Tnni3k modifies disease progression in murine models of cardiomyopathy
about
TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathyDissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conductionTroponin I-interacting protein kinase: a novel cardiac-specific kinase, emerging as a molecular target for the treatment of cardiac diseaseCharacterisation of a C1qtnf5 Ser163Arg knock-in mouse model of late-onset retinal macular degenerationStrain-specific modifier genes of Cecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genesAdditional sex combs-like family genes are required for normal cardiovascular developmentTranscription of a protein-coding gene on B chromosomes of the Siberian roe deer (Capreolus pygargus)Genetic variations strongly influence phenotypic outcome in the mouse retina.Identification of a cardiac disease modifier gene using forward genetics in the mouseAdenovirus-mediated overexpression of cardiac troponin I-interacting kinase promotes cardiomyocyte hypertrophy.Modifier genes and the plasticity of genetic networks in mice.Overexpression of TNNI3K, a cardiac-specific MAPKKK, promotes cardiac dysfunction.Defining the pathways underlying the prolonged PR interval in atrioventricular conduction disease.Distinct genetic regions modify specific muscle groups in muscular dystrophy.TNNI3K, a cardiac-specific kinase, promotes physiological cardiac hypertrophy in transgenic mice.Inhibition of the cardiomyocyte-specific kinase TNNI3K limits oxidative stress, injury, and adverse remodeling in the ischemic heartA founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformationsMapping genetic contributions to cardiac pathology induced by Beta-adrenergic stimulation in miceGenetics of common forms of heart failure: challenges and potential solutions.Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus LevelGenetic mutations and mechanisms in dilated cardiomyopathyA modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene.The CRISPR/Cas9 System and the Possibility of Genomic Edition for CardiologySystems Genetics Approach Identifies Gene Pathways and Adamts2 as Drivers of Isoproterenol-Induced Cardiac Hypertrophy and Cardiomyopathy in MiceThe genetic landscape of cardiomyopathy and its role in heart failure.Frequency of mononuclear diploid cardiomyocytes underlies natural variation in heart regeneration.Factors other than genotype account largely for the phenotypic variation of the pulmonary valve in Syrian hamsters.Genetically alike Syrian hamsters display both bifoliate and trifoliate aortic valves.Comparative phenotypic assessment of cardiac pathology, physiology, and gene expression in C3H/HeJ, C57BL/6J, and B6C3F1/J mice.Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia.
P2860
Q24299150-460D1E26-9B83-4A67-9661-D4E03B5FBC61Q24305930-8CE93BC1-13C6-4FE7-8395-F68CC1CDBB3EQ26864088-FBC3FAFF-EF7E-4150-9648-B713EA207E1EQ28478012-0FE2E516-6D1E-4CCF-84D9-11AB7B63282DQ28510741-16589B75-1B86-4BF9-907C-B1F0F284F064Q28585968-26782CDD-53FC-4B74-BF8E-2E8790DCAF11Q28681575-3A94ABEB-2EEB-4171-A4FD-A0E6E45C0D76Q30474767-662A6379-4C01-4A9E-ABA4-048D939A8738Q33504526-1942C571-DFEF-49B6-B2FB-D9C1E8829AA9Q34164033-F8C7D619-BD0E-4BA4-AD64-DBBF81BB45B8Q34236664-BC12BA76-A5EE-459C-A7F4-ECA61D4E9CB6Q34307352-F11EE4FA-BF03-4E89-BE81-D5A1A201E6D9Q34510215-6BC2D0AC-AD1D-4280-99D7-21F2CCBEB24BQ34518008-A9DD7FA5-0DA1-4331-A476-6591120C16D3Q34615034-104B3AF3-7102-4E72-B893-A85306A98C83Q35019445-89563482-829B-47D0-8753-C6B44CF06B67Q35093781-30DF7AC3-6789-4E5C-A45A-CAB98A790222Q35102230-4450950C-1FC3-4224-9641-F0E4A614642CQ35525031-DE647ED6-0CCA-4AAA-AF1E-B91E493C8F5BQ36063830-DA4D44BE-4A06-4FEA-8A1D-D40315C5160EQ36497170-F7C3C31D-2795-4AD9-85E1-EE7808F0DE1DQ37255814-54D0A8B2-253A-4648-B0E8-9EC32E6383EDQ37594531-AB47EE2B-F714-4398-AC3E-1CBD55F3A741Q37682494-92B3AFAC-1299-41F3-874F-E3B346F1A833Q38343935-C9070D1B-C52F-4E1D-B37F-6285C08EC166Q46345451-8F440FB3-4B3F-4927-B266-8631CD51CB41Q47756812-F4B5098B-4685-45E8-A735-15684E20C083Q51764243-E26A1800-1750-4F43-A314-81DE22FE1E60Q53452720-CF9A32E4-821F-4797-A95D-EC3916597619Q54982915-7A0A14C0-79DF-4EB7-8F9D-129D4496DDB9
P2860
Tnni3k modifies disease progression in murine models of cardiomyopathy
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Tnni3k modifies disease progression in murine models of cardiomyopathy
@ast
Tnni3k modifies disease progression in murine models of cardiomyopathy
@en
Tnni3k modifies disease progression in murine models of cardiomyopathy
@nl
type
label
Tnni3k modifies disease progression in murine models of cardiomyopathy
@ast
Tnni3k modifies disease progression in murine models of cardiomyopathy
@en
Tnni3k modifies disease progression in murine models of cardiomyopathy
@nl
prefLabel
Tnni3k modifies disease progression in murine models of cardiomyopathy
@ast
Tnni3k modifies disease progression in murine models of cardiomyopathy
@en
Tnni3k modifies disease progression in murine models of cardiomyopathy
@nl
P2093
P2860
P3181
P1433
P1476
Tnni3k modifies disease progression in murine models of cardiomyopathy
@en
P2093
Douglas A Marchuk
Ferrin C Wheeler
Howard A Rockman
Odessa A Marks
Pei-Lun Chu
Tracy N Hadnott
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1000647
P407
P577
2009-09-01T00:00:00Z