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Rabea Wagener

Showing results (41-50 of 49) with videos related to

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Blood|January 9, 2014
A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphomaItziar Salaverria, Idoia Martin-Guerrero, Rabea Wagener, et al.
Cancer Research|June 25, 2017
Functionally Null <i>RAD51D</i> Missense Mutation Associates Strongly with Ovarian CarcinomaBarbara Rivera, Massimo Di Iorio, Jessica Frankum, et al.
Genes, Chromosomes & Cancer|April 7, 2025
Subtyping Burkitt Lymphoma by DNA MethylationSelina Glaser, Rabea Wagener, Helene Kretzmer, et al.
Developmental Cell|March 20, 2018
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH MedulloblastomaDaniel J Merk, Jasmin Ohli, Natalie D Merk, et al.
Nature Genetics|November 13, 2012
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencingJulia Richter, Matthias Schlesner, Steve Hoffmann, et al.
Nature Communications|October 3, 2024
Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomasAnja Fischer, Thomas K Albert, Natalia Moreno, et al.
Nature Communications|March 31, 2019
Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphomaCristina López, Kortine Kleinheinz, Sietse M Aukema, et al.
Nature Genetics|October 6, 2015
DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional controlHelene Kretzmer, Stephan H Bernhart, Wei Wang, et al.
Leukemia|May 6, 2021
Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomasDaniel Hübschmann, Kortine Kleinheinz, Rabea Wagener, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Blood|January 9, 2014
A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphomaItziar Salaverria, Idoia Martin-Guerrero, Rabea Wagener, et al.
Cancer Research|June 25, 2017
Functionally Null <i>RAD51D</i> Missense Mutation Associates Strongly with Ovarian CarcinomaBarbara Rivera, Massimo Di Iorio, Jessica Frankum, et al.
Genes, Chromosomes & Cancer|April 7, 2025
Subtyping Burkitt Lymphoma by DNA MethylationSelina Glaser, Rabea Wagener, Helene Kretzmer, et al.
Developmental Cell|March 20, 2018
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH MedulloblastomaDaniel J Merk, Jasmin Ohli, Natalie D Merk, et al.
Nature Genetics|November 13, 2012
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencingJulia Richter, Matthias Schlesner, Steve Hoffmann, et al.
Nature Communications|October 3, 2024
Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomasAnja Fischer, Thomas K Albert, Natalia Moreno, et al.
Nature Communications|March 31, 2019
Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphomaCristina López, Kortine Kleinheinz, Sietse M Aukema, et al.
Nature Genetics|October 6, 2015
DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional controlHelene Kretzmer, Stephan H Bernhart, Wei Wang, et al.
Leukemia|May 6, 2021
Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomasDaniel Hübschmann, Kortine Kleinheinz, Rabea Wagener, et al.
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