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。Mitochondrial Metabolism in Aging Heart
Edward J. Lesnefsky et al.
CIRCULATION RESEARCH (2016)
On the origin of 3-methylglutaconic acid in disorders of mitochondrial energy metabolism
Nikita Ikon et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2016)
Cardiolipin remodeling: a regulatory hub for modulating cardiolipin metabolism and function
Cunqi Ye et al.
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2016)
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)
Metabolic annotation of 2-ethylhydracrylic acid
Robert O. Ryan
CLINICA CHIMICA ACTA (2015)
Left ventricular non-compaction cardiomyopathy
Jeffrey A. Towbin et al.
LANCET (2015)
The Role of Cardiolipin in Cardiovascular Health
Zheni Shen et al.
BIOMED RESEARCH INTERNATIONAL (2015)
Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome
Yan Huang et al.
PLOS ONE (2015)
Metabolic biology of 3-methylglutaconic acid-uria: a new perspective
Betty Su et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2014)
Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies
Gang Wang et al.
NATURE MEDICINE (2014)
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)
Seven functional classes of Barth syndrome mutation
Kevin Whited et al.
HUMAN MOLECULAR GENETICS (2013)
Cardiolipin-dependent Reconstitution of Respiratory Supercomplexes from Purified Saccharomyces cerevisiae Complexes III and IV
Soledad Bazan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Dysfunctional cardiac mitochondrial bioenergetic, lipidomic, and signaling in a murine model of Barth syndrome
Michael A. Kiebish et al.
JOURNAL OF LIPID RESEARCH (2013)
Barth syndrome
Sarah L. N. Clarke et al.
ORPHANET JOURNAL OF RARE DISEASES (2013)
Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle
Diti Ronvelia et al.
MOLECULAR GENETICS AND METABOLISM (2012)
The physical state of lipid substrates provides transacylation specificity for tafazzin
Michael Schlame et al.
NATURE CHEMICAL BIOLOGY (2012)
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)
Cardiac and Skeletal Muscle Defects in a Mouse Model of Human Barth Syndrome
Devrim Acehan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
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)
Specific metabolic rates of major organs and tissues across adulthood evaluation by mechanistic model of resting energy expenditure
ZiMian Wang et al.
AMERICAN JOURNAL OF CLINICAL NUTRITION (2010)
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)
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)
Identification of the Human Mitochondrial Linoleoyl-coenzyme A Monolysocardiolipin Acyltransferase (MLCL AT-1)
William A. Taylor et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria
Devrim Acehan et al.
MITOCHONDRION (2009)
Cardiolipin, the heart of mitochondrial metabolism
R. H. Houtkooper et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2008)
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)
Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography
Devrim Acehan et al.
LABORATORY INVESTIGATION (2007)
Role of cardiolipin alterations in mitochondrial dysfunction and disease
Adam J. Chicco et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)
The enzymatic function of tafazzin
Yang Xu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients
Matthew McKenzie et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
A Drosophila model of Barth syndrome
Yang Xu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Cardiac and clinical phenotype in Barth syndrome
Carolyn T. Spencer et al.
PEDIATRICS (2006)
A zebrafish model of human Barth syndrome reveals the essential role of tafazzin in cardiac development and function
Zaza Khuchua et al.
CIRCULATION RESEARCH (2006)
The thiolase superfamily: condensing enzymes with diverse reaction specificities
AM Haapalainen et al.
TRENDS IN BIOCHEMICAL SCIENCES (2006)
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)
Characterization of lymphoblast mitochondria from patients with Barth syndrome
Y Xu et al.
LABORATORY INVESTIGATION (2005)
Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis
F Valianpour et al.
JOURNAL OF LIPID RESEARCH (2005)
2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency:: Application to diagnosis and implications for the R-pathway of isoleucine oxidation
SH Korman et al.
CLINICAL CHEMISTRY (2005)
A novel cardiolipin-remodeling pathway revealed by a gene encoding an endoplasmic reticulum-associated acyl-CoA:lysocardiolipin acyltransferase (ALCAT1) in mouse
JS Cao et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome
ZM Gu et al.
MOLECULAR MICROBIOLOGY (2004)
Remodeling of cardiolipin by phospholipid transacylation
Y Xu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle
JJ Bissler et al.
LABORATORY INVESTIGATION (2002)
Metabolic cardiomyopathies
B Guertl et al.
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY (2000)
Predicting heart growth during puberty: The muscatine study
KF Janz et al.
PEDIATRICS (2000)