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Research 121–150 of 1000+
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Phylloid terminal hair nevus: A unique clinical entity
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Transforming growth factor-β in stem cells and tissue homeostasis
- The Role of Hormonal Imbalances in Amenorrhea
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Insight into the pathogensis of polycystic ovarian syndrome
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Gene-knockout mice with abnormal epidermal and hair follicular development
- TONGUE, RED
- Drug-induced male infertility: a real-world study using FAERS and EudraVigilance databases
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- The Role of MicroRNA, Long Non-Coding RNA and Circular RNA in the Pathogenesis of Polycystic Ovary Syndrome: A Literature Review
- Pregnancy, hair loss, and the pill.
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Anaesthetics and platelets.
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Idiopathic hypoparathyroidism with extensive intracranial calcification in children
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy