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Research 631–660 of 1000+
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- Congenital triangular alopecia - A case report
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Genetic analysis does not confirm non-classical congenital adrenal hyperplasia in more than a third of the women followed with this diagnosis
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Increased PHGDH expression promotes aberrant melanin accumulation
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Basal cell carcinomas in mice arise from hair follicle stem cells and multiple epithelial progenitor populations
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- The Dark Side of Gefitinib: Reflectance Confocal Microscopy Applied to Hair Hyperpigmentation
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Genetic Insights into Acne, Androgenetic Alopecia, and Alopecia Areata: Implications for Mechanisms and Precision Dermatology
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Male pattern hair loss: Taking one for the team: The selfless gene
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- Generalized atrophic benign epidermolysis bullosa.