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Research 391–420 of 1000+
- Antiandrogenic activity of Riboflavin 5′-phosphate (FMN) in 22Rv1 and LNCaP human prostate cancer cell lines
- New Horizons in the Genetics of Polycystic Ovary Syndrome: From Predisposition to Precision Medicine.
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- ACE2 and TMPRSS2 Potential Involvement in Genetic Susceptibility to SARS-COV-2 in Cancer Patients
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- [The effect of cgVEGF164 on the growth of murine hair follicles].
- A kindred with mutant IKAROS and autoimmunity
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- LB1053 Dysregulation of antioxidant enzyme PRDX5 in alopecia areata
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- An Updated Nomenclature for Keratin-Associated Proteins (KAPs)
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Ottawa, Ontario, Canada, February 13–16, 2013
- Abstracts
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Interplay between fibroblast growth factor 9 (FGF9) and CD44 underlies 46,XY disorders of sex development in Kruppel‐like factor 1 (KLF‐1)‐E325K‐associated congenital dyserythropoietic anaemia (CDA‐IV)
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women