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Research 721–750 of 1000+
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Finding Long-COVID: temporal topic modeling of electronic health records from the N3C and RECOVER programs
- Itpr3 Is Responsible for the Mouse Tufted (tf) Locus
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- 加齢に伴うミトコンドリア枯渇は皮膚老化と肥満を加速する
- PRZEWLEKŁY STAN KRYTYCZNY: WSPÓŁCZESNE SPOJRZENIE NA PROBLEM
- Policistisko olnīcu sindroms pusaudzēm – starppaaudžu, ģenētiskie, dzīves kvalitātes un negausīgas ēšanas aspekti. Promocijas darbs
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Genetically Altered Expression of Spermidine/Spermine N1-Acetyltransferase Affects Fat Metabolism in Mice via Acetyl-CoA
- Extracellular Matrix Degradation Products and Low-Oxygen Conditions Enhance the Regenerative Potential of Perivascular Stem Cells
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Clinical characteristics of polycystic ovary syndrome: investigating differences in White and South Asian women
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Vitamin D receptor ablation alters skin architecture and homeostasis of dendritic epidermal T cells
- Free androgen index (FAI)’s relations with oxidative stress and insulin resistance in polycystic ovary syndrome
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Pigmentary mosaicism: An update
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Clinical and Demographic Characteristics of Patients Diagnosed with Polycystic Ovary Syndrome: A Cross-Sectional Observational Study
- Polycystic Ovary Syndrome: Explaining the Gynecological Aspects and Treatment Options to Patients
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Proteomics Characterization of Primary Human Oral Epithelial Cells Using a Novel Culture Technique for Use in Tissue Regeneration