| Item Type | Name |
|
Concept
|
Base Sequence
|
|
Academic Article
|
The Id2 gene is a novel target of transcriptional activation by EWS-ETS fusion proteins in Ewing family tumors.
|
|
Academic Article
|
Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms.
|
|
Academic Article
|
Genetic variations in the gene encoding ELMO1 are associated with susceptibility to diabetic nephropathy.
|
|
Academic Article
|
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
|
|
Academic Article
|
Criterion values for multiplex SNP genotyping by the invader assay.
|
|
Academic Article
|
Expression of novel molecules, MICAL2-PV (MICAL2 prostate cancer variants), increases with high Gleason score and prostate cancer progression.
|
|
Academic Article
|
Differential quantification of CYP2D6 gene copy number by four different quantitative real-time PCR assays.
|
|
Academic Article
|
Common variation of IL28 affects gamma-GTP levels and inflammation of the liver in chronically infected hepatitis C virus patients.
|
|
Academic Article
|
Common variation in GPC5 is associated with acquired nephrotic syndrome.
|
|
Academic Article
|
Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese.
|
|
Academic Article
|
Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing.
|
|
Academic Article
|
Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese.
|
|
Academic Article
|
IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility.
|
|
Academic Article
|
Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese.
|
|
Academic Article
|
Involvement of epithelial cell transforming sequence-2 oncoantigen in lung and esophageal cancer progression.
|
|
Academic Article
|
Development of new HLA-B*3505 genotyping method using Invader assay.
|
|
Academic Article
|
Comparison of gene-expression profiles between diffuse- and intestinal-type gastric cancers using a genome-wide cDNA microarray.
|
|
Academic Article
|
Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene.
|
|
Academic Article
|
Functional haplotypes of IL-12B are associated with childhood atopic asthma.
|
|
Academic Article
|
Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus.
|
|
Academic Article
|
Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene.
|
|
Academic Article
|
TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.
|
|
Academic Article
|
Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetes.
|
|
Academic Article
|
Cyclin K as a direct transcriptional target of the p53 tumor suppressor.
|
|
Academic Article
|
The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation.
|
|
Academic Article
|
CD40 ligand gene and Kawasaki disease.
|
|
Academic Article
|
DKK1, a negative regulator of Wnt signaling, is a target of the beta-catenin/TCF pathway.
|
|
Academic Article
|
Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population.
|
|
Academic Article
|
Isolation and characterization of a novel gene CLUAP1 whose expression is frequently upregulated in colon cancer.
|
|
Academic Article
|
Molecular diagnosis of colorectal tumors by expression profiles of 50 genes expressed differentially in adenomas and carcinomas.
|
|
Academic Article
|
906 variations among 27 genes encoding cytochrome P450 (CYP) enzymes and aldehyde dehydrogenases (ALDHs) in the Japanese population.
|
|
Academic Article
|
p53RDL1 regulates p53-dependent apoptosis.
|
|
Academic Article
|
High-density SNP map of human ITR, a gene associated with vascular remodeling.
|
|
Academic Article
|
Glypican-3, overexpressed specifically in human hepatocellular carcinoma, is a novel tumor marker.
|
|
Academic Article
|
Activation of Holliday junction recognizing protein involved in the chromosomal stability and immortality of cancer cells.
|
|
Academic Article
|
Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathy.
|
|
Academic Article
|
hCDC4b, a regulator of cyclin E, as a direct transcriptional target of p53.
|
|
Academic Article
|
Catalog of 680 variations among eight cytochrome p450 ( CYP) genes, nine esterase genes, and two other genes in the Japanese population.
|
|
Academic Article
|
Nucleobindin 1 controls the unfolded protein response by inhibiting ATF6 activation.
|
|
Academic Article
|
Determination of splice-site mutations in Lynch syndrome (hereditary non-polyposis colorectal cancer) patients using functional splicing assay.
|
|
Academic Article
|
Overexpression of cohesion establishment factor DSCC1 through E2F in colorectal cancer.
|
|
Academic Article
|
Methylation at CpG islands in intron 1 of EGR2 confers enhancer-like activity.
|
|
Academic Article
|
The histone methyltransferase SMYD2 methylates PARP1 and promotes poly(ADP-ribosyl)ation activity in cancer cells.
|
|
Academic Article
|
Downregulation of the tumor suppressor HSPB7, involved in the p53 pathway, in renal cell carcinoma by hypermethylation.
|
|
Academic Article
|
A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes.
|
|
Academic Article
|
Identification of semaphorin3B as a direct target of p53.
|
|
Academic Article
|
Identification of SPARC as a candidate target antigen for immunotherapy of various cancers.
|
|
Academic Article
|
Identification of PDZK4, a novel human gene with PDZ domains, that is upregulated in synovial sarcomas.
|
|
Academic Article
|
SMYD3 encodes a histone methyltransferase involved in the proliferation of cancer cells.
|
|
Academic Article
|
A variable number of tandem repeats polymorphism in an E2F-1 binding element in the 5' flanking region of SMYD3 is a risk factor for human cancers.
|
|
Academic Article
|
Isolation of development and differentiation enhancing factor-like 1 (DDEFL1) as a drug target for hepatocellular carcinomas.
|
|
Academic Article
|
Identification of the interleukin 4 receptor alpha gene as a direct target for p73.
|
|
Academic Article
|
Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues.
|
|
Academic Article
|
Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor.
|
|
Academic Article
|
Mutated G-protein-coupled receptor GPR10 is responsible for the hyperphagia/dyslipidaemia/obesity locus of Dmo1 in the OLETF rat.
|
|
Academic Article
|
Cystatin C as a p53-inducible apoptotic mediator that regulates cathepsin L activity.
|
|
Academic Article
|
Diagnostic evaluation of RNA sequencing for the detection of genetic abnormalities associated with Ph-like acute lymphoblastic leukemia (ALL).
|
|
Academic Article
|
Characterization of a VNTR polymorphism in the coding region of the CEL gene.
|
|
Academic Article
|
HJURP is a cell-cycle-dependent maintenance and deposition factor of CENP-A at centromeres.
|
|
Academic Article
|
Bioinformatic prediction of potential T cell epitopes for SARS-Cov-2.
|
|
Academic Article
|
Plasma or Serum: Which Is Preferable for Mutation Detection in Liquid Biopsy?
|