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Research 751–780 of 1000+
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Thiopurines: Recent Topics and Their Role in the Treatment of Inflammatory Bowel Diseases
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Skin transcriptome reveals the periodic changes in genes underlying cashmere (ground hair) follicle transition in cashmere goats
- COVID-19 pandemic: what about the gonads?
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- Perspectives on Dermatopathology
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Research gaps in medical treatment of transgender/nonbinary people
- Current advances of <i>Dendrobium officinale</i> polysaccharides in dermatology: a literature review
- Local and Systemic Reduction by Topical Finasteride or Flutamide of Hamster Flank Organ Size and Enzyme Activity
- Where Have the Periods Gone? The Evaluation and Management of Functional Hypothalamic Amenorrhea
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- <i>Pten</i> loss in Lgr5<sup>+</sup> hair follicle stem cells promotes SCC development
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Epigenetic orchestration of RNA m<sup>6</sup>A methylation in wound healing and post-wound events
- Hyperandrogenism in Women: Polycystic Ovary Syndrome
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Immunoglobulin E and Serum Interleukin-13 and Bacteria in Patients with Alopecia Areata
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Examining the association of menarche and correlates in a rural polycystic ovary syndrome population: A cross-sectional study
- Existence of trichohyalin-keratohyalin hybrid granules: Co-localization of two major intermediate filament-associated proteins in non-follicular epithelia
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS