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Immunogenetics|August 6, 2017
On the feasibility of mining CD8+ T cell receptor patterns underlying immunogenic peptide recognitionNicolas De Neuter, Wout Bittremieux, Charlie Beirnaert, et al.Clinical Epigenetics|April 24, 2018
Large-scale analysis of DFNA5 methylation reveals its potential as biomarker for breast cancerLieselot Croes, Matthias Beyens, Erik Fransen, et al.Oncotarget|January 27, 2018
Large-scale copy number analysis reveals variations in genes not previously associated with malignant pleural mesotheliomaMarieke Hylebos, Guy Van Camp, Geert Vandeweyer, et al.Human Molecular Genetics|January 2, 2015
Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assemblyKatia Hardies, Patrick May, Tania Djémié, et al.American Journal of Medical Genetics. Part A|March 23, 2017
Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defectsCarla Marini, Katia Hardies, Tiziana Pisano, et al.British Journal of Cancer|August 24, 2024
IMPRESS: Improved methylation profiling using restriction enzymes and smMIP sequencing, combined with a new biomarker panel, creating a multi-cancer detection assayJanah Vandenhoeck, Isabelle Neefs, Thomas Vanpoucke, et al.Epilepsia|February 19, 2015
Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysisCorinna Hartmann, Sarah von Spiczak, Arvid Suls, et al.Epilepsia|November 22, 2007
Epilepsy as part of the phenotype associated with ATP1A2 mutationsLiesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, et al.Archives of Neurology|May 11, 2011
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsySaul A Mullen, Carla Marini, Arvid Suls, et al.Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.Pageof 7