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JAK2 V617F Mutation Prevalence in Myeloproliferative Neoplasms in Pernambuco, Brazil
(Mary Ann Liebert IncNew RochelleEUA, 2012)
SF3B1, a splicing factor is frequently mutated in refractory anemia with ring sideroblasts
(Nature Publishing GroupLondon, 2012)
Jak2 46/1 Haplotype Is Associated With Jak2 V617f-positive Myeloproliferative Neoplasms In Brazilian Patients
(WILEY-BLACKWELLHOBOKEN, 2015)
JAK2V617F mutation prevalence on chilean adults suffering from primary mesenteric and portal venous thromboses
(Wiley, 2020)
Introduction Mesenteric and portal venous thromboses are rare diseases with high mortality rates and are strongly associated with hepatic cirrhosis, and abdominal inflammatory or tumoral processes, but in some cases can ...
Frequência da mutação JAK2V617F em pacientes com trombocitose no interior do RS
(Universidade Federal de Santa MariaBrasilCiências da SaúdeUFSMPrograma de Pós-Graduação em Ciências FarmacêuticasCentro de Ciências da Saúde, 2020-03-06)
Myeloproliferative neoplasms (MPN) are unique hematopoietic stem-cell disorders, resulting in an
increased proliferation of single or multilineage mature hematopoietic cells. JAK2V617F mutation is a
diagnostic ...
Molecular analysis of 23 exons of the cftr gene in brazilian patients leads to the finding of rare cystic fibrosis mutations
(Wayne State University Press, 2012)
A mutação JAK2 V617F e as síndromes mieloproliferativasJAK2 V617F mutation and the myeloproliferative disorders
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2008)