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Marta Pineda

Showing results (81-90 of 150) with videos related to

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Familial Cancer|April 3, 2017
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteriaMaribel González-Acosta, Jesús Del Valle, Matilde Navarro, et al.
Cancers|April 3, 2020
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer PatientsJesús Del Valle, Paula Rofes, José Marcos Moreno-Cabrera, et al.
Familial Cancer|July 27, 2025
MLH1 c.27G>A (p.Arg9=) is a synonymous likely/pathogenic variant underlying variably mosaic constitutional MLH1 methylation in Lynch syndromeRocio Alvarez, Paula Climent-Cantó, GiWon Shin, et al.
Journal for Immunotherapy of Cancer|April 20, 2025
Discovery and validation of frameshift-derived neopeptides in Lynch syndrome: paving the way for novel cancer prevention strategiesCristina Bayó, Giancarlo Castellano, Fátima Marín, et al.
Scientific Reports|January 5, 2017
Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary CancerLídia Feliubadaló, Raúl Tonda, Mireia Gausachs, et al.
Occupational and Environmental Medicine|February 25, 2022
Night work, chronotype and risk of endometrial cancer in the Screenwide case-control studyLaura Costas, Jon Frias-Gomez, Yolanda Benavente Moreno, et al.
Nature Communications|April 3, 2026
Genomic analysis of T Cell receptors reveals lynch syndrome specific immune signaturesNan Deng, Fahriye Duzagac, Ana M Bolivar, et al.
Familial Cancer|July 20, 2024
Report of the sixth meeting of the European Consortium 'Care for CMMRD' (C<sub>4</sub>CMMRD), Paris, France, November 16th 2022Léa Guerrini-Rousseau, Richard Gallon, Marta Pineda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2015
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillanceFernando Bellido, Marta Pineda, Gemma Aiza, et al.
Cancers|October 2, 2020
Complete Loss of EPCAM Immunoexpression Identifies <i>EPCAM</i> Deletion Carriers in MSH2-Negative Colorectal NeoplasiaMíriam Cuatrecasas, Iñigo Gorostiaga, Cristina Riera, et al.
Pageof 15

Showing results (81-90 of 150) with videos related to

Sort By:
Pageof 15
Familial Cancer|April 3, 2017
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteriaMaribel González-Acosta, Jesús Del Valle, Matilde Navarro, et al.
Cancers|April 3, 2020
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer PatientsJesús Del Valle, Paula Rofes, José Marcos Moreno-Cabrera, et al.
Familial Cancer|July 27, 2025
MLH1 c.27G>A (p.Arg9=) is a synonymous likely/pathogenic variant underlying variably mosaic constitutional MLH1 methylation in Lynch syndromeRocio Alvarez, Paula Climent-Cantó, GiWon Shin, et al.
Journal for Immunotherapy of Cancer|April 20, 2025
Discovery and validation of frameshift-derived neopeptides in Lynch syndrome: paving the way for novel cancer prevention strategiesCristina Bayó, Giancarlo Castellano, Fátima Marín, et al.
Scientific Reports|January 5, 2017
Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary CancerLídia Feliubadaló, Raúl Tonda, Mireia Gausachs, et al.
Occupational and Environmental Medicine|February 25, 2022
Night work, chronotype and risk of endometrial cancer in the Screenwide case-control studyLaura Costas, Jon Frias-Gomez, Yolanda Benavente Moreno, et al.
Nature Communications|April 3, 2026
Genomic analysis of T Cell receptors reveals lynch syndrome specific immune signaturesNan Deng, Fahriye Duzagac, Ana M Bolivar, et al.
Familial Cancer|July 20, 2024
Report of the sixth meeting of the European Consortium 'Care for CMMRD' (C<sub>4</sub>CMMRD), Paris, France, November 16th 2022Léa Guerrini-Rousseau, Richard Gallon, Marta Pineda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2015
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillanceFernando Bellido, Marta Pineda, Gemma Aiza, et al.
Cancers|October 2, 2020
Complete Loss of EPCAM Immunoexpression Identifies <i>EPCAM</i> Deletion Carriers in MSH2-Negative Colorectal NeoplasiaMíriam Cuatrecasas, Iñigo Gorostiaga, Cristina Riera, et al.
Pageof 15