Expression and maintenance of mitochondrial DNA: new insights into human disease pathology
about
Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficienciesBRAT1 deficiency causes increased glucose metabolism and mitochondrial malfunctionMutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial diseaseStructural analysis and DNA binding of the HMG domains of the human mitochondrial transcription factor Ap32/gC1qR is indispensable for fetal development and mitochondrial translation: importance of its RNA-binding abilityRecombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxinRecombinant mitochondrial transcription factor A with N-terminal mitochondrial transduction domain increases respiration and mitochondrial gene expression.Mitochondrial stress engages E2F1 apoptotic signaling to cause deafnessElucidation of separate, but collaborative functions of the rRNA methyltransferase-related human mitochondrial transcription factors B1 and B2 in mitochondrial biogenesis reveals new insight into maternally inherited deafnessCKS proteins protect mitochondrial genome integrity by interacting with mitochondrial single-stranded DNA-binding protein.Variable copy number of mitochondrial DNA (mtDNA) predicts worse prognosis in advanced gastric cancer patients.Mitochondrial manganese superoxide dismutase mRNA expression in human chorioamniotic membranes and its association with labor, inflammation, and infection.Reassessing the role of mitochondrial DNA mutations in autism spectrum disorderA compendium of human mitochondrial gene expression machinery with links to disease.Core human mitochondrial transcription apparatus is a regulated two-component system in vitro.ERK-mediated phosphorylation of TFAM downregulates mitochondrial transcription: implications for Parkinson's diseaseERAL1 is associated with mitochondrial ribosome and elimination of ERAL1 leads to mitochondrial dysfunction and growth retardation.Reducing mitochondrial ROS improves disease-related pathology in a mouse model of ataxia-telangiectasia.Analysis of gene alterations of mitochondrial DNA D-loop regions to determine breast cancer clonality.Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthaseMitochondrial DNA copy number and chronic lymphocytic leukemia/small lymphocytic lymphoma risk in two prospective studiesRegulation of yeast chronological life span by TORC1 via adaptive mitochondrial ROS signaling.Peripheral blood mitochondrial DNA content, A10398G polymorphism, and risk of breast cancer in a Han Chinese population.Mitochondrial DNA copy number in peripheral blood leukocytes and the risk of clear cell renal cell carcinoma.Constitutive mitochondrial DNA copy number in peripheral blood of melanoma families with and without CDKN2A mutationsMitochondrial DNA copy number and risk of gastric cancer: a report from the Shanghai Women's Health Study.Energetics, epigenetics, mitochondrial genetics.High copy number of mitochondrial DNA (mtDNA) predicts good prognosis in glioma patients.LRP130 protein remodels mitochondria and stimulates fatty acid oxidation.Mechanism of transcription initiation by the yeast mitochondrial RNA polymeraseHitting the brakes: termination of mitochondrial transcription.A case-control study of maternal blood mitochondrial DNA copy number and preeclampsia riskA Proteomic Study of Memory After Imprinting in the Domestic Chick.No difference in mitochondrial distribution is observed in human oocytes after cryopreservation.Clinicopathological Implications of Mitochondrial Genome Alterations in Pediatric Acute Myeloid LeukemiaAssociation of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing lossp53 as guardian of the mitochondrial genomeHuman mitochondrial RNA polymerase: evaluation of the single-nucleotide-addition cycle on synthetic RNA/DNA scaffolds.Maternal blood mitochondrial DNA copy number and placental abruption risk: results from a preliminary study.Loss of p53 causes mitochondrial DNA depletion and altered mitochondrial reactive oxygen species homeostasis.
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P2860
Expression and maintenance of mitochondrial DNA: new insights into human disease pathology
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Expression and maintenance of ...... s into human disease pathology
@ast
Expression and maintenance of ...... s into human disease pathology
@en
type
label
Expression and maintenance of ...... s into human disease pathology
@ast
Expression and maintenance of ...... s into human disease pathology
@en
prefLabel
Expression and maintenance of ...... s into human disease pathology
@ast
Expression and maintenance of ...... s into human disease pathology
@en
P2860
P1476
Expression and maintenance of ...... s into human disease pathology
@en
P2093
Gerald S Shadel
P2860
P304
P356
10.2353/AJPATH.2008.071163
P407
P577
2008-05-05T00:00:00Z