Genetic causes of mitochondrial DNA depletion in humans.
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The maintenance of mitochondrial DNA integrity--critical analysis and updateMitochondrial disorders: challenges in diagnosis & treatmentHistorical perspective on mitochondrial medicineA cytoplasmic suppressor of a nuclear mutation affecting mitochondrial functions in Drosophila.Mitochondrial DNA copy number, but not haplogroup, confers a genetic susceptibility to leprosy in Han Chinese from Southwest China.Drosophila topo IIIalpha is required for the maintenance of mitochondrial genome and male germ-line stem cells.Exclusive neuronal expression of SUCLA2 in the human brain.Association of leukocyte mitochondrial DNA copy number with colorectal cancer risk: Results from the Shanghai Women's Health Study.Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle.Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthaseNitric oxide and mitochondria in metabolic syndrome.The "fast" and the "slow" modes of mitochondrial DNA degradation.Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia.Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies.The awakening of an advanced malignant cancer: an insult to the mitochondrial genomeNext-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions.Prevalent coordination of mitochondrial DNA transcription and initiation of replication with the cell cyclePersistent damage induces mitochondrial DNA degradation.Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defectsHerpes simplex encephalitis is linked with selective mitochondrial damage; a post-mortem and in vitro study.Syndromes associated with mitochondrial DNA depletion.Infantile-onset disorders of mitochondrial replication and protein synthesis.Quantitative Analysis of mtDNA Content in Formalin-Fixed Paraffin-Embedded Muscle Tissue.The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations.In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletion.Principal Aspects Regarding the Maintenance of Mammalian Mitochondrial Genome Integrity.Mitochondrial DNA 4977 bp deletion is a common phenomenon in hair and increases with age.Fishing in the (deoxyribonucleotide) pool.Melatonin as a mitochondrial protector in neurodegenerative diseases.A history of mitochondrial diseases.The Mitochondrial DNA Polymerase Promotes Elimination of Paternal Mitochondrial Genomes.
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P2860
Genetic causes of mitochondrial DNA depletion in humans.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 09 July 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genetic causes of mitochondrial DNA depletion in humans.
@en
Genetic causes of mitochondrial DNA depletion in humans.
@nl
type
label
Genetic causes of mitochondrial DNA depletion in humans.
@en
Genetic causes of mitochondrial DNA depletion in humans.
@nl
prefLabel
Genetic causes of mitochondrial DNA depletion in humans.
@en
Genetic causes of mitochondrial DNA depletion in humans.
@nl
P1476
Genetic causes of mitochondrial DNA depletion in humans.
@en
P2093
Joanna Poulton
P304
P356
10.1016/J.BBADIS.2009.06.009
P407
P50
P577
2009-07-09T00:00:00Z