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Marta Pineda

Showing results (61-70 of 150) with videos related to

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Journal of Medical Genetics|December 24, 2018
Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?Agostina Stradella, Jesús Del Valle, Paula Rofes, et al.
Human Mutation|November 15, 2013
ICO amplicon NGS data analysis: a Web tool for variant detection in common high-risk hereditary cancer genes analyzed by amplicon GS Junior next-generation sequencingAdriana Lopez-Doriga, Lídia Feliubadaló, Mireia Menéndez, et al.
Scientific Reports|January 5, 2017
A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscapeElisabeth Castellanos, Bernat Gel, Inma Rosas, et al.
The Journal of Antimicrobial Chemotherapy|July 26, 2020
Bone density, microarchitecture and tissue quality after 1 year of treatment with dolutegravir/abacavir/lamivudineJade Soldado-Folgado, Elisabeth Lerma-Chippirraz, Itziar Arrieta-Aldea, et al.
Cancer Epidemiology|November 21, 2022
Lessons learnt from the implementation of a colorectal cancer screening programme for lynch syndrome in a tertiary public hospitalNuria Dueñas, Matilde Navarro, Xavier Sanjuán, et al.
Cancer Prevention Research (Philadelphia, Pa.)|July 23, 2011
Characterization of new founder Alu-mediated rearrangements in MSH2 gene associated with a Lynch syndrome phenotypeLucia Pérez-Cabornero, Ester Borrás Flores, Mar Infante Sanz, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genesLídia Feliubadaló, Adriana Lopez-Doriga, Ester Castellsagué, et al.
Genome Medicine|January 14, 2025
TP53 germline testing and hereditary cancer: how somatic events and clinical criteria affect variant detection ratePaula Rofes, Carmen Castillo-Manzano, Mireia Menéndez, et al.
Clinical Epigenetics|December 31, 2024
Altered chromatin landscape and 3D interactions associated with primary constitutional MLH1 epimutationsPaula Climent-Cantó, Marc Subirana-Granés, Mireia Ramos-Rodríguez, et al.
Cancer Medicine|September 4, 2021
Sensitivity of cervical cytology in endometrial cancer detection in a tertiary hospital in SpainJon Frias-Gomez, Eva Tovar, August Vidal, et al.
Pageof 15

Showing results (61-70 of 150) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|December 24, 2018
Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?Agostina Stradella, Jesús Del Valle, Paula Rofes, et al.
Human Mutation|November 15, 2013
ICO amplicon NGS data analysis: a Web tool for variant detection in common high-risk hereditary cancer genes analyzed by amplicon GS Junior next-generation sequencingAdriana Lopez-Doriga, Lídia Feliubadaló, Mireia Menéndez, et al.
Scientific Reports|January 5, 2017
A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscapeElisabeth Castellanos, Bernat Gel, Inma Rosas, et al.
The Journal of Antimicrobial Chemotherapy|July 26, 2020
Bone density, microarchitecture and tissue quality after 1 year of treatment with dolutegravir/abacavir/lamivudineJade Soldado-Folgado, Elisabeth Lerma-Chippirraz, Itziar Arrieta-Aldea, et al.
Cancer Epidemiology|November 21, 2022
Lessons learnt from the implementation of a colorectal cancer screening programme for lynch syndrome in a tertiary public hospitalNuria Dueñas, Matilde Navarro, Xavier Sanjuán, et al.
Cancer Prevention Research (Philadelphia, Pa.)|July 23, 2011
Characterization of new founder Alu-mediated rearrangements in MSH2 gene associated with a Lynch syndrome phenotypeLucia Pérez-Cabornero, Ester Borrás Flores, Mar Infante Sanz, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genesLídia Feliubadaló, Adriana Lopez-Doriga, Ester Castellsagué, et al.
Genome Medicine|January 14, 2025
TP53 germline testing and hereditary cancer: how somatic events and clinical criteria affect variant detection ratePaula Rofes, Carmen Castillo-Manzano, Mireia Menéndez, et al.
Clinical Epigenetics|December 31, 2024
Altered chromatin landscape and 3D interactions associated with primary constitutional MLH1 epimutationsPaula Climent-Cantó, Marc Subirana-Granés, Mireia Ramos-Rodríguez, et al.
Cancer Medicine|September 4, 2021
Sensitivity of cervical cytology in endometrial cancer detection in a tertiary hospital in SpainJon Frias-Gomez, Eva Tovar, August Vidal, et al.
Pageof 15