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Kerstin Becker

Showing results (41-50 of 101) with videos related to

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Nucleic Acids Research|October 16, 2025
Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularizationGenevieve Trombly, Afaf Milad Said, Alexei P Kudin, et al.
Nucleic Acids Research|March 14, 2026
SMG1:SMG8:SMG9-complex integrity supports efficient execution of nonsense-mediated mRNA decaySabrina Kueckelmann, Sophie Theunissen, Fenja Meyer Zu Altenschildesche, et al.
Molecular Oncology|April 2, 2025
Multidimensional OMICs reveal ARID1A orchestrated control of DNA damage, splicing, and cell cycle in normal-like and malignant urothelial cellsRebecca M Schlösser, Florian Krumbach, Eyleen Corrales, et al.
Journal of Clinical Pathology|April 27, 2013
Deep ion sequencing of amplicon adapter ligated libraries: a novel tool in molecular diagnostics of formalin fixed and paraffin embedded tissuesKerstin Becker, Claudia Vollbrecht, Ulrike Koitzsch, et al.
Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.
Archives of Gynecology and Obstetrics|March 22, 2017
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center studyCornelia Meisel, Carolin Eva Sadowski, Daniela Kohlstedt, et al.
American Journal of Medical Genetics. Part A|November 6, 2020
Genotype-phenotype correlation in seven motor neuron disease families with novel ALS2 mutationsRosanne Sprute, Hannah Jergas, Akgün Ölmez, et al.
European Urology Focus|June 14, 2025
Evaluation of Different National Comprehensive Cancer Network Clinical Practice Guidelines in Prostate Cancer for Germline Genetic Testing in Localized and Locally Recurrent Prostate CancerMykyta Kachanov, Alexander E Volk, Fabian Falkenbach, et al.
Neuropediatrics|August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech DevelopmentWalid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Neuro-Oncology|February 16, 2017
Comprehensive molecular characterization of multifocal glioblastoma proves its monoclonal origin and reveals novel insights into clonal evolution and heterogeneity of glioblastomasKhalil Abou-El-Ardat, Michael Seifert, Kerstin Becker, et al.
Pageof 11

Showing results (41-50 of 101) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|October 16, 2025
Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularizationGenevieve Trombly, Afaf Milad Said, Alexei P Kudin, et al.
Nucleic Acids Research|March 14, 2026
SMG1:SMG8:SMG9-complex integrity supports efficient execution of nonsense-mediated mRNA decaySabrina Kueckelmann, Sophie Theunissen, Fenja Meyer Zu Altenschildesche, et al.
Molecular Oncology|April 2, 2025
Multidimensional OMICs reveal ARID1A orchestrated control of DNA damage, splicing, and cell cycle in normal-like and malignant urothelial cellsRebecca M Schlösser, Florian Krumbach, Eyleen Corrales, et al.
Journal of Clinical Pathology|April 27, 2013
Deep ion sequencing of amplicon adapter ligated libraries: a novel tool in molecular diagnostics of formalin fixed and paraffin embedded tissuesKerstin Becker, Claudia Vollbrecht, Ulrike Koitzsch, et al.
Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.
Archives of Gynecology and Obstetrics|March 22, 2017
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center studyCornelia Meisel, Carolin Eva Sadowski, Daniela Kohlstedt, et al.
American Journal of Medical Genetics. Part A|November 6, 2020
Genotype-phenotype correlation in seven motor neuron disease families with novel ALS2 mutationsRosanne Sprute, Hannah Jergas, Akgün Ölmez, et al.
European Urology Focus|June 14, 2025
Evaluation of Different National Comprehensive Cancer Network Clinical Practice Guidelines in Prostate Cancer for Germline Genetic Testing in Localized and Locally Recurrent Prostate CancerMykyta Kachanov, Alexander E Volk, Fabian Falkenbach, et al.
Neuropediatrics|August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech DevelopmentWalid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Neuro-Oncology|February 16, 2017
Comprehensive molecular characterization of multifocal glioblastoma proves its monoclonal origin and reveals novel insights into clonal evolution and heterogeneity of glioblastomasKhalil Abou-El-Ardat, Michael Seifert, Kerstin Becker, et al.
Pageof 11