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Stefano Lise

Showing results (11-20 of 33) with videos related to

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Cancer Discovery|July 24, 2020
Clinical <i>BRCA1/2</i> Reversion Analysis Identifies Hotspot Mutations and Predicted Neoantigens Associated with Therapy ResistanceStephen J Pettitt, Jessica R Frankum, Marco Punta, et al.
Nature Communications|January 31, 2020
Author Correction: Extreme intratumour heterogeneity and driver evolution in mismatch repair deficient gastro-oesophageal cancerKatharina von Loga, Andrew Woolston, Marco Punta, et al.
Nature Communications|January 18, 2020
Extreme intratumour heterogeneity and driver evolution in mismatch repair deficient gastro-oesophageal cancerKatharina von Loga, Andrew Woolston, Marco Punta, et al.
Oncoimmunology|December 21, 2023
Driver mutations in <i>GNAQ</i> and <i>GNA11</i> genes as potential targets for precision immunotherapy in uveal melanoma patientsSandra García-Mulero, Roberto Fornelino, Marco Punta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2012
Next-generation sequencing in health-care delivery: lessons from the functional analysis of rhodopsinWayne I L Davies, Susan M Downes, Josephine K Fu, et al.
Journal of Human Genetics|December 2, 2011
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequenciesAlistair T Pagnamenta, Stefano Lise, Victoria Harrison, et al.
European Journal of Human Genetics : EJHG|September 13, 2012
Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset diseaseMorag E Shanks, Susan M Downes, Richard R Copley, et al.
Nucleic Acids Research|December 21, 2004
The CATH Domain Structure Database and related resources Gene3D and DHS provide comprehensive domain family information for genome analysisFrances Pearl, Annabel Todd, Ian Sillitoe, et al.
The Journal of Clinical Investigation|March 10, 2020
Genome-wide plasma DNA methylation features of metastatic prostate cancerAnjui Wu, Paolo Cremaschi, Daniel Wetterskog, et al.
Journal of Visualized Experiments : Jove|December 30, 2017
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain MalformationsValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Cancer Discovery|July 24, 2020
Clinical <i>BRCA1/2</i> Reversion Analysis Identifies Hotspot Mutations and Predicted Neoantigens Associated with Therapy ResistanceStephen J Pettitt, Jessica R Frankum, Marco Punta, et al.
Nature Communications|January 31, 2020
Author Correction: Extreme intratumour heterogeneity and driver evolution in mismatch repair deficient gastro-oesophageal cancerKatharina von Loga, Andrew Woolston, Marco Punta, et al.
Nature Communications|January 18, 2020
Extreme intratumour heterogeneity and driver evolution in mismatch repair deficient gastro-oesophageal cancerKatharina von Loga, Andrew Woolston, Marco Punta, et al.
Oncoimmunology|December 21, 2023
Driver mutations in <i>GNAQ</i> and <i>GNA11</i> genes as potential targets for precision immunotherapy in uveal melanoma patientsSandra García-Mulero, Roberto Fornelino, Marco Punta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2012
Next-generation sequencing in health-care delivery: lessons from the functional analysis of rhodopsinWayne I L Davies, Susan M Downes, Josephine K Fu, et al.
Journal of Human Genetics|December 2, 2011
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequenciesAlistair T Pagnamenta, Stefano Lise, Victoria Harrison, et al.
European Journal of Human Genetics : EJHG|September 13, 2012
Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset diseaseMorag E Shanks, Susan M Downes, Richard R Copley, et al.
Nucleic Acids Research|December 21, 2004
The CATH Domain Structure Database and related resources Gene3D and DHS provide comprehensive domain family information for genome analysisFrances Pearl, Annabel Todd, Ian Sillitoe, et al.
The Journal of Clinical Investigation|March 10, 2020
Genome-wide plasma DNA methylation features of metastatic prostate cancerAnjui Wu, Paolo Cremaschi, Daniel Wetterskog, et al.
Journal of Visualized Experiments : Jove|December 30, 2017
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain MalformationsValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Pageof 4