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Research 181–210 of 1000+
- Vitamin D receptor gene polymorphisms are not associated with alopecia areata
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- 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
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Lack of association between Vitamin D receptor FokI polymorphism and alopecia areata.
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Cardiac biopsy in myocarditis
- The Influence of the MDR1 C3435T Polymorphism on Methotrexate Responsiveness in Rheumatoid Arthritis Patients
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese 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
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- ANALYSIS OF CTLA 4 GENE +49A/G AND CT60 A/G POLYMORPHISMS IN ALOPECIA AREATA PATIENTS
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- Association of insulin-like growth factor 2 Apa1 A820G gene (rs680) polymorphism with polycystic ovarian syndrome
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Testing for GHB in Hair by GC/MS/MS after a Single Exposure. Application to Document Sexual Assault
- Shorter CAG repeats in the androgen receptor gene may enhance hyperandrogenicity in polycystic ovary syndrome
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- 친환경농자재 개발을 위한 서양금혼초(Hypochaeris radicata L.)의 알레로패시 효과
- Notes from the Editor Emeritus: Finasteride: the downtrodden hero of hair transplantation emerges once again