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Peter Marynen

Showing results (61-70 of 92) with videos related to

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The Journal of Clinical Investigation|January 6, 2006
cIAP2 is a ubiquitin protein ligase for BCL10 and is dysregulated in mucosa-associated lymphoid tissue lymphomasShimin Hu, Ming-Qing Du, Sun-Mi Park, et al.
Haematologica|June 1, 2005
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinasesRoberta La Starza, Giorgina Specchia, Antonio Cuneo, et al.
Molecular Cell|July 11, 2008
Kinase activation and transformation by NUP214-ABL1 is dependent on the context of the nuclear poreKim De Keersmaecker, Jennifer L Rocnik, Rafael Bernad, et al.
Human Genetics|March 3, 2007
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic regionGuy Froyen, Marijke Bauters, Jackie Boyle, et al.
Nature Genetics|November 23, 2006
Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletionThomas De Raedt, Matthew Stephens, Ine Heyns, et al.
Human Molecular Genetics|June 19, 2003
CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behaviorSuzanna G M Frints, Peter Marynen, Dieter Hartmann, et al.
American Journal of Human Genetics|August 5, 2005
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in malesHilde Van Esch, Marijke Bauters, Jaakko Ignatius, et al.
American Journal of Human Genetics|December 17, 2009
Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombinationJoke Vandewalle, Hilde Van Esch, Karen Govaerts, et al.
Haematologica|January 2, 2008
Activity of imatinib in systemic mastocytosis with chronic basophilic leukemia and a PRKG2-PDGFRB fusionIdoya Lahortiga, Cem Akin, Jan Cools, et al.
Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.
Pageof 10

Showing results (61-70 of 92) with videos related to

Sort By:
Pageof 10
The Journal of Clinical Investigation|January 6, 2006
cIAP2 is a ubiquitin protein ligase for BCL10 and is dysregulated in mucosa-associated lymphoid tissue lymphomasShimin Hu, Ming-Qing Du, Sun-Mi Park, et al.
Haematologica|June 1, 2005
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinasesRoberta La Starza, Giorgina Specchia, Antonio Cuneo, et al.
Molecular Cell|July 11, 2008
Kinase activation and transformation by NUP214-ABL1 is dependent on the context of the nuclear poreKim De Keersmaecker, Jennifer L Rocnik, Rafael Bernad, et al.
Human Genetics|March 3, 2007
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic regionGuy Froyen, Marijke Bauters, Jackie Boyle, et al.
Nature Genetics|November 23, 2006
Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletionThomas De Raedt, Matthew Stephens, Ine Heyns, et al.
Human Molecular Genetics|June 19, 2003
CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behaviorSuzanna G M Frints, Peter Marynen, Dieter Hartmann, et al.
American Journal of Human Genetics|August 5, 2005
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in malesHilde Van Esch, Marijke Bauters, Jaakko Ignatius, et al.
American Journal of Human Genetics|December 17, 2009
Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombinationJoke Vandewalle, Hilde Van Esch, Karen Govaerts, et al.
Haematologica|January 2, 2008
Activity of imatinib in systemic mastocytosis with chronic basophilic leukemia and a PRKG2-PDGFRB fusionIdoya Lahortiga, Cem Akin, Jan Cools, et al.
Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.
Pageof 10