Literature DB >> 34797172

Understanding the molecular basis of cardiomyopathy.

Marie-Louise Bang1,2, Julius Bogomolovas3, Ju Chen3.   

Abstract

Inherited cardiomyopathies are a major cause of mortality and morbidity worldwide and can be caused by mutations in a wide range of proteins located in different cellular compartments. The present review is based on Dr. Ju Chen's 2021 Robert M. Berne Distinguished Lectureship of the American Physiological Society Cardiovascular Section, in which he provided an overview of the current knowledge on the cardiomyopathy-associated proteins that have been studied in his laboratory. The review provides a general summary of the proteins in different compartments of cardiomyocytes associated with cardiomyopathies, with specific focus on the proteins that have been studied in Dr. Chen's laboratory.

Entities:  

Keywords:  cardiomyopathy; genetics; murine models; protein mutations; translational research

Mesh:

Year:  2021        PMID: 34797172      PMCID: PMC8759964          DOI: 10.1152/ajpheart.00562.2021

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   5.125


  887 in total

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Journal:  Br J Dermatol       Date:  2011-08-09       Impact factor: 9.302

Review 2.  Getting to know the neighborhood: using proximity-dependent biotinylation to characterize protein complexes and map organelles.

Authors:  Anne-Claude Gingras; Kento T Abe; Brian Raught
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3.  A vinculin-containing cortical lattice in skeletal muscle: transverse lattice elements ("costameres") mark sites of attachment between myofibrils and sarcolemma.

Authors:  J V Pardo; J D Siliciano; S W Craig
Journal:  Proc Natl Acad Sci U S A       Date:  1983-02       Impact factor: 11.205

Review 4.  The SarcoEndoplasmic Reticulum Calcium ATPase.

Authors:  Joseph O Primeau; Gareth P Armanious; M'Lynn E Fisher; Howard S Young
Journal:  Subcell Biochem       Date:  2018

5.  Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

Authors:  Nadine Norton; Duanxiang Li; Mark J Rieder; Jill D Siegfried; Evadnie Rampersaud; Stephan Züchner; Steve Mangos; Jorge Gonzalez-Quintana; Libin Wang; Sean McGee; Jochen Reiser; Eden Martin; Deborah A Nickerson; Ray E Hershberger
Journal:  Am J Hum Genet       Date:  2011-02-25       Impact factor: 11.025

6.  Dilated cardiomyopathy in a patient with autosomal dominant EEF1A2-related neurodevelopmental disorder.

Authors:  Maki Kaneko; Tena Rosser; Gordana Raca
Journal:  Eur J Med Genet       Date:  2020-12-08       Impact factor: 2.708

7.  Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.

Authors:  Xianqin Zhang; Shenghan Chen; Shin Yoo; Susmita Chakrabarti; Teng Zhang; Tie Ke; Carlos Oberti; Sandro L Yong; Fang Fang; Lin Li; Roberto de la Fuente; Lejin Wang; Qiuyun Chen; Qing Kenneth Wang
Journal:  Cell       Date:  2008-12-12       Impact factor: 41.582

8.  Integrin-linked kinase is an adaptor with essential functions during mouse development.

Authors:  Anika Lange; Sara A Wickström; Madis Jakobson; Roy Zent; Kirsi Sainio; Reinhard Fässler
Journal:  Nature       Date:  2009-10-15       Impact factor: 49.962

9.  Integrin-linked kinase is localized to cell-matrix focal adhesions but not cell-cell adhesion sites and the focal adhesion localization of integrin-linked kinase is regulated by the PINCH-binding ANK repeats.

Authors:  F Li; Y Zhang; C Wu
Journal:  J Cell Sci       Date:  1999-12       Impact factor: 5.285

10.  Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.

Authors:  Rocio Toro; Alexandra Pérez-Serra; Oscar Campuzano; Javier Moncayo-Arlandi; Catarina Allegue; Anna Iglesias; Alipio Mangas; Ramon Brugada
Journal:  PLoS One       Date:  2016-07-08       Impact factor: 3.240

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  4 in total

Review 1.  CRISPR Modeling and Correction of Cardiovascular Disease.

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Journal:  Circ Res       Date:  2022-06-09       Impact factor: 23.213

2.  Ultrastructural Assessment and Proteomic Analysis in Myofibrillogenesis in the Heart Primordium After Heartbeat Initiation in Rats.

Authors:  Nobutoshi Ichise; Tatsuya Sato; Hiroyori Fusagawa; Hiroya Yamazaki; Taiki Kudo; Izaya Ogon; Noritsugu Tohse
Journal:  Front Physiol       Date:  2022-05-09       Impact factor: 4.755

3.  Integrated multi-omics analysis of adverse cardiac remodeling and metabolic inflexibility upon ErbB2 and ERRα deficiency.

Authors:  Catherine R Dufour; Hui Xia; Wafa B'chir; Marie-Claude Perry; Uros Kuzmanov; Anastasiia Gainullina; Kurt Dejgaard; Charlotte Scholtes; Carlo Ouellet; Dongmei Zuo; Virginie Sanguin-Gendreau; Christina Guluzian; Harvey W Smith; William J Muller; Etienne Audet-Walsh; Alexey A Sergushichev; Andrew Emili; Vincent Giguère
Journal:  Commun Biol       Date:  2022-09-12

4.  Subcellular Remodeling in Filamin C Deficient Mouse Hearts Impairs Myocyte Tension Development during Progression of Dilated Cardiomyopathy.

Authors:  Joseph D Powers; Natalie J Kirkland; Canzhao Liu; Swithin S Razu; Xi Fang; Adam J Engler; Ju Chen; Andrew D McCulloch
Journal:  Int J Mol Sci       Date:  2022-01-14       Impact factor: 6.208

  4 in total

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