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Showing results (341-350 of 444) with videos related to

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Journal of Medical Genetics|November 29, 2022
Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disordersEstela Carrasco, Adrià López-Fernández, Marta Codina-Sola, et al.
Frontiers in Genetics|September 21, 2018
Computational Tools for Splicing Defect Prediction in Breast/Ovarian Cancer Genes: How Efficient Are They at Predicting RNA Alterations?Alejandro Moles-Fernández, Laura Duran-Lozano, Gemma Montalban, et al.
Blood|September 22, 2025
Telomere content and genomics of myeloid neoplasia by whole-genome sequencingLuca Guarnera, Adam Wahida, Carmelo Gurnari, et al.
Human Mutation|September 13, 2013
Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility allelesAna Osorio, Massimo Bogliolo, Victoria Fernández, et al.
Cancer Discovery|August 24, 2012
PI3K inhibition impairs BRCA1/2 expression and sensitizes BRCA-proficient triple-negative breast cancer to PARP inhibitionYasir H Ibrahim, Celina García-García, Violeta Serra, et al.
JACC. Advances|July 4, 2025
Cardiologists' Perceptions of Cardiogenetic Testing and ManagementW H Wilson Tang, Quan M Bui, Allison L Cirino, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|March 14, 2020
Corrigendum to "Factors associated with sentinel lymph node status and prognostic role of completion lymph node dissection for thick melanoma" [Eur J Surg Oncol 46 2 (2019) 263-271]Aram Boada, Antonio Tejera-Vaquerizo, Simone Ribero, et al.
Clinical Chemistry|December 6, 2020
A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer PatientsLidia Feliubadaló, Alejandro Moles-Fernández, Marta Santamariña-Pena, et al.
The Journal of Molecular Diagnostics : JMD|October 21, 2023
A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical AnalysisLuz-Marina Porras, Natàlia Padilla, Alejandro Moles-Fernández, et al.
The Journal of Biological Chemistry|December 31, 2021
The ASCC2 CUE domain in the ALKBH3-ASCC DNA repair complex recognizes adjacent ubiquitins in K63-linked polyubiquitinPatrick M Lombardi, Sara Haile, Timur Rusanov, et al.
Pageof 45

Showing results (341-350 of 444) with videos related to

Sort By:
Pageof 45
Journal of Medical Genetics|November 29, 2022
Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disordersEstela Carrasco, Adrià López-Fernández, Marta Codina-Sola, et al.
Frontiers in Genetics|September 21, 2018
Computational Tools for Splicing Defect Prediction in Breast/Ovarian Cancer Genes: How Efficient Are They at Predicting RNA Alterations?Alejandro Moles-Fernández, Laura Duran-Lozano, Gemma Montalban, et al.
Blood|September 22, 2025
Telomere content and genomics of myeloid neoplasia by whole-genome sequencingLuca Guarnera, Adam Wahida, Carmelo Gurnari, et al.
Human Mutation|September 13, 2013
Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility allelesAna Osorio, Massimo Bogliolo, Victoria Fernández, et al.
Cancer Discovery|August 24, 2012
PI3K inhibition impairs BRCA1/2 expression and sensitizes BRCA-proficient triple-negative breast cancer to PARP inhibitionYasir H Ibrahim, Celina García-García, Violeta Serra, et al.
JACC. Advances|July 4, 2025
Cardiologists' Perceptions of Cardiogenetic Testing and ManagementW H Wilson Tang, Quan M Bui, Allison L Cirino, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|March 14, 2020
Corrigendum to "Factors associated with sentinel lymph node status and prognostic role of completion lymph node dissection for thick melanoma" [Eur J Surg Oncol 46 2 (2019) 263-271]Aram Boada, Antonio Tejera-Vaquerizo, Simone Ribero, et al.
Clinical Chemistry|December 6, 2020
A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer PatientsLidia Feliubadaló, Alejandro Moles-Fernández, Marta Santamariña-Pena, et al.
The Journal of Molecular Diagnostics : JMD|October 21, 2023
A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical AnalysisLuz-Marina Porras, Natàlia Padilla, Alejandro Moles-Fernández, et al.
The Journal of Biological Chemistry|December 31, 2021
The ASCC2 CUE domain in the ALKBH3-ASCC DNA repair complex recognizes adjacent ubiquitins in K63-linked polyubiquitinPatrick M Lombardi, Sara Haile, Timur Rusanov, et al.
Pageof 45