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Molecular drug targets in myeloproliferative neoplasms: mutant ABL1, JAK2, MPL, KIT, PDGFRA, PDGFRB and FGFR1.
Tefferi A. Tefferi A. J Cell Mol Med. 2009 Feb;13(2):215-37. doi: 10.1111/j.1582-4934.2008.00559.x. Epub 2008 Oct 23. J Cell Mol Med. 2009. PMID: 19175693 Free PMC article. Review.
FIP1L1-PDGFRA) or inter-chromosomal (e.g. ETV6-PDGFRB) gene fusions. BCR-ABL1 is associated with chronic myelogenous leukaemia (CML) and mutant PDGFR with an MPN phenotype characterized by eosinophilia and in addition, in case of FIP1L1-PDGFRA, bone marrow mastocyto …
FIP1L1-PDGFRA) or inter-chromosomal (e.g. ETV6-PDGFRB) gene fusions. BCR-ABL1 is associated with chronic myelogenous leukaemia …
Oncogenic signals as treatment targets in classic myeloproliferative neoplasms.
Tefferi A, Levine RL, Kantarjian H. Tefferi A, et al. Biol Blood Marrow Transplant. 2009 Jan;15(1 Suppl):114-9. doi: 10.1016/j.bbmt.2008.10.010. Biol Blood Marrow Transplant. 2009. PMID: 19147089 Free article. Review.
Therapeutically validated oncoproteins in myeloproliferative neoplasms (MPNs) include BCR-ABL in chronic myelogenous leukemia (CML) and a spectrum of PDGFRA/B mutant proteins that are products of intra- (eg, FIP1L1-PDGFRA) or interchromosomal (eg, ETV6-PDGFRB) gene …
Therapeutically validated oncoproteins in myeloproliferative neoplasms (MPNs) include BCR-ABL in chronic myelogenous leukemia (CML) and a sp …
Myeloid Neoplasms with t(5;12) and ETV6-ACSL6 Gene Fusion, Potential Mimickers of Myeloid Neoplasm with PDGFRB Rearrangement: Case Report with Imatinib Therapy and Review of the Literature.
De Luca-Johnson J, Ninfea JI, Pearson L, Conant J, Bryant R, Zakai NA, Tang ME. De Luca-Johnson J, et al. Case Rep Med. 2016;2016:8324791. doi: 10.1155/2016/8324791. Epub 2016 Sep 26. Case Rep Med. 2016. PMID: 27746819 Free PMC article.
ETV6-ACSL6 gene fusion is a rare abnormality that most often presents as a myeloproliferative-type disorder with prominent eosinophilia or basophilia. Review of the literature yielded a total of 11 previous cases. This gene fusion results in a t(5;12)(q31~33;p13) that mimi …
ETV6-ACSL6 gene fusion is a rare abnormality that most often presents as a myeloproliferative-type disorder with prominent eosinophilia or b …
Myeloid neoplasm with ETV6::ACSl6 fusion: landscape of molecular and clinical features.
Su Z, Liu X, Hu W, Yang J, Yin X, Hou F, Wang Y, Zhang J. Su Z, et al. Hematology. 2022 Dec;27(1):1010-1018. doi: 10.1080/16078454.2022.2117206. Hematology. 2022. PMID: 36069745 Free article. Review.
OBJECTIVES: Since the publication of the third edition, the WHO classification of tumors of hematopoietic and lymphoid disorders has introduced the disease entity of 'myeloid/lymphoid neoplasms with eosinophilia and PDGFRB rearrangement', in which the most common chromosomal abno …
OBJECTIVES: Since the publication of the third edition, the WHO classification of tumors of hematopoietic and lymphoid disorders has introdu …
Fusion genes in leukemia: an emerging network.
Bohlander SK. Bohlander SK. Cytogenet Cell Genet. 2000;91(1-4):52-6. doi: 10.1159/000056818. Cytogenet Cell Genet. 2000. PMID: 11173830 Review.
Not only does one find star-shaped topologies, with one gene forming fusions with several others (e.g. ETV6/PDGFRB, ETV6/JAK2, ETV6/ABL etc.), but also networks connecting several genes with more than one fusion partner (e.g. ...
Not only does one find star-shaped topologies, with one gene forming fusions with several others (e.g. ETV6/PDGFRB, ETV6/JAK2, …
[The hematological malignancies related to primary hypereosinophilia and their diagnostics].
Skonieczka K, Matiakowska K, Haus O. Skonieczka K, et al. Postepy Hig Med Dosw (Online). 2014 Dec 29;68:1530-7. doi: 10.5604/17322693.1134167. Postepy Hig Med Dosw (Online). 2014. PMID: 25834096 Free article. Review. Polish.
In differential diagnosis of hypereosinophilia, the analysis of characteristic gene mutations (e.g., cKIT) and gene fusions (e.g., ETV6-PDGFRB) is also applied, using molecular genetic methods....
In differential diagnosis of hypereosinophilia, the analysis of characteristic gene mutations (e.g., cKIT) and gene fusions (e.g., ETV6
[ABL1, SRC and other non-receptor protein tyrosine kinases as new targets for specific anticancer therapy].
Klener P, Klener P Jr. Klener P, et al. Klin Onkol. 2010;23(4):203-9. Klin Onkol. 2010. PMID: 20806817 Review. Czech.
Small molecule tyrosine kinase inhibitors interfere with these pathophysiological circuits by blocking the signalling cascades triggered by the aberrantly activated protein tyrosine kinases (e.g. BCR-ABL1, FIP1L1-PDGFRA or ETV6-PDGFRB).Tyrosine kinase inhibitors (im …
Small molecule tyrosine kinase inhibitors interfere with these pathophysiological circuits by blocking the signalling cascades triggered by …