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Research 61–90 of 1000+
- Research gaps in medical treatment of transgender/nonbinary people
- Cutaneous extramedullary haematopoiesis: Implications in human disease and treatment
- Impacts of Anabolic-androgenic steroid supplementation on female health and offspring: Mechanisms, side effects, and medical perspectives
- Metastatic Embryonal Cell Carcinoma with High Testosterone and Absence of Secondary Sexual Characteristics
- Game Changers: Blockbuster Small-Molecule Drugs Approved by the FDA in 2024
- Effect of injectable calcium alginate-amelogenin hydrogel on macrophage polarization and promotion of jaw bone osteogenesis
- Society for Endocrinology guidelines for testosterone replacement therapy in male hypogonadism
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Transdifferentiation of Human Hair Follicle Mesenchymal Stem Cells into Red Blood Cells by OCT4
- The Pharmacology of Regenerative Medicine
- Three-Dimensional Bioprinting: A Comprehensive Review for Applications in Tissue Engineering and Regenerative Medicine
- Role of regeneration in tissue repairing and therapies
- Safety of testosterone treatment in postmenopausal women
- The Role of Nutrition on Thyroid Function
- Androgen Treatment in Adolescent Males With Hypogonadism
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- Research on the balance of thiol-disulfide in blood serum in women with telogen effluvium
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps
- Melanocytes in regenerative medicine applications and disease modeling
- Testosterone: The Male Sex Hormone
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- An Update of Congenital Adrenal Hyperplasia
- Methimazole, Carbimazole, and Congenital Skin Defects
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions