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Peter Marynen

Showing results (81-90 of 92) with videos related to

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Genome Research|March 26, 2017
Small chromosomal regions position themselves autonomously according to their chromatin classHarmen J G van de Werken, Josien C Haan, Yana Feodorova, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 geneSuzanna G M Frints, Lin Jun, Jean-Pierre Fryns, et al.
Genome Research|April 4, 2008
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repairMarijke Bauters, Hilde Van Esch, Michael J Friez, et al.
Blood|February 1, 2003
MALT1 is deregulated by both chromosomal translocation and amplification in B-cell non-Hodgkin lymphomaDolors Sanchez-Izquierdo, Gerard Buchonnet, Reiner Siebert, et al.
The Journal of Experimental Medicine|October 22, 2008
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocationMarina Bousquet, Cathy Quelen, Roberto Rosati, et al.
Nature Genetics|September 14, 2004
Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemiaC Graux, J Cools, C Melotte, et al.
Cancer Cell|June 5, 2003
PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRα-induced myeloproliferative diseaseJan Cools, Elizabeth H Stover, Christina L Boulton, et al.
The New England Journal of Medicine|March 28, 2003
A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndromeJan Cools, Daniel J DeAngelo, Jason Gotlib, et al.
American Journal of Human Genetics|July 31, 2012
Copy-number gains of HUWE1 due to replication- and recombination-based rearrangementsGuy Froyen, Stefanie Belet, Francisco Martinez, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expressionSuzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Genome Research|March 26, 2017
Small chromosomal regions position themselves autonomously according to their chromatin classHarmen J G van de Werken, Josien C Haan, Yana Feodorova, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 geneSuzanna G M Frints, Lin Jun, Jean-Pierre Fryns, et al.
Genome Research|April 4, 2008
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repairMarijke Bauters, Hilde Van Esch, Michael J Friez, et al.
Blood|February 1, 2003
MALT1 is deregulated by both chromosomal translocation and amplification in B-cell non-Hodgkin lymphomaDolors Sanchez-Izquierdo, Gerard Buchonnet, Reiner Siebert, et al.
The Journal of Experimental Medicine|October 22, 2008
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocationMarina Bousquet, Cathy Quelen, Roberto Rosati, et al.
Nature Genetics|September 14, 2004
Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemiaC Graux, J Cools, C Melotte, et al.
Cancer Cell|June 5, 2003
PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRα-induced myeloproliferative diseaseJan Cools, Elizabeth H Stover, Christina L Boulton, et al.
The New England Journal of Medicine|March 28, 2003
A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndromeJan Cools, Daniel J DeAngelo, Jason Gotlib, et al.
American Journal of Human Genetics|July 31, 2012
Copy-number gains of HUWE1 due to replication- and recombination-based rearrangementsGuy Froyen, Stefanie Belet, Francisco Martinez, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expressionSuzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
Pageof 10