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Research 391–420 of 1000+
- Prevalence and Predictors of Impaired Glucose Tolerance and Diabetes Mellitus Type 2 in Patients with Polycystic Ovary Syndrome
- Metabolic Aspects of Polycystic Ovary Syndrome
- Workup and Management of Polycystic Ovary Syndrome
- Skin-Associated Cartilage Is a Distinct Type of Lipid-Filled Tissue
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review
- Scalp Microbiome Composition in Young Women: Associations with Scalp Type, Sensitivity, and Lifestyle Factors
- Noggin overexpression inhibits eyelid opening by altering epidermal apoptosis and differentiation
- Effect of a transcriptional inactive or absent vitamin D receptor on beta-cell function and glucose homeostasis in mice
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes
- American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the Diagnosis and Treatment of Hyperandrogenic Disorders
- p53 Involvement in the Control of Murine Hair Follicle Regression
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Descriptive Study of Hairline Patterns amongst Etche People of Rivers State, Nigeria
- An enzyme-linked immunosorbent assay for detection of botulinum toxin antibodies
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Hair matrix germinative epidermal cells confer follicle-inducing capabilities on dermal sheath and high passage papilla cells
- Expression of the Orphan Protein Plet-1 during Trichilemmal Differentiation of Anagen Hair Follicles
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Comment on: The Gabrin sign
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Boron deficiency responses in maize (<i>Zea mays</i> L.) roots
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Intrauterine botulinum toxin A administration promotes endometrial regeneration mediated by IGFBP3-dependent OPN proteolytic cleavage in thin endometrium
- Growth hormone-responsive alopecia in dogs
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Structure and expression of the ovine Hoxc-13 gene
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia