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Research 331–360 of 1000+
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Role of Iron Deficiency in Chronic Hair Loss
- Gene Variant in Amish a Clue to Better Aging
- Molecular Mechanisms Regulating Hair Follicle Development
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Polycystic ovary syndrome
- Challenges and Strategies for Improving the Regenerative Effects of Mesenchymal Stromal Cell-Based Therapies
- Androgenetic alopecia: pathogenesis and potential for therapy
- Biotin and biotinidase deficiency
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Aging of the hair follicle pigmentation system
- 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.
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Bioengineered Plants Can Be a Useful Source of Omega-3 Fatty Acids
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- New approach to the understanding of keloid: psychoneuroimmune–endocrine aspects
- Clinical Case Seminar: Postmenopausal androgen excess-challenges in diagnostic work-up and management of ovarian thecosis
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)