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Sam Behjati

Showing results (51-60 of 126) with videos related to

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Science (New York, N.Y.)|September 16, 2017
Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancerJarno Drost, Ruben van Boxtel, Francis Blokzijl, et al.
Pediatric Blood & Cancer|October 9, 2024
A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumorShathar Mahmood, Sarah M Leiter, Poe Phyu, et al.
Cancer Medicine|May 28, 2014
Fibroblastic growth factor receptor 1 amplification in osteosarcoma is associated with poor response to neo-adjuvant chemotherapyM Fernanda Amary, Hongtao Ye, Fitim Berisha, et al.
The Journal of Pathology|November 25, 2022
Recurrent FOSL1 rearrangements in desmoplastic fibroblastomaSolange De Noon, Robert Piggott, Jamie Trotman, et al.
British Journal of Haematology|March 25, 2026
Single-cell transcriptional consequences of leukaemogenic SETBP1 mutationsMi K Trinh, Nathaniel D Anderson, Matthew D Young, et al.
The Journal of Pathology. Clinical Research|August 9, 2016
Diagnostic value of H3F3A mutations in giant cell tumour of bone compared to osteoclast-rich mimicsNadège Presneau, Daniel Baumhoer, Sam Behjati, et al.
Nature|March 1, 2022
Author Correction: Inherent mosaicism and extensive mutation of human placentasTim H H Coorens, Thomas R W Oliver, Rashesh Sanghvi, et al.
The Lancet. Child & Adolescent Health|January 23, 2021
Predisposition to cancer in children and adolescentsChristian P Kratz, Marjolijn C Jongmans, Hélène Cavé, et al.
Translational Oncology|December 31, 2024
Wilms tumor primary cultures capture phenotypic heterogeneity and facilitate preclinical screeningLisa Götz, Jenny Wegert, Alireza Paikari, et al.
Nature|March 11, 2021
Inherent mosaicism and extensive mutation of human placentasTim H H Coorens, Thomas R W Oliver, Rashesh Sanghvi, et al.
Pageof 13

Showing results (51-60 of 126) with videos related to

Sort By:
Pageof 13
Science (New York, N.Y.)|September 16, 2017
Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancerJarno Drost, Ruben van Boxtel, Francis Blokzijl, et al.
Pediatric Blood & Cancer|October 9, 2024
A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumorShathar Mahmood, Sarah M Leiter, Poe Phyu, et al.
Cancer Medicine|May 28, 2014
Fibroblastic growth factor receptor 1 amplification in osteosarcoma is associated with poor response to neo-adjuvant chemotherapyM Fernanda Amary, Hongtao Ye, Fitim Berisha, et al.
The Journal of Pathology|November 25, 2022
Recurrent FOSL1 rearrangements in desmoplastic fibroblastomaSolange De Noon, Robert Piggott, Jamie Trotman, et al.
British Journal of Haematology|March 25, 2026
Single-cell transcriptional consequences of leukaemogenic SETBP1 mutationsMi K Trinh, Nathaniel D Anderson, Matthew D Young, et al.
The Journal of Pathology. Clinical Research|August 9, 2016
Diagnostic value of H3F3A mutations in giant cell tumour of bone compared to osteoclast-rich mimicsNadège Presneau, Daniel Baumhoer, Sam Behjati, et al.
Nature|March 1, 2022
Author Correction: Inherent mosaicism and extensive mutation of human placentasTim H H Coorens, Thomas R W Oliver, Rashesh Sanghvi, et al.
The Lancet. Child & Adolescent Health|January 23, 2021
Predisposition to cancer in children and adolescentsChristian P Kratz, Marjolijn C Jongmans, Hélène Cavé, et al.
Translational Oncology|December 31, 2024
Wilms tumor primary cultures capture phenotypic heterogeneity and facilitate preclinical screeningLisa Götz, Jenny Wegert, Alireza Paikari, et al.
Nature|March 11, 2021
Inherent mosaicism and extensive mutation of human placentasTim H H Coorens, Thomas R W Oliver, Rashesh Sanghvi, et al.
Pageof 13