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Research 601–630 of 1000+
- 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
- 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)
- EVALUATION OF ASSOCIATION OF ANTHROPOMETRIC INDICES WITH STRESS RESPONSE IN PCOS POPULATION
- 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
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- [The complex detection of AB(O)-system antigens and of keratin polymorphism in the forensic medical study of hair].
- 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
- Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome
- Oligomenorrhoea in Exercising Women
- 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
- 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
- Policistisko olnīcu sindroms pusaudzēm – starppaaudžu, ģenētiskie, dzīves kvalitātes un negausīgas ēšanas aspekti. Promocijas darbs
- 1379 Cell of origin contributes to the melanoma diversity
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- 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