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Douglas Wallace

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Publications

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Vesa Jouni; Su Hailing; Watts Giles D; Krause Sabine; Walter Maggie C; Martin Barbara; Smith Charles; Wallace Douglas C; Kimonis Virginia E
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts.
Wallace Douglas C; Fan Weiwei
The pathophysiology of mitochondrial disease as modeled in the mouse.
Brandon Marty C; Wallace Douglas C; Baldi Pierre
Data structures and compression algorithms for genomic sequence data.

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All Publications

2009: Vesa Jouni; Su Hailing; Watts Giles D; Krause Sabine; Walter Maggie C; Martin Barbara; Smith Charles; Wallace Douglas C; Kimonis Virginia E
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts.
Neuromuscular disorders : NMD 2009;19(11):766-72.
2009: Wallace Douglas C; Fan Weiwei
The pathophysiology of mitochondrial disease as modeled in the mouse.
Genes & development 2009;23(15):1714-36.
2009: Brandon Marty C; Wallace Douglas C; Baldi Pierre
Data structures and compression algorithms for genomic sequence data.
Bioinformatics (Oxford, England) 2009;25(14):1731-8.
2009: Hendrickson Sher L; Kingsley Lawrence A; Ruiz-Pesini Eduardo; Poole Jason C; Jacobson Lisa P; Palella Frank J; Bream Jay H; Wallace Douglas C; O'Brien Stephen J
Mitochondrial DNA haplogroups influence lipoatrophy after highly active antiretroviral therapy.
Journal of acquired immune deficiency syndromes (1999) 2009;51(2):111-6.
2009: Udar Nitin; Atilano Shari R; Memarzadeh Masood; Boyer David S; Chwa Marilyn; Lu Stephanie; Maguen Barak; Langberg Jonathan; Coskun Pinar; Wallace Douglas C; Nesburn Anthony B; Khatibi Nikan; Hertzog Dieter; Le Khoi; Hwang Daniel; Kenney M Cristina
Mitochondrial DNA haplogroups associated with age-related macular degeneration.
Investigative ophthalmology & visual science 2009;50(6):2966-74.
2009: Suissa Sarit; Wang Zhibo; Poole Jason; Wittkopp Sharine; Feder Jeanette; Shutt Timothy E; Wallace Douglas C; Shadel Gerald S; Mishmar Dan
Ancient mtDNA genetic variants modulate mtDNA transcription and replication.
PLoS genetics 2009;5(5):e1000474.
2009: Atilano Shari R; Chwa Marilyn; Kim Dae W; Jordan Nicole; Udar N; Coskun Pinar; Jester J V; Wallace Douglas C; Kenney M Cristina
Hydrogen peroxide causes mitochondrial DNA damage in corneal epithelial cells.
Cornea 2009;28(4):426-33.
2009: Lee Jaewon; Schriner Samuel E; Wallace Douglas C
Adenine nucleotide translocator 1 deficiency increases resistance of mouse brain and neurons to excitotoxic insults.
Biochimica et biophysica acta 2009;1787(5):364-70.
2009: Potluri Prasanth; Davila Antonio; Ruiz-Pesini Eduardo; Mishmar Dan; O'Hearn Sean; Hancock Saege; Simon Mariella; Scheffler Immo E; Wallace Douglas C; Procaccio Vincent
A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease.
Molecular genetics and metabolism 2009;96(4):189-95.
2009: Brandon Marty C; Ruiz-Pesini Eduardo; Mishmar Dan; Procaccio Vincent; Lott Marie T; Nguyen Kevin Cuong; Spolim Syawal; Patil Upen; Baldi Pierre; Wallace Douglas C
MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequences.
Human mutation 2009;30(1):1-6.
2009: Rollins Brandi; Martin Maureen V; Sequeira P Adolfo; Moon Emily A; Morgan Ling Z; Watson Stanley J; Schatzberg Alan; Akil Huda; Myers Richard M; Jones Edward G; Wallace Douglas C; Bunney William E; Vawter Marquis P
Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder.
PloS one 2009;4(3):e4913.
2009: Tang Sha; Le Phung Khanh; Tse Stephanie; Wallace Douglas C; Huang Taosheng
Heterozygous mutation of Opa1 in Drosophila shortens lifespan mediated through increased reactive oxygen species production.
PloS one 2009;4(2):e4492.
2008: Khusnutdinova Elza; Gilyazova Irina; Ruiz-Pesini Eduardo; Derbeneva Olga; Khusainova Rita; Khidiyatova Irina; Magzhanov Rim; Wallace Douglas C
A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease.
Annals of the New York Academy of Sciences 2008;1147():1-20.
2008: Hendrickson Sher L; Hutcheson Holli B; Ruiz-Pesini Eduardo; Poole Jason C; Lautenberger James; Sezgin Efe; Kingsley Lawrence; Goedert James J; Vlahov David; Donfield Sharyne; Wallace Douglas C; O'Brien Stephen J
Mitochondrial DNA haplogroups influence AIDS progression.
AIDS (London, England) 2008;22(18):2429-39.
2008: Khidr Lily; Wu Guikai; Davila Antonio; Procaccio Vincent; Wallace Douglas; Lee Wen-Hwa
Role of SUV3 helicase in maintaining mitochondrial homeostasis in human cells.
The Journal of biological chemistry 2008;283(40):27064-73.
2008: Subramaniam Vaidya; Golik Pawel; Murdock Deborah G; Levy Shawn; Kerstann Keith W; Coskun Pinar E; Melkonian Goarik A; Wallace Douglas C
MITOCHIP assessment of differential gene expression in the skeletal muscle of Ant1 knockout mice: coordinate regulation of OXPHOS, antioxidant, and apoptotic genes.
Biochimica et biophysica acta 2008;1777(7-8):666-75.
2008: Wallace Douglas C
Mitochondria as chi.
Genetics 2008;179(2):727-35.
2008: Volodko Natalia V; Starikovskaya Elena B; Mazunin Ilya O; Eltsov Nikolai P; Naidenko Polina V; Wallace Douglas C; Sukernik Rem I
Mitochondrial genome diversity in arctic Siberians, with particular reference to the evolutionary history of Beringia and Pleistocenic peopling of the Americas.
American journal of human genetics 2008;82(5):1084-100.
2008: Cornille Karen; Milea Dan; Amati-Bonneau Patrizia; Procaccio Vincent; Zazoun Lydie; Guillet Virginie; El Achouri Ghizlane; Delettre Cécile; Gueguen Naïg; Loiseau Dominique; Muller Agnès; Ferré Marc; Chevrollier Arnaud; Wallace Douglas C; Bonneau Dominique; Hamel Christian; Reynier Pascal; Lenaers Guy
Reversible optic neuropathy with OPA1 exon 5b mutation.
Annals of neurology 2008;63(5):667-71.
2008: Bannwarth S; Procaccio V; Rouzier C; Fragaki K; Poole J; Chabrol B; Desnuelle C; Pouget J; Azulay J P; Attarian S; Pellissier J F; Gargus J J; Abdenur J E; Mozaffar T; Calvas P; Labauge P; Pages M; Wallace D C; Lambert J C; Paquis-Flucklinger V
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy.
Mitochondrion 2008;8(2):136-45.
2008: Fan Weiwei; Waymire Katrina G; Narula Navneet; Li Peng; Rocher Christophe; Coskun Pinar E; Vannan Mani A; Narula Jagat; Macgregor Grant R; Wallace Douglas C
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.
Science (New York, N.Y.) 2008;319(5865):958-62.
2008: Yarosh Will; Monserrate Jessica; Tong James Jiayuan; Tse Stephanie; Le Phung Khanh; Nguyen Kimberly; Brachmann Carrie B; Wallace Douglas C; Huang Taosheng
The molecular mechanisms of OPA1-mediated optic atrophy in Drosophila model and prospects for antioxidant treatment.
PLoS genetics 2008;4(1):e6.
2007: Ortiz Gustavo A; Koch Sebastian; Wallace Douglas M; Lopez-Alberola Robert
Successful intravenous thrombolysis for acute stroke in a child.
Journal of child neurology 2007;22(6):749-52.
2007: Tong James Jiayuan; Schriner Samuel E; McCleary David; Day Brian J; Wallace Douglas C
Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster.
Nature genetics 2007;39(4):476-85.
2007: Ruiz-Pesini Eduardo; Lott Marie T; Procaccio Vincent; Poole Jason C; Brandon Marty C; Mishmar Dan; Yi Christina; Kreuziger James; Baldi Pierre; Wallace Douglas C
An enhanced MITOMAP with a global mtDNA mutational phylogeny.
Nucleic acids research 2007;35(Database issue):D823-8.
2007: Rodriguez-Iturbe Bernardo; Sepassi Lili; Quiroz Yasmir; Ni Zhenmin; Wallace Douglas C; Vaziri Nosratola D
Association of mitochondrial SOD deficiency with salt-sensitive hypertension and accelerated renal senescence.
Journal of applied physiology (Bethesda, Md. : 1985) 2007;102(1):255-60.
2007: Lind Joanne M; Hutcheson-Dilks Holli B; Williams Scott M; Moore Jason H; Essex Myron; Ruiz-Pesini Eduardo; Wallace Douglas C; Tishkoff Sarah A; O'Brien Stephen J; Smith Michael W
Elevated male European and female African contributions to the genomes of African American individuals.
Human genetics 2007;120(5):713-22.
2007: Wallace Douglas C
Why do we still have a maternally inherited mitochondrial DNA? Insights from evolutionary medicine.
Annual review of biochemistry 2007;76():781-821.
2006: Ruiz-Pesini Eduardo; Wallace Douglas C
Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA.
Human mutation 2006;27(11):1072-81.
2006: Brandon M; Baldi P; Wallace D C
Mitochondrial mutations in cancer.
Oncogene 2006;25(34):4647-62.
2006: Mishmar Dan; Ruiz-Pesini Eduardo; Mondragon-Palomino Mariana; Procaccio Vincent; Gaut Brandon; Wallace Douglas C
Adaptive selection of mitochondrial complex I subunits during primate radiation.
Gene 2006;378():11-8.
2006: Naïmi Mourad; Bannwarth Sylvie; Procaccio Vincent; Pouget Jean; Desnuelle Claude; Pellissier Jean-François; Rötig Agnes; Munnich Arnold; Calvas Patrick; Richelme Christian; Jonveaux Philippe; Castelnovo Giovanni; Simon Mariella; Clanet Michel; Wallace Douglas; Paquis-Flucklinger Véronique
Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay.
European journal of human genetics : EJHG 2006;14(8):917-22.
2006: Pedram Ali; Razandi Mahnaz; Wallace Douglas C; Levin Ellis R
Functional estrogen receptors in the mitochondria of breast cancer cells.
Molecular biology of the cell 2006;17(5):2125-37.
2006: Montiel-Sosa Francisco; Ruiz-Pesini Eduardo; Enríquez José Antonio; Marcuello Ana; Díez-Sánchez Carmen; Montoya Julio; Wallace Douglas C; López-Pérez Manuel José
Differences of sperm motility in mitochondrial DNA haplogroup U sublineages.
Gene 2006;368():21-7.
2006: Volod'ko N V; L'vova M A; Starikovskaia E B; Derbeneva O A; Bychkov I Iu; Mikhailovskaia I E; Pogozheva I V; Fedotov F F; Soyan G V; Procaccio V; Wallace D C; Sukernik R I
[Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia]
Genetika 2006;42(1):89-97.
2006: Procaccio Vincent; Neckelmann Nicolas; Paquis-Flucklinger Veronique; Bannwarth Sylvie; Jimenez Richard; Davila Antonio; Poole Jason C; Wallace Douglas C
Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.
Molecular diagnosis & therapy 2006;10(6):381-9.
2005: Crimi Marco; O'Hearn Sean F; Wallace Douglas C; Comi Giacomo P
Molecular research technologies in mitochondrial diseases: the microarray approach.
IUBMB life 2005;57(12):811-8.
2005: Loeb Lawrence A; Wallace Douglas C; Martin George M
The mitochondrial theory of aging and its relationship to reactive oxygen species damage and somatic mtDNA mutations.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(52):18769-70.
2005: Yin Hang; Stahl John S; Andrade Francisco H; McMullen Colleen A; Webb-Wood Sarah; Newman Nancy J; Biousse Valerie; Wallace Douglas C; Pardue Machelle T
Eliminating the Ant1 isoform produces a mouse with CPEO pathology but normal ocular motility.
Investigative ophthalmology & visual science 2005;46(12):4555-62.
2005: Wallace Douglas M; Ross Bruce H; Thomas Christine K
Motor unit behavior during clonus.
Journal of applied physiology (Bethesda, Md. : 1985) 2005;99(6):2166-72.
2005: Brand Martin D; Pakay Julian L; Ocloo Augustine; Kokoszka Jason; Wallace Douglas C; Brookes Paul S; Cornwall Emma J
The basal proton conductance of mitochondria depends on adenine nucleotide translocase content.
The Biochemical journal 2005;392(Pt 2):353-62.
2005: Wallace Douglas C
The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.
Gene 2005;354():169-80.
2005: Schriner Samuel E; Linford Nancy J; Martin George M; Treuting Piper; Ogburn Charles E; Emond Mary; Coskun Pinar E; Ladiges Warren; Wolf Norman; Van Remmen Holly; Wallace Douglas C; Rabinovitch Peter S
Extension of murine life span by overexpression of catalase targeted to mitochondria.
Science (New York, N.Y.) 2005;308(5730):1909-11.
2005: Atilano Shari R; Coskun Pinar; Chwa Marilyn; Jordan Nicole; Reddy Vinitha; Le Khoi; Wallace Douglas C; Kenney M Cristina
Accumulation of mitochondrial DNA damage in keratoconus corneas.
Investigative ophthalmology & visual science 2005;46(4):1256-63.
2005: Flierl A; Chen Y; Coskun P E; Samulski R J; Wallace D C
Adeno-associated virus-mediated gene transfer of the heart/muscle adenine nucleotide translocator (ANT) in mouse.
Gene therapy 2005;12(7):570-8.
2005: Petros John A; Baumann Amanda K; Ruiz-Pesini Eduardo; Amin Mahul B; Sun Carrie Qi; Hall John; Lim SoDug; Issa Muta M; Flanders W Dana; Hosseini Seyed H; Marshall Fray F; Wallace Douglas C
mtDNA mutations increase tumorigenicity in prostate cancer.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(3):719-24.
2005: Starikovskaya Elena B; Sukernik Rem I; Derbeneva Olga A; Volodko Natalia V; Ruiz-Pesini Eduardo; Torroni Antonio; Brown Michael D; Lott Marie T; Hosseini Seyed H; Huoponen Kirsi; Wallace Douglas C
Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups.
Annals of human genetics 2005;69(Pt 1):67-89.
2005: Brandon Marty C; Lott Marie T; Nguyen Kevin Cuong; Spolim Syawal; Navathe Shamkant B; Baldi Pierre; Wallace Douglas C
MITOMAP: a human mitochondrial genome database--2004 update.
Nucleic acids research 2005;33(Database issue):D611-3.
2005: Wallace D C
Mitochondria and cancer: Warburg addressed.
Cold Spring Harbor symposia on quantitative biology 2005;70():363-74.
2005: Wallace Douglas C
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine.
Annual review of genetics 2005;39():359-407.
2004: Vallance H D; Jeven G; Wallace D C; Brown M D
A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.
Pediatric cardiology 2004;25(5):538-40.
2004: Coskun Pinar E; Beal M Flint; Wallace Douglas C
Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(29):10726-31.
2004: Procaccio Vincent; Wallace Douglas C
Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations.
Neurology 2004;62(10):1899-901.
2004: Brown Michael D; Hosseini Seyed; Steiner Israel; Wallace Douglas C; Korn-Lubetzki Isabelle
Complete mitochondrial DNA sequence analysis in a family with early-onset dystonia and optic atrophy.
Movement disorders : official journal of the Movement Disorder Society 2004;19(2):235-7.
2004: Mishmar Dan; Ruiz-Pesini Eduardo; Brandon Martin; Wallace Douglas C
Mitochondrial DNA-like sequences in the nucleus (NUMTs): insights into our African origins and the mechanism of foreign DNA integration.
Human mutation 2004;23(2):125-33.
2004: Kokoszka Jason E; Waymire Katrina G; Levy Shawn E; Sligh James E; Cai Jiyang; Jones Dean P; MacGregor Grant R; Wallace Douglas C
The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore.
Nature 2004;427(6973):461-5.
2004: Law Alick K T; Gupta Deepak; Levy Shawn; Wallace Douglas C; McKeon Robert J; Buck Charles R
TGF-beta1 induction of the adenine nucleotide translocator 1 in astrocytes occurs through Smads and Sp1 transcription factors.
BMC neuroscience 2004;5():1.
2004: Ruiz-Pesini Eduardo; Mishmar Dan; Brandon Martin; Procaccio Vincent; Wallace Douglas C
Effects of purifying and adaptive selection on regional variation in human mtDNA.
Science (New York, N.Y.) 2004;303(5655):223-6.
2003: Gu Guangyu; Deutch Ariel Y; Franklin Jeff; Levy Shawn; Wallace Douglas C; Zhang Jing
Profiling genes related to mitochondrial function in mice treated with N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine.
Biochemical and biophysical research communications 2003;308(1):197-205.
2003: Buck Charles R; Jurynec Michael J; Gupta Deepak K; Law Alick K T; Bilger Johannes; Wallace Douglas C; McKeon Robert J
Increased adenine nucleotide translocator 1 in reactive astrocytes facilitates glutamate transport.
Experimental neurology 2003;181(2):149-58.
2003: Flierl A; Jackson C; Cottrell B; Murdock D; Seibel P; Wallace D C
Targeted delivery of DNA to the mitochondrial compartment via import sequence-conjugated peptide nucleic acid.
Molecular therapy : the journal of the American Society of Gene Therapy 2003;7(4):550-7.
2003: Coskun Pinar E; Ruiz-Pesini Eduardo; Wallace Douglas C
Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(5):2174-6.
2003: Mishmar Dan; Ruiz-Pesini Eduardo; Golik Pawel; Macaulay Vincent; Clark Andrew G; Hosseini Seyed; Brandon Martin; Easley Kirk; Chen Estella; Brown Michael D; Sukernik Rem I; Olckers Antonel; Wallace Douglas C
Natural selection shaped regional mtDNA variation in humans.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(1):171-6.
2003: Wallace D C; Ruiz-Pesini E; Mishmar D
mtDNA variation, climatic adaptation, degenerative diseases, and longevity.
Cold Spring Harbor symposia on quantitative biology 2003;68():479-86.
2002: Biousse Valérie; Pardue Machelle T; Wallace Douglas C; Newman Nancy J
The eyes of mito-mouse: mouse models of mitochondrial disease.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2002;22(4):279-85.
2002: Derbeneva O A; Starikovskaia E B; Volod'ko N V; Wallace D C; Sukernik R I
[Mitochondrial DNA variation in Kets and Nganasans and the early peoples of Northern Eurasia]
Genetika 2002;38(11):1554-60.
2002: Gearing Marla; Juncos Jorge L; Procaccio Vincent; Gutekunst Claire-Anne; Marino-Rodriguez Elaine M; Gyure Kymberly A; Ono Shoichiro; Santoianni Robert; Krawiecki Nicolas S; Wallace Douglas C; Wainer Bruce H
Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia.
Annals of neurology 2002;52(4):465-76.
2002: Derbeneva Olga A; Sukernik Rem I; Volodko Natalia V; Hosseini Seyed H; Lott Marie T; Wallace Douglas C
Analysis of mitochondrial DNA diversity in the aleuts of the commander islands and its implications for the genetic history of beringia.
American journal of human genetics 2002;71(2):415-21.
2002: Schurr Theodore G; Wallace Douglas C
Mitochondrial DNA diversity in Southeast Asian populations.
Human biology; an international record of research 2002;74(3):431-52.
2002: Cruciani Fulvio; Santolamazza Piero; Shen Peidong; Macaulay Vincent; Moral Pedro; Olckers Antonel; Modiano David; Holmes Susan; Destro-Bisol Giovanni; Coia Valentina; Wallace Douglas C; Oefner Peter J; Torroni Antonio; Cavalli-Sforza L Luca; Scozzari Rosaria; Underhill Peter A
A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes.
American journal of human genetics 2002;70(5):1197-214.
2002: Derbeneva Olga A; Starikovskaya Elena B; Wallace Douglas C; Sukernik Rem I
Traces of early Eurasians in the Mansi of northwest Siberia revealed by mitochondrial DNA analysis.
American journal of human genetics 2002;70(4):1009-14.
2002: Brown Michael D; Starikovskaya Elena; Derbeneva Olga; Hosseini Seyed; Allen Jon C; Mikhailovskaya Irina E; Sukernik Rem I; Wallace Douglas C
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
Human genetics 2002;110(2):130-8.
2002: Sukernik R I; Derbeneva O A; Starikovskaia E B; Volod'ko N V; Mikhailovskaia I E; Bychkov I Iu; Lott M; Brown M; Wallace D
[The mitochondrial genome and human mitochondrial diseases]
Genetika 2002;38(2):161-70.
2002: Sharer J Daniel; Shern Jack F; Van Valkenburgh Hillary; Wallace Douglas C; Kahn Richard A
ARL2 and BART enter mitochondria and bind the adenine nucleotide transporter.
Molecular biology of the cell 2002;13(1):71-83.
2002: Lell Jeffrey T; Sukernik Rem I; Starikovskaya Yelena B; Su Bing; Jin Li; Schurr Theodore G; Underhill Peter A; Wallace Douglas C
The dual origin and Siberian affinities of Native American Y chromosomes.
American journal of human genetics 2002;70(1):192-206.
2002: Murdock Deborah G; Wallace Douglas C
PNA-mediated PCR clamping. Applications and methods.
Methods in molecular biology (Clifton, N.J.) 2002;208():145-64.
2002: Wallace Douglas C
Animal models for mitochondrial disease.
Methods in molecular biology (Clifton, N.J.) 2002;197():3-54.
2001: Brown M D; Allen J C; Van Stavern G P; Newman N J; Wallace D C
Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
American journal of medical genetics 2001;104(4):331-8.
2001: Jessie B C; Sun C Q; Irons H R; Marshall F F; Wallace D C; Petros J A
Accumulation of mitochondrial DNA deletions in the malignant prostate of patients of different ages.
Experimental gerontology 2001;37(1):169-74.
2001: Melov S; Doctrow S R; Schneider J A; Haberson J; Patel M; Coskun P E; Huffman K; Wallace D C; Malfroy B
Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimetics.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2001;21(21):8348-53.
2001: Huoponen K; Schurr T G; Chen Y; Wallace D C
Mitochondrial DNA variation in an aboriginal Australian population: evidence for genetic isolation and regional differentiation.
Human immunology 2001;62(9):954-69.
2001: Sandbach J M; Coscun P E; Grossniklaus H E; Kokoszka J E; Newman N J; Wallace D C
Ocular pathology in mitochondrial superoxide dismutase (Sod2)-deficient mice.
Investigative ophthalmology & visual science 2001;42(10):2173-8.
2001: Brown M D; Zhadanov S; Allen J C; Hosseini S; Newman N J; Atamonov V V; Mikhailovskaya I E; Sukernik R I; Wallace D C
Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families.
Human genetics 2001;109(1):33-9.
2001: Ke Y; Su B; Song X; Lu D; Chen L; Li H; Qi C; Marzuki S; Deka R; Underhill P; Xiao C; Shriver M; Lell J; Wallace D; Wells R S; Seielstad M; Oefner P; Zhu D; Jin J; Huang W; Chakraborty R; Chen Z; Jin L
African origin of modern humans in East Asia: a tale of 12,000 Y chromosomes.
Science (New York, N.Y.) 2001;292(5519):1151-3.
2001: Kokoszka J E; Coskun P; Esposito L A; Wallace D C
Increased mitochondrial oxidative stress in the Sod2 (+/-) mouse results in the age-related decline of mitochondrial function culminating in increased apoptosis.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(5):2278-83.
2001: Wallace D C
Mouse models for mitochondrial disease.
American journal of medical genetics 2001;106(1):71-93.
2001: Wallace D C
Mitochondrial defects in neurodegenerative disease.
Mental retardation and developmental disabilities research reviews 2001;7(3):158-66.
2001: Wallace D C
A mitochondrial paradigm for degenerative diseases and ageing.
Novartis Foundation symposium 2001;235():247-63; discussion 263-6.
2000: Sligh J E; Levy S E; Waymire K G; Allard P; Dillehay D L; Nusinowitz S; Heckenlively J R; MacGregor G R; Wallace D C
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(26):14461-6.
2000: Lell J T; Wallace D C
The peopling of Europe from the maternal and paternal perspectives.
American journal of human genetics 2000;67(6):1376-81.
2000: Brown M D; Trounce I A; Jun A S; Allen J C; Wallace D C
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation.
The Journal of biological chemistry 2000;275(51):39831-6.
2000: Murdock D G; Christacos N C; Wallace D C
The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method.
Nucleic acids research 2000;28(21):4350-5.
2000: Melov S; Ravenscroft J; Malik S; Gill M S; Walker D W; Clayton P E; Wallace D C; Malfroy B; Doctrow S R; Lithgow G J
Extension of life-span with superoxide dismutase/catalase mimetics.
Science (New York, N.Y.) 2000;289(5484):1567-9.
2000: Cai J; Wallace D C; Zhivotovsky B; Jones D P
Separation of cytochrome c-dependent caspase activation from thiol-disulfide redox change in cells lacking mitochondrial DNA.
Free radical biology & medicine 2000;29(3-4):334-42.
2000: Levy S E; Chen Y S; Graham B H; Wallace D C
Expression and sequence analysis of the mouse adenine nucleotide translocase 1 and 2 genes.
Gene 2000;254(1-2):57-66.
2000: Saunders A M; Trowers M K; Shimkets R A; Blakemore S; Crowther D J; Mansfield T A; Wallace D M; Strittmatter W J; Roses A D
The role of apolipoprotein E in Alzheimer's disease: pharmacogenomic target selection.
Biochimica et biophysica acta 2000;1502(1):85-94.
2000: McMahon F J; Chen Y S; Patel S; Kokoszka J; Brown M D; Torroni A; DePaulo J R; Wallace D C
Mitochondrial DNA sequence diversity in bipolar affective disorder.
The American journal of psychiatry 2000;157(7):1058-64.
2000: Pettus E H; Betarbet R; Cottrell B; Wallace D C; Madyastha V; Greenamyre J T
Immunocytochemical characterization of the mitochondrially encoded ND1 subunit of complex I (NADH : ubiquinone oxidoreductase) in rat brain.
Journal of neurochemistry 2000;75(1):383-92.
2000: Trounce I; Schmiedel J; Yen H C; Hosseini S; Brown M D; Olson J J; Wallace D C
Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells.
Nucleic acids research 2000;28(10):2164-70.
2000: Chen Y S; Olckers A; Schurr T G; Kogelnik A M; Huoponen K; Wallace D C
mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations.
American journal of human genetics 2000;66(4):1362-83.
2000: Esposito L A; Kokoszka J E; Waymire K G; Cottrell B; MacGregor G R; Wallace D C
Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene.
Free radical biology & medicine 2000;28(5):754-66.
2000: Wallace D C
Mitochondrial defects in cardiomyopathy and neuromuscular disease.
American heart journal 2000;139(2 Pt 3):S70-85.
1999: Jiang S; Cai J; Wallace D C; Jones D P
Cytochrome c-mediated apoptosis in cells lacking mitochondrial DNA. Signaling pathway involving release and caspase 3 activation is conserved.
The Journal of biological chemistry 1999;274(42):29905-11.
1999: Melov S; Schneider J A; Coskun P E; Bennett D A; Wallace D C
Mitochondrial DNA rearrangements in aging human brain and in situ PCR of mtDNA.
Neurobiology of aging 1999;20(5):565-71.
1999: Wallace D C; Brown M D; Lott M T
Mitochondrial DNA variation in human evolution and disease.
Gene 1999;238(1):211-30.
1999: Scozzari R; Cruciani F; Santolamazza P; Malaspina P; Torroni A; Sellitto D; Arredi B; Destro-Bisol G; De Stefano G; Rickards O; Martinez-Labarga C; Modiano D; Biondi G; Moral P; Olckers A; Wallace D C; Novelletto A
Combined use of biallelic and microsatellite Y-chromosome polymorphisms to infer affinities among African populations.
American journal of human genetics 1999;65(3):829-46.
1999: Rekate H L; Nadkarni T D; Teaford P A; Wallace D
Brainstem dysfunction in chiari malformation presenting as profound hypoglycemia: presentation of four cases, review of the literature, and conjecture as to mechanism.
Neurosurgery 1999;45(2):386-91.
1999: Heddi A; Stepien G; Benke P J; Wallace D C
Coordinate induction of energy gene expression in tissues of mitochondrial disease patients.
The Journal of biological chemistry 1999;274(33):22968-76.
1999: Melov S; Coskun P E; Wallace D C
Mouse models of mitochondrial disease, oxidative stress, and senescence.
Mutation research 1999;434(3):233-42.
1999: Murdock D G; Boone B E; Esposito L A; Wallace D C
Up-regulation of nuclear and mitochondrial genes in the skeletal muscle of mice lacking the heart/muscle isoform of the adenine nucleotide translocator.
The Journal of biological chemistry 1999;274(20):14429-33.
1999: Levy S E; Waymire K G; Kim Y L; MacGregor G R; Wallace D C
Transfer of chloramphenicol-resistant mitochondrial DNA into the chimeric mouse.
Transgenic research 1999;8(2):137-45.
1999: Esposito L A; Melov S; Panov A; Cottrell B A; Wallace D C
Mitochondrial disease in mouse results in increased oxidative stress.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(9):4820-5.
1999: Wallace D C
Mitochondrial diseases in man and mouse.
Science (New York, N.Y.) 1999;283(5407):1482-8.
1999: Wallace D C; Murdock D G
Mitochondria and dystonia: the movement disorder connection?
Proceedings of the National Academy of Sciences of the United States of America 1999;96(5):1817-9.
1999: Melov S; Coskun P; Patel M; Tuinstra R; Cottrell B; Jun A S; Zastawny T H; Dizdaroglu M; Goodman S I; Huang T T; Miziorko H; Epstein C J; Wallace D C
Mitochondrial disease in superoxide dismutase 2 mutant mice.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(3):846-51.
1999: Schurr T G; Sukernik R I; Starikovskaya Y B; Wallace D C
Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic.
American journal of physical anthropology 1999;108(1):1-39.
1998: Brown M D; Hosseini S H; Torroni A; Bandelt H J; Allen J C; Schurr T G; Scozzari R; Cruciani F; Wallace D C
mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America?
American journal of human genetics 1998;63(6):1852-61.
1998: Starikovskaya Y B; Sukernik R I; Schurr T G; Kogelnik A M; Wallace D C
mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New World.
American journal of human genetics 1998;63(5):1473-91.
1998: Melov S; Schneider J A; Day B J; Hinerfeld D; Coskun P; Mirra S S; Crapo J D; Wallace D C
A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase.
Nature genetics 1998;18(2):159-63.
1998: Kogelnik A M; Lott M T; Brown M D; Navathe S B; Wallace D C
MITOMAP: a human mitochondrial genome database--1998 update.
Nucleic acids research 1998;26(1):112-5.
1998: Wallace D C; Brown M D; Melov S; Graham B; Lott M
Mitochondrial biology, degenerative diseases and aging.
BioFactors (Oxford, England) 1998;7(3):187-90.
1997: Wallace D C; Stugard C; Murdock D; Schurr T; Brown M D
Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(26):14900-5.
1997: Lell J T; Brown M D; Schurr T G; Sukernik R I; Starikovskaya Y B; Torroni A; Moore L G; Troup G M; Wallace D C
Y chromosome polymorphisms in native American and Siberian populations: identification of native American Y chromosome haplotypes.
Human genetics 1997;100(5-6):536-43.
1997: Biousse V; Brown M D; Newman N J; Allen J C; Rosenfeld J; Meola G; Wallace D C
De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy.
Neurology 1997;49(4):1136-8.
1997: Scozzari R; Cruciani F; Malaspina P; Santolamazza P; Ciminelli B M; Torroni A; Modiano D; Wallace D C; Kidd K K; Olckers A; Moral P; Terrenato L; Akar N; Qamar R; Mansoor A; Mehdi S Q; Meloni G; Vona G; Cole D E; Cai W; Novelletto A
Differential structuring of human populations for homologous X and Y microsatellite loci.
American journal of human genetics 1997;61(3):719-33.
1997: Wallace D C
Mitochondrial DNA in aging and disease.
Scientific American 1997;277(2):40-7.
1997: Pratt V M; Jackson C E; Wallace D C; Gurley D S; Feit A; Feldman G L
DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene.
American journal of human genetics 1997;61(1):231-3.
1997: Graham B H; Waymire K G; Cottrell B; Trounce I A; MacGregor G R; Wallace D C
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.
Nature genetics 1997;16(3):226-34.
1997: Melov S; Hinerfeld D; Esposito L; Wallace D C
Multi-organ characterization of mitochondrial genomic rearrangements in ad libitum and caloric restricted mice show striking somatic mitochondrial DNA rearrangements with age.
Nucleic acids research 1997;25(5):974-82.
1997: Brown M D; Sun F; Wallace D C
Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
American journal of human genetics 1997;60(2):381-7.
1997: Huoponen K; Torroni A; Wickman P R; Sellitto D; Gurley D S; Scozzari R; Wallace D C
Mitochondrial DNA and Y chromosome-specific polymorphisms in the Seminole Tribe of Florida.
European journal of human genetics : EJHG 1997;5(1):25-34.
1997: Kogelnik A M; Lott M T; Brown M D; Navathe S B; Wallace D C
MITOMAP: an update on the status of the human mitochondrial genome database.
Nucleic acids research 1997;25(1):196-9.
1996: Muth J; Williams P M; Williams S J; Brown M D; Wallace D C; Karger B L
Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy.
Electrophoresis 1996;17(12):1875-83.
1996: Torroni A; Huoponen K; Francalacci P; Petrozzi M; Morelli L; Scozzari R; Obinu D; Savontaus M L; Wallace D C
Classification of European mtDNAs from an analysis of three European populations.
Genetics 1996;144(4):1835-50.
1996: Heddi A; Faure-Vigny H; Wallace D C; Stepien G
Coordinate expression of nuclear and mitochondrial genes involved in energy production in carcinoma and oncocytoma.
Biochimica et biophysica acta 1996;1316(3):203-9.
1996: Torroni A; Carelli V; Petrozzi M; Terracina M; Barboni P; Malpassi P; Wallace D C; Scozzari R
Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.
American journal of human genetics 1996;59(1):248-52.
1996: Gebhart S S; Shoffner J M; Koontz D; Kaufman A; Wallace D
Insulin resistance associated with maternally inherited diabetes and deafness.
Metabolism: clinical and experimental 1996;45(4):526-31.
1996: Jun A S; Trounce I A; Brown M D; Shoffner J M; Wallace D C
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.
Molecular and cellular biology 1996;16(3):771-7.
1996: Horton T M; Petros J A; Heddi A; Shoffner J; Kaufman A E; Graham S D; Gramlich T; Wallace D C
Novel mitochondrial DNA deletion found in a renal cell carcinoma.
Genes, chromosomes & cancer 1996;15(2):95-101.
1996: Brown M D; Shoffner J M; Kim Y L; Jun A S; Graham B H; Cabell M F; Gurley D S; Wallace D C
Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients.
American journal of medical genetics 1996;61(3):283-9.
1996: Trounce I; Wallace D C
Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells.
Somatic cell and molecular genetics 1996;22(1):81-5.
1996: Kogelnik A M; Lott M T; Brown M D; Navathe S B; Wallace D C
MITOMAP: a human mitochondrial genome database.
Nucleic acids research 1996;24(1):177-9.
1996: Mili F; Flanders W D; Sherman S L; Go R C; Wallace D C
Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders.
Genetic epidemiology 1996;13(6):605-14.
1996: Trounce I A; Kim Y L; Jun A S; Wallace D C
Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines.
Methods in enzymology 1996;264():484-509.
1995: Li Y; Huang T T; Carlson E J; Melov S; Ursell P C; Olson J L; Noble L J; Yoshimura M P; Berger C; Chan P H; Wallace D C; Epstein C J
Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase.
Nature genetics 1995;11(4):376-81.
1995: Melov S; Shoffner J M; Kaufman A; Wallace D C
Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle.
Nucleic acids research 1995;23(20):4122-6.
1995: Horton T M; Graham B H; Corral-Debrinski M; Shoffner J M; Kaufman A E; Beal M F; Wallace D C
Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients.
Neurology 1995;45(10):1879-83.
1995: Wallace D C
1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging.
American journal of human genetics 1995;57(2):201-23.
1995: Chen Y S; Torroni A; Excoffier L; Santachiara-Benerecetti A S; Wallace D C
Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups.
American journal of human genetics 1995;57(1):133-49.
1995: Torroni A; Wallace D C
MtDNA haplogroups in Native Americans.
American journal of human genetics 1995;56(5):1234-8.
1995: Wallace D C; Shoffner J M; Trounce I; Brown M D; Ballinger S W; Corral-Debrinski M; Horton T; Jun A S; Lott M T
Mitochondrial DNA mutations in human degenerative diseases and aging.
Biochimica et biophysica acta 1995;1271(1):141-51.
1995: Shoffner J M; Voljavec A S; Dixon J; Kaufman A; Wallace D C; Mitch W E
Renal amino acid transport in adults with oxidative phosphorylation diseases.
Kidney international 1995;47(4):1101-7.
1995: Shoffner J M; Bialer M G; Pavlakis S G; Lott M; Kaufman A; Dixon J; Teichberg S; Wallace D C
Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene.
Neurology 1995;45(2):286-92.
1995: Newman N J; Torroni A; Brown M D; Lott M T; Wallace D C; Philen R; Roman G C
Cuban optic neuropathy.
Neurology 1995;45(2):397.
1995: Kim Y L; Brown M D; Wallace D C
Single-strand conformation polymorphism analysis for the detection of point mutations in the mitochondrial DNA.
Analytical biochemistry 1995;224(2):608-11.
1995: Brown M D; Torroni A; Reckord C L; Wallace D C
Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
Human mutation 1995;6(4):311-25.
1995: Deans Z; Dawson S J; Buttery L; Polak J M; Wallace D; Latchman D S
Direct evidence that the POU family transcription factor Oct-2 represses the cellular tyrosine hydroxylase gene in neuronal cells.
Journal of molecular neuroscience : MN 1995;6(3):159-67.
1995: Torroni A; Brown M D; Lott M T; Newman N J; Wallace D C
African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Cuba Neuropathy Field Investigation Team.
Human mutation 1995;5(4):310-7.
1995: Shoffner J M; Kaufman A; Koontz D; Krawiecki N; Smith E; Topp M; Wallace D C
Oxidative phosphorylation diseases and cerebellar ataxia.
Clinical neuroscience (New York, N.Y.) 1995;3(1):43-53.
1994: Torroni A; Lott M T; Cabell M F; Chen Y S; Lavergne L; Wallace D C
mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.
American journal of human genetics 1994;55(4):760-76.
1994: Wallace D C
Mitochondrial DNA sequence variation in human evolution and disease.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(19):8739-46.
1994: Corral-Debrinski M; Horton T; Lott M T; Shoffner J M; McKee A C; Beal M F; Graham B H; Wallace D C
Marked changes in mitochondrial DNA deletion levels in Alzheimer brains.
Genomics 1994;23(2):471-6.
1994: Trounce I; Neill S; Wallace D C
Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(18):8334-8.
1994: Newman N J; Torroni A; Brown M D; Lott M T; Fernandez M M; Wallace D C
Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team.
American journal of ophthalmology 1994;118(2):158-68.
1994: Brown M D; Torroni A; Huoponen K; Chen Y S; Lott M T; Wallace D C
Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.
American journal of human genetics 1994;55(2):410-2.
1994: Ballinger S W; Shoffner J M; Gebhart S; Koontz D A; Wallace D C
Mitochondrial diabetes revisited.
Nature genetics 1994;7(4):458-9.
1994: Brown M D; Wallace D C
Molecular basis of mitochondrial DNA disease.
Journal of bioenergetics and biomembranes 1994;26(3):273-89.
1994: Wallace D C
Mitochondrial DNA mutations in diseases of energy metabolism.
Journal of bioenergetics and biomembranes 1994;26(3):241-50.
1994: Jun A S; Brown M D; Wallace D C
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(13):6206-10.
1994: Torroni A; Wallace D C
Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance.
Journal of bioenergetics and biomembranes 1994;26(3):261-71.
1994: Heddi A; Lestienne P; Wallace D C; Stepien G
Steady state levels of mitochondrial and nuclear oxidative phosphorylation transcripts in Kearns-Sayre syndrome.
Biochimica et biophysica acta 1994;1226(2):206-12.
1994: Haraguchi Y; Chung A B; Neill S; Wallace D C
OXBOX and REBOX, overlapping promoter elements of the mitochondrial F0F1-ATP synthase beta subunit gene. OXBOX/REBOX in the ATPsyn beta promoter.
The Journal of biological chemistry 1994;269(12):9330-4.
1994: Torroni A; Chen Y S; Semino O; Santachiara-Beneceretti A S; Scott C R; Lott M T; Winter M; Wallace D C
mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico.
American journal of human genetics 1994;54(2):303-18.
1994: Torroni A; Neel J V; Barrantes R; Schurr T G; Wallace D C
Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(3):1158-62.
1994: Torroni A; Miller J A; Moore L G; Zamudio S; Zhuang J; Droma T; Wallace D C
Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude.
American journal of physical anthropology 1994;93(2):189-99.
1994: Wallace D C; Lott M T; Shoffner J M; Ballinger S
Mitochondrial DNA mutations in epilepsy and neurological disease.
Epilepsia 1994;35 Suppl 1():S43-50.
1994: Shoffner J M; Wallace D C
Oxidative phosphorylation diseases and mitochondrial DNA mutations: diagnosis and treatment.
Annual review of nutrition 1994;14():535-68.
1993: Ortiz R G; Newman N J; Shoffner J M; Kaufman A E; Koontz D A; Wallace D C
Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutation.
Archives of ophthalmology 1993;111(11):1525-30.
1993: Mecocci P; MacGarvey U; Kaufman A E; Koontz D; Shoffner J M; Wallace D C; Beal M F
Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain.
Annals of neurology 1993;34(4):609-16.
1993: Shoffner J M; Wallace D C
Oxidative phosphorylation diseases and stroke.
Heart disease and stroke : a journal for primary care physicians 1993;2(5):439-45.
1993: Torroni A; Sukernik R I; Schurr T G; Starikorskaya Y B; Cabell M F; Crawford M H; Comuzzie A G; Wallace D C
mtDNA variation of aboriginal Siberians reveals distinct genetic affinities with Native Americans.
American journal of human genetics 1993;53(3):591-608.
1993: Torroni A; Schurr T G; Cabell M F; Brown M D; Neel J V; Larsen M; Smith D G; Vullo C M; Wallace D C
Asian affinities and continental radiation of the four founding Native American mtDNAs.
American journal of human genetics 1993;53(3):563-90.
1993: Heddi A; Lestienne P; Wallace D C; Stepien G
Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP production.
The Journal of biological chemistry 1993;268(16):12156-63.
1993: Weiner N C; Newman N J; Lessell S; Johns D R; Lott M T; Wallace D C
Atypical Leber's hereditary optic neuropathy with molecular confirmation.
Archives of neurology 1993;50(5):470-3.
1993: Wallace D C
Mitochondrial diseases: genotype versus phenotype.
Trends in genetics : TIG 1993;9(4):128-33.
1992: Shoffner J M; Wallace D C
Mitochondrial genetics: principles and practice.
American journal of human genetics 1992;51(6):1179-86.
1992: Corral-Debrinski M; Horton T; Lott M T; Shoffner J M; Beal M F; Wallace D C
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age.
Nature genetics 1992;2(4):324-9.
1992: Chung A B; Stepien G; Haraguchi Y; Li K; Wallace D C
Transcriptional control of nuclear genes for the mitochondrial muscle ADP/ATP translocator and the ATP synthase beta subunit. Multiple factors interact with the OXBOX/REBOX promoter sequences.
The Journal of biological chemistry 1992;267(29):21154-61.
1992: Robinson B H; Petrova-Benedict R; Buncic J R; Wallace D C
Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.
Biochemical medicine and metabolic biology 1992;48(2):122-6.
1992: Corral-Debrinski M; Shoffner J M; Lott M T; Wallace D C
Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease.
Mutation research 1992;275(3-6):169-80.
1992: Brown M D; Torroni A; Shoffner J M; Wallace D C
Mitochondrial tRNA(Thr) mutations and lethal infantile mitochondrial myopathy.
American journal of human genetics 1992;51(2):446-7.
1992: Brown M D; Yang C C; Trounce I; Torroni A; Lott M T; Wallace D C
A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.
American journal of human genetics 1992;51(2):378-85.
1992: Wallace D C; Shoffner J M; Watts R L; Juncos J L; Torroni A
Mitochondrial oxidative phosphorylation defects in Parkinson's disease.
Annals of neurology 1992;32(1):113-4.
1992: Brown M D; Voljavec A S; Lott M T; MacDonald I; Wallace D C
Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 1992;6(10):2791-9.
1992: Stepien G; Torroni A; Chung A B; Hodge J A; Wallace D C
Differential expression of adenine nucleotide translocator isoforms in mammalian tissues and during muscle cell differentiation.
The Journal of biological chemistry 1992;267(21):14592-7.
1992: Shoffner J M; Wallace D C
Heart disease and mitochondrial DNA mutations.
Heart disease and stroke : a journal for primary care physicians 1992;1(4):235-41.
1992: Wallace D C; Torroni A
American Indian prehistory as written in the mitochondrial DNA: a review.
Human biology; an international record of research 1992;64(3):403-16.
1992: Ortiz R G; Newman N J; Manoukian S V; Diesenhouse M C; Lott M T; Wallace D C
Optic disk cupping and electrocardiographic abnormalities in an American pedigree with Leber's hereditary optic neuropathy.
American journal of ophthalmology 1992;113(5):561-6.
1992: Wallace D C
Mitochondrial genetics: a paradigm for aging and degenerative diseases?
Science (New York, N.Y.) 1992;256(5057):628-32.
1992: Rosenfeld J V; Wallace D; Klug G L; Danks A
Transnasal stereotactic biopsy of a clivus tumor. Technical note.
Journal of neurosurgery 1992;76(5):878-9.
1992: Ballinger S W; Shoffner J M; Hedaya E V; Trounce I; Polak M A; Koontz D A; Wallace D C
Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.
Nature genetics 1992;1(1):11-5.
1992: Wallace D M; Magnuson D J; Gray T S
Organization of amygdaloid projections to brainstem dopaminergic, noradrenergic, and adrenergic cell groups in the rat.
Brain research bulletin 1992;28(3):447-54.
1992: Weissman J D; Constantinitis I; Hudgins P; Wallace D C
31P magnetic resonance spectroscopy suggests impaired mitochondrial function in AZT-treated HIV-infected patients.
Neurology 1992;42(3 Pt 1):619-23.
1992: Stone E M; Newman N J; Miller N R; Johns D R; Lott M T; Wallace D C
Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.
Journal of clinical neuro-ophthalmology 1992;12(1):10-4.
1992: Brown M D; Voljavec A S; Lott M T; Torroni A; Yang C C; Wallace D C
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
Genetics 1992;130(1):163-73.
1992: Ballinger S W; Schurr T G; Torroni A; Gan Y Y; Hodge J A; Hassan K; Chen K H; Wallace D C
Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations.
Genetics 1992;130(1):139-52.
1992: Wallace D C; Lott M T; Shoffner J M; Brown M D
Diseases resulting from mitochondrial DNA point mutations.
Journal of inherited metabolic disease 1992;15(4):472-9.
1992: Wallace D C
Diseases of the mitochondrial DNA.
Annual review of biochemistry 1992;61():1175-212.
1991: Merriwether D A; Clark A G; Ballinger S W; Schurr T G; Soodyall H; Jenkins T; Sherry S T; Wallace D C
The structure of human mitochondrial DNA variation.
Journal of molecular evolution 1991;33(6):543-55.
1991: Corral-Debrinski M; Stepien G; Shoffner J M; Lott M T; Kanter K; Wallace D C
Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease.
JAMA : the journal of the American Medical Association 1991;266(13):1812-6.
1991: Shoffner J M; Watts R L; Juncos J L; Torroni A; Wallace D C
Mitochondrial oxidative phosphorylation defects in Parkinson's disease.
Annals of neurology 1991;30(3):332-9.
1991: Newman N J; Lott M T; Wallace D C
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
American journal of ophthalmology 1991;111(6):750-62.
1991: Wallace D C
Mitochondrial genes and neuromuscular disease.
Research publications - Association for Research in Nervous and Mental Disease 1991;69():101-20.
1991: Shoffner J M; Lott M T; Wallace D C
MERRF: a model disease for understanding the principles of mitochondrial genetics.
Revue neurologique 1991;147(6-7):431-5.
1990: Li K; Hodge J A; Wallace D C
OXBOX, a positive transcriptional element of the heart-skeletal muscle ADP/ATP translocator gene.
The Journal of biological chemistry 1990;265(33):20585-8.
1990: Torroni A; Stepien G; Hodge J A; Wallace D C
Neoplastic transformation is associated with coordinate induction of nuclear and cytoplasmic oxidative phosphorylation genes.
The Journal of biological chemistry 1990;265(33):20589-93.
1990: Wallace D C; Lott M T; Lezza A M; Seibel P; Voljavec A S; Shoffner J M
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction.
Pediatric research 1990;28(5):525-8.
1990: Zheng X X; Shoffner J M; Voljavec A S; Wallace D C
Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies.
Biochimica et biophysica acta 1990;1019(1):1-10.
1990: Newman N J; Wallace D C
Mitochondria and Leber's hereditary optic neuropathy.
American journal of ophthalmology 1990;109(6):726-30.
1990: Lott M T; Voljavec A S; Wallace D C
Variable genotype of Leber's hereditary optic neuropathy patients.
American journal of ophthalmology 1990;109(6):625-31.
1990: Shoffner J M; Lott M T; Lezza A M; Seibel P; Ballinger S W; Wallace D C
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
Cell 1990;61(6):931-7.
1990: Webster K A; Gunning P; Hardeman E; Wallace D C; Kedes L
Coordinate reciprocal trends in glycolytic and mitochondrial transcript accumulations during the in vitro differentiation of human myoblasts.
Journal of cellular physiology 1990;142(3):566-73.
1990: Schurr T G; Ballinger S W; Gan Y Y; Hodge J A; Merriwether D A; Lawrence D N; Knowler W C; Weiss K M; Wallace D C
Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages.
American journal of human genetics 1990;46(3):613-23.
1990: Shoffner J M; Wallace D C
Oxidative phosphorylation diseases. Disorders of two genomes.
Advances in human genetics 1990;19():267-330.
1990: Wallace D C
Report of the committee on human mitochondrial DNA.
Cytogenetics and cell genetics 1990;55(1-4):395-405.
1989: Shoffner J M; Lott M T; Voljavec A S; Soueidan S A; Costigan D A; Wallace D C
Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(20):7952-6.
1989: Zheng X; Shoffner J M; Lott M T; Voljavec A S; Krawiecki N S; Winn K; Wallace D C
Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV.
Neurology 1989;39(9):1203-9.
1989: Li K; Warner C K; Hodge J A; Minoshima S; Kudoh J; Fukuyama R; Maekawa M; Shimizu Y; Shimizu N; Wallace D C
A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressed.
The Journal of biological chemistry 1989;264(24):13998-4004.
1989: Singh G; Lott M T; Wallace D C
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.
The New England journal of medicine 1989;320(20):1300-5.
1989: Wallace D M; Magnuson D J; Gray T S
The amygdalo-brainstem pathway: selective innervation of dopaminergic, noradrenergic and adrenergic cells in the rat.
Neuroscience letters 1989;97(3):252-8.
1989: Wallace D C
Mitochondrial DNA mutations and neuromuscular disease.
Trends in genetics : TIG 1989;5(1):9-13.
1989: Wallace D C
Report of the committee on human mitochondrial DNA.
Cytogenetics and cell genetics 1989;51(1-4):612-21.
1988: Wallace D C; Singh G; Lott M T; Hodge J A; Schurr T G; Lezza A M; Elsas L J; Nikoskelainen E K
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
Science (New York, N.Y.) 1988;242(4884):1427-30.
1988: Wallace D C; Zheng X X; Lott M T; Shoffner J M; Hodge J A; Kelley R I; Epstein C M; Hopkins L C
Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease.
Cell 1988;55(4):601-10.
1988: Shuster R C; Rubenstein A J; Wallace D C
Mitochondrial DNA in anucleate human blood cells.
Biochemical and biophysical research communications 1988;155(3):1360-5.
1988: Santachiara Benerecetti A S; Scozzari R; Semino O; Torroni A; Brega A; Wallace D C
Mitochondrial DNA polymorphisms in Italy. II. Molecular analysis of new and rare morphs from Sardinia and Rome.
Annals of human genetics 1988;52(Pt 1):39-56.
1987: Neckelmann N; Li K; Wade R P; Shuster R; Wallace D C
cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(21):7580-4.
1987: Singh G; Neckelmann N; Wallace D C
Conformational mutations in human mitochondrial DNA.
Nature 1987;329(6136):270-2.
1987: Wallace D C
Maternal genes: mitochondrial diseases.
Birth defects original article series 1987;23(3):137-90.
1987: Wallace D C; Ye J H; Neckelmann S N; Singh G; Webster K A; Greenberg B D
Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations.
Current genetics 1987;12(2):81-90.
1986: Wallace D C
Mitochondrial genes and disease.
Hospital practice (Office ed.) 1986;21(10):77-87, 90-2.
1986: Brega A; Gardella R; Semino O; Morpurgo G; Astaldi Ricotti G B; Wallace D C; Santachiara Benerecetti A S
Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mitochondrial DNA.
American journal of human genetics 1986;39(4):502-12.
1986: Brega A; Scozzari R; Maccioni L; Iodice C; Wallace D C; Bianco I; Cao A; Santachiara Benerecetti A S
Mitochondrial DNA polymorphisms in Italy. I. Population data from Sardinia and Rome.
Annals of human genetics 1986;50(Pt 4):327-38.
1986: Novotny E J; Singh G; Wallace D C; Dorfman L J; Louis A; Sogg R L; Steinman L
Leber's disease and dystonia: a mitochondrial disease.
Neurology 1986;36(8):1053-60.
1986: Wallace D C; Yang J H; Ye J H; Lott M T; Oliver N A; McCarthy J
Computer prediction of peptide maps: assignment of polypeptides to human and mouse mitochondrial DNA genes by analysis of two-dimensional-proteolytic digest gels.
American journal of human genetics 1986;38(4):461-81.
1986: Bonné-Tamir B; Johnson M J; Natali A; Wallace D C; Cavalli-Sforza L L
Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level.
American journal of human genetics 1986;38(3):341-51.
1986: Wallace D C
Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance.
Somatic cell and molecular genetics 1986;12(1):41-9.
1985: Lott T J; Yang J H; Ye J H; Wallace D C
The use of microcomputers for the quantitation of light intensity patterns using digitized video signals.
Computer applications in the biosciences : CABIOS 1985;1(4):249-52.
1985: Wallace D C; Garrison K; Knowler W C
Dramatic founder effects in Amerindian mitochondrial DNAs.
American journal of physical anthropology 1985;68(2):149-55.
1985: Rosing H S; Hopkins L C; Wallace D C; Epstein C M; Weidenheim K
Maternally inherited mitochondrial myopathy and myoclonic epilepsy.
Annals of neurology 1985;17(3):228-37.
1984: Oliver N; McCarthy J; Wallace D C
Comparison of mitochondrially synthesized polypeptides of human, mouse, and monkey cell lines by a two-dimensional protease gel system.
Somatic cell and molecular genetics 1984;10(6):639-43.
1984: Yang J H; Ye J H; Wallace D C
Computer selection of oligonucleotide probes from amino acid sequences for use in gene library screening.
Nucleic acids research 1984;12(1 Pt 2):837-43.
1983: Oliver N A; Greenberg B D; Wallace D C
Assignment of a polymorphic polypeptide to the human mitochondrial DNA unidentified reading frame 3 gene by a new peptide mapping strategy.
The Journal of biological chemistry 1983;258(9):5834-9.
1983: Blanc H; Chen K H; D'Amore M A; Wallace D C
Amino acid change associated with the major polymorphic Hinc II site of Oriental and Caucasian mitochondrial DNAs.
American journal of human genetics 1983;35(2):167-76.
1983: Johnson M J; Wallace D C; Ferris S D; Rattazzi M C; Cavalli-Sforza L L
Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns.
Journal of molecular evolution 1983;19(3-4):255-71.
1982: Wallace D C
Structure and evolution of organelle genomes.
Microbiological reviews 1982;46(2):208-40.
1982: Webster K A; Oliver N A; Wallace D C
Assignment of an oligomycin-resistance locus to human chromosome 10.
Somatic cell genetics 1982;8(2):223-44.
1982: Oliver N A; Wallace D C
Assignment of two mitochondrially synthesized polypeptides to human mitochondrial DNA and their use in the study of intracellular mitochondrial interaction.
Molecular and cellular biology 1982;2(1):30-41.
1982: Wallace D C; Surti U; Adams C W; Szulman A E
Complete moles have paternal chromosomes but maternal mitochondrial DNA.
Human genetics 1982;61(2):145-7.
1981: Blanc H; Adams C W; Wallace D C
Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines.
Nucleic acids research 1981;9(21):5785-95.
1981: Denaro M; Blanc H; Johnson M J; Chen K H; Wilmsen E; Cavalli-Sforza L L; Wallace D C
Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA.
Proceedings of the National Academy of Sciences of the United States of America 1981;78(9):5768-72.
1981: Wallace D C
Assignment of the chloramphenicol resistance gene to mitochondrial deoxyribonucleic acid and analysis of its expression in cultured human cells.
Molecular and cellular biology 1981;1(8):697-710.
1981: Blanc H; Wright C T; Bibb M J; Wallace D C; Clayton D A
Mitochondrial DNA of chloramphenicol-resistant mouse cells contains a single nucleotide change in the region encoding the 3' end of the large ribosomal RNA.
Proceedings of the National Academy of Sciences of the United States of America 1981;78(6):3789-93.
1981: Case J T; Wallace D C
Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblasts.
Somatic cell genetics 1981;7(1):103-8.
1980: Giles R E; Blanc H; Cann H M; Wallace D C
Maternal inheritance of human mitochondrial DNA.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(11):6715-9.
1980: Giles R E; Stroynowski I; Wallace D C
Characterization of mitochondrial DNA in chloramphenicol-resistant interspecific hybrids and a cybrid.
Somatic cell genetics 1980;6(4):543-554.
1977: Wallace D C; Bunn C L; Eisenstadt J M
Mitotic segregation of cytoplasmic determinants for chloramphenicol resistance in mammalian cells II: Fusions with human cell lines.
Somatic cell genetics 1977;3(1):93-119.
1977: Bunn C L; Wallace D C; Eisenstadt J M
Mitotic segregation of cytoplasmic determinants for chloramphenicol resistance in mammalian cells. I: Fusion with mouse cell lines.
Somatic cell genetics 1977;3(1):71-92.
1976: Wallace D C; Pollack Y; Bunn C L; Eisenstadt J M
Cytoplasmic inheritance in mammalian tissue culture cells.
In vitro 1976;12(11):758-76.
1975: Wallace D C; Bunn C L; Eisenstadt J M
Cytoplasmic transfer of chloramphenicol resistance in human tissue culture cells.
The Journal of cell biology 1975;67(1):174-88.

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