Related references
Note: Only part of the references are listed.Elevated glutamate and decreased glutamine levels in the cerebrospinal fluid of patients with MELAS syndrome
Maria Paz Guerrero-Molina et al.
JOURNAL OF NEUROLOGY (2022)
Identification of a novel m.3955G > A variant in MT-ND1 associated with Leigh syndrome
Manting Xu et al.
MITOCHONDRION (2022)
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutation
Stefania Evangelisti et al.
MOLECULAR GENETICS AND METABOLISM (2022)
Rewiring cell signalling pathways in pathogenic mtDNA mutations
Chih-Yao Chung et al.
TRENDS IN CELL BIOLOGY (2022)
Targeted A-to-G base editing in human mitochondrial DNA with programmable deaminases
Sung-Ik Cho et al.
CELL (2022)
CRISPR-free base editors with enhanced activity and expanded targeting scope in mitochondrial and nuclear DNA
Beverly Y. Mok et al.
NATURE BIOTECHNOLOGY (2022)
Mitochondrial base editor DdCBE causes substantial DNA off-target editing in nuclear genome of embryos
Yinghui Wei et al.
CELL DISCOVERY (2022)
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia
Chengxian Xu et al.
JCI INSIGHT (2022)
Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome
Marius Hippen et al.
NEUROLOGY-GENETICS (2022)
Mitochondrial ATP6 and ND3 genes are associated with type 2 diabetic peripheral neuropathy
Devi Kasinathan et al.
DIABETES & METABOLIC SYNDROME-CLINICAL RESEARCH & REVIEWS (2022)
Leber's hereditary optic neuropathy plus dystonia caused by the mitochondrial ND1 gene m.4160 T > C mutation
Hong Ren et al.
NEUROLOGICAL SCIENCES (2022)
Modeling of mitochondrial bioenergetics and autophagy impairment in MELAS-mutant iPSC-derived retinal pigment epithelial cells
Sujoy Bhattacharya et al.
STEM CELL RESEARCH & THERAPY (2022)
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy
Alberto Danese et al.
CELL REPORTS (2022)
A Primer Genetic Toolkit for Exploring Mitochondrial Biology and Disease Using Zebrafish
Ankit Sabharwal et al.
GENES (2022)
Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body Exposure
Sophie Belal et al.
BIOMEDICINES (2022)
The Role of Mitochondrial Mutations in Chronification of Inflammation: Hypothesis and Overview of Own Data
Alexander N. Orekhov et al.
LIFE-BASEL (2022)
Mitochondrial DNA CRISPR/CAS9 editing: An approach to establishing the role of mitochondrial mutations in atherogenesis
V.N. Sukhorukov et al.
ATHEROSCLEROSIS (2022)
Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation
Haruna Tani et al.
NUCLEIC ACIDS RESEARCH (2022)
A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism
Feilong Meng et al.
NUCLEIC ACIDS RESEARCH (2022)
Varied Responses to a High m.3243A>G Mutation Load and Respiratory Chain Dysfunction in Patient-Derived Cardiomyocytes
Sanna Ryytty et al.
CELLS (2022)
Enhanced mitochondrial DNA editing in mice using nuclear-exported TALE-linked deaminases and nucleases
Seonghyun Lee et al.
GENOME BIOLOGY (2022)
Current progress with mammalian models of mitochondrial DNA disease
James Bruce Stewart
JOURNAL OF INHERITED METABOLIC DISEASE (2021)
Quality control of the mitochondrial proteome
Jiyao Song et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2021)
Mitochondrial DNA copy number in human disease: the more the better?
Roberta Filograna et al.
FEBS LETTERS (2021)
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
Margherita Protasoni et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
Sanjiban Chakrabarty et al.
JOURNAL OF NEUROLOGY (2021)
Evaluating the Bioenergetics Health Index Ratio in Leigh Syndrome Fibroblasts to Understand Disease Severity
Ajibola B. Bakare et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
Structural basis for a complex I mutation that blocks pathological ROS production
Zhan Yin et al.
NATURE COMMUNICATIONS (2021)
Mitochondrial DNA editing in mice with DddA-TALE fusion deaminases
Hyunji Lee et al.
NATURE COMMUNICATIONS (2021)
Constitutive activation of the PI3K-Akt-mTORC1 pathway sustains the m.3243 A > G mtDNA mutation
Chih-Yao Chung et al.
NATURE COMMUNICATIONS (2021)
Precision modeling of mitochondrial disease in rats via DdCBE-mediated mtDNA editing
Xiaolong Qi et al.
CELL DISCOVERY (2021)
Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G > A mutation
Xiaolin Yu et al.
NEUROLOGICAL SCIENCES (2021)
Approach to edit mitochondrial DNA mutations associated with atherosclerosis
V.N. Sukhorukov et al.
ATHEROSCLEROSIS (2021)
Modelling Mitochondrial Disease in Human Pluripotent Stem Cells: What Have We Learned?
Cameron L. McKnight et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
Quantifying Mitochondrial Dynamics in Patient Fibroblasts with Multiple Developmental Defects and Mitochondrial Disorders
Ajibola B. Bakare et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
Clinical features, pathogenesis, and management of stroke-like episodes due to MELAS
Syuichi Tetsuka et al.
METABOLIC BRAIN DISEASE (2021)
A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome
Yoshihito Kishita et al.
SCIENTIFIC REPORTS (2021)
Leber Hereditary Optic Neuropathy: Review of Treatment and Management
Rabih Hage et al.
FRONTIERS IN NEUROLOGY (2021)
Precision modeling of mitochondrial diseases in zebrafish via DdCBE-mediated mtDNA base editing
Jiayin Guo et al.
CELL DISCOVERY (2021)
Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations
Nicolas Gutierrez Cortes et al.
HUMAN MOLECULAR GENETICS (2020)
The cell biology of mitochondrial membrane dynamics
Marta Giacomello et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2020)
Molecular basis of Leigh syndrome: a current look
Manuela Baldo Schubert et al.
ORPHANET JOURNAL OF RARE DISEASES (2020)
Mitochondrial TCA cycle metabolites control physiology and disease
Inmaculada Martinez-Reyes et al.
NATURE COMMUNICATIONS (2020)
Mitochondrial DNA mutations induce mitochondrial biogenesis and increase the tumorigenic potential of Hodgkin and Reed-Sternberg cells
Sophie Haumann et al.
CARCINOGENESIS (2020)
Mitochondrial transport mediates survival of retinal ganglion cells in affected LHON patients
Tien-Chun Yang et al.
HUMAN MOLECULAR GENETICS (2020)
Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons
Teresa Galera-Monge et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)
Testosterone increases apoptotic cell death and decreases mitophagy in Leber's hereditary optic neuropathy cells
Elona Jankauskaite et al.
JOURNAL OF APPLIED GENETICS (2020)
Novel MT-ND Gene Variants Causing Adult-Onset Mitochondrial Disease and Isolated Complex I Deficiency
Yi Shiau Ng et al.
FRONTIERS IN GENETICS (2020)
Possible Role of Mitochondrial DNA Mutations in Chronification of Inflammation: Focus on Atherosclerosis
Alexander N. Orekhov et al.
JOURNAL OF CLINICAL MEDICINE (2020)
Molecular Basis of the Pathogenic Mechanism Induced by the m.9191T>C Mutation in Mitochondrial ATP6Gene
Xin Su et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)
A Single Intravenous Injection of AAV-PHP.B-hNDUFS4 Ameliorates the Phenotype of Ndufs4(-/-) Mice
Pedro Silva-Pinheiro et al.
MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT (2020)
Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy
Yanchun Ji et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2020)
A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing
Beverly Y. Mok et al.
NATURE (2020)
Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors
Andrew V. Anzalone et al.
NATURE BIOTECHNOLOGY (2020)
Distal control of mitochondrial biogenesis and respiratory activity by extracellular lactate caused by large-scale deletion of mitochondrial DNA
Emi Ogasawara et al.
PHARMACOLOGICAL RESEARCH (2020)
A novel acceptor stem variant in mitochondrial tRNATyr impairs mitochondrial translation and is associated with a severe phenotype
Kimberly A. Kripps et al.
MOLECULAR GENETICS AND METABOLISM (2020)
Mitochondrial Nuclear Retrograde Regulator 1 (MNRR1) rescues the cellular phenotype of MELAS by inducing homeostatic mechanisms
Siddhesh Aras et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
Maternal transmission of mitochondrial diseases
Marcos R. Chiaratti et al.
GENETICS AND MOLECULAR BIOLOGY (2020)
Clinical and demographic features of chronic progressive external ophthalmoplegia in a large adult-onset cohort
Julia N. Heighton et al.
MITOCHONDRION (2019)
Mitochondrial dysfunction caused by m.2336T > C mutation with hypertrophic cardiomyopathy in cybrid cell lines
Dan Li et al.
MITOCHONDRION (2019)
Correlation between hepatic oxidative damage and clinical severity and mitochondrial gene sequencing results in biliary atresia
Junfeng Wang et al.
HEPATOLOGY RESEARCH (2019)
Knock-In Strategy for Editing Human and Zebrafish Mitochondrial DNA Using Mito-CRISPR/Cas9 System
Wan-Ping Bian et al.
ACS SYNTHETIC BIOLOGY (2019)
Mitochondrial DNA: Distribution, Mutations, and Elimination
Chaojun Yan et al.
CELLS (2019)
Glutamate Stimulation Dysregulates AMPA Receptors-Induced Signal Transduction Pathway in Leber's Inherited Optic Neuropathy Patient-Specific hiPSC-Derived Retinal Ganglion Cells
Yi-Ping Yang et al.
CELLS (2019)
Creation of Cybrid Cultures Containing mtDNA Mutations m.12315G>A and m.1555G>A, Associated with Atherosclerosis
Margarita A. Sazonova et al.
BIOMOLECULES (2019)
The Mitochondrial Genome-on Selective Constraints and Signatures at the Organism, Cell, and Single Mitochondrion Levels
Noam Shtolz et al.
FRONTIERS IN ECOLOGY AND EVOLUTION (2019)
Search-and-replace genome editing without double-strand breaks or donor DNA
Andrew V. Anzalone et al.
NATURE (2019)
Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy
Yanchun Ji et al.
HUMAN MOLECULAR GENETICS (2019)
A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis
Zidong Jia et al.
NUCLEIC ACIDS RESEARCH (2019)
Oxidative Insults and Mitochondrial DNA Mutation Promote Enhanced Autophagy and Mitophagy Compromising Cell Viability in Pluripotent Cell Model of Mitochondrial Disease
Dar-Shong Lin et al.
CELLS (2019)
A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function
Mi Zhou et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2018)
Molecular basis of diseases caused by the mtDNA mutation m.8969G > A in I the subunit a of ATP synthase
Natalia Skoczen et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2018)
SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype
C. Quadalti et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2018)
Mitophagy and Quality Control Mechanisms in Mitochondrial Maintenance
Sarah Pickles et al.
CURRENT BIOLOGY (2018)
Assembly of mammalian oxidative phosphorylation complexes I-V and supercomplexes
Alba Signes et al.
MITOCHONDRIAL DISEASES (2018)
Bioactivity and gene expression profiles of hiPSC-generated retinal ganglion cells in MT-ND4 mutated Leber's hereditary optic neuropathy
You-Ren Wu et al.
EXPERIMENTAL CELL RESEARCH (2018)
Mitochondrial tRNALeu(UUR) C3275T, tRNAGln T4363C and tRNALys A8343G mutations may be associated with PCOS and metabolic syndrome
Yu Ding et al.
GENE (2018)
The multifaceted contributions of mitochondria to cellular metabolism
Jessica B. Spinelli et al.
NATURE CELL BIOLOGY (2018)
MERRF Classification: Implications for Diagnosis and Clinical Trials
Josef Finsterer et al.
PEDIATRIC NEUROLOGY (2018)
Assembly of the membrane domain of ATP synthase in human mitochondria
Jiuya He et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized
Payam A. Gammage et al.
TRENDS IN GENETICS (2018)
Linear mitochondrial DNA is rapidly degraded by components of the replication machinery
Viktoriya Peeva et al.
NATURE COMMUNICATIONS (2018)
MitoTALEN reduces mutant mtDNA load and restores tRNAAla levels in a mouse model of heteroplasmic mtDNA mutation
Sandra R. Bacman et al.
NATURE MEDICINE (2018)
Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo
Payam A. Gammage et al.
NATURE MEDICINE (2018)
Clinical, biochemical, and genetic analysis of the mitochondrial respiratory chain complex I deficiency
Yan-Yan Ma et al.
MEDICINE (2018)
Mitochondrial DNA mutation m.3243A > GHeterogeneous clinical picture for cardiologists (m.3243A > G: A phenotypic chameleon)
Katharina Niedermayr et al.
CONGENITAL HEART DISEASE (2018)
Mitochondrial Disease: Advances in Clinical Diagnosis, Management, Therapeutic Development, and Preventative Strategies
Colleen C. Muraresku et al.
CURRENT GENETIC MEDICINE REPORTS (2018)
Programmable base editing of A.T to G.C in genomic DNA without DNA cleavage
Nicole M. Gaudelli et al.
NATURE (2017)
Hypoxia treatment reverses neurodegenerative disease in a mouse model of Leigh syndrome
Michele Ferrari et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders
Carmen Lorenz et al.
CELL STEM CELL (2017)
Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy
Raymond C. B. Wong et al.
AGING-US (2017)
Mitochondrial fatty acid synthesis, fatty acids and mitochondrial physiology
Alexander J. Kastaniotis et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2017)
The Mitochondrial tRNALeu(UUR) A3302G Mutation may be Associated With Insulin Resistance in Woman With Polycystic Ovary Syndrome
Yu Ding et al.
REPRODUCTIVE SCIENCES (2016)
Maintenance and Expression of Mammalian Mitochondrial DNA
Claes M. Gustafsson et al.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 85 (2016)
Mitochondrial cytochrome c oxidase deficiency
Malgorzata Rak et al.
CLINICAL SCIENCE (2016)
NOVEL GENETIC AND NEUROPATHOLOGICAL INSIGHTS IN NEUROGENIC MUSCLE WEAKNESS, ATAXIA, AND RETINITIS PIGMENTOSA (NARP)
Kristl G. Claeys et al.
MUSCLE & NERVE (2016)
G7731A mutation in mouse mitochondrial tRNALYs regulates late-onset disorders in transmitochondrial mice
Akinori Shimizu et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2015)
Structure and function of mitochondrial membrane protein complexes
Werner Kuehlbrandt
BMC BIOLOGY (2015)
Genetic mosaic analysis of a deleterious mitochondrial DNA mutation in Drosophila reveals novel aspects of mitochondrial regulation and function
Zhe Chen et al.
MOLECULAR BIOLOGY OF THE CELL (2015)
Impaired respiratory function in MELAS-induced pluripotent stem cells with high heteroplasmy levels
Masaki Kodaira et al.
FEBS OPEN BIO (2015)
MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNALeu(UUR) gene
Masahide Goto et al.
BRAIN & DEVELOPMENT (2014)
A review of maternally inherited diabetes and deafness
Hui-Zhen Li et al.
FRONTIERS IN BIOSCIENCE-LANDMARK (2014)
An update on complex I assembly: the assembly of players
Rasika S. Vartak et al.
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2014)
Architecture of mammalian respiratory complex I
Kutti R. Vinothkumar et al.
NATURE (2014)
Distal weakness with respiratory insufficiency caused by the m.8344A > G MERRF mutation
Emma L. Blakely et al.
NEUROMUSCULAR DISORDERS (2014)
Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming
Martin Picard et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Mitochondrial genetics
Patrick Francis Chinnery et al.
BRITISH MEDICAL BULLETIN (2013)
Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs
Sandra R. Bacman et al.
NATURE MEDICINE (2013)
Mitochondrial DNA Genetics and the Heteroplasmy Conundrum in Evolution and Disease
Douglas C. Wallace et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2013)
Does Mitochondrial DNA Play a Role in Parkinson's Disease? A Review of Cybrid and Other Supportive Evidence
Russell H. Swerdlow
ANTIOXIDANTS & REDOX SIGNALING (2012)
Mitochondrial Stress Engages E2F1 Apoptotic Signaling to Cause Deafness
Nuno Raimundo et al.
CELL (2012)
Mitochondrial Mutations are Associated with Atherosclerotic Lesions in the Human Aorta
Igor A. Sobenin et al.
CLINICAL & DEVELOPMENTAL IMMUNOLOGY (2012)
Mitochondrial ATP synthase: architecture, function and pathology
An I. Jonckheere et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2012)
Human mitochondrial DNA: roles of inherited and somatic mutations
Eric A. Schon et al.
NATURE REVIEWS GENETICS (2012)
Specific mitochondrial DNA mutation in mice regulates diabetes and lymphoma development
Osamu Hashizume et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside
Rajeshwari D. Koilkonda et al.
JOURNAL OF OPHTHALMOLOGY (2011)
Succinate dehydrogenase - Assembly, regulation and role in human disease
Jared Rutter et al.
MITOCHONDRION (2010)
Mitochondrial protein import: from proteomics to functional mechanisms
Oliver Schmidt et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2010)
Mitochondrial tRNALeu(UUR) mutation m.3302A>G presenting as childhood-onset severe myopathy: threshold determination through segregation study
Diana Ballhausen et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2010)
Mitochondrial DNA Defects and Selective Extraocular Muscle Involvement in CPEO
Laura C. Greaves et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
Mitochondrial DNA G8363A mutation in the tRNALys gene: Clinical, biochemical and pathological study
Roberta Virgilio et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2009)
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome -: Evidence from 12 cases
Sara Shanske et al.
ARCHIVES OF NEUROLOGY (2008)
Mice with mitochondrial complex I deficiency develop a fatal encephalomyopathy
Shane E. Kruse et al.
CELL METABOLISM (2008)
Manipulating the metazoan mitochondrial genome with targeted restriction enzymesu
Hong Xu et al.
SCIENCE (2008)
Experimental strategies towards treating mitochondrial DNA disorders
Julie L. Gardner et al.
BIOSCIENCE REPORTS (2007)
Increased longevity and refractoriness to Ca2+-dependent neurodegeneration in Surf1 knockout mice
Carlotta Dell'Agnello et al.
HUMAN MOLECULAR GENETICS (2007)
Generation of trans-mitochondrial mice carrying homoplasmic mtDNAs with a missense mutation in a structural gene using ES cells
A Kasahara et al.
HUMAN MOLECULAR GENETICS (2006)
Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA Leu(UUR) gene
WM Hutchison et al.
ARCHIVES OF NEUROLOGY (2005)
Contrasting phenotypes in three patients with novel mutations in mitochondrial tRNA genes
R Anitori et al.
MOLECULAR GENETICS AND METABOLISM (2005)
Tissue dependent co-segregation of the novel pathogenic G12276A mitochondrial tRNALeu(CUN) mutation with the A185G D-loop polymorphism -: art. no. e124
G Zsurka et al.
JOURNAL OF MEDICAL GENETICS (2004)
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
M Chol et al.
JOURNAL OF MEDICAL GENETICS (2003)
Manipulating mitochondrial DNA heteroplasmy by a mitochondrially targeted restriction endonuclease
S Srivastava et al.
HUMAN MOLECULAR GENETICS (2001)
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation
MD Brown et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Mitochondria and calcium: from cell signalling to cell death
MR Duchen
JOURNAL OF PHYSIOLOGY-LONDON (2000)
Share Paper
