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Alexander Kohlmann

Showing results (41-50 of 102) with videos related to

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Haematologica|August 11, 2011
Prognostic relevance of RUNX1 mutations in T-cell acute lymphoblastic leukemiaVera Grossmann, Wolfgang Kern, Stefan Harbich, et al.
British Journal of Haematology|October 25, 2011
TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining alleleUlrike Bacher, Sandra Weissmann, Alexander Kohlmann, et al.
Journal of Virology|September 29, 2004
Identification of differentially expressed genes in scrapie-infected mouse brains by using global gene expression technologyWei Xiang, Otto Windl, Gerda Wünsch, et al.
Genes, Chromosomes & Cancer|August 14, 2012
Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia casesClaudia Haferlach, Ulrike Bacher, Vera Grossmann, et al.
Critical Reviews in Oncology/Hematology|May 16, 2018
Genetic alterations crossing the borders of distinct hematopoetic lineages and solid tumors: Diagnostic challenges in the era of high-throughput sequencing in hemato-oncologyEvgenii Shumilov, Johanna Flach, Thomas Pabst, et al.
BMC Genomics|June 26, 2007
New data on robustness of gene expression signatures in leukemia: comparison of three distinct total RNA preparation proceduresMarta Campo Dell'Orto, Andrea Zangrando, Luca Trentin, et al.
Journal of Theoretical Biology|August 8, 2006
PQN and DQN: algorithms for expression microarraysWei-min Liu, Rui Li, James Z Sun, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2002
Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profilesClaudia Schoch, Alexander Kohlmann, Susanne Schnittger, et al.
Haematologica|April 19, 2012
Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflowSusanne Schnittger, Ulrike Bacher, Christiane Eder, et al.
Genes, Chromosomes & Cancer|March 13, 2014
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%Verena Mühlbacher, Melanie Zenger, Susanne Schnittger, et al.
Pageof 11

Showing results (41-50 of 102) with videos related to

Sort By:
Pageof 11
Haematologica|August 11, 2011
Prognostic relevance of RUNX1 mutations in T-cell acute lymphoblastic leukemiaVera Grossmann, Wolfgang Kern, Stefan Harbich, et al.
British Journal of Haematology|October 25, 2011
TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining alleleUlrike Bacher, Sandra Weissmann, Alexander Kohlmann, et al.
Journal of Virology|September 29, 2004
Identification of differentially expressed genes in scrapie-infected mouse brains by using global gene expression technologyWei Xiang, Otto Windl, Gerda Wünsch, et al.
Genes, Chromosomes & Cancer|August 14, 2012
Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia casesClaudia Haferlach, Ulrike Bacher, Vera Grossmann, et al.
Critical Reviews in Oncology/Hematology|May 16, 2018
Genetic alterations crossing the borders of distinct hematopoetic lineages and solid tumors: Diagnostic challenges in the era of high-throughput sequencing in hemato-oncologyEvgenii Shumilov, Johanna Flach, Thomas Pabst, et al.
BMC Genomics|June 26, 2007
New data on robustness of gene expression signatures in leukemia: comparison of three distinct total RNA preparation proceduresMarta Campo Dell'Orto, Andrea Zangrando, Luca Trentin, et al.
Journal of Theoretical Biology|August 8, 2006
PQN and DQN: algorithms for expression microarraysWei-min Liu, Rui Li, James Z Sun, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2002
Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profilesClaudia Schoch, Alexander Kohlmann, Susanne Schnittger, et al.
Haematologica|April 19, 2012
Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflowSusanne Schnittger, Ulrike Bacher, Christiane Eder, et al.
Genes, Chromosomes & Cancer|March 13, 2014
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%Verena Mühlbacher, Melanie Zenger, Susanne Schnittger, et al.
Pageof 11