Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Thrombocytopenia and RUNX1[original query] |
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Clinical effect of point mutations in myelodysplastic syndromes. The New England journal of medicine 2011 Jun 364 (26): 2496-506. Bejar Rafael, Stevenson Kristen, Abdel-Wahab Omar, Galili Naomi, Nilsson Björn, Garcia-Manero Guillermo, Kantarjian Hagop, Raza Azra, Levine Ross L, Neuberg Donna, Ebert Benjamin |
Impact of somatic and germline mutations on the outcome of systemic mastocytosis. Blood advances 2018 11 2 (21): 2814-2828. Muñoz-González Javier I, Jara-Acevedo María, Alvarez-Twose Iván, Merker Jason D, Teodosio Cristina, Hou Yanli, Henriques Ana, Roskin Krishna M, Sanchez-Muñoz Laura, Tsai Albert G, Caldas Carolina, Matito Almudena, Sánchez-Gallego J Ignacio, Mayado Andrea, Dasilva-Freire Noelia, Gotlib Jason R, Escribano Luis, Orfao Alberto, García-Montero Andrés |
Genotypic and phenotypic evolution in a patient with chronic myelomonocytic leukemia. Leukemia research reports 2019 12 12 100185. Geissler Klaus, Jäger Eva, Gurbisz Micha |
A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome. Aging clinical and experimental research 2020 9 33 (7): 1987-1992. Ferrari Silvia, Regazzo Daniela, Omenetto Elisabetta, Scaroni Carla, Semenzato Gianpietro, Fabris Fabrizio, Vianello Fabriz |
A family case series of inherited thrombocytopenia. Proceedings (Baylor University. Medical Center) 2022 12 36 (1): 93-95. Borkowski Artur, Gawry? Jakub, Iwanek Gracjan, Dybko Jaros? |
A RUNX1-FPDMM rhesus macaque model reproduces the human phenotype and predicts challenges to curative gene therapies. Blood 2022 11 141 (3): 231-237. Lee Byung-Chul, Zhou Yifan, Bresciani Erica, Ozkaya Neval, Dulau-Florea Alina, Carrington Blake, Shin Tae-Hoon, Baena Valentina, Syed Zulfeqhar A, Hong So Gun, Zhen Tao, Calvo Katherine R, Liu Paul, Dunbar Cynthia |
The clinical phenotype of germline RUNX1 mutations in relation to the accompanying somatic variants and RUNX1 isoform expression. Genes, chromosomes & cancer 2023 6 . David Cabrerizo Granados, Indira Barbosa, Panagiotis Baliakas, Eva Hellström-Lindberg, Vanessa Lund |
Unrelated hematopoietic stem cell transplantation for familial platelet disorder/acute myeloid leukemia with germline RUNX1 mutations. International journal of hematology 2023 3 . Toratani Kazunori, Watanabe Mizuki, Kanda Junya, Oka Tomomi, Hyuga Mizuki, Arai Yasuyuki, Iwasaki Makoto, Sakurada Maki, Nannya Yasuhito, Ogawa Seishi, Yamada Takahiro, Takaori-Kondo Akifu |
Germline RUNX1 variants in paediatric patients in a French specialised centre. EJHaem 2023 2 4 (1): 145-152. Liu Cécile, Ballerini Paola, Nguyen Guillaume, Mincheva Zoia, Copin Bruno, Bouslama Boutheina, Leverger Guy, Petit Arnaud, Favier Rémi, Lapillonne Hélène, Boutroux Hélè |
Mutated IKZF1 is an independent marker of adverse risk in acute myeloid leukemia. Leukemia 2023 10 . Jan-Niklas Eckardt, Sebastian Stasik, Christoph Röllig, Andreas Petzold, Tim Sauer, Sebastian Scholl, Andreas Hochhaus, Martina Crysandt, Tim H Brümmendorf, Ralph Naumann, Björn Steffen, Volker Kunzmann, Hermann Einsele, Markus Schaich, Andreas Burchert, Andreas Neubauer, Kerstin Schäfer-Eckart, Christoph Schliemann, Stefan W Krause, Regina Herbst, Mathias Hänel, Maher Hanoun, Ulrich Kaiser, Martin Kaufmann, Zdenek Rácil, Jiri Mayer, Uta Oelschlägel, Wolfgang E Berdel, Gerhard Ehninger, Hubert Serve, Carsten Müller-Tidow, Uwe Platzbecker, Claudia D Baldus, Andreas Dahl, Johannes Schetelig, Martin Bornhäuser, Jan Moritz Middeke, Christian Thie |
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- Page last updated:Apr 29, 2024
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