Lack of complex I is associated with oncocytic thyroid tumours
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Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies.Inhibition of Neuroblastoma Tumor Growth by Ketogenic Diet and/or Calorie Restriction in a CD1-Nu Mouse Model.Identification of an mtDNA mutation hot spot in UV-induced mouse skin tumors producing altered cellular biochemistry.High-resolution genomic profiling of thyroid lesions uncovers preferential copy number gains affecting mitochondrial biogenesis loci in the oncocytic variants.Alterations of oxidative phosphorylation in meningiomas and peripheral nerve sheath tumorsRelevance of mitochondrial genetics and metabolism in cancer development.Impaired mitochondrial metabolism and mammary carcinogenesisCombination of metronomic cyclophosphamide and dietary intervention inhibits neuroblastoma growth in a CD1-nu mouse model.Mitochondrial dysfunction: a neglected component of skin diseases.Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation.Oxidative Phosphorylation System in Gastric Carcinomas and Gastritis.Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III DeficienciesThe ketogenic diet is not feasible as a therapy in a CD-1 nu/nu mouse model of renal cell carcinoma with features of Stauffer's syndrome.Changes in mitochondrial DNA alter expression of nuclear encoded genes associated with tumorigenesisThe genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization.Whole-exome sequencing identifies a variant of the mitochondrial MT-ND1 gene associated with epileptic encephalopathy: west syndrome evolving to Lennox-Gastaut syndrome.Placing mitochondrial DNA mutations within the progression model of type I endometrial carcinoma.Mitochondrial Dysfunction: A Novel Potential Driver of Epithelial-to-Mesenchymal Transition in Cancer.Near-haploidization significantly associates with oncocytic adrenocortical, thyroid, and parathyroid tumors but not with mitochondrial DNA mutations.Alterations of Oxidative Phosphorylation Complexes in Papillary Thyroid Carcinoma.Mitochondrial Markers for Cancer: Relevance to Diagnosis, Therapy, and Prognosis and General Understanding of Malignant Disease Mechanisms
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Lack of complex I is associated with oncocytic thyroid tumours
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 07 April 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Lack of complex I is associated with oncocytic thyroid tumours
@en
Lack of complex I is associated with oncocytic thyroid tumours.
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type
label
Lack of complex I is associated with oncocytic thyroid tumours
@en
Lack of complex I is associated with oncocytic thyroid tumours.
@nl
prefLabel
Lack of complex I is associated with oncocytic thyroid tumours
@en
Lack of complex I is associated with oncocytic thyroid tumours.
@nl
P2093
P2860
P356
P1476
Lack of complex I is associated with oncocytic thyroid tumours
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P2093
D Neureiter
F A Zimmermann
R Feichtinger
P2860
P2888
P304
P356
10.1038/SJ.BJC.6605028
P407
P577
2009-04-07T00:00:00Z