Douglas C Wallace


Ontology type: schema:Person     


Person Info

NAME

Douglas C

SURNAME

Wallace

Publications in SciGraph latest 50 shown

  • 2018-10-29 Mitochondrial genetic medicine in NATURE GENETICS
  • 2017 Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease in PHARMACOLOGY OF MITOCHONDRIA
  • 2016-12 Cristae remodeling causes acidification detected by integrated graphene sensor during mitochondrial outer membrane permeabilization in SCIENTIFIC REPORTS
  • 2016-07-06 Genetics: Mitochondrial DNA in evolution and disease in NATURE
  • 2015-12 Trans-mitochondrial coordination of cristae at regulated membrane junctions in NATURE COMMUNICATIONS
  • 2015-12 Corrigendum: Landscape of the mitochondrial Hsp90 metabolome in tumours in NATURE COMMUNICATIONS
  • 2015-10 Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia in JOURNAL OF GENETIC COUNSELING
  • 2015 Fluorescence Analysis of Single Mitochondria with Nanofluidic Channels in MITOCHONDRIAL MEDICINE
  • 2013-12 Landscape of the mitochondrial Hsp90 metabolome in tumours in NATURE COMMUNICATIONS
  • 2013-02 Mitochondrial genome instability resulting from SUV3 haploinsufficiency leads to tumorigenesis and shortened lifespan in ONCOGENE
  • 2012-12 Comparison of male chimeric mice generated from microinjection of JM8.N4 embryonic stem cells into C57BL/6J and C57BL/6NTac blastocysts in TRANSGENIC RESEARCH
  • 2012-10 Mitochondria and cancer in NATURE REVIEWS CANCER
  • 2011-06 Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss in NATURE GENETICS
  • 2011-02 Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-05 Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-04 Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster in NATURE GENETICS
  • 2007-03-20 Drosophila aconitase activity and reactivation in PROTOCOL EXCHANGE
  • 2007-03-20 Mitochondrial respiration measurement in PROTOCOL EXCHANGE
  • 2007-01 Elevated male European and female African contributions to the genomes of African American individuals in HUMAN GENETICS
  • 2006-11 Detection of Low Levels of the Mitochondrial tRNALeu(UUR) 3243A>G Mutation in Blood Derived from Patients with Diabetes in MOLECULAR DIAGNOSIS & THERAPY
  • 2006-08 Mitochondrial mutations in cancer in ONCOGENE
  • 2006-08 Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2006-01 Spectrum of pathogenic mtDNA mutations in Leber’s hereditary optic neuropathy families from Siberia in RUSSIAN JOURNAL OF GENETICS
  • 2005-04 Adeno-associated virus-mediated gene transfer of the heart/muscle adenine nucleotide translocator (ANT) in mouse in GENE THERAPY
  • 2004-12 TGF-β1 induction of the adenine nucleotide translocator 1 in astrocytes occurs through Smads and Sp1 transcription factors in BMC NEUROSCIENCE
  • 2004-01 The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore in NATURE
  • 2002-11 Mitochondrial DNA Variation in the Kets and Nganasans and Its Implications for the Initial Peopling of Northern Eurasia in RUSSIAN JOURNAL OF GENETICS
  • 2002-07-23 PNA-Mediated PCR Clamping: Applications and Methods in PEPTIDE NUCLEIC ACIDS
  • 2002-04-02 Animal Models for Mitochondrial Disease in MITOCHONDRIAL DNA
  • 2002-02 The Mitochondrial Genome and Human Mitochondrial Diseases in RUSSIAN JOURNAL OF GENETICS
  • 2002-02 The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J in HUMAN GENETICS
  • 2001-07 Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families in HUMAN GENETICS
  • 1999-04 Transfer of chloramphenicol‐resistant mitochondrial DNA into the chimeric mouse in TRANSGENIC RESEARCH
  • 1999 Aging and Degenerative Diseases in FRONTIERS OF CELLULAR BIOENERGETICS
  • 1998-06 Radicals r'aging in NATURE GENETICS
  • 1998-02 A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase in NATURE GENETICS
  • 1997-09 Y chromosome polymorphisms in Native American and Siberian populations: identification of Native American Y chromosome haplotypes in HUMAN GENETICS
  • 1997-07 A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator in NATURE GENETICS
  • 1996-01 Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells in SOMATIC CELL AND MOLECULAR GENETICS
  • 1995-12 Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase in NATURE GENETICS
  • 1995-04 Renal amino acid transport in adults with oxidative phosphorylation diseases in KIDNEY INTERNATIONAL
  • 1994-08 Mitochondrial diabetes revisited in NATURE GENETICS
  • 1994-06 Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance in JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
  • 1994-06 Mitochondrial DNA mutations in diseases of energy metabolism in JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
  • 1994-06 Molecular basis of mitochondrial DNA disease in JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
  • 1992-12 Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age in NATURE GENETICS
  • 1992-07 Diseases resulting from mitochondrial DNA point mutations in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1992-04 Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion in NATURE GENETICS
  • 1991-12 The structure of human mitochondrial DNA variation in JOURNAL OF MOLECULAR EVOLUTION
  • 1990-11 Mitochondrial DNA Mutations Associated with Neuromuscular Diseases: Analysis and Diagnosis Using the Polymerase Chain Reaction in PEDIATRIC RESEARCH
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