نتایج جستجو برای: ژن myh7

تعداد نتایج: 16107  

Journal: :Circulation. Cardiovascular genetics 2015
Matthew N Bainbridge Erica E Davis Wen-Yee Choi Amy Dickson Hugo R Martinez Min Wang Huyen Dinh Donna M Muzny Ricardo Pignatelli Nicholas Katsanis Eric Boerwinkle Richard A Gibbs John L Jefferies

BACKGROUND Left ventricular noncompaction (LVNC) is an autosomal-dominant, genetically heterogeneous cardiomyopathy with variable severity, which may co-occur with cardiac hypertrophy. METHODS AND RESULTS Here, we generated whole exome sequence data from multiple members from 5 families with LVNC. In 4 of 5 families, the candidate causative mutation segregates with disease in known LVNC genes...

Journal: :Circulation. Cardiovascular genetics 2012
Jessica R Golbus Megan J Puckelwartz John P Fahrenbach Lisa M Dellefave-Castillo Don Wolfgeher Elizabeth M McNally

BACKGROUND Hypertrophic cardiomyopathy and dilated cardiomyopathy arise from mutations in genes encoding sarcomere proteins including MYH7, MYBPC3, and TTN. Genetic diagnosis of cardiomyopathy relies on complete sequencing of the gene coding regions, and most pathogenic variation is rare. The 1000 Genomes Project is an ongoing consortium designed to deliver whole genome sequence information fro...

2017
Ce Wang Yukiko Hata Keiichi Hirono Asami Takasaki Sayaka Watanabe Ozawa Hideyuki Nakaoka Kazuyoshi Saito Nariaki Miyao Mako Okabe Keijiro Ibuki Naoki Nishida Hideki Origasa Xianyi Yu Neil E. Bowles Fukiko Ichida

BACKGROUND Left ventricular noncompaction (LVNC) has since been classified as a primary genetic cardiomyopathy, but the genetic basis is not fully evaluated. The aim of the present study was to identify the genetic spectrum using next-generation sequencing and to evaluate genotype-phenotype correlations in LVNC patients. METHODS AND RESULTS Using next-generation sequencing, we targeted and se...

2011
Pavel Capek Jiri Vondrasek Jiri Skvor Radim Brdicka

AIM To analyze the genesis of hypertrophic cardiomyopathy on a large cohort of patients from molecular genetics point of view and perform the functional analysis of the 3D molecular model of defective myosin-7 protein in silico. METHODS The study enrolled 153 patients with diagnosed hypertrophic cardiomyopathy from different parts of the Czech Republic. DNA samples were analyzed for mutations...

Journal: :Heart 2015
Diego García-Giustiniani Michael Arad Martín Ortíz-Genga Roberto Barriales-Villa Xusto Fernández Isabel Rodríguez-García Andrea Mazzanti Elena Veira Emilia Maneiro Paula Rebolo Iván Lesende Laura Cazón Dov Freimark Juan Ramón Gimeno-Blanes Christine Seidman Jonathan Seidman William McKenna Lorenzo Monserrat

OBJECTIVES The prognostic value of genetic studies in cardiomyopathies is still controversial. Our objective was to evaluate the outcome of patients with cardiomyopathy with mutations in the converter domain of β myosin heavy chain (MYH7). METHODS Clinical characteristics and survival of 117 affected members with mutations in the converter domain of MYH7 were compared with 409 patients descri...

Journal: :The Journal of Cell Biology 1996
A Kurz S Lampel J E Nickolenko J Bradl A Benner R M Zirbel T Cremer P Lichter

The intranuclear position of a set of genes was analyzed with respect to the territories occupied by the whole chromosomes in which these genes are localized. Genes and their respective chromosome territories were simultaneously visualized in three-dimensionally preserved nuclei applying dual color fluorescence in situ hybridization. Three coding (DMD, MYH7, and HBB) and two noncoding sequences...

Journal: :Clinica chimica acta; international journal of clinical chemistry 2015
Andrey S Glotov Sergey V Kazakov Elena A Zhukova Anton V Alexandrov Oleg S Glotov Vladimir S Pakin Maria M Danilova Irina V Poliakova Svetlana S Niyazova Natalia N Chakova Svetlana M Komissarova Elena A Kurnikova Andrey M Sarana Sergey G Sherbak Alexey A Sergushichev Anatoly A Shalyto Vladislav S Baranov

BACKGROUND Hypertrophic cardiomyopathy is a common genetic cardiac disease. Prevention and early diagnosis of this disease are very important. Because of the large number of causative genes and the high rate of mutations involved in the pathogenesis of this disease, traditional methods of early diagnosis are ineffective. METHODS We developed a custom AmpliSeq panel for NGS sequencing of the c...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2015
Nicholas L Reyes Glen B Banks Mark Tsang Daciana Margineantu Haiwei Gu Danijel Djukovic Jacky Chan Michelle Torres H Denny Liggitt Dinesh K Hirenallur-S David M Hockenbery Daniel Raftery Brian M Iritani

Mammalian skeletal muscle is broadly characterized by the presence of two distinct categories of muscle fibers called type I "red" slow twitch and type II "white" fast twitch, which display marked differences in contraction strength, metabolic strategies, and susceptibility to fatigue. The relative representation of each fiber type can have major influences on susceptibility to obesity, diabete...

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