is-rSNP: a novel technique for in silico regulatory SNP detection.
about
HOCOMOCO: a comprehensive collection of human transcription factor binding sites modelsCandidate gene association studies: a comprehensive guide to useful in silico toolsBioinformatics for personal genome interpretationHaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variantsGenome-wide analysis of blood pressure variability and ischemic stroke.Non-homologous end-joining pathway associated with occurrence of myocardial infarction: gene set analysis of genome-wide association study data.Toll-like receptor 9 polymorphisms are associated with severity variables in a cohort of meningococcal meningitis survivors.Post-GWAS functional characterization of susceptibility variants for chronic lymphocytic leukemia.Linking disease associations with regulatory information in the human genome.Large-scale computational identification of regulatory SNPs with rSNP-MAPPER.Single nucleotide polymorphisms in noncoding regions of Rad51C do not change the risk of unselected breast cancer but they modulate the level of oxidative stress and the DNA damage characteristics: a case-control study.Associating disease-related genetic variants in intergenic regions to the genes they impactIdentified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese populationRole of non-coding sequence variants in cancer.Variation Interpretation Predictors: Principles, Types, Performance, and Choice.Network graph analysis of gene-gene interactions in genome-wide association study data.Genetic variation of the transthyretin gene in wild-type transthyretin amyloidosis (ATTRwt).Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk.Identifying functional single nucleotide polymorphisms in the human CArGomeGenome-wide analysis distinguishes hyperglycemia regulated epigenetic signatures of primary vascular cells.A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary interventionIdentification of cis-regulatory sequence variations in individual genome sequences.Genetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population.Obesity-related known and candidate SNP markers can significantly change affinity of TATA-binding protein for human gene promoters.In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci.TEMPLE: analysing population genetic variation at transcription factor binding sites.Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancerMonoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal.Negative selection maintains transcription factor binding motifs in human cancer.Candidate SNP markers of aggressiveness-related complications and comorbidities of genetic diseases are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters.atSNP: transcription factor binding affinity testing for regulatory SNP detection.The single nucleotide variant rs12722489 determines differential estrogen receptor binding and enhancer properties of an IL2RA intronic regionCandidate SNP Markers of Gender-Biased Autoimmune Complications of Monogenic Diseases Are Predicted by a Significant Change in the Affinity of TATA-Binding Protein for Human Gene PromotersGWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M)Candidate SNP Markers of Chronopathologies Are Predicted by a Significant Change in the Affinity of TATA-Binding Protein for Human Gene Promoters.Fulvestrant up regulates UGT1A4 and MRPs through ERα and c-Myb pathways: a possible primary drug disposition mechanism.Evaluating the impact of single nucleotide variants on transcription factor binding.Non-coding single nucleotide variants affecting estrogen receptor binding and activitySNP2TFBS - a database of regulatory SNPs affecting predicted transcription factor binding site affinity.
P2860
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P2860
is-rSNP: a novel technique for in silico regulatory SNP detection.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
is-rSNP: a novel technique for in silico regulatory SNP detection.
@en
is-rSNP: a novel technique for in silico regulatory SNP detection.
@nl
type
label
is-rSNP: a novel technique for in silico regulatory SNP detection.
@en
is-rSNP: a novel technique for in silico regulatory SNP detection.
@nl
prefLabel
is-rSNP: a novel technique for in silico regulatory SNP detection.
@en
is-rSNP: a novel technique for in silico regulatory SNP detection.
@nl
P2093
P2860
P356
P1433
P1476
is-rSNP: a novel technique for in silico regulatory SNP detection.
@en
P2093
Adam Kowalczyk
Geoff Macintyre
Izhak Haviv
James Bailey
P2860
P304
P356
10.1093/BIOINFORMATICS/BTQ378
P407
P577
2010-09-01T00:00:00Z