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- Association of Human Beta – Defensin 1 Gene Polymorphisms with Alopecia Areata Patients
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Reversible Alopecia Universalis During Treatment with PEG-Interferon and Ribavirin for Chronic Hepatitis C
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- c-Myc activation in transgenic mouse epidermis results in mobilization of stem cells and differentiation of their progeny
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Factors Related to Premature Canities; A Cross-sectional Study in Lagos State, Nigeria
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- Identification of the Ovine Keratin-Associated Protein 26-1 Gene and Its Association with Variation in Wool Traits
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- Regulatory T cells are required for normal and activin‐promoted wound repair in mice
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Skin Adipocyte Stem Cell Self-Renewal Is Regulated by a PDGFA/AKT-Signaling Axis
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- YAP and TAZ are essential for basal and squamous cell carcinoma initiation
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep