about
Antimutator alleles of yeast DNA polymerase gamma modulate the balance between DNA synthesis and excisionLRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAsThe role of oxidative stress in Parkinson's diseaseDNA ligase III: a spotty presence in eukaryotes, but an essential function where testedConnecting the Dots: From DNA Damage and Repair to AgingReview: can diet influence the selective advantage of mitochondrial DNA haplotypes?The Role of Mitochondrial DNA in Mediating Alveolar Epithelial Cell Apoptosis and Pulmonary FibrosisOrganellar RNA editingMechanisms of chemotherapy-induced behavioral toxicitiesMitochondrial disorders: challenges in diagnosis & treatmentStructural basis for S-adenosylmethionine binding and methyltransferase activity by mitochondrial transcription factor B1An Overview of Genetic Changes and Risk of Pancreatic Ductal AdenocarcinomaThe Red Queen in mitochondria: cyto-nuclear co-evolution, hybrid breakdown and human diseaseProtein instability and functional defects caused by mutations of dihydro-orotate dehydrogenase in Miller syndrome patientsDihydro-orotate dehydrogenase is physically associated with the respiratory complex and its loss leads to mitochondrial dysfunctionAlkyladenine DNA glycosylase (AAG) localizes to mitochondria and interacts with mitochondrial single-stranded binding protein (mtSSB)Toward a mtDNA locus-specific mutation database using the LOVD platformPathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathy.A novel m.7539C>T point mutation in the mt-tRNA(Asp) gene associated with multisystemic mitochondrial disease.The elusive nature of adaptive mitochondrial DNA evolution of an arctic lineage prone to frequent introgression.Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.Disease-associated mitochondrial mutations and the evolution of primate mitogenomes.DNA damage related crosstalk between the nucleus and mitochondria.Mitochondrial Transfer from Wharton's Jelly Mesenchymal Stem Cell to MERRF Cybrid Reduces Oxidative Stress and Improves Mitochondrial Bioenergetics.Saturation of the human phenomeA yeast-based assay identifies drugs active against human mitochondrial disordersAssociation between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort.The mitochondrial genome: dynamics, mechanisms of repair, and a target in disease and therapyMitochondrial abnormality associates with type-specific neuronal loss and cell morphology changes in the pedunculopontine nucleus in Parkinson diseaseDNA mismatch repair and oxidative DNA damage: implications for cancer biology and treatment.Unraveling biochemical pathways affected by mitochondrial dysfunctions using metabolomic approaches.An appraisal of human mitochondrial DNA instability: new insights into the role of non-canonical DNA structures and sequence motifs.Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease.MitoBreak: the mitochondrial DNA breakpoints database.In vivo quantification reveals extensive natural variation in mitochondrial form and function in Caenorhabditis briggsae.Variable penetrance of metabolic phenotypes and development of high-fat diet-induced adiposity in NEIL1-deficient mice.Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia.Mitochondrial DNA copy number and risk of gastric cancer: a report from the Shanghai Women's Health Study.Transfection of plant mitochondria and in organello gene integration.Mitochondrial DNA disease: new options for prevention.
P2860
Q21134954-824137FA-29B1-4922-AFF9-CB3DDF5AE4D5Q24295176-0F936F62-D3C4-4817-9B3B-EB4C54A117E4Q24307946-9071951A-78CB-475C-ABBE-EA12FCDE49C6Q24603339-70321876-10D5-4159-82E7-23551C1DA4E2Q26750854-90F4DFDB-9835-41C2-913F-D5F4B78C0A6FQ26778950-9043614B-561D-4463-B331-5FB0EB3F518FQ26786969-4CF73F41-B57B-41BD-9B6D-A7DD805A9656Q26827664-9445EEFD-56C4-4758-8857-A3FD12DE892BQ26998870-E3682755-C3AF-4C75-8F6A-40D23B016F7AQ27000484-6573A7F5-A0F1-42A3-AE5A-F51D658D9788Q27678821-3498E4D9-67AA-488F-9E85-C509D7984FD1Q28076342-58297143-DF9B-46DF-9759-A0497A239081Q28086964-67198F06-0CBD-4723-88B4-86A21D1D7C20Q28274852-7A31445B-58DC-437F-AFC9-0BBAFB9170C3Q28280768-6DAE4082-F1F3-452E-96A1-82F90FAC4E07Q28282687-3D089B82-A56B-4759-A682-6D1437097704Q28649774-7B78DF9A-ACA4-4BDD-B6AD-CA5DB4BE5E4AQ30316651-F0EC1456-FDB8-4EDA-A629-E90C621BA38BQ30316940-19994F2A-9314-4E01-9B29-65E232B3B255Q30360946-437CD65B-C32E-420B-AB4C-47A5660E39C0Q30459704-4D63CCFD-AB6D-44AB-9CA7-1018E427133FQ33693717-46F41563-D4B1-47F4-9689-0E8BEB7A5032Q33740063-05628695-C921-4CE6-A603-474E210128C9Q33760222-18C45D9E-D467-45B2-AEDB-223ACC1EEA05Q33885880-05732A2A-7803-4CDE-B81B-227E71E2590BQ33946234-DB78BC94-1055-4C64-8A73-C762C2E2B444Q34054660-E5C74975-016C-468C-869A-E47C781D3827Q34133150-714A647A-D92D-40E6-A4DB-B9614C3FC8B2Q34299923-CCEC3664-F3E4-4DF5-8A39-0511EAA03A61Q34309933-CC515BBF-8B07-471F-BD59-ECA38012537FQ34318248-721BB6AF-E98D-45C5-8C99-C5A1EB80182EQ34337096-E2228A80-D3DF-43BA-BEE4-E0B5FB0ADBB6Q34346045-C7C6A572-2DEF-4320-8822-3C6539EB0A7CQ34381089-68761375-84CE-4735-B9F8-9EC557CBDB17Q34405677-262F5DEB-C595-46C4-8ACA-2C05D376E18CQ34783521-0882447F-786D-42EB-9E9A-5F90AFBE6B9AQ34785735-64A24770-1017-40E2-8010-B6BD36FBBAE6Q35204650-D90D7DE0-BCF7-456F-8ACE-B2262B3244A0Q35224425-28E5EE0F-9306-465F-8796-E78547C0FB34Q35230167-47BB3F9E-DE21-4742-87AA-EF45FA4FD631
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 15 September 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Mitochondrial DNA mutations and human disease.
@en
Mitochondrial DNA mutations and human disease.
@nl
type
label
Mitochondrial DNA mutations and human disease.
@en
Mitochondrial DNA mutations and human disease.
@nl
prefLabel
Mitochondrial DNA mutations and human disease.
@en
Mitochondrial DNA mutations and human disease.
@nl
P2093
P1476
Mitochondrial DNA mutations and human disease.
@en
P2093
Douglass M Turnbull
Helen A L Tuppen
Robert W Taylor
P304
P356
10.1016/J.BBABIO.2009.09.005
P407
P577
2009-09-15T00:00:00Z