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Rolf Marschalek

Showing results (61-70 of 187) with videos related to

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British Journal of Haematology|August 23, 2018
Prenatal origin of KRAS mutation in a child with an acute myelomonocytic leukaemia bearing the KMT2A/MLL-AFDN/MLLT4/AF6 fusion transcriptNellina Andriano, Valeria Iachelli, Paola Bonaccorso, et al.
Cancer Genetics and Cytogenetics|April 6, 2010
Nebulette is the second member of the nebulin family fused to the MLL gene in infant leukemiaVirginia M Cóser, Claus Meyer, Rosania Basegio, et al.
Cancer Genetics|November 12, 2015
Long-term remission of therapy-related acute myeloid leukemia with a new t(11;18)(q23;q21.2) translocation and KMT2A-ME2 (MLL-ME2) fusion geneTomáš Szotkowski, Marie Jarošová, Olga Zimmermannová, et al.
Prostaglandins & Other Lipid Mediators|August 15, 2017
TGFβ/SMAD signalling modulates MLL and MLL-AF4 mediated 5-lipoxygenase promoter activationMeike J Saul, Florian Groher, Anett B Hegewald, et al.
Cancer Genetics and Cytogenetics|December 16, 2010
Therapy-related acute myeloid leukemia with t(2;11)(q37;q23) after treatment for osteosarcomaBella Bielorai, Claus Meyer, Luba Trakhtenbrot, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 4, 2009
An interstitial deletion at 3p21.3 results in the genetic fusion of MLH1 and ITGA9 in a Lynch syndrome familyClaus Meyer, Angela Brieger, Guido Plotz, et al.
Cytogenetic and Genome Research|March 3, 2017
Identification of a Cryptic Insertion ins(11;X)(q23;q28q12) Resulting in a KMT2A-FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic LeukemiaJana Lentes, Kathrin Thomay, Dominik T Schneider, et al.
British Journal of Haematology|January 24, 2015
Subclonality and prenatal origin of RAS mutations in KMT2A (MLL)-rearranged infant acute lymphoblastic leukaemiaMariana Emerenciano, Thayana da C Barbosa, Bruno de Almeida Lopes, et al.
The Journal of Biological Chemistry|November 19, 2010
Cell-based analysis of structure-function activity of threonine aspartase 1Carolin Bier, Shirley K Knauer, Alexander Klapthor, et al.
British Journal of Haematology|April 26, 2002
Low frequency of clonotypic Ig and T-cell receptor gene rearrangements in t(4;11) infant acute lymphoblastic leukaemia and its implication for the detection of minimal residual diseaseMartina Peham, Simon Panzer, Karin Fasching, et al.
Pageof 19

Showing results (61-70 of 187) with videos related to

Sort By:
Pageof 19
British Journal of Haematology|August 23, 2018
Prenatal origin of KRAS mutation in a child with an acute myelomonocytic leukaemia bearing the KMT2A/MLL-AFDN/MLLT4/AF6 fusion transcriptNellina Andriano, Valeria Iachelli, Paola Bonaccorso, et al.
Cancer Genetics and Cytogenetics|April 6, 2010
Nebulette is the second member of the nebulin family fused to the MLL gene in infant leukemiaVirginia M Cóser, Claus Meyer, Rosania Basegio, et al.
Cancer Genetics|November 12, 2015
Long-term remission of therapy-related acute myeloid leukemia with a new t(11;18)(q23;q21.2) translocation and KMT2A-ME2 (MLL-ME2) fusion geneTomáš Szotkowski, Marie Jarošová, Olga Zimmermannová, et al.
Prostaglandins & Other Lipid Mediators|August 15, 2017
TGFβ/SMAD signalling modulates MLL and MLL-AF4 mediated 5-lipoxygenase promoter activationMeike J Saul, Florian Groher, Anett B Hegewald, et al.
Cancer Genetics and Cytogenetics|December 16, 2010
Therapy-related acute myeloid leukemia with t(2;11)(q37;q23) after treatment for osteosarcomaBella Bielorai, Claus Meyer, Luba Trakhtenbrot, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 4, 2009
An interstitial deletion at 3p21.3 results in the genetic fusion of MLH1 and ITGA9 in a Lynch syndrome familyClaus Meyer, Angela Brieger, Guido Plotz, et al.
Cytogenetic and Genome Research|March 3, 2017
Identification of a Cryptic Insertion ins(11;X)(q23;q28q12) Resulting in a KMT2A-FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic LeukemiaJana Lentes, Kathrin Thomay, Dominik T Schneider, et al.
British Journal of Haematology|January 24, 2015
Subclonality and prenatal origin of RAS mutations in KMT2A (MLL)-rearranged infant acute lymphoblastic leukaemiaMariana Emerenciano, Thayana da C Barbosa, Bruno de Almeida Lopes, et al.
The Journal of Biological Chemistry|November 19, 2010
Cell-based analysis of structure-function activity of threonine aspartase 1Carolin Bier, Shirley K Knauer, Alexander Klapthor, et al.
British Journal of Haematology|April 26, 2002
Low frequency of clonotypic Ig and T-cell receptor gene rearrangements in t(4;11) infant acute lymphoblastic leukaemia and its implication for the detection of minimal residual diseaseMartina Peham, Simon Panzer, Karin Fasching, et al.
Pageof 19