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Research 631–660 of 1000+
- Enhancing the diagnostic yield of monogenic diabetes in unresolved cases with early-onset hyperglycemia
- Auxin Input Pathway Disruptions Are Mitigated by Changes in Auxin Biosynthetic Gene Expression in Arabidopsis
- The evolutionary impact of androgen levels on prostate cancer in a multi-scale mathematical model
- The Molecular Basis of Androgen Insensitivity
- Single-Cell RNA Sequencing Reveals Cellular and Transcriptional Changes Associated With M1 Macrophage Polarization in Hidradenitis Suppurativa
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Oligomenorrhoea in Exercising Women
- Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Itpr3 Is Responsible for the Mouse Tufted (tf) Locus
- Finding Long-COVID: temporal topic modeling of electronic health records from the N3C and RECOVER programs
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Uncharted waters
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- PRZEWLEKŁY STAN KRYTYCZNY: WSPÓŁCZESNE SPOJRZENIE NA PROBLEM
- Policistisko olnīcu sindroms pusaudzēm – starppaaudžu, ģenētiskie, dzīves kvalitātes un negausīgas ēšanas aspekti. Promocijas darbs
- 1379 Cell of origin contributes to the melanoma diversity
- 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
- The agouti mouse model: an epigenetic biosensor for nutritional and environmental alterations on the fetal epigenome
- Whole-genome sequencing of eight goat populations for the detection of selection signatures underlying production and adaptive traits
- Trichoscopy of Dark Scalp
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- WNT Signaling in the Control of Hair Growth and Structure
- 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