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  • 36 Hits
  • Search Condition : Filter (MeSH = Genetic Predisposition to Disease)
Species Resource Title
Human and Animal Cells THP-1(RCB1189) An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.
DNA material CSII-EF-MCS-IRES2-Venus (RDB04384) The Molecular Basis of Chemical Chaperone Therapy for Oculocutaneous Albinism Type 1A.
Human and Animal Cells Ba/F3(RCB0805) Next-generation cDNA screening for oncogene and resistance phenotypes.
Human and Animal Cells Control iPS Functional evaluation of the pathological significance of MEFV variants using induced pluripotent stem cell-derived macrophages.
Drosophila Discovering human diabetes-risk gene function with genetics and physiological assays.
Mice RBRC02759 Posttranscriptional regulation of colonic epithelial repair by RNA binding protein IMP1/IGF2BP1.
Drosophila 6459R-1,6459R-7 Twin CHCH Proteins, CHCHD2, and CHCHD10: Key Molecules of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Frontotemporal Dementia.
C.elegans An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes.
C.elegans tm3768 The tumour suppressor CYLD regulates the p53 DNA damage response.
Human and Animal Cells MKN45(RCB1001) Autophagy-related genes in Helicobacter pylori infection.
Human and Animal Cells MKN7(RCB0999) , A431 Gene amplification of CCNE1, CCND1, and CDK6 in gastric cancers detected by multiplex ligation-dependent probe amplification and fluorescence in situ hybridization.
C.elegans tm794 Regulation of ATG4B stability by RNF5 limits basal levels of autophagy and influences susceptibility to bacterial infection.
Mice RBRC01828 Propagation of trimethylated H3K27 regulated by polycomb protein EED is required for embryogenesis, hematopoietic maintenance, and tumor suppression.
C.elegans tm1086 Exploring the link between MORF4L1 and risk of breast cancer.
Human and Animal Cells SSP-25(RCB1293) , RBE(RCB1292) Activation-induced cytidine deaminase links bile duct inflammation to human cholangiocarcinoma.
Human and Animal Cells Nucleotide change of codon 38 in the X gene of hepatitis B virus genotype C is associated with an increased risk of hepatocellular carcinoma.
Human and Animal Cells A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese.
DNA material p3xFLAG-CMV-10-Pemt (RDB14190) , pcDNA3-myc-CHC(232-340) (RDB14191) , pcDNA3-myc-CHC(1074-1406) (RDB14192) , pcDNA3-myc-CHC(1267-1513) (RDB14193) , pcDNA3-myc-CHC(1-1676) (RDB14194) , pcDNA3.1-p53-HA (RDB14195) , pcDNA3.1-FLAG-Pemt-HA (RDB14196). Insufficiency of phosphatidylethanolamine N-methyltransferase is risk for lean non-alcoholic steatohepatitis.
Drosophila DGRC#113334 MiR-980 Is a Memory Suppressor MicroRNA that Regulates the Autism-Susceptibility Gene A2bp1.
DNA material pGL4.17 Tyk2 WT (RDB13913) , pGL4.17 Tyk2 mutant (RDB13914). Reduced Tyk2 gene expression in β-cells due to natural mutation determines susceptibility to virus-induced diabetes.