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Research 601–630 of 1000+
- holistic view of management of polycystic ovarian syndrome
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Aging of hair
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Pseudofolliculitis barbae; current treatment options
- Genetically predicted levels of circulating cytokines and the risk of six immune skin diseases: a two-sample Mendelian randomization study
- The Menopausal Transition: Is the Hair Follicle “Going through Menopause”?
- An updated landscape of Female Pattern Hair Loss
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- In Vitro Culture Methods of Skin Cells for Optimal Skin Reconstruction by Tissue Engineering
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Modulating the stem cell niche for tissue regeneration
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Tcf3 promotes cell migration and wound repair through regulation of lipocalin 2
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- Female pattern hair loss
- Review on Hair Problem and its Solution
- Hair regeneration: Mechano-activation and related therapeutic approaches.
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Use of Exosomes for Cosmetics Applications
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- The First Visit: Consult and Workup Before Sperm Banking
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Advances in Stem Cell Therapy: Specific Applications in the Treatment of Cutaneous Radiation Syndrome
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France