Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease

scientific article published on 28 August 2009

Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.HRTHM.2009.08.031
P932PMC publication ID2789271
P698PubMed publication ID19959123
P5875ResearchGate publication ID40446139

P50authorJeffrey E OlginQ89825592
Bradley AouizeratQ92638520
Zian H TsengQ98297936
Stacy L. MusoneQ114427827
Dean WhitemanQ117251729
Pui-Yan KwokQ30348364
Ludmila PawlikowskaQ32653026
P2093author name stringEric Vittinghoff
Feng Lin
P2860cites workFamilial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patientsQ44612518
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1Q55670706
Sudden Cardiac DeathQ56593283
Elevation of Expression of Smads 2, 3, and 4, Decorin and TGF-βin the Chronic Phase of Myocardial Infarct Scar HealingQ58047304
Differential effects of transforming growth factor-beta 1 and phorbol myristate acetate on cardiac fibroblasts. Regulation of fibrillar collagen mRNAs and expression of early transcription factorsQ64966731
Changes in extracellular matrix and in transforming growth factor beta isoforms after coronary artery ligation in ratsQ74162665
Predicting sudden death in the population: the Paris Prospective Study IQ77342545
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease lociQ21145042
Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4Q24538382
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsQ24550675
Narcolepsy is strongly associated with the T-cell receptor alpha locusQ24649513
PLINK: a tool set for whole-genome association and population-based linkage analysesQ24677407
Pirfenidone prevents the development of a vulnerable substrate for atrial fibrillation in a canine model of heart failureQ24684669
Principal components analysis corrects for stratification in genome-wide association studiesQ27860975
TGFβ2 knockout mice have multiple developmental defects that are non-overlapping with other TGFβ knockout phenotypesQ28592444
Specificity, diversity, and regulation in TGF-beta superfamily signaling.Q33792305
Induction of cardiac fibrosis by transforming growth factor-beta(1).Q34043223
Sudden cardiac death in the United States, 1989 to 1998.Q34099663
Heterozygous TGFBR2 mutations in Marfan syndromeQ34331334
Family history as a risk factor for primary cardiac arrestQ34454002
Sudden death due to cardiac arrhythmiasQ34496008
Genomic control, a new approach to genetic-based association studiesQ34539204
PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposesQ34974290
Of mice and dogs: species-specific differences in the inflammatory response following myocardial infarction.Q35083426
TGF-beta-induced SMAD signaling and gene regulation: consequences for extracellular matrix remodeling and wound healingQ35841836
Expression of transforming growth factor-beta 1 in specific cells and tissues of adult and neonatal miceQ36220077
Transforming growth factor-beta 1 induces alpha-smooth muscle actin expression in granulation tissue myofibroblasts and in quiescent and growing cultured fibroblastsQ36232642
Ambulatory sudden cardiac death: mechanisms of production of fatal arrhythmia on the basis of data from 157 casesQ36416908
The role of TGF-beta signaling in myocardial infarction and cardiac remodelingQ36655326
Extracellular control of TGFbeta signalling in vascular development and diseaseQ36951674
The effects of ABCG5/G8 polymorphisms on plasma HDL cholesterol concentrations depend on smoking habit in the Boston Puerto Rican Health StudyQ37089123
Transforming growth factor beta receptor type II inactivation induces the malignant transformation of intestinal neoplasms initiated by Apc mutation.Q38508373
Expression cloning of the TGF-β type II receptor, a functional transmembrane serine/threonine kinaseQ41639273
P433issue12
P921main subjectcardiac arrestQ202837
P304page(s)1745-1750
P577publication date2009-08-28
P1433published inHeart RhythmQ2058605
P1476titleAssociation of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease
P478volume6

Reverse relations

cites work (P2860)
Q35683200A Common Polymorphism of the Human Cardiac Sodium Channel Alpha Subunit (SCN5A) Gene Is Associated with Sudden Cardiac Death in Chronic Ischemic Heart Disease
Q38735806A comparison of gene expression profiles in patients with coronary artery disease, type 2 diabetes, and their coexisting conditions
Q64289639A generally conserved response to hypoxia in iPSC-derived cardiomyocytes from humans and chimpanzees
Q54587757Association between TGFBR2 gene polymorphism (rs2228048, Asn389Asn) and intracerebral hemorrhage in Korean population.
Q37706936Association of CASQ2 polymorphisms with sudden cardiac arrest and heart failure in patients with coronary artery disease
Q36819566Autophagy inhibition of hsa-miR-19a-3p/19b-3p by targeting TGF-β R II during TGF-β1-induced fibrogenesis in human cardiac fibroblasts
Q54179932Epigenome-wide association study reveals differential DNA methylation in individuals with a history of myocardial infarction.
Q21261953GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease
Q44853264GWAS or Gee Whiz, PSAS or Pshaw: elucidating the biologic and clinical significance of genetic variation in cardiovascular disease.
Q52866707Genetic variations involved in sudden cardiac death and their associations and interactions.
Q33352008Genetics in arterial calcification: pieces of a puzzle and cogs in a wheel
Q57244819High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations
Q26859562Nitric Oxide Synthase 1 Adaptor Protein, an Emerging New Genetic Marker for QT Prolongation and Sudden Cardiac Death
Q35069518Observational cohort study of ventricular arrhythmia in adults with Marfan syndrome caused by FBN1 mutations
Q41264353Transforming growth factor beta receptor II polymorphisms are associated with Kawasaki disease
Q42670499Transforming growth factor-β signaling pathway-associated genes SMAD2 and TGFBR2 are implicated in metabolic syndrome in a Taiwanese population

Search more.