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Norovirus-mediated translation repression promotes macrophage cell death.
- Published in:
- PLoS Pathogens, 2024, v. 20, n. 9, p. 1, doi. 10.1371/journal.ppat.1012480
- By:
- Publication type:
- Article
Severe infantile parkinsonism because of a de novo mutation on DLP1 mitochondrial-peroxisomal protein.
- Published in:
- 2017
- By:
- Publication type:
- case study
Human Nasal Epithelium Organoids for Assessing Neutralizing Antibodies to a Protective SARS-CoV-2 Virus-like Particle Vaccine.
- Published in:
- Organoids, 2024, v. 5, n. 1, p. 18, doi. 10.3390/organoids3010002
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- Publication type:
- Article
Reflexiones acerca del retorno financiero, social y ambiental del sector cultivo del café en Colombia.
- Published in:
- Libre Empresa, 2021, v. 18, n. 2, p. 11, doi. 10.18041/1657-2815/libreempresa.2021v18n2.8970
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- Publication type:
- Article
Sistema de compensación de los docentes ocasionales y catedráticos de las universidades públicas de la ciudad de Palmira - Valle del Cauca - 2017.
- Published in:
- Libre Empresa, 2018, v. 15, n. 2, p. 99, doi. 10.18041/1657-2815/libreempresa.2018v15n2.5350
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- Publication type:
- Article
Uridine Prevents Negative Effects of OXPHOS Xenobiotics on Dopaminergic Neuronal Differentiation.
- Published in:
- Cells (2073-4409), 2019, v. 8, n. 11, p. 1407, doi. 10.3390/cells8111407
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- Publication type:
- Article
NIVEL DE CONOCIMIENTO DE LOS MICROEMPRESARIOS DE LA INDUSTRIA DE MUEBLES DE MADERA (PALMIRA - VALLE) SOBRE POLíTICA PúBLICA PARA EL FORTALECIMIENTO DE SI PRODUCTIVIDAD Y COMPETITIVIDAD, 2011.
- Published in:
- Revista Entramado, 2011, v. 7, n. 2, p. 14
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- Publication type:
- Article
Ketogenic treatment reduces the percentage of a LHON heteroplasmic mutation and increases mtDNA amount of a LHON homoplasmic mutation.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Spatial and Temporal Expression of High Mobility Group Nucleosome‐Binding (HMGN) Genes in Brain Areas Associated with Cognition in Individuals with Down Syndrome.
- Published in:
- FASEB Journal, 2021, v. 35, p. N.PAG, doi. 10.1096/fasebj.2021.35.S1.03240
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- Publication type:
- Article
Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies.
- Published in:
- BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-91
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- Publication type:
- Article
Infectious stress triggers a POLG-related mitochondrial disease.
- Published in:
- Neurogenetics, 2020, v. 21, n. 1, p. 19, doi. 10.1007/s10048-019-00593-2
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- Publication type:
- Article
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
- Published in:
- Neurogenetics, 2012, v. 13, n. 3, p. 245, doi. 10.1007/s10048-012-0322-0
- By:
- Publication type:
- Article
FK506 affects mitochondrial protein synthesis and oxygen consumption in human cells.
- Published in:
- Cell Biology & Toxicology, 2013, v. 29, n. 6, p. 407, doi. 10.1007/s10565-013-9263-0
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- Publication type:
- Article
EFECTO DE LA COMPLEMENTACIÓN CON MICRONUTRIENTES ANTIOXIDANTES DURANTE LA GESTACIÓN SOBRE INDICADORES MATERNOS DE OBESIDAD, INFLAMACIÓN Y ANEMIA.
- Published in:
- Revista Gastrohnup, 2015, v. 17, n. 1, p. 19
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- Publication type:
- Article
Plasma coenzyme Q<sub>10</sub> status is impaired in selected genetic conditions.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-37542-2
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- Publication type:
- Article
Expanding the clinical phenotypes of MT-ATP6 mutations.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 23, p. 6191
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- Publication type:
- Article
Mitochondrial antibiograms in personalized medicine.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 6, p. 1132, doi. 10.1093/hmg/dds517
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- Publication type:
- Article
‘Progress’ renders detrimental an ancient mitochondrial DNA genetic variant.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4224, doi. 10.1093/hmg/ddr350
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- Publication type:
- Article
Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 17, p. 3343
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- Publication type:
- Article
Validez predictiva del Cuestionario de Conocimientos y Actitudes hacia la Medicina de Familia abreviado.
- Published in:
- Salud Pública de México, 2017, v. 59, n. 5, p. 508, doi. 10.21149/8536
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- Publication type:
- Article
Prevalencia de lesiones por arma de fuego en pacientes pediátricos tratados en el servicio de urgencias de pediatría del Hospital Universitario Dr. José Eleuterio González.
- Published in:
- Salud Pública de México, 2010, v. 52, n. 1, p. 1
- By:
- Publication type:
- Article
Enfermedades genéticas del ADN mitocondrial humano.
- Published in:
- Salud Pública de México, 2001, v. 43, n. 2, p. 151, doi. 10.1590/S0036-36342001000200010
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- Publication type:
- Article
Stressed cybrids model demyelinated axons in multiple sclerosis.
- Published in:
- Metabolic Brain Disease, 2013, v. 28, n. 4, p. 639, doi. 10.1007/s11011-013-9410-6
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- Publication type:
- Article
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Mitochondrial Genetic Background May Impact Statins Side Effects and Atherosclerosis Development in Familial Hypercholesterolemia.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 1, p. 471, doi. 10.3390/ijms24010471
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- Publication type:
- Article
Pathological Features in Paediatric Patients with TK2 Deficiency.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 11002, doi. 10.3390/ijms231911002
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- Publication type:
- Article
Oxidative Phosphorylation Dysfunction Modifies the Cell Secretome.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 9, p. 3374, doi. 10.3390/ijms21093374
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- Publication type:
- Article
Rebooting the human mitochondrial phylogeny: an automated and scalable methodology with expert knowledge.
- Published in:
- BMC Bioinformatics, 2011, v. 12, n. 1, p. 174, doi. 10.1186/1471-2105-12-174
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- Publication type:
- Article
Global differential expression of genes located in the Down Syndrome Critical Region in normal human brain.
- Published in:
- 2014
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- Publication type:
- Journal Article
Global differential expression of genes located in the Down Syndrome Critical Region in normal human brain.
- Published in:
- Colombia Medica, 2014, v. 45, n. 4, p. 154, doi. 10.25100/cm.v45i4.1640
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- Publication type:
- Article
Genomic study of the critical region of chromosome 21 associated to Down syndrome.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Genomic study of the critical region of chromosome 21 associated to Down syndrome.
- Published in:
- Colombia Medica, 2011, v. 42, n. 1, p. 26, doi. 10.25100/cm.v42i1.748
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- Publication type:
- Article
Las células dendríticas en la infección por el VIH-1.
- Published in:
- Colombia Medica, 2007, v. 38, n. 4, p. 421, doi. 10.25100/cm.v38i4.529
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- Publication type:
- Article
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction.
- Published in:
- Acta Neuropathologica, 2003, v. 105, n. 1, p. 69, doi. 10.1007/s00401-002-0604-y
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- Publication type:
- Article
El principio de la confianza legítima como modo de prevenir el impacto del cambio en la posición de las autoridades.
- Published in:
- Revista Pensamiento Americano, 2022, v. 15, n. 30, p. 1, doi. 10.21803/penamer.15.30.537
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- Publication type:
- Article
An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations.
- Published in:
- Frontiers in Genetics, 2015, v. 5, p. 1, doi. 10.3389/fgene.2014.00469
- By:
- Publication type:
- Article
Integrated Quantitative Neuro-Transcriptome Analysis of Several Brain Areas in Human Trisomy 21.
- Published in:
- Genes, 2022, v. 13, n. 4, p. 628, doi. 10.3390/genes13040628
- By:
- Publication type:
- Article
Spatial and Temporal Expression of High-Mobility-Group Nucleosome-Binding (HMGN) Genes in Brain Areas Associated with Cognition in Individuals with Down Syndrome.
- Published in:
- Genes, 2021, v. 12, n. 12, p. 2000, doi. 10.3390/genes12122000
- By:
- Publication type:
- Article
The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call.
- Published in:
- Genes, 2021, v. 12, n. 10, p. 1590, doi. 10.3390/genes12101590
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- Publication type:
- Article
Molecular Insights into Mitochondrial Protein Translocation and Human Disease.
- Published in:
- Genes, 2021, v. 12, n. 7, p. 1031, doi. 10.3390/genes12071031
- By:
- Publication type:
- Article
Leigh Syndrome in a Pedigree Harboring the m.1555A>G Mutation in the Mitochondrial 12S rRNA.
- Published in:
- Genes, 2020, v. 11, n. 9, p. 1007, doi. 10.3390/genes11091007
- By:
- Publication type:
- Article
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers.
- Published in:
- BMC Research Notes, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13104-018-4025-y
- By:
- Publication type:
- Article
Effect of mitochondrial haplogroups on ranibizumab response in neovascular age‐related macular degeneration patients: a pilot study.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Infección por el virus de la hepatitis B en individuos con factores de exposición en Quibdó y Apartadó, Colombia.
- Published in:
- Revista Colombiana de Gastroenterología, 2015, v. 30, n. 1, p. 11
- By:
- Publication type:
- Article
Machine learning classifier for identification of damaging missense mutations exclusive to human mitochondrial DNA-encoded polypeptides.
- Published in:
- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-017-1562-7
- By:
- Publication type:
- Article
Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter.
- Published in:
- 2012
- By:
- Publication type:
- Correction notice
Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter.
- Published in:
- Nature Structural & Molecular Biology, 2011, v. 18, n. 11, p. 1281, doi. 10.1038/nsmb.2160
- By:
- Publication type:
- Article
Human mitochondrial mTERF wraps around DNA through a left-handed superhelical tandem repeat.
- Published in:
- Nature Structural & Molecular Biology, 2010, v. 17, n. 7, p. 891, doi. 10.1038/nsmb.1859
- By:
- Publication type:
- Article
Variants Ala307Ala and Ser680Ser of 307 and 680 FSHr polymorphisms negatively influence on assisted reproductive techniques outcome and determine high probability of non-pregnancy in Caucasian patients.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 10, p. 2769, doi. 10.1007/s10815-021-02276-0
- By:
- Publication type:
- Article
tRNA punctuation model of RNA processing in human mitochondria.
- Published in:
- Nature, 1981, v. 290, n. 5806, p. 470, doi. 10.1038/290470a0
- By:
- Publication type:
- Article