Found: 37
Select item for more details and to access through your institution.
HIF-1α induction, proliferation and glycolysis of T heileria-infected leukocytes.
- Published in:
- Cellular Microbiology, 2015, v. 17, n. 4, p. 467, doi. 10.1111/cmi.12421
- By:
- Publication type:
- Article
S100A8-mediated metabolic adaptation controls HIV-1 persistence in macrophages in vivo.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33401-x
- By:
- Publication type:
- Article
Use of H 2 O 2 to Cause Oxidative Stress, the Catalase Issue.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 23, p. 9149, doi. 10.3390/ijms21239149
- By:
- Publication type:
- Article
Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization.
- Published in:
- International Journal of Molecular Sciences, 2018, v. 19, n. 3, p. 764, doi. 10.3390/ijms19030764
- By:
- Publication type:
- Article
Clinical and Biochemical Studies on Cytochrome Oxidase Deficienciesa.
- Published in:
- Annals of the New York Academy of Sciences, 1988, v. 550, n. 1, p. 348, doi. 10.1111/j.1749-6632.1988.tb35349.x
- By:
- Publication type:
- Article
Separate fusion of outer and inner mitochondrial membranes.
- Published in:
- EMBO Reports, 2005, v. 6, n. 9, p. 853, doi. 10.1038/sj.embor.7400488
- By:
- Publication type:
- Article
QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.17163
- By:
- Publication type:
- Article
Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome.
- Published in:
- Nucleic Acids Research, 2013, v. 41, n. 1, p. 418, doi. 10.1093/nar/gks965
- By:
- Publication type:
- Article
Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria.
- Published in:
- Nucleic Acids Research, 2011, v. 39, n. 18, p. 8173, doi. 10.1093/nar/gkr546
- By:
- Publication type:
- Article
A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.
- Published in:
- Nature Genetics, 2001, v. 29, n. 1, p. 57, doi. 10.1038/ng706
- By:
- Publication type:
- Article
Tissue- and Cell-Specific Mitochondrial Defect in Parkin-Deficient Mice.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099898
- By:
- Publication type:
- Article
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?
- Published in:
- 2018
- By:
- Publication type:
- journal article
D-loop mutations in mitochondrial DNA: link with mitochondrial DNA depletion?
- Published in:
- Human Genetics, 2002, v. 110, n. 5, p. 479, doi. 10.1007/s00439-002-0708-4
- By:
- Publication type:
- Article
Functional characterization of novel mutations in the human cytochrome b gene.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 7, p. 510, doi. 10.1038/sj.ejhg.5200678
- By:
- Publication type:
- Article
Kinetic analysis of ATP hydrolysis by complex V in four murine tissues: Towards an assay suitable for clinical diagnosis.
- Published in:
- PLoS ONE, 2019, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0221886
- By:
- Publication type:
- Article
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 12, p. 3614, doi. 10.1093/brain/aws298
- By:
- Publication type:
- Article
Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?
- Published in:
- Brain: A Journal of Neurology, 2007, v. 130, n. 6, p. 1516, doi. 10.1093/brain/awm067
- By:
- Publication type:
- Article
Increased dNTP pools rescue mtDNA depletion in human POLG-deficient fibroblasts.
- Published in:
- FASEB Journal, 2019, v. 33, n. 6, p. 7168, doi. 10.1096/fj.201801591R
- By:
- Publication type:
- Article
Genetic diagnosis of Mendelian disorders via RNA sequencing.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/ncomms15824
- By:
- Publication type:
- Article
Probenecid potentiates MPTP/ MPP<sup>+</sup> toxicity by interference with cellular energy metabolism.
- Published in:
- Journal of Neurochemistry, 2013, v. 127, n. 6, p. 782, doi. 10.1111/jnc.12343
- By:
- Publication type:
- Article
Incidence and predictors of total mortality in 267 adults presenting with mitochondrial diseases.
- Published in:
- Journal of Inherited Metabolic Disease, 2020, v. 43, n. 3, p. 459, doi. 10.1002/jimd.12185
- By:
- Publication type:
- Article
Erratum to: Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project.
- Published in:
- 2018
- By:
- Publication type:
- Erratum
Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project.
- Published in:
- Journal of Inherited Metabolic Disease, 2017, v. 40, n. 3, p. 403, doi. 10.1007/s10545-017-0035-5
- By:
- Publication type:
- Article
Potentiation of mitotane action by rosuvastatin: New insights for adrenocortical carcinoma management.
- Published in:
- International Journal of Oncology, 2019, v. 54, n. 6, p. 2149, doi. 10.3892/ijo.2019.4770
- By:
- Publication type:
- Article
Metalloprotease-mediated OPA1 processing is modulated by the mitochondrial membrane potential.
- Published in:
- Biology of the Cell (Wiley-Blackwell), 2008, v. 100, n. 5, p. 315, doi. 10.1042/BC20070110
- By:
- Publication type:
- Article
Hypoxia Promotes Mitochondrial Complex I Abundance via HIF-1α in Complex III and Complex IV Deficient Cells.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 10, p. 2197, doi. 10.3390/cells9102197
- By:
- Publication type:
- Article
Engrailed protects mouse midbrain dopaminergic neurons against mitochondrial complex I insults.
- Published in:
- Nature Neuroscience, 2011, v. 14, n. 10, p. 1260, doi. 10.1038/nn.2916
- By:
- Publication type:
- Article
Respiratory mutations lead to different pleiotropic effects on OXPHOS complexes in yeast and in human cells
- Published in:
- FEBS Letters, 2008, v. 582, n. 23/24, p. 3489, doi. 10.1016/j.febslet.2008.09.016
- By:
- Publication type:
- Article
PGC-1α/β induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 10, p. 1805, doi. 10.1093/hmg/ddp093
- By:
- Publication type:
- Article
Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseases.
- Published in:
- European Heart Journal, 2015, v. 36, n. 42, p. 2886, doi. 10.1093/eurheartj/ehv307
- By:
- Publication type:
- Article
Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.
- Published in:
- Annals of Neurology, 2001, v. 49, n. 5, p. 607, doi. 10.1002/ana.1002
- By:
- Publication type:
- Article
Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: Neuropathology, biochemistry, and molecular genetics.
- Published in:
- Annals of Neurology, 1989, v. 26, n. 1, p. 20, doi. 10.1002/ana.410260104
- By:
- Publication type:
- Article
The mitochondrial complex I inhibitor rotenone triggers a cerebral tauopathy.
- Published in:
- Journal of Neurochemistry, 2005, v. 95, n. 4, p. 930, doi. 10.1111/j.1471-4159.2005.03493.x
- By:
- Publication type:
- Article
Annonacin, a lipophilic inhibitor of mitochondrial complex I, induces nigral and striatal neurodegeneration in rats: possible relevance for atypical parkinsonism in Guadeloupe.
- Published in:
- Journal of Neurochemistry, 2004, v. 88, n. 1, p. 63, doi. 10.1046/j.1471-4159.2003.02138.x
- By:
- Publication type:
- Article
Dysfunction of mitochondrial complex I and the proteasome: interactions between two biochemical deficits in a cellular model of Parkinson's disease.
- Published in:
- Journal of Neurochemistry, 2003, v. 86, n. 5, p. 1297, doi. 10.1046/j.1471-4159.2003.01952.x
- By:
- Publication type:
- Article
Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 1, p. 33, doi. 10.1093/hmg/7.1.33
- By:
- Publication type:
- Article
Physiopathologie des maladies mitochondriales.
- Published in:
- Biologie Aujourd'hui, 2015, v. 209, n. 2, p. 125, doi. 10.1051/jbio/2015014
- By:
- Publication type:
- Article