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Research 871–900 of 1000+
- The Management of Postacne Scarring
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Principles and mechanisms of regeneration in the mouse model for wound‐induced hair follicle neogenesis
- Alopecia in patients treated with molecularly targeted anticancer therapies
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Prevalence and accurate diagnosis of polycystic ovary syndrome in adolescents across world regions: a systematic review and meta-analysis
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- The regeneration blastema of lizards: an amniote model for the study of appendage replacement
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- Scalp hypothermia as a preventative measure for chemotherapy‐induced alopecia: a review of controlled clinical trials
- Prediction of male-pattern baldness from genotypes
- Aromatase deficiency in a male patient - Case report and review of the literature.
- An Update on Medical Treatment Options for Hidradenitis Suppurativa
- Polycystic ovary syndrome and its management: In view of oxidative stress
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Multipotent Nestin-Positive Stem Cells Reside in the Stroma of Human Eccrine and Apocrine Sweat Glands and Can Be Propagated Robustly In Vitro
- The Clinical Presentation of Systemic Lupus Erythematosus
- A systematic review of antiandrogens and feminization in transgender women
- Three-Dimensional Analysis of Cell Division Orientation in Epidermal Basal Layer Using Intravital Two-Photon Microscopy
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Evidence for various calcium sites in human hair shaft revealed by sub-micrometer X-ray fluorescence
- The influence of sulfur and hair growth on stable isotope diet estimates for grizzly bears
- Genetic Fate Mapping Using Site-Specific Recombinases
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Revisiting hyper- and hypo-androgenism by tandem mass spectrometry
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression