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R Schweiger

Showing results (81-90 of 94) with videos related to

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Oncotarget|July 21, 2016
A cancer specific hypermethylation signature of the TERT promoter predicts biochemical relapse in prostate cancer: a retrospective cohort studyPedro Castelo-Branco, Ricardo Leão, Tatiana Lipman, et al.
Scientific Reports|September 23, 2020
Maternal exercise conveys protection against NAFLD in the offspring via hepatic metabolic programmingInga Bae-Gartz, Philipp Kasper, Nora Großmann, et al.
Genome Medicine|July 22, 2018
Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistanceSabrina Grasse, Matthias Lienhard, Steffen Frese, et al.
Journal of the American Society of Nephrology : JASN|January 15, 2022
Claudin-10a Deficiency Shifts Proximal Tubular Cl<sup>-</sup> Permeability to Cation Selectivity <i>via</i> Claudin-2 RedistributionTilman Breiderhoff, Nina Himmerkus, Luca Meoli, et al.
Cancer Discovery|August 30, 2012
Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylationStefan T Börno, Axel Fischer, Martin Kerick, et al.
Science Translational Medicine|September 5, 2014
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genomeTomasz Zemojtel, Sebastian Köhler, Luisa Mackenroth, et al.
Leukemia|June 18, 2011
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratoriesA Kohlmann, H-U Klein, S Weissmann, et al.
Nature Genetics|August 31, 2010
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndromePeter M Krawitz, Michal R Schweiger, Christian Rödelsperger, et al.
The Journal of Pathology|July 21, 2017
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndromeHans Binder, Lydia Hopp, Michal R Schweiger, et al.
Clinical Chemistry and Laboratory Medicine|January 3, 2025
Behind the scenes of EQA - characteristics, capabilities, benefits and assets of external quality assessment (EQA)Christoph Buchta, Barbara De la Salle, Rachel Marrington, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Oncotarget|July 21, 2016
A cancer specific hypermethylation signature of the TERT promoter predicts biochemical relapse in prostate cancer: a retrospective cohort studyPedro Castelo-Branco, Ricardo Leão, Tatiana Lipman, et al.
Scientific Reports|September 23, 2020
Maternal exercise conveys protection against NAFLD in the offspring via hepatic metabolic programmingInga Bae-Gartz, Philipp Kasper, Nora Großmann, et al.
Genome Medicine|July 22, 2018
Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistanceSabrina Grasse, Matthias Lienhard, Steffen Frese, et al.
Journal of the American Society of Nephrology : JASN|January 15, 2022
Claudin-10a Deficiency Shifts Proximal Tubular Cl<sup>-</sup> Permeability to Cation Selectivity <i>via</i> Claudin-2 RedistributionTilman Breiderhoff, Nina Himmerkus, Luca Meoli, et al.
Cancer Discovery|August 30, 2012
Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylationStefan T Börno, Axel Fischer, Martin Kerick, et al.
Science Translational Medicine|September 5, 2014
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genomeTomasz Zemojtel, Sebastian Köhler, Luisa Mackenroth, et al.
Leukemia|June 18, 2011
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratoriesA Kohlmann, H-U Klein, S Weissmann, et al.
Nature Genetics|August 31, 2010
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndromePeter M Krawitz, Michal R Schweiger, Christian Rödelsperger, et al.
The Journal of Pathology|July 21, 2017
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndromeHans Binder, Lydia Hopp, Michal R Schweiger, et al.
Clinical Chemistry and Laboratory Medicine|January 3, 2025
Behind the scenes of EQA - characteristics, capabilities, benefits and assets of external quality assessment (EQA)Christoph Buchta, Barbara De la Salle, Rachel Marrington, et al.
Pageof 10