نتایج جستجو برای: cardiac conduction system disease

تعداد نتایج: 3736785  

Journal: :Development 2009
Nikhil V Munshi John McAnally Svetlana Bezprozvannaya Jeff M Berry James A Richardson Joseph A Hill Eric N Olson

The cardiac conduction system comprises a specialized tract of electrically coupled cardiomyocytes responsible for impulse propagation through the heart. Abnormalities in cardiac conduction are responsible for numerous forms of cardiac arrhythmias, but relatively little is known about the gene regulatory mechanisms that control the formation of the conduction system. We demonstrate that a dista...

Background and Aim: Smoking stimulates adrenergic depletion in circulation and, theoretically, it can increase incidence and prevalence of cardiac conduction defects. In this study we wanted to know if smoking affected cardiac conduction defects in patients with acute inferior myocardial infarction (MI). Materials and Methods: In this cross- sectional study, 40 smokers and 40 non – smokers wit...

Journal: :Global Journal of Science Frontier Research 2020

Journal: :COJ Technical & Scientific Research 2018

Journal: :Circulation research 2012
Catherine A Risebro Louisa K Petchey Nicola Smart John Gomes James Clark Joaquim M Vieira Joseph Yanni Halina Dobrzynski Sean Davidson Zia Zuberi Andrew Tinker Bo Shui Yvonne I Tallini Michael I Kotlikoff Lucile Miquerol Robert J Schwartz Paul R Riley

RATIONALE Nkx2.5 is one of the most widely studied cardiac-specific transcription factors, conserved from flies to man, with multiple essential roles in both the developing and adult heart. Specific dominant mutations in NKX2.5 have been identified in adult congenital heart disease patients presenting with conduction system anomalies and recent genome-wide association studies implicate the NKX2...

Journal: :Journal of the American College of Cardiology 2019

2003
Heather M. MacLeod Mary R. Culley Jill M. Huber Elizabeth M. McNally Emery Dreifuss

Background: Mutations in the gene encoding the nuclear membrane protein lamin A/C have been associated with at least 7 distinct diseases including dilated cardiomyopathy with conduction system disease, autosomal dominant Emery Dreifuss Muscular Dystrophy, limb girdle muscular dystrophy, Charcot Marie Tooth, Mandibuloacral dysplasia, lipodystrophy and progeria. Methods: We used mutation detectio...

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