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Research 61–90 of 1000+
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Congenital Atrichia: A Case Report
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Acne
- British Hair and Nail Society
- Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Trichoscopy in genetic hair shaft abnormalities
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Time-dependent 53BP1 foci kinetics in X-irradiated human hair follicle dermal papilla cells
- Protective Effect of Conditioned Medium of Immortalized Human Stem Cells from Exfoliated Deciduous Teeth Against Hair Graying Caused by X-Ray Irradiation via Its Antioxidative Activity
- Sex-limited chromosomes and non-reproductive traits
- Trichoscopy in Hair Shaft Disorders
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Infertility and teratogenicity after paternal exposure to systemic dermatologic medications: A systematic review
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice