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Michael Parsons

Showing results (61-70 of 69) with videos related to

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European Journal of Human Genetics : EJHG|October 14, 2024
Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centresCristina Fortuno, Elisa J Cops, Aimee L Davidson, et al.
Cell Reports|October 26, 2023
Differential DNA damage repair and PARP inhibitor vulnerability of the mammary epithelial lineagesHyeyeon Kim, Kazeera Aliar, Pirashaanthy Tharmapalan, et al.
Cell Reports|October 17, 2023
Differential DNA damage repair and PARP inhibitor vulnerability of the mammary epithelial lineagesHyeyeon Kim, Kazeera Aliar, Pirashaanthy Tharmapalan, et al.
The Lancet. Oncology|December 25, 2025
A comprehensive framework for glioma surgery by the PIONEER Consortium and RANO resect group, part 2: perioperative recommendations for neurological, language, functional, and quality-of-life assessmentJasper K W Gerritsen, Philipp Karschnia, Lorenzo Bello, et al.
The Lancet. Oncology|December 25, 2025
A comprehensive framework for glioma surgery by the PIONEER Consortium and RANO resect group, part 1: intraoperative recommendations for mapping, monitoring, and decision makingJasper K W Gerritsen, Philipp Karschnia, Lorenzo Bello, et al.
Journal of Medical Genetics|April 10, 2016
Naturally occurring BRCA2 alternative mRNA splicing events in clinically relevant samplesJames D Fackenthal, Toshio Yoshimatsu, Bifeng Zhang, et al.
Cell|February 24, 2018
A Hematogenous Route for Medulloblastoma Leptomeningeal MetastasesLivia Garzia, Noriyuki Kijima, A Sorana Morrissy, et al.
Cell|June 2, 2018
A Hematogenous Route for Medulloblastoma Leptomeningeal MetastasesLivia Garzia, Noriyuki Kijima, A Sorana Morrissy, et al.
Human Molecular Genetics|March 25, 2016
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithmsMiguel de la Hoya, Omar Soukarieh, Irene López-Perolio, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
European Journal of Human Genetics : EJHG|October 14, 2024
Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centresCristina Fortuno, Elisa J Cops, Aimee L Davidson, et al.
Cell Reports|October 26, 2023
Differential DNA damage repair and PARP inhibitor vulnerability of the mammary epithelial lineagesHyeyeon Kim, Kazeera Aliar, Pirashaanthy Tharmapalan, et al.
Cell Reports|October 17, 2023
Differential DNA damage repair and PARP inhibitor vulnerability of the mammary epithelial lineagesHyeyeon Kim, Kazeera Aliar, Pirashaanthy Tharmapalan, et al.
The Lancet. Oncology|December 25, 2025
A comprehensive framework for glioma surgery by the PIONEER Consortium and RANO resect group, part 2: perioperative recommendations for neurological, language, functional, and quality-of-life assessmentJasper K W Gerritsen, Philipp Karschnia, Lorenzo Bello, et al.
The Lancet. Oncology|December 25, 2025
A comprehensive framework for glioma surgery by the PIONEER Consortium and RANO resect group, part 1: intraoperative recommendations for mapping, monitoring, and decision makingJasper K W Gerritsen, Philipp Karschnia, Lorenzo Bello, et al.
Journal of Medical Genetics|April 10, 2016
Naturally occurring BRCA2 alternative mRNA splicing events in clinically relevant samplesJames D Fackenthal, Toshio Yoshimatsu, Bifeng Zhang, et al.
Cell|February 24, 2018
A Hematogenous Route for Medulloblastoma Leptomeningeal MetastasesLivia Garzia, Noriyuki Kijima, A Sorana Morrissy, et al.
Cell|June 2, 2018
A Hematogenous Route for Medulloblastoma Leptomeningeal MetastasesLivia Garzia, Noriyuki Kijima, A Sorana Morrissy, et al.
Human Molecular Genetics|March 25, 2016
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithmsMiguel de la Hoya, Omar Soukarieh, Irene López-Perolio, et al.
Pageof 7