4.2 Review

Barth Syndrome: Connecting Cardiolipin to Cardiomyopathy

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Cardiac & Cardiovascular Systems

Mitochondrial Metabolism in Aging Heart

Edward J. Lesnefsky et al.

CIRCULATION RESEARCH (2016)

Article Endocrinology & Metabolism

On the origin of 3-methylglutaconic acid in disorders of mitochondrial energy metabolism

Nikita Ikon et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2016)

Review Biophysics

Cardiolipin remodeling: a regulatory hub for modulating cardiolipin metabolism and function

Cunqi Ye et al.

JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2016)

Article Biochemistry & Molecular Biology

Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome

Gerard J. Gaspard et al.

CHEMISTRY AND PHYSICS OF LIPIDS (2015)

Review Medical Laboratory Technology

Metabolic annotation of 2-ethylhydracrylic acid

Robert O. Ryan

CLINICA CHIMICA ACTA (2015)

Article Medicine, General & Internal

Left ventricular non-compaction cardiomyopathy

Jeffrey A. Towbin et al.

LANCET (2015)

Review Biotechnology & Applied Microbiology

The Role of Cardiolipin in Cardiovascular Health

Zheni Shen et al.

BIOMED RESEARCH INTERNATIONAL (2015)

Article Multidisciplinary Sciences

Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome

Yan Huang et al.

PLOS ONE (2015)

Article Endocrinology & Metabolism

Metabolic biology of 3-methylglutaconic acid-uria: a new perspective

Betty Su et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2014)

Article Biochemistry & Molecular Biology

Barth syndrome: Cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation

Francois Gonzalvez et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2013)

Article Biochemistry & Molecular Biology

Seven functional classes of Barth syndrome mutation

Kevin Whited et al.

HUMAN MOLECULAR GENETICS (2013)

Article Biochemistry & Molecular Biology

Cardiolipin-dependent Reconstitution of Respiratory Supercomplexes from Purified Saccharomyces cerevisiae Complexes III and IV

Soledad Bazan et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2013)

Article Biochemistry & Molecular Biology

Dysfunctional cardiac mitochondrial bioenergetic, lipidomic, and signaling in a murine model of Barth syndrome

Michael A. Kiebish et al.

JOURNAL OF LIPID RESEARCH (2013)

Review Genetics & Heredity

Barth syndrome

Sarah L. N. Clarke et al.

ORPHANET JOURNAL OF RARE DISEASES (2013)

Article Biochemistry & Molecular Biology

The physical state of lipid substrates provides transacylation specificity for tafazzin

Michael Schlame et al.

NATURE CHEMICAL BIOLOGY (2012)

Article Cardiac & Cardiovascular Systems

Impaired cardiac reserve and severely diminished skeletal muscle O2 utilization mediate exercise intolerance in Barth syndrome

Carolyn T. Spencer et al.

AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2011)

Article Biochemistry & Molecular Biology

Cardiac and Skeletal Muscle Defects in a Mouse Model of Human Barth Syndrome

Devrim Acehan et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2011)

Article Multidisciplinary Sciences

Cardiolipin microdomains localize to negatively curved regions of Escherichia coli membranes

Lars D. Renner et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)

Article Biochemistry & Molecular Biology

Formation of molecular species of mitochondrial cardiolipin 2. A mathematical model of pattern formation by phospholipid transacylation

Michael Schlame

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2009)

Article Biochemistry & Molecular Biology

Formation of molecular species of mitochondrial cardiolipin. 1. A novel transacylation mechanism to shuttle fatty acids between sn-1 and sn-2 positions of multiple phospholipid species

Ashim Malhotra et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2009)

Article Biochemistry & Molecular Biology

Identification of the Human Mitochondrial Linoleoyl-coenzyme A Monolysocardiolipin Acyltransferase (MLCL AT-1)

William A. Taylor et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2009)

Review Biochemistry & Molecular Biology

Cardiolipin, the heart of mitochondrial metabolism

R. H. Houtkooper et al.

CELLULAR AND MOLECULAR LIFE SCIENCES (2008)

Article Cardiac & Cardiovascular Systems

Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse α-cardiac myosin in the laser trap assay

Edward P. Debold et al.

AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2007)

Review Cell Biology

Role of cardiolipin alterations in mitochondrial dysfunction and disease

Adam J. Chicco et al.

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)

Article Biochemistry & Molecular Biology

The enzymatic function of tafazzin

Yang Xu et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2006)

Article Biochemistry & Molecular Biology

Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients

Matthew McKenzie et al.

JOURNAL OF MOLECULAR BIOLOGY (2006)

Article Multidisciplinary Sciences

A Drosophila model of Barth syndrome

Yang Xu et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Pediatrics

Cardiac and clinical phenotype in Barth syndrome

Carolyn T. Spencer et al.

PEDIATRICS (2006)

Review Biochemistry & Molecular Biology

The thiolase superfamily: condensing enzymes with diverse reaction specificities

AM Haapalainen et al.

TRENDS IN BIOCHEMICAL SCIENCES (2006)

Article Biochemistry & Molecular Biology

Cardiolipin is essential for organization of complexes III and IV into a supercomplex in intact yeast mitochondria

M Zhang et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2005)

Article Medicine, Research & Experimental

Characterization of lymphoblast mitochondria from patients with Barth syndrome

Y Xu et al.

LABORATORY INVESTIGATION (2005)

Article Biochemistry & Molecular Biology

Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis

F Valianpour et al.

JOURNAL OF LIPID RESEARCH (2005)

Article Biochemistry & Molecular Biology

Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome

ZM Gu et al.

MOLECULAR MICROBIOLOGY (2004)

Article Biochemistry & Molecular Biology

Remodeling of cardiolipin by phospholipid transacylation

Y Xu et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2003)

Review Pathology

Metabolic cardiomyopathies

B Guertl et al.

INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY (2000)

Article Pediatrics

Predicting heart growth during puberty: The muscatine study

KF Janz et al.

PEDIATRICS (2000)