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David Malkin

Showing results (221-230 of 270) with videos related to

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Cancer Genetics|September 4, 2012
Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortiumPhuong L Mai, David Malkin, Judy E Garber, et al.
Acta Neuropathologica|October 16, 2014
Alternative lengthening of telomeres is enriched in, and impacts survival of TP53 mutant pediatric malignant brain tumorsJoshua Mangerel, Aryeh Price, Pedro Castelo-Branco, et al.
Clinical Genetics|August 2, 2019
Comprehensive characterization of a Canadian cohort of von Hippel-Lindau disease patientsYasser Salama, Saleh Albanyan, Marta Szybowska, et al.
Cancer Cell|June 24, 2014
Quiescent sox2(+) cells drive hierarchical growth and relapse in sonic hedgehog subgroup medulloblastomaRobert J Vanner, Marc Remke, Marco Gallo, et al.
Journal of the National Cancer Institute|January 5, 2006
Cancer survivorship--genetic susceptibility and second primary cancers: research strategies and recommendationsLois B Travis, Charles S Rabkin, Linda Morris Brown, et al.
Cell Genomics|February 13, 2023
CanDIG: Federated network across Canada for multi-omic and health data discovery and analysisL Jonathan Dursi, Zoltan Bozoky, Richard de Borja, et al.
Nature Medicine|March 18, 2023
Diagnostic classification of childhood cancer using multiscale transcriptomicsFederico Comitani, Joshua O Nash, Sarah Cohen-Gogo, et al.
The American Journal of Gastroenterology|January 6, 2016
Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International ConsortiumMelyssa Aronson, Steven Gallinger, Zane Cohen, et al.
Oncotarget|April 9, 2016
Medulloblastoma-associated DDX3 variant selectively alters the translational response to stressSekyung Oh, Ryan A Flynn, Stephen N Floor, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 11, 2015
BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade gliomaMatthew Mistry, Nataliya Zhukova, Daniele Merico, et al.
Pageof 27

Showing results (221-230 of 270) with videos related to

Sort By:
Pageof 27
Cancer Genetics|September 4, 2012
Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortiumPhuong L Mai, David Malkin, Judy E Garber, et al.
Acta Neuropathologica|October 16, 2014
Alternative lengthening of telomeres is enriched in, and impacts survival of TP53 mutant pediatric malignant brain tumorsJoshua Mangerel, Aryeh Price, Pedro Castelo-Branco, et al.
Clinical Genetics|August 2, 2019
Comprehensive characterization of a Canadian cohort of von Hippel-Lindau disease patientsYasser Salama, Saleh Albanyan, Marta Szybowska, et al.
Cancer Cell|June 24, 2014
Quiescent sox2(+) cells drive hierarchical growth and relapse in sonic hedgehog subgroup medulloblastomaRobert J Vanner, Marc Remke, Marco Gallo, et al.
Journal of the National Cancer Institute|January 5, 2006
Cancer survivorship--genetic susceptibility and second primary cancers: research strategies and recommendationsLois B Travis, Charles S Rabkin, Linda Morris Brown, et al.
Cell Genomics|February 13, 2023
CanDIG: Federated network across Canada for multi-omic and health data discovery and analysisL Jonathan Dursi, Zoltan Bozoky, Richard de Borja, et al.
Nature Medicine|March 18, 2023
Diagnostic classification of childhood cancer using multiscale transcriptomicsFederico Comitani, Joshua O Nash, Sarah Cohen-Gogo, et al.
The American Journal of Gastroenterology|January 6, 2016
Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International ConsortiumMelyssa Aronson, Steven Gallinger, Zane Cohen, et al.
Oncotarget|April 9, 2016
Medulloblastoma-associated DDX3 variant selectively alters the translational response to stressSekyung Oh, Ryan A Flynn, Stephen N Floor, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 11, 2015
BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade gliomaMatthew Mistry, Nataliya Zhukova, Daniele Merico, et al.
Pageof 27