• 58 Hits
  • 検索条件 : 絞込み (MeSH = Genetic Predisposition to Disease)
生物種 リソース名 タイトル
ヒト・動物細胞 CGM1(RCB0566) A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese.
ヒト・動物細胞 CGM1(RCB0566) Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese.
線虫 Punctuated Loci on Chromosome IV Determine Natural Variation in Orsay Virus Susceptibility of Caenorhabditis elegans Strains Bristol N2 and Hawaiian CB4856.
ヒト・動物細胞 HEV0050 , HEV0049 , HEV0048 , HEV0045 , HEV0043 , HEV0042 , HEV0041 , HEV0040 , HEV0039 , HEV0038 , ... Genome-wide association study of coronary artery disease in the Japanese.
ショウジョウバエ Functional Studies of Genetic Variants Associated with Human Diseases in Notch Signaling-Related Genes Using Drosophila.
ヒト・動物細胞 SF8543(RCB0608) Genome-wide association studies in Japanese women identified genetic loci associated with wrinkles and sagging.
ゼブラフィッシュ Tg(cmlc2:Mermaid) Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases.
ヒト・動物細胞 THP-1(RCB1189) An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.
遺伝子材料 CSII-EF-MCS-IRES2-Venus (RDB04384) The Molecular Basis of Chemical Chaperone Therapy for Oculocutaneous Albinism Type 1A.
ヒト・動物細胞 293(RCB1637) Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia.
ヒト・動物細胞 OP9(RCB1124) Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia.
ヒト・動物細胞 409B2(HPS0076) Vulnerability to shear stress caused by altered peri-endothelial matrix is a key feature of Moyamoya disease.
ヒト・動物細胞 Ba/F3(RCB0805) Next-generation cDNA screening for oncogene and resistance phenotypes.
実験動物マウス RBRC01834 UTX maintains the functional integrity of the murine hematopoietic system by globally regulating aging-associated genes.
ニワトリ・ウズラ JB , GSP/Cp Combined deletions of IHH and NHEJ1 cause chondrodystrophy and embryonic lethality in the Creeper chicken.
ヒト・動物細胞 Control iPS Functional evaluation of the pathological significance of MEFV variants using induced pluripotent stem cell-derived macrophages.
ショウジョウバエ DGRC#111506 A Drosophila model to study retinitis pigmentosa pathology associated with mutations in the core splicing factor Prp8.
ショウジョウバエ Discovering human diabetes-risk gene function with genetics and physiological assays.
実験動物マウス RBRC02759 Posttranscriptional regulation of colonic epithelial repair by RNA binding protein IMP1/IGF2BP1.
ヒト・動物細胞 SRA 01/04(RCB1591) The impact of GJA8 SNPs on susceptibility to age-related cataract.