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M Schoenmakers

Showing results (51-60 of 79) with videos related to

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Oncogene|February 3, 2005
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplificationsMarkus Heidenblad, David Lindgren, Joris A Veltman, et al.
Journal of Medical Genetics|February 12, 2002
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactylyP Debeer, E F P M Schoenmakers, W O Twal, et al.
Human Reproduction (Oxford, England)|October 23, 2008
Constitutional DNA copy number changes in ICSI childrenG H Woldringh, I M Janssen, J Y Hehir-Kwa, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Heterogeneity of structural abnormalities in the 7q31.3 approximately q34 region in myeloid malignanciesM Belén González, Norma C Gutiérrez, Juan L García, et al.
Human Molecular Genetics|July 3, 2003
Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitutionRoland P Kuiper, Marga Schepens, José Thijssen, et al.
Leukemia|April 20, 2007
High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progressionR P Kuiper, E F P M Schoenmakers, S V van Reijmersdal, et al.
Human Molecular Genetics|May 27, 2005
Fusion of the SUMO/Sentrin-specific protease 1 gene SENP1 and the embryonic polarity-related mesoderm development gene MESDC2 in a patient with an infantile teratoma and a constitutional t(12;15)(q13;q25)Imke M Veltman, Lilian A Vreede, Jinke Cheng, et al.
British Journal of Pharmacology|February 5, 2014
The electromechanical window is no better than QT prolongation to assess risk of Torsade de Pointes in the complete atrioventricular block model in dogsT R G Stams, V J A Bourgonje, H D M Beekman, et al.
Genes, Chromosomes & Cancer|September 12, 2012
Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyomaEric F P M Schoenmakers, Jens Bunt, Lianne Hermers, et al.
American Journal of Human Genetics|December 17, 2009
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia geneLudovica Volpi, Gaia Roversi, Elisa Adele Colombo, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Oncogene|February 3, 2005
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplificationsMarkus Heidenblad, David Lindgren, Joris A Veltman, et al.
Journal of Medical Genetics|February 12, 2002
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactylyP Debeer, E F P M Schoenmakers, W O Twal, et al.
Human Reproduction (Oxford, England)|October 23, 2008
Constitutional DNA copy number changes in ICSI childrenG H Woldringh, I M Janssen, J Y Hehir-Kwa, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Heterogeneity of structural abnormalities in the 7q31.3 approximately q34 region in myeloid malignanciesM Belén González, Norma C Gutiérrez, Juan L García, et al.
Human Molecular Genetics|July 3, 2003
Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitutionRoland P Kuiper, Marga Schepens, José Thijssen, et al.
Leukemia|April 20, 2007
High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progressionR P Kuiper, E F P M Schoenmakers, S V van Reijmersdal, et al.
Human Molecular Genetics|May 27, 2005
Fusion of the SUMO/Sentrin-specific protease 1 gene SENP1 and the embryonic polarity-related mesoderm development gene MESDC2 in a patient with an infantile teratoma and a constitutional t(12;15)(q13;q25)Imke M Veltman, Lilian A Vreede, Jinke Cheng, et al.
British Journal of Pharmacology|February 5, 2014
The electromechanical window is no better than QT prolongation to assess risk of Torsade de Pointes in the complete atrioventricular block model in dogsT R G Stams, V J A Bourgonje, H D M Beekman, et al.
Genes, Chromosomes & Cancer|September 12, 2012
Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyomaEric F P M Schoenmakers, Jens Bunt, Lianne Hermers, et al.
American Journal of Human Genetics|December 17, 2009
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia geneLudovica Volpi, Gaia Roversi, Elisa Adele Colombo, et al.
Pageof 8