Search
for
Sort by
Research 901–930 of 1000+
- КЛІНІЧНІ ФЕНОТИПИ ВИСОКОГО РИЗИКУ НАЯВНОСТІ ПЕРВИННИХ МІТОХОНДРІАЛЬНИХ ЦИТОПАТІЙ (частина 2)
- Clinical features and presentation of polycystic ovary syndrome
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- A Transcriptome Sequencing Study on Genome-Wide Gene Expression Differences of Lung Cancer Cells Modulated by Fucoidan
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- [The complex detection of AB(O)-system antigens and of keratin polymorphism in the forensic medical study of hair].
- MmuPV1 infection and tumor development of T cell-deficient mice is prevented by passively transferred hyperimmune sera from normal congenic mice immunized with MmuPV1 virus-like particles (VLPs)
- 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
- 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
- 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
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- 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
- Epidermal pigmentation in the human lineage is an adaptation to ultraviolet radiation
- Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome
- Finding Long-COVID: temporal topic modeling of electronic health records from the N3C and RECOVER programs
- 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
- 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
- Genetically Altered Expression of Spermidine/Spermine N1-Acetyltransferase Affects Fat Metabolism in Mice via Acetyl-CoA