نتایج جستجو برای: mybpc3

تعداد نتایج: 307  

1999
Pascale Richard Richard Isnard Lucie Carrier Olivier Dubourg Yves Donatien Bénédicte Mathieu Gisèle Bonne Françoise Gary Philippe Charron Albert Hagege Michel Komajda Ketty Schwartz Bernard Hainque

Familial hypertrophic cardiomyopathy is a genetically heterogeneous autosomal dominant disease, caused by mutations in several sarcomeric protein genes. So far, seven genes have been shown to be associated with the disease with the â-myosin heavy chain (MYH7) and the cardiac myosin binding protein C (MYBPC3) genes being the most frequently involved. We performed electrocardiography (ECG) and ec...

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: :Circulation. Cardiovascular genetics 2016
Annalisa Milano Marieke T Blom Elisabeth M Lodder Daniel A van Hoeijen Julien Barc Tamara T Koopmann Abdennasser Bardai Leander Beekman Peter Lichtner Maarten P van den Berg Arthur A M Wilde Connie R Bezzina Hanno L Tan

BACKGROUND Sudden cardiac arrest (SCA) ranks among the most common causes of death worldwide. Because SCA is most often lethal, yet mostly occurs in individuals without previously known cardiac disease, the identification of patients at risk for SCA could save many lives. In unselected SCA victims from the community, common genetic variants (which are not disease-causing per se, but may increas...

Journal: :Circulation journal : official journal of the Japanese Circulation Society 2005
Masami Shimizu Hidekazu Ino Toshihiko Yasuda Noboru Fujino Katsuharu Uchiyama Tomohito Mabuchi Tetsuo Konno Tomoya Kaneda Takashi Fujita Eiichi Masuta Masahiro Katoh Akira Funada Hiroshi Mabuchi

BACKGROUND Some patients with dilated cardiomyopathy (DCM) have mutations of the genes that encode sarcomeric or cytoskeletal proteins of cardiomyocytes, but the prevalence of these mutations in Japan remains unclear. METHODS AND RESULTS A group of 99 unrelated adult patients with DCM (familial n=27, sporadic n=72) were screened for the following genes: cardiac beta-myosin heavy chain, cardia...

Journal: :Cardiogenetics 2011
Quinn S Wells Natalie L Ausborn Birgit H Funke Jean P Pfotenhauer Joseph L Fredi Samantha Baxter Thomas D Disalvo Charles C Hong

Idiopathic dilated cardiomyopathy (DCM) is a primary myocardial disorder characterized by ventricular chamber enlargement and systolic dysfunction. Twenty to fifty percent of idiopathic DCM cases are thought to have a genetic cause. Of more than 30 genes known to be associated with DCM, rare variants in the VCL and MYBPC3 genes have been reported in several cases of DCM. In this report, we desc...

2015
Matthew J. Birket Marcelo C. Ribeiro Georgios Kosmidis Dorien Ward Ana Rita Leitoguinho Vera van de Pol Cheryl Dambrot Harsha D. Devalla Richard P. Davis Pier G. Mastroberardino Douwe E. Atsma Robert Passier Christine L. Mummery

Maximizing baseline function of human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) is essential for their effective application in models of cardiac toxicity and disease. Here, we aimed to identify factors that would promote an adequate level of function to permit robust single-cell contractility measurements in a human induced pluripotent stem cell (hiPSC) model of hypertrophic card...

ژورنال: :مجله دانشگاه علوم پزشکی اراک 0
بهناز سادات عابدی behnaz sadat abedi department of genetics, shahrekord azad university, shahrekord, iranگروه ژنتیک، دانشگاه آزاد شهرکرد، شهرکرد، ایران زهره کیانی zohreh kiyani department of genetics, shahrekord azad university, shahrekord, iranگروه ژنتیک، دانشگاه آزاد شهرکرد، شهرکرد، ایران شهربانو پرچمی shahrbanoo parchami department of human genetics, cellular and molecular research center, shahrekord university of medical sciences, shahrekord, iranگروه ژنتیک، مرکز تحقیقات سلولی و مولکولی، دانشگاه علوم پزشکی شهرکرد، شهرکرد، ایران مرتضی هاشم زاده چالشتری morteza hashemzade chaloshtari cellular and molecular research center, shahrekord university of medical sciences, shahrekotd, iranایران، شهرکرد، دانشگاه علوم پزشکی شهرکرد، مرکزتحقیقات سلولی و مولکولیسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهرکرد (shahr kord university of medical sciences) عباس دوستی abbas doosti department of genetics, cellular and molecular research center, shahrekord azad university, shahrekord, iranگروه ژنتیک، مرکز تحقیقات سلولی و مولکولی، دانشگاه آزاد شهرکرد، شهرکرد، ایرانسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهرکرد (shahr kord university of medical sciences)

زمینه و هدف: کاردیومایوپاتی هایپرتروفیک (hcm) مجموعه ای متنوع از بیماری های قلبی با توارث آتوزومی غالب است که 2/0 درصد از جمعیت جهان را تحت تأثیر قرار داده و شایع ترین علت مرگ قلبی ناگهانی در جوانان زیر 35 سال می باشد. حدود 40 درصد از موارد بیماری مربوط به جهش در ژن mybpc3 است. هدف از این مطالعه بررسی جهش های ژن mybpc3 در اگزون های 15 و 18 بیماران hcm در استان چهارمحال و بختیاری می باشد. مواد و...

2015
Nawel Jaafar Francesca Girolami Ihsen Zairi Sondes Kraiem Mohamed Hammami Iacopo Olivotto

We recently performed next generation sequencing (NGS) genetic screening in 11 consecutive and unrelated Tunisian HCM probands seen at Habib Thameur Hospital in Tunis in the first 6 months of 2014, as part of a cooperative study between our Institutions. The clinical diagnosis of HCM was made according to standard criteria. Using the Illumina platform, a panel of 12 genes was analyzed including...

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