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Research 661–690 of 1000+
- Oral Presentations: Abstracts of the Urological Society of Australia and New Zealand Annual Scientific Meeting, 25–28 February 2023, Melbourne, Australia
- Frontal fibrosing alopecia: A review of disease pathogenesis
- ORAL AND TOPICAL FINASTERIDE IN THE TREATMENT OF MALE ANDROGENETIC ALOPECIA – NARRATIVE REVIEW
- Gastrointestinal bezoars: two distinct cases illustrating diagnostic and surgical challenges
- Platelet-Rich Plasma (PRP): Molecular Mechanisms, Actions and Clinical Applications in Human Body
- Mendelian randomization studies of testosterone exposure: A systematic review
- Androgenetic Alopecia: A Review
- Stimulation by exosomes from hypoxia-preconditioned hair follicle mesenchymal stem cells facilitates mitophagy by inhibiting the PI3K/AKT/mTOR signaling pathway to alleviate ulcerative colitis
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- The effects of infrared radiation on the human skin
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Discreet monilethrix: De novo mutation on the example of polish families
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Skin Development and Disease: A Molecular Perspective
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Zebrafish Model of Hereditary Pigmentary Disorders
- Early-onset Male Androgenetic Alopecia and Metabolic Syndrome: Are They Associated?
- Frizzled Receptors in Development and Disease
- Ptosis in childhood
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- A Review of the Use of Biotin for Hair Loss
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer
- Lysophospholipid Mediators in Health and Disease
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities