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Research 181–210 of 1000+
- Association of methionine synthase gene polymorphisms with wool production and quality traits in Chinese Merino population12
- Vitamin D receptor gene polymorphisms are not associated with alopecia areata
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
- The Influence of the MDR1 C3435T Polymorphism on Methotrexate Responsiveness in Rheumatoid Arthritis Patients
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- ANALYSIS OF CTLA 4 GENE +49A/G AND CT60 A/G POLYMORPHISMS IN ALOPECIA AREATA PATIENTS
- Association of insulin-like growth factor 2 Apa1 A820G gene (rs680) polymorphism with polycystic ovarian syndrome
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- 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
- 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
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- 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
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</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
- THERAPEUTIC HOTLINE: Genetic variations in the androgen receptor gene and finasteride response in women with androgenetic alopecia mediated by epigenetics