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S Schnittger

Showing results (81-90 of 131) with videos related to

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Genes, Chromosomes & Cancer|May 1, 1995
dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemiaH Rieder, S Schnittger, H Bodenstein, et al.
British Journal of Haematology|September 6, 2000
Mapping of leukaemia-associated breakpoints in chromosome band 3q21 using a newly established PAC contigR Wieser, A Volz, S Schnittger, et al.
Leukemia|July 30, 2015
Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPNS Jeromin, A Kohlmann, M Meggendorfer, et al.
Leukemia|May 10, 2000
Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AMLS Schnittger, U Kinkelin, C Schoch, et al.
Blood Cancer Journal|March 12, 2013
Imatinib failure and response to dasatinib in a patient with chronic myeloid leukemia in blast crisis and a novel, nine-nucleotide BCR-ABL insertion mutationM Sigl, S Spoerl, S Schnittger, et al.
Leukemia|March 29, 2013
High incidence of RAS signalling pathway mutations in MLL-rearranged acute myeloid leukemiaV Grossmann, S Schnittger, F Poetzinger, et al.
Leukemia|January 22, 2011
Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedureV Grossmann, A Kohlmann, H-U Klein, et al.
British Journal of Haematology|October 29, 1998
Cell lineage specific involvement in acute promyelocytic leukaemia (APL) using a combination of May-Grünwald-Giemsa staining and fluorescence in situ hybridization techniques for the detection of the translocation t(15;17)(q22;q12)T Haferlach, H Löffler, C Nickenig, et al.
Nature Genetics|March 10, 2001
Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemiaT Pabst, B U Mueller, P Zhang, et al.
Leukemia|August 21, 2013
Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant diseaseA Kohlmann, N Nadarajah, T Alpermann, et al.
Pageof 14

Showing results (81-90 of 131) with videos related to

Sort By:
Pageof 14
Genes, Chromosomes & Cancer|May 1, 1995
dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemiaH Rieder, S Schnittger, H Bodenstein, et al.
British Journal of Haematology|September 6, 2000
Mapping of leukaemia-associated breakpoints in chromosome band 3q21 using a newly established PAC contigR Wieser, A Volz, S Schnittger, et al.
Leukemia|July 30, 2015
Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPNS Jeromin, A Kohlmann, M Meggendorfer, et al.
Leukemia|May 10, 2000
Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AMLS Schnittger, U Kinkelin, C Schoch, et al.
Blood Cancer Journal|March 12, 2013
Imatinib failure and response to dasatinib in a patient with chronic myeloid leukemia in blast crisis and a novel, nine-nucleotide BCR-ABL insertion mutationM Sigl, S Spoerl, S Schnittger, et al.
Leukemia|March 29, 2013
High incidence of RAS signalling pathway mutations in MLL-rearranged acute myeloid leukemiaV Grossmann, S Schnittger, F Poetzinger, et al.
Leukemia|January 22, 2011
Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedureV Grossmann, A Kohlmann, H-U Klein, et al.
British Journal of Haematology|October 29, 1998
Cell lineage specific involvement in acute promyelocytic leukaemia (APL) using a combination of May-Grünwald-Giemsa staining and fluorescence in situ hybridization techniques for the detection of the translocation t(15;17)(q22;q12)T Haferlach, H Löffler, C Nickenig, et al.
Nature Genetics|March 10, 2001
Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemiaT Pabst, B U Mueller, P Zhang, et al.
Leukemia|August 21, 2013
Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant diseaseA Kohlmann, N Nadarajah, T Alpermann, et al.
Pageof 14