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Helmut Hanenberg

Showing results (131-140 of 159) with videos related to

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Nature Communications|December 12, 2025
G-CSF/NAMPT signaling drives neutrophil dysfunction and enhances bacterial infection susceptibility in cancer patientsEkaterina Pylaeva, Lea Tollrian, Jana Riedesel, et al.
Molecular Cancer Research : MCR|July 10, 2020
Exposure of Patient-Derived Mesenchymal Stromal Cells to TGFB1 Supports Fibrosis Induction in a Pediatric Acute Megakaryoblastic Leukemia ModelTheresa Hack, Stefanie Bertram, Helen Blair, et al.
Journal of Extracellular Vesicles|April 6, 2019
Optimisation of imaging flow cytometry for the analysis of single extracellular vesicles by using fluorescence-tagged vesicles as biological reference materialAndré Görgens, Michel Bremer, Rita Ferrer-Tur, et al.
Cells|August 28, 2020
Subcellular Localization and Mitotic Interactome Analyses Identify SIRT4 as a Centrosomally Localized and Microtubule Associated ProteinLaura Bergmann, Alexander Lang, Christoph Bross, et al.
Nature Genetics|April 20, 2010
Mutation of the RAD51C gene in a Fanconi anemia-like disorderFiona Vaz, Helmut Hanenberg, Beatrice Schuster, et al.
Cell Stem Cell|September 24, 2019
NHEJ-Mediated Repair of CRISPR-Cas9-Induced DNA Breaks Efficiently Corrects Mutations in HSPCs from Patients with Fanconi AnemiaFrancisco José Román-Rodríguez, Laura Ugalde, Lara Álvarez, et al.
Blood|November 4, 2004
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from SpainElsa Callén, José A Casado, Marc D Tischkowitz, et al.
Communications Biology|July 30, 2024
A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastomaTatsiana Ryl, Elena Afanasyeva, Till Hartmann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 26, 2015
Defects in the Fanconi Anemia Pathway in Head and Neck Cancer Cells Stimulate Tumor Cell Invasion through DNA-PK and Rac1 SignalingLindsey E Romick-Rosendale, Elizabeth E Hoskins, Lisa M Privette Vinnedge, et al.
JCI Insight|May 20, 2016
Proteomics analysis reveals a Th17-prone cell population in presymptomatic graft-versus-host diseaseWei Li, Liangyi Liu, Aurelie Gomez, et al.
Pageof 16

Showing results (131-140 of 159) with videos related to

Sort By:
Pageof 16
Nature Communications|December 12, 2025
G-CSF/NAMPT signaling drives neutrophil dysfunction and enhances bacterial infection susceptibility in cancer patientsEkaterina Pylaeva, Lea Tollrian, Jana Riedesel, et al.
Molecular Cancer Research : MCR|July 10, 2020
Exposure of Patient-Derived Mesenchymal Stromal Cells to TGFB1 Supports Fibrosis Induction in a Pediatric Acute Megakaryoblastic Leukemia ModelTheresa Hack, Stefanie Bertram, Helen Blair, et al.
Journal of Extracellular Vesicles|April 6, 2019
Optimisation of imaging flow cytometry for the analysis of single extracellular vesicles by using fluorescence-tagged vesicles as biological reference materialAndré Görgens, Michel Bremer, Rita Ferrer-Tur, et al.
Cells|August 28, 2020
Subcellular Localization and Mitotic Interactome Analyses Identify SIRT4 as a Centrosomally Localized and Microtubule Associated ProteinLaura Bergmann, Alexander Lang, Christoph Bross, et al.
Nature Genetics|April 20, 2010
Mutation of the RAD51C gene in a Fanconi anemia-like disorderFiona Vaz, Helmut Hanenberg, Beatrice Schuster, et al.
Cell Stem Cell|September 24, 2019
NHEJ-Mediated Repair of CRISPR-Cas9-Induced DNA Breaks Efficiently Corrects Mutations in HSPCs from Patients with Fanconi AnemiaFrancisco José Román-Rodríguez, Laura Ugalde, Lara Álvarez, et al.
Blood|November 4, 2004
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from SpainElsa Callén, José A Casado, Marc D Tischkowitz, et al.
Communications Biology|July 30, 2024
A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastomaTatsiana Ryl, Elena Afanasyeva, Till Hartmann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 26, 2015
Defects in the Fanconi Anemia Pathway in Head and Neck Cancer Cells Stimulate Tumor Cell Invasion through DNA-PK and Rac1 SignalingLindsey E Romick-Rosendale, Elizabeth E Hoskins, Lisa M Privette Vinnedge, et al.
JCI Insight|May 20, 2016
Proteomics analysis reveals a Th17-prone cell population in presymptomatic graft-versus-host diseaseWei Li, Liangyi Liu, Aurelie Gomez, et al.
Pageof 16