Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marten Gehlhaar"'
Autor:
Marten Gehlhaar, Hartmut Döhner, Rabia Shahswar, Gudrun Göhring, Aylin Kirchner, Anuhar Chaturvedi, Robin Bollin, Frederik Damm, Arnold Ganser, Felicitas Thol, Lutz Wiehlmann, Liu Huang, Carolin Walter, Martin Wichmann, Brigitte Schlegelberger, Richard F. Schlenk, K.J. Suchanek, Michael Heuser, Martin Dugas, Konstanze Döhner, Jürgen Krauter
Publikováno v:
Blood. 123(6)
Mutations in the cohesin complex are novel, genetic lesions in acute myeloid leukemia (AML) that are not well characterized. In this study, we analyzed the frequency, clinical, and prognostic implications of mutations in STAG1, STAG2, SMC1A, SMC3, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e39ec0b5fdf94578725a7d83c5b4467e
https://pubmed.ncbi.nlm.nih.gov/24335498
https://pubmed.ncbi.nlm.nih.gov/24335498
Autor:
Victoria Panagiota, Nicolaus Kroeger, Tatjana Zabelina, Felicitas Thol, Michael Heuser, Robin Bollin, Anita Badbaran, Boris Fehse, Gudrun Göhring, Michelle Maria Araujo Cruz, Christian Koenecke, Haefaa Alchalby, Anuhar Chaturvedi, Matthias Eder, Marten Gehlhaar, Maximilian Christopeit, Francis Ayuk, Rabia Shahswar, Ulrich Lehmann, Ioanna Triviai, Michael Koenigsmann, Arnold Ganser, Brigitte Schlegelberger, Christine Wolschke, Hans Kreipe, Michael Stadler
Publikováno v:
Blood. 126:352-352
Introduction Primary or post-ET/post-PV myelofibrosis is one of the Philadelphia chromosome-negative chronic myeloproliferative neoplasia characterized by significantly reduced overall survival. More recently several mutated genes have been detected,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ee8ddcc5f47f534c56652cf6d719a63
https://doi.org/10.1182/blood.v126.23.352.352
https://doi.org/10.1182/blood.v126.23.352.352
Autor:
Hartmut Döhner, Martin Wichmann, Arnold Ganser, Jürgen Krauter, Liu Huang, Brigitte Schlegelberger, K.J. Suchanek, Konstanze Döhner, Gudrun Goehring, Marten Gehlhaar, Anuhar Chaturvedi, Frederik Damm, Aylin Kirchner, Michael Heuser, Robin Bollin, Felicitas Thol, Lutz Wiehlmann, Carolin Walter, Martin Dugas, Richard F. Schlenk
Publikováno v:
Blood. 122:1314-1314
Background The cohesin complex presents a ring structure that regulates chromosome segregation during meiosis and mitosis and is thus essential for cell division. Genes that belong to the cohesin complex in somatic vertebrate cells are SMC1A, SMC3, R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f190d503febecf687e236d58e7c7650
https://doi.org/10.1182/blood.v122.21.1314.1314
https://doi.org/10.1182/blood.v122.21.1314.1314
Autor:
Francis Ayuk, Vera Dobbernack, Christian Koenecke, Christine Wolschke, Robin Bollin, Michael Heuser, Marten Gehlhaar, Haefaa Alchalby, Felicitas Thol, Tatjana Zabelina, Liu Huang, Sofia Kade, Nicolaus Kröger, Arnold Ganser
Publikováno v:
ResearcherID
Abstract 1740 Mutations in the additional sex combs like 1 gene (ASXL1) have been described recently in patients with myelodysplastic and myeloproliferative syndromes. While in MDS ASXL1 is associated with worse prognosis, the role in MPN is not well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ceeaef3afc7ab0e4b5e0deba814d445
https://doi.org/10.1182/blood.v120.21.1740.1740
https://doi.org/10.1182/blood.v120.21.1740.1740
Autor:
Robin Bollin, Anita Badbaran, Tatjana Zabelina, Lutz Wiehlmann, Carolin Walter, Rabia Shahswar, Michelle Maria Araujo Cruz, Felicitas Thol, Gudrun Göhring, Francis Ayuk, Victoria Panagiota, Anuhar Chaturvedi, Ioanna Triviai, Hans-Heinrich Kreipe, Martin Dugas, Boris Fehse, Christian Koenecke, Christine Wolschke, Michael Heuser, Carol Stocking, Max Christopeit, Ulrich Lehmann, Michael Koenigsmann, Matthias Eder, Marten Gehlhaar, Nicolaus Kröger, Arnold Ganser, Brigitte Schlegelberger, Michael Stadler, Haefaa Alchalby
Publikováno v:
Biology of Blood and Marrow Transplantation
Molecular genetics may influence outcome for patients with myelofibrosis. To determine the impact of molecular genetics on outcome after allogeneic stem cell transplantation, we screened 169 patients with primary myelofibrosis (n = 110), post-essenti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bab2cf87f83e14b3a48c62a47eff568