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Cancer Research
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January 14, 2010
Insertional mutagenesis in mice deficient for p15Ink4b, p16Ink4a, p21Cip1, and p27Kip1 reveals cancer gene interactions and correlations with tumor phenotypes
Jaap Kool, Anthony G Uren, Carla P Martins, et al.
Genome Research
|
April 25, 2014
Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis
Henne Holstege, Wayne Pfeiffer, Daoud Sie, et al.
Neuropathology and Applied Neurobiology
|
March 13, 2015
Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours
Avanita S Prabowo, Hinke Foka van Thuijl, Ilari Scheinin, et al.
The Journal of Molecular Diagnostics : JMD
|
August 28, 2021
PCR-Free Shallow Whole Genome Sequencing for Chromosomal Copy Number Detection from Plasma of Cancer Patients Is an Efficient Alternative to the Conventional PCR-Based Approach
Jamie J Beagan, Esther E E Drees, Phylicia Stathi, et al.
Lung Cancer (Amsterdam, Netherlands)
|
August 10, 2013
EGFR mutation analysis in sputum of lung cancer patients: a multitechnique study
A Jasmijn Hubers, Daniëlle A M Heideman, Yasushi Yatabe, et al.
International Journal of Cancer
|
September 8, 2018
Genome-wide microRNA analysis of HPV-positive self-samples yields novel triage markers for early detection of cervical cancer
Barbara C Snoek, Wina Verlaat, Iris Babion, et al.
British Journal of Cancer
|
December 16, 2021
Molecular pathways in post-colonoscopy versus detected colorectal cancers: results from a nested case-control study
Roel M M Bogie, Chantal M C le Clercq, Quirinus J M Voorham, et al.
Genome Biology
|
September 24, 2014
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Hinke F van Thuijl, Ilari Scheinin, Daoud Sie, et al.
Molecular Oncology
|
January 25, 2015
Proper genomic profiling of (BRCA1-mutated) basal-like breast carcinomas requires prior removal of tumor infiltrating lymphocytes
Maarten P G Massink, Irsan E Kooi, Saskia E van Mil, et al.
Gigascience
|
December 10, 2021
Fusion transcripts and their genomic breakpoints in polyadenylated and ribosomal RNA-minus RNA sequencing data
Youri Hoogstrate, Malgorzata A Komor, René Böttcher, et al.
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of 6
Search research articles
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Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Cancer Research
|
January 14, 2010
Insertional mutagenesis in mice deficient for p15Ink4b, p16Ink4a, p21Cip1, and p27Kip1 reveals cancer gene interactions and correlations with tumor phenotypes
Jaap Kool, Anthony G Uren, Carla P Martins, et al.
Genome Research
|
April 25, 2014
Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis
Henne Holstege, Wayne Pfeiffer, Daoud Sie, et al.
Neuropathology and Applied Neurobiology
|
March 13, 2015
Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours
Avanita S Prabowo, Hinke Foka van Thuijl, Ilari Scheinin, et al.
The Journal of Molecular Diagnostics : JMD
|
August 28, 2021
PCR-Free Shallow Whole Genome Sequencing for Chromosomal Copy Number Detection from Plasma of Cancer Patients Is an Efficient Alternative to the Conventional PCR-Based Approach
Jamie J Beagan, Esther E E Drees, Phylicia Stathi, et al.
Lung Cancer (Amsterdam, Netherlands)
|
August 10, 2013
EGFR mutation analysis in sputum of lung cancer patients: a multitechnique study
A Jasmijn Hubers, Daniëlle A M Heideman, Yasushi Yatabe, et al.
International Journal of Cancer
|
September 8, 2018
Genome-wide microRNA analysis of HPV-positive self-samples yields novel triage markers for early detection of cervical cancer
Barbara C Snoek, Wina Verlaat, Iris Babion, et al.
British Journal of Cancer
|
December 16, 2021
Molecular pathways in post-colonoscopy versus detected colorectal cancers: results from a nested case-control study
Roel M M Bogie, Chantal M C le Clercq, Quirinus J M Voorham, et al.
Genome Biology
|
September 24, 2014
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Hinke F van Thuijl, Ilari Scheinin, Daoud Sie, et al.
Molecular Oncology
|
January 25, 2015
Proper genomic profiling of (BRCA1-mutated) basal-like breast carcinomas requires prior removal of tumor infiltrating lymphocytes
Maarten P G Massink, Irsan E Kooi, Saskia E van Mil, et al.
Gigascience
|
December 10, 2021
Fusion transcripts and their genomic breakpoints in polyadenylated and ribosomal RNA-minus RNA sequencing data
Youri Hoogstrate, Malgorzata A Komor, René Böttcher, et al.
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of 6