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Research 211–240 of 1000+
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Keratin disorders: from gene to therapy
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- THE PATHOGENESIS OF ALOPECIA AREATA
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- The Function of LPR1 is Controlled by an Element in the Promoter and is Independent of SUMO E3 Ligase SIZ1 in Response to Low Pi Stress in Arabidopsis thaliana
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- FGFR2 is associated with hair thickness in Asian populations
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Associations between single-nucleotide polymorphisms of RFC-1, GGH, MTHFR , TYMS, and TCII genes and the efficacy and toxicity of methotrexate treatment in patients with rheumatoid arthritis
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- <i>WNT10A</i> , dermatology and dentistry
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Somatostatin Expression in Human Hair Follicles and Its Potential Role in Immune Privilege
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- The Genetic Architecture of Alopecia Areata
- Ulcerative colitis and total alopecia in a mother and her son