Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors. - Wikidata - wikimedia - TriplyDB

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

http://www.wikidata.org/entity/Q34630607

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Mitochondrial DNA mutations in oxyphilic and chief cell parathyroid adenomas Investigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal disease Mitochondrial haplogroup N1a phylogeography, with implication to the origin of European farmers Decoding Warburg's hypothesis: tumor-related mutations in the mitochondrial respiratory chain Mitochondrial complex I and cell death: a semi-automatic shotgun model Population history of the Red Sea--genetic exchanges between the Arabian Peninsula and East Africa signaled in the mitochondrial DNA HV1 haplogroup Cardiolipins are biomarkers of mitochondria-rich thyroid oncocytic tumors Somatic mitochondrial DNA mutations in cancer escape purifying selection and high pathogenicity mutations lead to the oncocytic phenotype: pathogenicity analysis of reported somatic mtDNA mutations in tumors.Following mitochondrial footprints through a long mucosal path to lung cancer.Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma.Oxidative stress and mitochondrial dysfunction across broad-ranging pathologies: toward mitochondria-targeted clinical strategies.ATP synthesis, mitochondrial function, and steroid biosynthesis in rodent primary and tumor Leydig cells Rebooting the human mitochondrial phylogeny: an automated and scalable methodology with expert knowledge.Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies.Using mitochondrial DNA to test the hypothesis of a European post-glacial human recolonization from the Franco-Cantabrian refuge Complete mitochondrial genomes reveal neolithic expansion into Europe.Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells.Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma.Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.Mitochondrial DNA somatic mutation in cancer Investigation of cyanine dyes for in vivo optical imaging of altered mitochondrial membrane potential in tumors.Reduced mitochondrial DNA content associates with poor prognosis of prostate cancer in African American men.Mitochondrial dysfunction impairs tumor suppressor p53 expression/function.A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors.Mitochondrial dynamics protein Drp1 is overexpressed in oncocytic thyroid tumors and regulates cancer cell migration Identification of an mtDNA mutation hot spot in UV-induced mouse skin tumors producing altered cellular biochemistry.mtDNA lineage analysis of mouse L-cell lines reveals the accumulation of multiple mtDNA mutants and intermolecular recombination.Mitochondrial subversion in cancer.High-resolution genomic profiling of thyroid lesions uncovers preferential copy number gains affecting mitochondrial biogenesis loci in the oncocytic variants.Quantitative analysis of energy metabolic pathways in MCF-7 breast cancer cells by selected reaction monitoring assay.Mitochondrial DNA mutations distinguish bilateral multifocal renal oncocytomas from familial Birt-Hogg-Dubé tumors MtDNA analysis of global populations support that major population expansions began before Neolithic Time.A multi-parametric workflow for the prioritization of mitochondrial DNA variants of clinical interest Osteopontin expression in papillary thyroid carcinoma and its relationship with the BRAF mutation and tumor characteristics Relevance of mitochondrial genetics and metabolism in cancer development.The Genomic Landscape of Renal Oncocytoma Identifies a Metabolic Barrier to Tumorigenesis Combination of metronomic cyclophosphamide and dietary intervention inhibits neuroblastoma growth in a CD1-nu mouse model.A Case of Oncocytic Adrenocortical Neoplasm of Borderline (Uncertain) Malignant Potential.Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.Lack of complex I is associated with oncocytic thyroid tumours

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P2860

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

http://www.wikidata.org/entity/Q34630607

description

2007 nî lūn-bûn

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2007 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2007 թվականի մայիսին հրատարակված գիտական հոդված

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2007年の論文

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Disruptive mitochondrial DNA m ...... c phenotype in thyroid tumors.

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Proceedings of the National Academy of Sciences of the United States of America

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Disruptive mitochondrial DNA m ...... ic phenotype in thyroid tumors

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Alberto Rinaldi Ceroni

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Anna Ghelli

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Anna Maria Porcelli

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Christine M Betts

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Giovanni Romeo

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Giuseppe Gasparre

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Giuseppe Nicola Martinelli

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Lucia Fiammetta Pennisi

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Massimo Moretti

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Matteo Toller

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P2860

MITOMAP: a human mitochondrial genome database--2004 update

A critical reassessment of the role of mitochondria in tumorigenesis

OligoWiz 2.0--integrating sequence feature annotation into the design of microarray probes.

A role for mitochondrial enzymes in inherited neoplasia and beyond

Why do cancers have high aerobic glycolysis?

Human non-synonymous SNPs: server and survey

HmtDB, a human mitochondrial genomic resource based on variability studies supporting population genetics and biomedical research.

mtDNA mutations increase tumorigenicity in prostate cancer.

Mitochondrial DNA in human malignancy.

Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

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Giovanni Tallini

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mitochondrial DNA

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