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Research 151–180 of 1000+
- Common Variants in the Sex Hormone-Binding Globulin (SHBG) Gene Influence SHBG Levels in Women with Polycystic Ovary Syndrome
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease
- Association of Androgen Receptor CAG Repeat Length with Polycystic Ovary Syndrome in an Iranian Female Population
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males”
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Alopecia Areata
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Application of PCR Technique to Detect Polymorphism of the KRTAP1.1 Gene in Three Sheep Breeds - A Review
- An evaluation of the RapidHIT™ ID system for hair roots stained with Diamond™ Nucleic Acid Dye
- Epigenetic control of adult stem cell function
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Landmark native breed of the Orenburg goats: progress in its breeding and genetics and future prospects
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Ulcerative colitis and total alopecia in a mother and her son
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- Association of psoriasis and psoriatic arthritis with human leukocyte antigen and killer cell immunoglobulin–like receptor gene frequency: A multiethnic population study
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Topical metformin as a novel therapy for alopecia areata due to its immunologic effects
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle