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Research 211–240 of 1000+
- Beyond Appearances: The Hidden Coat Diversity of the Sicilian Mastiff Revealed by Integrated Phenotypic and Genetic Analyses
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- THERAPEUTIC HOTLINE: Genetic variations in the androgen receptor gene and finasteride response in women with androgenetic alopecia mediated by epigenetics
- Joint study of the associations of HLA‐B and the transmembrane short tandem repeat polymorphism of MICA protein with alopecia areata shows independent associations of both with the disease
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Polymorphism of keratin-associated protein (KAP) 7 gene and its association with wool traits in Rambouillet sheep
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- FGFR2 is associated with hair thickness in Asian populations
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- Association of Androgen Receptor CAG Repeat Length with Polycystic Ovary Syndrome in an Iranian Female Population
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Cross-species amplification of human microsatellite markers in pig-tailed and stump-tailed macaques
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Transgenic mouse models support HCR as an effector gene in the PSORS1 locus
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- Polymorphisms of OCT1 and metformin effects in Iraqi women with polycystic ovary syndrome in Karbala city
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss