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Research 751–780 of 1000+
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Intrinsic and Extrinsic Factors Associated with Hair Graying (Canities) and Therapeutic Potential of Plant Extracts and Phytochemicals
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Evaluation of the Awareness, Beliefs, and Psychological Impact of Patients with Alopecia Areata in Makkah City, Saudi Arabia
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- The role of the skin microbiome in the development of alopecia areata
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Acne Vulgaris
- Australasian Society for Dermatology Research Meeting, May 2006
- Androgenic alopecia and dutasteride in hair mesotherapy: A short review
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Wound repair at a glance
- Polycystic ovary syndrome
- The Pathobiology of Skin Aging
- Neural Potential of a Stem Cell Population in the Hair Follicle
- ROOT HAIR DEFECTIVE SIX‐LIKE4 (RSL4) promotes root hair elongation by transcriptionally regulating the expression of genes required for cell growth
- 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.
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Gsdma3 is required for hair follicle differentiation in mice
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Immunology of alopecia areata
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Pseudofolliculitis barbae; current treatment options