Eric A. Schon
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(Suggest an Edit or Addition)Eric A. Schon's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (2012) (2913)
- Mitochondrial respiratory-chain diseases. (2003) (1494)
- Human mitochondrial DNA: roles of inherited and somatic mutations (2012) (625)
- mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases. (1991) (594)
- Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene (1999) (565)
- A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA. (1989) (546)
- Mitochondrial disorders in the nervous system. (2008) (528)
- Mitochondria: The Next (Neurode)Generation (2011) (514)
- Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy (1991) (513)
- Upregulated function of mitochondria-associated ER membranes in Alzheimer disease (2012) (495)
- MELAS: Clinical features, biochemistry, and molecular genetics (1992) (481)
- Deletions of mitochondrial DNA in Kearns‐Sayre syndrome (1988) (450)
- Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. (1992) (433)
- Mitochondrial DNA Mutations and Pathogenesis (1997) (432)
- α-Synuclein Is Localized to Mitochondria-Associated ER Membranes (2014) (394)
- Neuronal degeneration and mitochondrial dysfunction. (2003) (348)
- Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients (2002) (347)
- Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondria. (2009) (331)
- Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA. (1990) (330)
- The kinase domain of mitochondrial PINK1 faces the cytoplasm (2008) (314)
- Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy. (1994) (306)
- Transthyretin: A choroid plexus‐specific transport protein in human brain The 1986 S. Weir Mitchell Award (1986) (305)
- The clinical maze of mitochondrial neurology (2013) (298)
- NAD+-Dependent Activation of Sirt1 Corrects the Phenotype in a Mouse Model of Mitochondrial Disease (2014) (294)
- The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle. (1992) (273)
- Mitochondrial encephalomyopathies. (1989) (268)
- Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus (2002) (265)
- In Vivo Correction of COX Deficiency by Activation of the AMPK/PGC-1α Axis (2011) (263)
- RNA-mediated gene duplication: the rat preproinsulin I gene is a functional retroposon (1985) (255)
- Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy (2002) (254)
- Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR. (1992) (245)
- Demonstration of transthyretin mRNA in the brain and other extrahepatic tissues in the rat. (1985) (233)
- Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA (1993) (231)
- Mitochondria-associated ER membranes in Alzheimer disease (2013) (231)
- Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot? (1993) (229)
- Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome. (1989) (218)
- Mitochondrial DNA genotypes in nuclear transfer-derived cloned sheep (1999) (213)
- Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA (1992) (208)
- Risk of developing a mitochondrial DNA deletion disorder (2004) (200)
- Mitochondrial DNA mutations in human disease. (2001) (181)
- Mitochondrial involvement in Alzheimer's disease. (1999) (178)
- Mitochondrial iron chelation ameliorates cigarette-smoke induced bronchitis and emphysema in mice (2015) (177)
- Mitochondrial genetics and disease. (2000) (173)
- Two direct repeats cause most human mtDNA deletions. (2004) (171)
- A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissues. (1989) (164)
- A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency (1999) (163)
- Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation (2008) (163)
- Mitochondrial abnormalities in temporal lobe of autistic brain (2013) (156)
- Rearranged mitochondrial genomes are present in human oocytes. (1995) (155)
- Mitochondria in neuromuscular disorders. (1998) (153)
- The retinal pigment epithelium is the unique site of transthyretin synthesis in the rat eye. (1990) (151)
- A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene (1995) (148)
- Increased localization of APP‐C99 in mitochondria‐associated ER membranes causes mitochondrial dysfunction in Alzheimer disease (2017) (147)
- Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibition. (2012) (145)
- Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cells (2004) (140)
- Cybrids in Alzheimer's disease: A cellular model of the disease? (1998) (138)
- A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease (2018) (135)
- Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis. (1990) (134)
- Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes. (1997) (133)
- Nonidentical distribution of transferrin and ferric iron in human brain (1988) (132)
- Conformation of promoter DNA: Fine mapping of S1-hypersensitive sites (1983) (131)
- Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection? (2000) (127)
- Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression. (2000) (127)
- Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243. (1994) (126)
- Evidence for the presence of 5S rRNA in mammalian mitochondria. (1998) (126)
- Pathogenesis of primary defects in mitochondrial ATP synthesis. (2001) (120)
- Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease. (2002) (120)
- Power, sex, suicide Mitochondria and the meaning of life (2006) (118)
- A mitochondrial tRNA anticodon swap associated with a muscle disease (1993) (113)
- Therapeutic prospects for mitochondrial disease. (2010) (112)
- S1-hypersensitive sites in eukaryotic promoter regions. (1984) (112)
- In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes (1995) (111)
- An algorithm based on graph theory for the assembly of contigs in physical mapping of DNA (1994) (108)
- A functionally dominant mitochondrial DNA mutation. (2008) (107)
- Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome (1991) (107)
- ApoE4 upregulates the activity of mitochondria‐associated ER membranes (2015) (101)
- Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defects (2009) (101)
- Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging. (1996) (99)
- Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome. (1989) (99)
- On the Pathogenesis of Alzheimer's Disease: The MAM Hypothesis (2017) (98)
- Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidase. (1987) (97)
- Crystal Structure of Human SCO1 (2005) (97)
- A T → C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndrome (1994) (97)
- Oligomycin Induces a Decrease in the Cellular Content of a Pathogenic Mutation in the Human Mitochondrial ATPase 6 Gene* (1999) (96)
- Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice. (2010) (94)
- Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines. (2000) (93)
- Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations. (2004) (90)
- A human SCO2 mutation helps define the role of Sco1p in the cytochrome oxidase assembly pathway. (2000) (90)
- Mitochondria-associated ER membranes and Alzheimer disease. (2016) (87)
- Hypocitrullinemia in patients with MELAS: an insight into the “MELAS paradox” (2005) (87)
- Differential diagnosis of fatal and benign cytochrome c oxidase‐deficient myopathies of infancy (1991) (85)
- Is Alzheimer's disease a disorder of mitochondria-associated membranes? (2010) (85)
- Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome. (2002) (83)
- Clinical syndromes associated with ragged red fibers. (1991) (79)
- The fate of human sperm-derived mtDNA in somatic cells. (1997) (77)
- Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging? (2006) (77)
- Widespread expression of amyloid beta-protein precursor gene in rat brain. (1989) (77)
- Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses (1998) (76)
- Structure and evolution of goat γ-, β C- and β A-globin genes: Three developmentally regulated genes contain inserted elements (1981) (75)
- Mitochondria, OxPhos, and neurodegeneration: cells are not just running out of gas. (2019) (75)
- Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutations. (2002) (75)
- Mitochondrial DNA and RNA processing in MELAS (1996) (74)
- Gene conversion of two functional goat alpha-globin genes preserves only minimal flanking sequences. (1982) (71)
- The mitochondrial tRNA(Leu)(UUR)) mutation in MELAS: a model for pathogenesis. (1992) (71)
- Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2. (2010) (71)
- Association of myopathy with large‐scale mitochondrial dna duplications and deletions: Which is pathogenic? (1997) (69)
- New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reporters. (2003) (68)
- Clinical manifestations of mitochondrial DNA depletion. (1998) (68)
- Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome (1991) (68)
- Low-dose rapamycin extends lifespan in a mouse model of mtDNA depletion syndrome (2017) (66)
- Cytochrome Oxidase Deficiency: Clinical and Biochemical Heterogeneity a (1986) (66)
- MFN2 mutations in Charcot–Marie–Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics (2019) (66)
- Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutase. (1987) (64)
- Transthyretin is synthesized in the mammalian eye. (1988) (62)
- A new role for α‐synuclein in Parkinson's disease: Alteration of ER–mitochondrial communication (2015) (62)
- An algal nucleus-encoded subunit of mitochondrial ATP synthase rescues a defect in the analogous human mitochondrial-encoded subunit. (2002) (61)
- Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effects (2002) (61)
- Clinical manifestations of mitochondria1 DNA depletion (1998) (60)
- Functional complementation of mitochondrial DNAs: mobilizing mitochondrial genetics against dysfunction. (2010) (60)
- Natural underlying mtDNA heteroplasmy as a potential source of intra‐person hiPSC variability (2016) (59)
- Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase. (1992) (59)
- Kearns–Sayre syndrome: oncocytic transformation of choroid plexus epithelium (2000) (58)
- Distribution of transthyretin in the rat eye. (1990) (57)
- Identification of a mutation in the mitochondrial tRNACys gene associated with mitochondrial encephalopathy (1996) (56)
- Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease. (1992) (55)
- The many clinical faces of cytochrome c oxidase deficiency. (2012) (54)
- Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR. (1996) (54)
- Tales from the crypt. (2003) (53)
- Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region (1991) (52)
- Sequence and linkage of the goat εI and εII β-globin genes* (1983) (52)
- Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene (1995) (51)
- Isolation of a cDNA encoding the B isozyme of human phosphoglycerate mutase (PGAM) and characterization of the PGAM gene family. (1988) (51)
- Germ-Line Therapy to Cure Mitochondrial Disease: Protocol and Ethics of In Vitro Ovum Nuclear Transplantation (1995) (50)
- Medicinal and genetic approaches to the treatment of mitochondrial disease. (2003) (48)
- Three-Dimensional Analysis of Mitochondrial Crista Ultrastructure in a Patient with Leigh Syndrome by In Situ Cryoelectron Tomography (2018) (48)
- Novel subcellular localization for α-synuclein: possible functional consequences (2015) (47)
- Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathy. (2000) (47)
- Mitochondrial DNA Mutations in Cancer (2005) (45)
- Congenital megaconial myopathy due to a novel defect in the choline kinase Beta gene. (2012) (45)
- SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency (2018) (42)
- Two related pseudogenes are the result of a gene duplication in the goat β-globin locus (1981) (42)
- Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS. (1993) (41)
- Molecular defects in cytochrome oxidase in mitochondrial diseases (1988) (41)
- Transthyretin (1986) (41)
- Mitochondrial encephalomyopathies: therapeutic approaches (2000) (41)
- Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidase. (1988) (40)
- Mitochondrial DNA and Diseases of the Nervous System: The Spectrum (1998) (39)
- Heavy breathing: energy conversion by mitochondrial respiratory supercomplexes. (2009) (39)
- Subunit Va of human and bovine cytochrome c oxidase is highly conserved. (1988) (39)
- Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNA (1992) (39)
- Sequence of a cDNA specifying subunit VIIa of human cytochrome c oxidase. (1989) (39)
- Phenotype–genotype correlations in skeletal muscle of patients with mtDNA deletions (1995) (38)
- Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation. (2002) (37)
- Mitochondrial Genetics and Disease (2014) (36)
- Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidase. (1992) (36)
- High proportions of mtDNA duplications in patients with Kearns-Sayre syndrome occur in the heart. (1997) (36)
- Retinol-binding protein is synthesized in the mammalian eye. (1988) (35)
- Structure of the gene encoding the muscle-specific subunit of human phosphoglycerate mutase. (1989) (33)
- Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356 (2016) (33)
- Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with sco2 mutations (2012) (32)
- High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathy (1995) (32)
- mechanisms of disease Mitochondrial Respiratory-Chain Diseases (2003) (32)
- Deletions of mitochondrial DNA in Kearns-Sayre syndrome (1998) (32)
- Efficient and specific amplification of identified partial duplications of human mitochondrial DNA by long PCR. (1996) (32)
- Transcription of the β-like globin genes and pseudogenes of the goat in a cell-free system (1981) (29)
- Sequence of a cDNA specifying subunit VIIc of human cytochrome c oxidase. (1990) (29)
- High-resolution YAC-cosmid-STS map of human chromosome 13. (1998) (26)
- The gene for human muscle-specific phosphoglycerate mutase, PGAM2, mapped to chromosome 7 by polymerase chain reaction. (1989) (25)
- A cDNA specifying the human amyloid beta precursor protein (ABPP) encodes a 95-kDa polypeptide. (1988) (24)
- Renal oncocytomas with rearrangements involving 11q13 contain breakpoints near CCND1. (2004) (24)
- ATP‐binding cassette transporters and sterol O‐acyltransferases interact at membrane microdomains to modulate sterol uptake and esterification (2015) (23)
- Biochemical and molecular aspects of cytochrome C oxidase deficiency. (1988) (22)
- Eliminating mitochondrial DNA from sperm. (2012) (22)
- Cytochrome oxidase deficiency: progress and problems (1994) (21)
- Mitochondria (2003) (20)
- Neurotrophin‐4 is up‐regulated in ragged‐red fibers associated with pathogenic mitochondrial DNA mutations (1998) (20)
- Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: A new approach to the study of mitochondrial myopathies (1991) (20)
- Differential expression of nuclear genes for cytochrome c oxidase during myogenesis (1990) (20)
- Immunocytochemical study of nebulin in Duchenne muscular dystrophy (1988) (19)
- Both heavy strand replication origins are active in partially duplicated human mitochondrial DNAs. (2001) (19)
- Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry? (1991) (18)
- Point mutations in the mitochondrial tRNA Lys gene: Implications for pathogenesis and mechanism (1997) (18)
- Paucity of deleted mitochondrial DNAs in brain regions of Huntington's disease patients. (1995) (18)
- Mitochondrial DNA and the genetics of mitochondrial disease (1994) (18)
- Cardiac deficiency of single cytochrome oxidase assembly factor scox induces p53-dependent apoptosis in a Drosophila cardiomyopathy model. (2015) (17)
- Identification by nucleotide sequence analysis of a goat pseudoglobin gene. (1980) (16)
- Mitophagy in cells with mtDNA mutations (2012) (16)
- Mitochondrial mutations: genotype to phenotype. (2007) (16)
- The mitochondrial respiratory chain and its disorders (2006) (15)
- The isolation of the beta A-, beta C-, and gamma-globin genes and a presumptive embryonic globin gene from a goat DNA recombinant library. (1980) (14)
- Mixing and matching mitochondrial aminoacyl synthetases and their tRNAs: a new way to treat respiratory chain disorders? (2014) (13)
- Rat LINE1: The origin and evolution of a family of long interspersed middle repetitive DNA elements (2005) (13)
- Mitochondrial encephalomyopathies: biochemical approach. (1991) (13)
- Loss of ROS—a radical response (1998) (13)
- Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegia (1997) (13)
- Replication of a heteroplasmic population of normal and partially-deleted human mitochondrial genomes (1995) (12)
- Mitochondrial single nucleotide polymorphism genotyping by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using cleavable biotinylated dideoxynucleotides. (2012) (12)
- Bacterial Conjugation in the Cytoplasm of Mouse Cells (2008) (12)
- Unexpected vascular enrichment of SCO1 over SCO2 in mammalian tissues: implications for human mitochondrial disease. (2010) (12)
- Structure and evolution of goat gamma-, beta C- and beta A-globin genes: three developmentally regulated genes contain inserted elements. (1981) (11)
- Alterations of Mitochondrial DNA in Liver Diseases (2015) (11)
- RNA-binding patterns in total human tissue proteins: analysis by northwestern blotting. (1993) (11)
- Nucleotide sequence of cDNA encoding subunit Va from rat heart cytochrome c oxidase. (1989) (10)
- Complements of the house. (2004) (10)
- Alzheimer Disease. (2017) (9)
- Isolation of a cDNA specifying subunit VIIb of human cytochrome c oxidase. (1993) (9)
- Sequence of a cDNA specifying subunit VIa of human cytochrome c oxidase. (1989) (8)
- The mitochondrial genome (2020) (8)
- Primary Disorders of Mitochondrial DNA and the Pathophysiology of mtDNA-Related Disorders (2002) (8)
- Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiency. (2004) (8)
- Identification of mutations in mtDNA from patients suffering mitochondrial diseases. (2002) (8)
- tRNA processing in human mitochondrial disorders (2004) (7)
- Nucleoid autonomy (2008) (7)
- Mitochondrial dysfunction as a mechanism of CNS injury (1991) (7)
- Chapter 3 Molecular Genetic Basis of the Mitochondrial Encephalomyopathies (2002) (6)
- No Evidence for Association of SCO2 Heterozygosity with High-Grade Myopia or Other Diseases with Possible Mitochondrial Dysfunction. (2016) (6)
- Appendix 5. Gene products present in mitochondria of yeast and animal cells. (2007) (6)
- Sequence and linkage of the goat epsilon I and epsilon II beta-globin genes. (1983) (5)
- IMPLICATIONS FOR REDOX SIGNALING BY A MITOCHONDRIAL CYTOCHROME c OXIDASE "ASSEMBLY" PROTEIN*□ S (2005) (5)
- Point mutations in the mitochondrial tRNALys gene: Implications for pathogenesis and mechanism (2004) (4)
- Congenital Megaconial Myopathy Due to a Novel Defect in the Choline Kinase beta (CHKB) Gene (P01.116) (2012) (4)
- Transcription of the beta-like globin genes and pseudogenes of the goat in a cell-free system. (1981) (4)
- Response to “Germ Line Therapy to Cure Mitochondrial Disease: Protocol and Ethics of In Vitro Ovum Nuclear Transplantation” by Donald S. Rubenstein, David C. Thomasma, Eric A. Schon, and Michael J. Zinaman (CQ Vol 4, No 3) (1999) (4)
- Deletions of mitochondrial DNA in Kearns‐Sayre syndrome (1988) (3)
- Mitochondrial disease: Replace or edit? (2021) (3)
- Deletions of mitochondrial DNA in Kearns-Sayre syndrome (2011) (3)
- Mitochondrial disorders in muscle. (1993) (3)
- Introduction: the birth of mitochondrial medicine (2006) (3)
- Drug Effects in Patients with Mitochondrial Diseases (2008) (3)
- A toolkit for the cell's powerhouse (2008) (2)
- Erratum: Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy (Human Molecular Genetics (1994) 3 (13-19)) (1994) (2)
- Appendix 4. Mitochondrial genetic codes in various organisms. (2007) (1)
- A calcium signalling defect in the pathogenesis of a mtDNA-inherited oxidative phosphorylation deficiency. (1999) (1)
- Nucleotide sequence of a cDNA for bovine cytochrome c oxidase subunit VIIc. (1989) (1)
- Mitochondrial Changes in Aging with Particular Reference to Muscle, and Possible Clinical Consequences (2011) (1)
- Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (1992) (1)
- Analysis of giant deletions of human mitochondrial DNA in progressive external ophthalmoplegia (1991) (1)
- Metabolic myopathies. (1986) (1)
- Isolation of cDNA Clones Encoding the M and B Subunits of Human Phosphoglycerate Mutase (1987) (1)
- Appendix 6. Changes in the mitochondrial transcriptome and proteome under various stresses and growth conditions. (2007) (1)
- Bioenergetics through thick and thin (2018) (1)
- [Molecular biology of mitochondrial myopathies]. (1991) (0)
- Molecular cloning of human phosphoglycerate mutase complementary dna (1985) (0)
- Mitochondrial myopathy associated with high levels of mitochondrial DNA harboring a 260 bp tandem duplication in the D-loop region (1994) (0)
- Phenotypical expression and molecular genetics of the nt-3243 mutation in the mitochondrial tRNA(LEU(UUR)) gene (1995) (0)
- 33 – Mitochondrial Disorders (2007) (0)
- Use of single strand conformation polymorphisms to detect point mutations in human mitochondrial dna (1991) (0)
- Erratum: SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency (Brain (2018) 141 (662-672) DOI: 10.1093/brain/awx369) (2018) (0)
- A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease (2018) (0)
- Developmental Cell Previews Eliminating Mitochondrial DNA from Sperm (2012) (0)
- Exploring the use of the bacterial conjugation system to deliver DNA to mitochondria (2004) (0)
- NEUROSCIENCE FOR NEUROLOGISTS Mitochondria (2003) (0)
- Nucleic Acids Research (2008) (0)
- Response to “Germ Line Therapy to Cure Mitochondrial Disease: Protocol and Ethics of In Vitro Ovum Nuclear Transplantation” by Donald S. Rubenstein, David C. Thomasma, Eric A. Schon, and Michael J. Zinaman (CQ Vol. 4, No. 3) (1999) (0)
- Three-dimensional analysis of mitochondrial crista ultrastructure in a Leigh Syndrome patient by in situ cryo-electron tomography (2018) (0)
- Oxidative Phosphorylation at the fin de siècle Matti Saraste (1999) (0)
- Novel diagnostic and treatment method for Alzheimer ' s disease Technology # 2312 (0)
- Rolf Luft, MD, PhD (1914-2007) (2007) (0)
- List of contributors. (2019) (0)
- Appendix 3. Linearized maps of circular mitochondrial genomes from representative organisms. (2007) (0)
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