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Matthias Schlesner

Showing results (41-50 of 167) with videos related to

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Cancers|September 30, 2020
Cancer Predisposition Genes in Cancer-Free FamiliesGuoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, et al.
Hereditary Cancer in Clinical Practice|January 20, 2021
A rare large duplication of MLH1 identified in Lynch syndromeAbhishek Kumar, Nagarajan Paramasivam, Obul Reddy Bandapalli, et al.
Cells|January 8, 2023
Investigation of Rare Non-Coding Variants in Familial Multiple MyelomaYasmeen Niazi, Nagarajan Paramasivam, Joanna Blocka, et al.
Haematologica|May 11, 2019
Cryptic insertion of <i>MYC</i> exons 2 and 3 into the immunoglobulin heavy chain locus detected by whole genome sequencing in a case of "<i>MYC</i>-negative" Burkitt lymphomaRabea Wagener, Susanne Bens, Umut H Toprak, et al.
Pharmacological Research|December 1, 2021
iTReX: Interactive exploration of mono- and combination therapy dose response profiling dataDina ElHarouni, Yannick Berker, Heike Peterziel, et al.
Oncotarget|November 2, 2017
Patient-specific molecular alterations are associated with metastatic clear cell renal cell cancer progressing under tyrosine kinase inhibitor therapySteffen Dietz, Holger Sültmann, YueJun Du, et al.
Journal of Personalized Medicine|August 6, 2021
Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic CancerEmily P Slater, Lisa M Wilke, Lutz Benedikt Böhm, et al.
Haematologica|May 11, 2023
Transcriptomic profiling does not refine mastocytosis diagnosisLars Buschhorn, Dorett I Odoni, Johanna Geuder, et al.
Leukemia & Lymphoma|September 9, 2022
Exploration of whole genome and transcriptome sequencing data lacks evidence for oncogenic viral elements to drive the pathogenesis of T-cell prolymphocytic leukemiaPaurnima Patil, Umut H Toprak, Julian Seufert, et al.
The American Journal of Surgical Pathology|October 25, 2016
Recurrent Somatic PDGFRB Mutations in Sporadic Infantile/Solitary Adult Myofibromas But Not in Angioleiomyomas and MyopericytomasAbbas Agaimy, Matthias Bieg, Michael Michal, et al.
Pageof 17

Showing results (41-50 of 167) with videos related to

Sort By:
Pageof 17
Cancers|September 30, 2020
Cancer Predisposition Genes in Cancer-Free FamiliesGuoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, et al.
Hereditary Cancer in Clinical Practice|January 20, 2021
A rare large duplication of MLH1 identified in Lynch syndromeAbhishek Kumar, Nagarajan Paramasivam, Obul Reddy Bandapalli, et al.
Cells|January 8, 2023
Investigation of Rare Non-Coding Variants in Familial Multiple MyelomaYasmeen Niazi, Nagarajan Paramasivam, Joanna Blocka, et al.
Haematologica|May 11, 2019
Cryptic insertion of <i>MYC</i> exons 2 and 3 into the immunoglobulin heavy chain locus detected by whole genome sequencing in a case of "<i>MYC</i>-negative" Burkitt lymphomaRabea Wagener, Susanne Bens, Umut H Toprak, et al.
Pharmacological Research|December 1, 2021
iTReX: Interactive exploration of mono- and combination therapy dose response profiling dataDina ElHarouni, Yannick Berker, Heike Peterziel, et al.
Oncotarget|November 2, 2017
Patient-specific molecular alterations are associated with metastatic clear cell renal cell cancer progressing under tyrosine kinase inhibitor therapySteffen Dietz, Holger Sültmann, YueJun Du, et al.
Journal of Personalized Medicine|August 6, 2021
Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic CancerEmily P Slater, Lisa M Wilke, Lutz Benedikt Böhm, et al.
Haematologica|May 11, 2023
Transcriptomic profiling does not refine mastocytosis diagnosisLars Buschhorn, Dorett I Odoni, Johanna Geuder, et al.
Leukemia & Lymphoma|September 9, 2022
Exploration of whole genome and transcriptome sequencing data lacks evidence for oncogenic viral elements to drive the pathogenesis of T-cell prolymphocytic leukemiaPaurnima Patil, Umut H Toprak, Julian Seufert, et al.
The American Journal of Surgical Pathology|October 25, 2016
Recurrent Somatic PDGFRB Mutations in Sporadic Infantile/Solitary Adult Myofibromas But Not in Angioleiomyomas and MyopericytomasAbbas Agaimy, Matthias Bieg, Michael Michal, et al.
Pageof 17