about
Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestryA regulatory polymorphism in HAVCR2 modulates susceptibility to HIV-1 infectionData on the evolutionary history of the V(D)J recombination-activating protein 1 - RAG1 coupled with sequence and variant analysesOncoCis: annotation of cis-regulatory mutations in cancer.An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer's disease in the Han Chinese population.Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy AdultsAssociation between IL7R polymorphisms and severe liver disease in HIV/HCV coinfected patients: a cross-sectional studyObesity-related known and candidate SNP markers can significantly change affinity of TATA-binding protein for human gene promoters.Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.Dissecting ancestry genomic background in substance dependence genome-wide association studiesrVarBase: an updated database for regulatory features of human variants.RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins.GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.Relationship of TRIM5 and TRIM22 polymorphisms with liver disease and HCV clearance after antiviral therapy in HIV/HCV coinfected patientsAutophagy-related gene LRRK2 is likely a susceptibility gene for systemic lupus erythematosus in northern Han Chinese.Genomic alterations as mediators of miRNA dysregulation in ovarian cancer.Confirmation of five novel susceptibility loci for systemic lupus erythematosus (SLE) and integrated network analysis of 82 SLE susceptibility loci.The effect of non-coding DNA variations on P53 and cMYC competitive inhibition at cis-overlapping motifs.Integrative genomics and transcriptomics analysis of human embryonic and induced pluripotent stem cells.Human aging in the post-GWAS era: further insights reveal potential regulatory variants.Multiple Genetic Associations with Irish Wolfhound Dilated Cardiomyopathy.Fine-mapping of antipsychotic response genome-wide association studies reveals novel regulatory mechanisms.Genome-wide association study of body mass index in subjects with alcohol dependence.Association of a 3' Untranslated Region Polymorphism in PCSK9 with HIV Viral Load and CD4+ Levels in HIV/Hepatitis C Virus Co-Infected Women.SCN11A variants may influence postoperative pain sensitivity after gynecological surgery in Chinese Han female patients.Fatty acid amide hydrolase-morphine interaction influences ventilatory response to hypercapnia and postoperative opioid outcomes in children.DEFA gene variants associated with IgA nephropathy in a Chinese population.A validated gene regulatory network and GWAS identifies early regulators of T cell-associated diseases.Principles and methods of in-silico prioritization of non-coding regulatory variants.rSNPBase 3.0: an updated database of SNP-related regulatory elements, element-gene pairs and SNP-based gene regulatory networks.Genetic variants of 20q12 contributed to non-syndromic orofacial clefts susceptibility.A Novel Polymorphism in the Promoter of the CYP4A11 Gene Is Associated with Susceptibility to Coronary Artery Disease.The polymorphism rs6918289 located in the downstream region of the TREM2 gene is associated with TNF-α levels and IMT-F.GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.Genetic polymorphisms in are associated with endometrial carcinoma susceptibility among Chinese Han womenDNA Motif Recognition Modeling from Protein SequencesAdvances in Human Biology: Combining Genetics and Molecular Biophysics to Pave the Way for Personalized Diagnostics and Medicine
P2860
Q27315831-C0DB5897-A9EA-46E0-9B0A-5800C7590AAFQ27316407-FD23B912-C1F0-4390-80E8-B9B0EC003AEEQ28542702-2F88D395-06E8-4889-8955-D1F605CEC07AQ28601961-6255A4E0-8A2D-4FED-ADF2-A5A99BF98B96Q34474391-AB6484F9-6892-4867-BAB0-7977ACA3EEFAQ35755004-0118171A-D9B8-4485-AD71-A49548C9B6CCQ35775152-D90D423F-5C7B-44A8-9429-45B22668514FQ35803583-6FEF55BD-0929-49B3-8E56-9FDD40B3D6A1Q35875387-B913559E-1994-4F74-B386-48929266BAABQ35882594-288D9644-F002-4D34-94C4-3F6CF735ED9DQ36248052-709FB3E8-E98C-4CEB-AC55-ACEB2512BCB9Q36434636-4D022013-C3BF-460D-8CDE-1A4A3C788897Q36434990-84EEB51E-7510-477A-80DB-A20B0F7740A1Q36435017-284D2145-9F0B-4E17-9516-CFF1671D9B3EQ37230823-B65E0954-E2DE-44CD-B19D-528672C817DEQ37706696-9200B794-FB47-4A99-BDB5-7FCCDFB0CEB7Q38256465-4B207E14-65E2-4AE5-8F97-075022824983Q38437890-2B2D746F-713E-4529-9608-94292D6968F5Q38450687-DA40500C-F08D-4070-AC91-959B872E60FCQ38467233-3AC1A7E5-DDC1-4279-8D58-D90A959E45BDQ39015956-52054CB2-A056-4B3E-B7E7-FD2C27D80FFEQ39923993-863B73CF-28CF-4784-98BD-BFCF0787CE8EQ40418374-1FECD5CF-F7A7-46F7-8E4F-C327C2A1B090Q41232551-99A17882-F2D4-4FA0-8907-F1149399A224Q41934639-D26D0530-4A0F-43E1-84B7-555A0BF24940Q42283374-6452EFC5-5BC2-42C2-AE09-DA7F527B4C62Q44341989-B9B9059C-57A8-4A3F-8B5A-FD9DFA61A2DEQ44817385-84ED86E5-2B72-4E5C-93C8-069F92C9AB1CQ46523543-4C62DDC7-B7F7-42CC-95EC-E72A400AB71EQ47210541-6E4AF8A9-0237-4156-AF8E-A8DEBD441261Q47574201-B273ECEF-A6DA-47B5-9B28-3EBD8933F074Q48564298-2B675082-CFC3-4324-B9D0-DE27820C4F9DQ51150942-3637AF29-93C9-48DB-8640-30A87E8ADE1CQ55017597-512FD7C7-5E0B-4F11-9D48-C8F06492CB4CQ55474442-EAF3AC07-B3EB-4D4D-A420-711A5D2344AEQ58571946-A1348216-6669-4C9A-8154-03ADB3579006Q58753645-567CFDAE-0C9A-4324-8695-71B3513B546EQ59042601-9636F037-66F2-4380-8A7B-A5CFC74AD636
P2860
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh
2013年學術文章
@zh-hant
name
rSNPBase: a database for curated regulatory SNPs.
@en
rSNPBase: a database for curated regulatory SNPs.
@nl
type
label
rSNPBase: a database for curated regulatory SNPs.
@en
rSNPBase: a database for curated regulatory SNPs.
@nl
prefLabel
rSNPBase: a database for curated regulatory SNPs.
@en
rSNPBase: a database for curated regulatory SNPs.
@nl
P2093
P2860
P356
P1476
rSNPBase: a database for curated regulatory SNPs.
@en
P2093
Kunlin Zhang
Liyuan Guo
Suhua Chang
P2860
P304
P356
10.1093/NAR/GKT1167
P407
P433
Database issue
P577
2013-11-26T00:00:00Z