Related references
Note: Only part of the references are listed.Coenzyme Q biosynthesis in health and disease
Manuel Jesus Acosta et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2016)
Mitochondrial dysfunction in inherited renal disease and acute kidney injury
Francesco Emma et al.
NATURE REVIEWS NEPHROLOGY (2016)
Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure
Maria Andrea Desbats et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2015)
Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency
Maria Andrea Desbats et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2015)
Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis
Theresa P. T. Nguyen et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2014)
Coenzyme Q supplementation or over-expression of the yeast Coq8 putative kinase stabilizes multi-subunit Coq polypeptide complexes in yeast coq null mutants
Cuiwen H. He et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2014)
Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Qw deficiency
Mara Doimo et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2014)
Vitamin K2 Biosynthetic Enzyme, UBIAD1 Is Essential for Embryonic Development of Mice
Kimie Nakagawa et al.
PLOS ONE (2014)
Structural Insights into Ubiquinone Biosynthesis in Membranes
Wei Cheng et al.
SCIENCE (2014)
Structure of a Membrane-Embedded Prenyltransferase Homologous to UBIAD1
Hua Huang et al.
PLOS BIOLOGY (2014)
Ubiad1 Is an Antioxidant Enzyme that Regulates eNOS Activity by CoQ10 Synthesis
Vera Mugoni et al.
CELL (2013)
Simultaneous Sequencing of 24 Genes Associated with Steroid-Resistant Nephrotic Syndrome
Hugh J. McCarthy et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2013)
Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice
Catarina M. Quinzii et al.
FASEB JOURNAL (2013)
Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome
Darrell L. Dinwiddie et al.
GENOMICS (2013)
A novel mutation in COQ2 leading to fatal infantile multisystem disease
Bernadette S. Jakobs et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2013)
Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy
Jun Mitsui et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells
Marco Spinazzi et al.
NATURE PROTOCOLS (2012)
Effects of Inhibiting CoQ10 Biosynthesis with 4-nitrobenzoate in Human Fibroblasts
Catarina M. Quinzii et al.
PLOS ONE (2012)
Renal involvement in mitochondrial cytopathies
Francesco Emma et al.
PEDIATRIC NEPHROLOGY (2012)
Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant mice
Marni J. Falk et al.
EMBO MOLECULAR MEDICINE (2011)
Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency
Catarina M. Quinzii et al.
FASEB JOURNAL (2010)
Treatment of CoQ10 Deficient Fibroblasts with Ubiquinone, CoQ Analogs, and Vitamin C: Time- and Compound-Dependent Effects
Luis C. Lopez et al.
PLOS ONE (2010)
Antioxidant Probucol Attenuates Myocardial Oxidative Stress and Collagen Expressions in Post-Myocardial Infarction Rats
Shu-xian Zhou et al.
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY (2009)
LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability
Kai Stefan Dimmer et al.
HUMAN MOLECULAR GENETICS (2008)
COQ2 nephropathy:: A newly described inherited mitochondriopathy with primary renal involvement
Francesca Diomedi-Camassei et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)
Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis
Jose M. Lopez-Martin et al.
HUMAN MOLECULAR GENETICS (2007)
Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders
Julie Mollet et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Organelle isolation: functional mitochondria from mouse liver, muscle and cultured filroblasts
Christian Frezza et al.
NATURE PROTOCOLS (2007)
A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency
C Quinzii et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
The Saccharomyces cerevisiae COQ10 gene encodes a START domain protein required for function of coenzyme Q in respiration
MH Barros et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
hCOX18 and hCOX19:: Two human genes involved in cytochrome c oxidase assembly
S Sacconi et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
Metabolism and function of coenzyme Q
M Turunen et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2004)
Isolation and functional expression of human COQ2, a gene encoding a polyprenyl transferase involved in the synthesis of CoQ
M Forsgren et al.
BIOCHEMICAL JOURNAL (2004)
Ubiquinone biosynthesis in rat liver peroxisomes
M Tekle et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2002)
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency
A Rötig et al.
LANCET (2000)
Share Paper
