Resultados da busca - Santibanez-Koref, Mauro

Human Chondrocytes Respond Discordantly to the Protein Encoded by the Osteoarthritis Susceptibility Gene GDF5 por Ratnayake, Madhushika, Plöger, Frank, Santibanez-Koref, Mauro, Loughlin, John

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Circulating cell-free mitochondrial DNA levels in Parkinson’s disease are influenced by treatment por Lowes, Hannah, Pyle, Angela, Santibanez-Koref, Mauro, Hudson, Gavin

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Functional Characterization of the Osteoarthritis Susceptibility Mapping to CHST11—A Bioinformatics and Molecular Study por Reynard, Louise N., Ratnayake, Madhushika, Santibanez-Koref, Mauro, Loughlin, John

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Association of stroke and bleed events in non-valvular atrial fibrillation patients with direct oral anticoagulant prescriptions in NHS England between 2013 and 2016 por Sheth, Harsh, McNally, Daniel, Santibanez-Koref, Mauro, Burn, John

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Inhibition of O(6)-methylguanine-DNA methyltransferase by an alkyltransferase-like protein from Escherichia coli por Pearson, Steven J., Ferguson, Jennifer, Santibanez-Koref, Mauro, Margison, Geoffrey P.

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Comparing Methods for Mapping cis Acting Polymorphisms Using Allelic Expression Ratios por Teare, Marion Dawn, Pinyakorn, Suteeraporn, Heighway, James, Santibanez Koref, Mauro F.

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Finding genes that influence quantitative traits with tree-based clustering por Wilson, Ian J, Howey, Richard AJ, Houniet, Darren T, Santibanez-Koref, Mauro

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Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression por Cunnington, Michael S., Santibanez Koref, Mauro, Mayosi, Bongani M., Burn, John, Keavney, Bernard

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Interactions between nuclear and mitochondrial SNPs and Parkinson’s disease risk por Pickett, Sarah J., Deen, Dasha, Pyle, Angela, Santibanez-Koref, Mauro, Hudson, Gavin

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Allelic expression analysis of the osteoarthritis susceptibility locus that maps to MICAL3 por Ratnayake, Madhushika, Reynard, Louise N, Raine, Emma VA, Santibanez-Koref, Mauro, Loughlin, John

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Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution por Santibanez-Koref, Mauro, Griffin, Helen, Turnbull, Douglass M., Chinnery, Patrick F., Herbert, Mary, Hudson, Gavin

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Erratum to: PTESFinder: a computational method to identify post-transcriptional exon shuffling (PTES) events por Izuogu, Osagie G., Alhasan, Abd A., Alafghani, Hani M., Santibanez-Koref, Mauro, Elliott, David J., Jackson, Michael S.

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Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans por Pyle, Angela, Hudson, Gavin, Wilson, Ian J., Coxhead, Jonathan, Smertenko, Tania, Herbert, Mary, Santibanez-Koref, Mauro, Chinnery, Patrick F.

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How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future Strategies por Gallon, Richard, Gawthorpe, Peter, Phelps, Rachel L., Hayes, Christine, Borthwick, Gillian M., Santibanez-Koref, Mauro, Jackson, Michael S., Burn, John

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Using population data for assessing next-generation sequencing performance por Houniet, Darren T., Rahman, Thahira J., Al Turki, Saeed, Hurles, Matthew E., Xu, Yaobo, Goodship, Judith, Keavney, Bernard, Santibanez Koref, Mauro

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Impact of Month of Birth on the Risk of Development of Autoimmune Addison's Disease por Pazderska, Agnieszka, Fichna, Marta, Mitchell, Anna L., Napier, Catherine M., Gan, Earn, Ruchała, Marek, Santibanez-Koref, Mauro, Pearce, Simon H.

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Late-onset sacsinopathy diagnosed by exome sequencing and comparative genomic hybridisation por Pyle, Angela, Griffin, Helen, Duff, Jennifer, Zwolinski, Simon, Smertenko, Tania, Yu-Wai-Man, Patrick, Santibanez-Koref, Mauro, Horvath, Rita, Chinnery, Patrick F.

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Evidence for Widespread Reticulate Evolution within Human Duplicons por Jackson, Michael S. , Oliver, Karen , Loveland, Jane , Humphray, Sean , Dunham, Ian , Rocchi, Mariano , Viggiano, Luigi , Park, Jonathan P. , Hurles, Matthew E. , Santibanez-Koref, Mauro 

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Using MRI to predict future adverse cardiac remodelling in a male mouse model of myocardial infarction por Redgrave, Rachael E., Tual-Chalot, Simon, Davison, Benjamin J., Greally, Elizabeth, Santibanez-Koref, Mauro, Schneider, Jurgen E., Blamire, Andrew M., Arthur, Helen M.

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Diverse presentations of cutaneous mosaicism occur in CYLD cutaneous syndrome and may result in parent-to-child transmission por Arefi, Majid, Wilson, Valerie, Muthiah, Siobhan, Zwolinski, Simon, Bajwa, Dalvir, Brennan, Paul, Blasdale, Katie, Bourn, David, Burn, John, Santibanez-Koref, Mauro, Rajan, Neil

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