Search
for
Sort by
Research 181–210 of 1000+
- Molecular cloning, characterization, and expression of sheep FGF5 gene
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- CPK1 activates CNGCs through phosphorylation for Ca2+ signaling to promote root hair growth in Arabidopsis
- The Genetic Architecture of Alopecia Areata
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Transcriptional and epigenetic mechanisms governing epidermal stem cell regulation
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Thiopurines: Recent Topics and Their Role in the Treatment of Inflammatory Bowel Diseases
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Spectrum of Phenotypes Associated with Human MC1R Variations
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Vitamin D Receptor, UVR, and Skin Cancer: A Potential Protective Mechanism
- SnapshotDx Quiz: August 2019
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Interferon in the treatment of cutaneous T-cell lymphoma
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- What does acne genetics teach us about disease pathogenesis?
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Genetic basis of polycystic ovary syndrome
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing