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Genome Biology
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October 15, 2008
Distinct transcriptional MYCN/c-MYC activities are associated with spontaneous regression or malignant progression in neuroblastomas
Frank Westermann, Daniel Muth, Axel Benner, et al.
BMC Bioinformatics
|
May 22, 2010
Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline
Joachim M De Schrijver, Kim De Leeneer, Steve Lefever, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 21, 2012
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis
Frauke Coppieters, Bram De Wilde, Steve Lefever, et al.
Plos One
|
August 27, 2013
Effective Alu repeat based RT-Qpcr normalization in cancer cell perturbation experiments
Ali Rihani, Tom Van Maerken, Filip Pattyn, et al.
BMC Bioinformatics
|
May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays
Björn Menten, Filip Pattyn, Katleen De Preter, et al.
Biotechnology and Bioengineering
|
October 16, 2019
Unraveling and resolving inefficient glucolipid biosurfactants production through quantitative multiomics analyses of Starmerella bombicola strains
Sofie Lodens, Sophie L K W Roelants, Katarzyna Ciesielska, et al.
Plos One
|
October 8, 2011
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics
Kim De Leeneer, Joachim De Schrijver, Lieven Clement, et al.
Nucleic Acids Research
|
April 30, 2013
MYCN and HDAC2 cooperate to repress miR-183 signaling in neuroblastoma
Marco Lodrini, Ina Oehme, Christina Schroeder, et al.
BMC Medical Genomics
|
May 22, 2012
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform
Sarah De Keulenaer, Jan Hellemans, Steve Lefever, et al.
International Journal of Cancer
|
July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas
Annelies Fieuw, Candy Kumps, Alexander Schramm, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 4
Genome Biology
|
October 15, 2008
Distinct transcriptional MYCN/c-MYC activities are associated with spontaneous regression or malignant progression in neuroblastomas
Frank Westermann, Daniel Muth, Axel Benner, et al.
BMC Bioinformatics
|
May 22, 2010
Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline
Joachim M De Schrijver, Kim De Leeneer, Steve Lefever, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 21, 2012
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis
Frauke Coppieters, Bram De Wilde, Steve Lefever, et al.
Plos One
|
August 27, 2013
Effective Alu repeat based RT-Qpcr normalization in cancer cell perturbation experiments
Ali Rihani, Tom Van Maerken, Filip Pattyn, et al.
BMC Bioinformatics
|
May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays
Björn Menten, Filip Pattyn, Katleen De Preter, et al.
Biotechnology and Bioengineering
|
October 16, 2019
Unraveling and resolving inefficient glucolipid biosurfactants production through quantitative multiomics analyses of Starmerella bombicola strains
Sofie Lodens, Sophie L K W Roelants, Katarzyna Ciesielska, et al.
Plos One
|
October 8, 2011
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics
Kim De Leeneer, Joachim De Schrijver, Lieven Clement, et al.
Nucleic Acids Research
|
April 30, 2013
MYCN and HDAC2 cooperate to repress miR-183 signaling in neuroblastoma
Marco Lodrini, Ina Oehme, Christina Schroeder, et al.
BMC Medical Genomics
|
May 22, 2012
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform
Sarah De Keulenaer, Jan Hellemans, Steve Lefever, et al.
International Journal of Cancer
|
July 29, 2011
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas
Annelies Fieuw, Candy Kumps, Alexander Schramm, et al.
Page
of 4