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Peter Papenhausen

Showing results (1-10 of 17) with videos related to

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Genes|April 6, 2017
The Role of c-MYC in B-Cell Lymphomas: Diagnostic and Molecular AspectsLynh Nguyen, Peter Papenhausen, Haipeng Shao
International Journal of Clinical and Experimental Pathology|July 21, 2015
Therapy-related acute myeloid leukemia with eosinophilia, basophilia, t(4;14)(q12;q24) and PDGFRA rearrangement: a case report and review of the literatureJun Zhou, Peter Papenhausen, Haipeng Shao
Cancer Genetics|March 26, 2023
Mitotic recombinatory evolution in acute leukemiaPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
Archives of Pathology & Laboratory Medicine|January 2, 2013
Burkitt lymphoma arising from lymphoplasmacytic lymphoma following acquisition of MYC translocation and loss of the ETV6 tumor suppressor geneDeniz Peker, Brian Quigley, Dahui Qin, et al.
Cancer Genetics|September 18, 2012
Microarray, gene sequencing, and reverse transcriptase-polymerase chain reaction analyses of a cryptic PML-RARA translocationJason Koshy, You-Wen Qian, Gayathri Bhagwath, et al.
Cancer Genetics|February 27, 2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusionsPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
International Journal of Clinical and Experimental Pathology|January 19, 2013
Double-hit mantle cell lymphoma with MYC gene rearrangement or amplification: a report of four cases and review of the literatureReza Setoodeh, Stuart Schwartz, Peter Papenhausen, et al.
Cancer Genetics|March 25, 2015
MYC amplification in multiple marker chromosomes and EZH2 microdeletion in a man with acute myeloid leukemiaZhifu Xiang, Al-Ola Abdallah, Rangaswamy Govindarajan, et al.
Cancer Genetics|December 3, 2014
Concurrence of B-lymphoblastic leukemia and myeloproliferative neoplasm with copy neutral loss of heterozygosity at chromosome 1p harboring a MPL W515S mutationJiangchuan Tao, Xiaohui Zhang, Jeffrey Lancet, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCNRachel D Burnside, Sharon Molinari, Christina Botti, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Genes|April 6, 2017
The Role of c-MYC in B-Cell Lymphomas: Diagnostic and Molecular AspectsLynh Nguyen, Peter Papenhausen, Haipeng Shao
International Journal of Clinical and Experimental Pathology|July 21, 2015
Therapy-related acute myeloid leukemia with eosinophilia, basophilia, t(4;14)(q12;q24) and PDGFRA rearrangement: a case report and review of the literatureJun Zhou, Peter Papenhausen, Haipeng Shao
Cancer Genetics|March 26, 2023
Mitotic recombinatory evolution in acute leukemiaPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
Archives of Pathology & Laboratory Medicine|January 2, 2013
Burkitt lymphoma arising from lymphoplasmacytic lymphoma following acquisition of MYC translocation and loss of the ETV6 tumor suppressor geneDeniz Peker, Brian Quigley, Dahui Qin, et al.
Cancer Genetics|September 18, 2012
Microarray, gene sequencing, and reverse transcriptase-polymerase chain reaction analyses of a cryptic PML-RARA translocationJason Koshy, You-Wen Qian, Gayathri Bhagwath, et al.
Cancer Genetics|February 27, 2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusionsPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
International Journal of Clinical and Experimental Pathology|January 19, 2013
Double-hit mantle cell lymphoma with MYC gene rearrangement or amplification: a report of four cases and review of the literatureReza Setoodeh, Stuart Schwartz, Peter Papenhausen, et al.
Cancer Genetics|March 25, 2015
MYC amplification in multiple marker chromosomes and EZH2 microdeletion in a man with acute myeloid leukemiaZhifu Xiang, Al-Ola Abdallah, Rangaswamy Govindarajan, et al.
Cancer Genetics|December 3, 2014
Concurrence of B-lymphoblastic leukemia and myeloproliferative neoplasm with copy neutral loss of heterozygosity at chromosome 1p harboring a MPL W515S mutationJiangchuan Tao, Xiaohui Zhang, Jeffrey Lancet, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCNRachel D Burnside, Sharon Molinari, Christina Botti, et al.
Pageof 2