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Oncotarget
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July 21, 2016
A cancer specific hypermethylation signature of the TERT promoter predicts biochemical relapse in prostate cancer: a retrospective cohort study
Pedro 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 programming
Inga 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 resistance
Sabrina 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 Redistribution
Tilman 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 hypermethylation
Stefan 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 genome
Tomasz 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 laboratories
A 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 syndrome
Peter 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 syndrome
Hans 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.
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of 10
Search research articles
Search
Showing results (81-90 of 94) with videos related to
Sort By:
Page
of 10
Oncotarget
|
July 21, 2016
A cancer specific hypermethylation signature of the TERT promoter predicts biochemical relapse in prostate cancer: a retrospective cohort study
Pedro 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 programming
Inga 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 resistance
Sabrina 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 Redistribution
Tilman 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 hypermethylation
Stefan 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 genome
Tomasz 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 laboratories
A 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 syndrome
Peter 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 syndrome
Hans 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.
Page
of 10