoma
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Dermoscopy of neoplastic alopecia secondary to cutaneous metastasis from breast carcinoma
- Temporal Triangular Alopecia—Clinical and Dermoscopic Features of a Rare Entity
- Acquired non-scarring vertex alopecia in three women revealing trichotillomania: Diagnostic accuracy of trichoscopy
- ROOT HAIR DEFECTIVE SIX‐LIKE4 (RSL4) promotes root hair elongation by transcriptionally regulating the expression of genes required for cell growth
- Exploring nanobioceramics in wound healing as effective and economical alternatives
- Determination of protonation state in molecular salt of minoxidil and 2,4-dihydroxybenzoic acid through a combined experimental and theoretical study: influence of proton transfer on biological activities
- Preparation, solubility, and anti-inflammatory effects of a complex of diphenylcyclopropenone/β-cyclodextrin derivatives as the treatment of alopecia areata
- Novel anti‐dandruff shampoo incorporated with ketoconazole‐coated zinc oxide nanoparticles using green tea extract
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Barley disease susceptibility factor RACB acts in epidermal cell polarity and positioning of the nucleus
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Uncharted waters
- Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA?
- Usefulness of Dermoscopy to Provide Accurate Assessment of Skin Cancers
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- Dissecting the Impact of α-MSH-MC1R-cAMP Signaling on UVA-Induced Stress in Fibroblasts - Implications for Regulation of Cutaneous Photoaging
- Synthesis of Analogues of Cercidin, an Antimicrobial Compound of <i>Cercidiphyllum japonicum</i> : Glycosylation of Methyl Gallate with Ulosyl Bromides