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Research 601–630 of 1000+
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- 5‐Alpha reductase inhibitor related litigation: A legal database review
- A Gender Hypothesis of sex disparities in adverse drug events
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Improved health-span and lifespan in mtDNA mutator mice treated with the mitochondrially targeted antioxidant SkQ1
- Pathophysiology of the Behçet's Disease
- The role of WNT10B in physiology and disease: A 10-year update
- Evaluation of the effect of injection of dutasteride as mesotherapeutic tool in treatment of androgenetic alopecia in males
- Microglia: sculptors of the polycystic ovary syndrome (PCOS)-like brain?
- Lean Women with Polycystic Ovary Syndrome
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Endocrinology
- Mineral Deficiencies: A Root Cause for Reduced Longevity in Mammals
- Existence of Neural Crest–Derived Progenitor Cells in Normal and Fuchs Endothelial Dystrophy Corneal Endothelium
- Mood and Sexual Function in Polycystic Ovary Syndrome
- Keratin 6A promotes skin inflammation through JAK1-STAT3 activation in keratinocytes
- Metabolic Syndrome, Hepatic Steatosis and Testosterone: A Matter of Sex
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- The Hormonal Background of Hair Loss in Non-Scarring Alopecias
- Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Controversies Regarding Transdermal Androgen Therapy in Postmenopausal Women
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- On the geographies of hair: Exploring the entangled margins of the bordered body
- Mood disorders and quality of life in polycystic ovary syndrome