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4 research outputs found

Genomic profile of patients with triple negative (JAK2, CALR and MPL) essential thrombocythemia and primary myelofibrosis

Whole exome sequencing of philadelphia-negative (Ph-negative) myeloproliferative neoplasms (MPNs) and myelodysplastic/myeloproliferative disorders (MDS/MPD)

Incidence and impact of activating mutations of the RAS-RAF- MEK-ERK pathway in patients with philadelphia-negative (Ph-negative) myeloproliferative neoplasms (MPNs) and myelodysplastic/myeloproliferative disorders-unclassified (MDS/MPD-U)

The presence of ASXL1 mutations as well as a total number of myeloid driver mutations higher than two is strongly associated with the diagnosis of primary myelofibrosis as opposed to essential thrombocythemia

Author: Ascendino Evelyn Helena
Bacal Nydia
Bello Isabel C.
Bezerra Alanna Mara P. S.
Bollman Patricia W.
Campregher Paulo Vidal
Cordeiro De Farias Danielle Leao
Costa Erika M. M.
Costa Fernando Ferreira
Datoguia Tarcila S.
De Souza Santos Fabio Pires
Diniz Michelli Silva
Fadel Adriana Valente
Guerra Joao Carlos
Hamerschlak Nelson
Helman Ricardo
Higashi Marcia
Kassab Carolina
Lima Marinus de Moraes
Lisboa Bianca
Mattos Vinicius R. P.
Miyagi Mariana
Musacchio Juliane
Padua Leandro
Pasqualin Denise da Cunha
Pereira Welbert Oliveira
Perini Guilherme Fleury
Perobelli Leila Martins
Petroni Roberta Cardoso
Puga Renato D.
Salvino Marco A.
Santucci Rodrigo
Schriefer Ana Fernandes
Silveira Paulo A. A.
Soares Rodolfo
Souto Eizabeth Xisto
Tiburcio Manuela Pinto
Velloso Elvira
Yoshida Sandra Nakashima
Publication venue: Amer Soc Hematology
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