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Research 241–270 of 1000+
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Current and prospective strategies for advancing the targeted delivery of CRISPR/Cas system via extracellular vesicles
- Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- Defining the identity of mouse embryonic dermal fibroblasts
- Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis
- Associations between genetically predicted sex and growth hormones and facial aging in the UK Biobank: a two−sample Mendelian randomization study
- Alopecia Areata in 12 years old female treated with Oral Azathioprine: A case report and review
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Genetic basis of polycystic ovary syndrome
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- DNA Methylation‐Regulated ZDHHC17 Promotes the Risk of Facial Skin Aging
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Gut Microbiota and Its Association with Alopecia Areata: Insights from a Two-Sample Mendelian Randomization Study
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü