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P Marynen

Showing results (71-80 of 185) with videos related to

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The American Journal of Pathology|April 7, 2000
The product of the t(11;18), an API2-MLT fusion, marks nearly half of gastric MALT type lymphomas without large cell proliferationM Baens, B Maes, A Steyls, et al.
The Journal of Clinical Investigation|April 1, 1995
Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal alleleC Guo, B Van Damme, Y Vanrenterghem, et al.
Leukemia|February 13, 2009
FIP1L1-PDGFRalpha D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRalpha T674I eosinophilic leukemia with single agent sorafenibE Lierman, L Michaux, E Beullens, et al.
Leukemia|January 1, 1996
Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21)S P Romana, M Le Coniat, H Poirel, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemiaJ Cools, P Peeters, T Voet, et al.
Blood|August 12, 2000
Translocation t(11;18) absent in early gastric marginal zone B-cell lymphoma of MALT type responding to eradication of Helicobacter pylori infectionB Alpen, A Neubauer, J Dierlamm, et al.
Cell Biology International Reports|September 1, 1981
Role of the alpha 2M-receptor in attachment and spreading of human fibroblastsJ J Cassiman, P Marynen, M Brugmans, et al.
Human Genetics|June 1, 1997
Interstitial telomeric sequences at the junction site of a jumping translocationJ R Vermeesch, P Petit, F Speleman, et al.
Human Genetics|January 27, 2000
Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded maleJ R Vermeesch, H Duhamel, P Petit, et al.
Journal of Medical Genetics|April 1, 1995
Encephalocraniocutaneous lipomatosis with a mutation in the NF1 geneE Legius, R Wu, M Eyssen, et al.
Pageof 19

Showing results (71-80 of 185) with videos related to

Sort By:
Pageof 19
The American Journal of Pathology|April 7, 2000
The product of the t(11;18), an API2-MLT fusion, marks nearly half of gastric MALT type lymphomas without large cell proliferationM Baens, B Maes, A Steyls, et al.
The Journal of Clinical Investigation|April 1, 1995
Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal alleleC Guo, B Van Damme, Y Vanrenterghem, et al.
Leukemia|February 13, 2009
FIP1L1-PDGFRalpha D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRalpha T674I eosinophilic leukemia with single agent sorafenibE Lierman, L Michaux, E Beullens, et al.
Leukemia|January 1, 1996
Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21)S P Romana, M Le Coniat, H Poirel, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemiaJ Cools, P Peeters, T Voet, et al.
Blood|August 12, 2000
Translocation t(11;18) absent in early gastric marginal zone B-cell lymphoma of MALT type responding to eradication of Helicobacter pylori infectionB Alpen, A Neubauer, J Dierlamm, et al.
Cell Biology International Reports|September 1, 1981
Role of the alpha 2M-receptor in attachment and spreading of human fibroblastsJ J Cassiman, P Marynen, M Brugmans, et al.
Human Genetics|June 1, 1997
Interstitial telomeric sequences at the junction site of a jumping translocationJ R Vermeesch, P Petit, F Speleman, et al.
Human Genetics|January 27, 2000
Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded maleJ R Vermeesch, H Duhamel, P Petit, et al.
Journal of Medical Genetics|April 1, 1995
Encephalocraniocutaneous lipomatosis with a mutation in the NF1 geneE Legius, R Wu, M Eyssen, et al.
Pageof 19