Molecular Monitoring of 8p11 Myeloproliferative Syndrome in an Infant-Reference-Cited by-同舟云学术

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Molecular Monitoring of 8p11 Myeloproliferative Syndrome in an Infant

Published:2009-11 Issue:11 Volume:31 Page:879-883
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Zhang Wenyong W.,Habeebu Sultan,Sheehan Andrea M.,Naeem Rizwan,Hernandez Vivian S.,Dreyer ZoAnn E.,López-Terrada Dolores

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference40 articles.

1. WHO Classification of Tumours of the Haematopoietic and Lymphoid Tissues. 4th ed;Bain,2008

2. FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome;Xiao;Nat Genet,1998

3. The t(8;13)(p11;q11–12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP;Smedley;Hum Mol Genet,1998

4. Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12);Popovici;Proc Natl Acad Sci USA,1998

5. ZNF198-FGFR1 transforms Ba/F3 cells to growth factor independence and results in high level tyrosine phosphorylation of STATS 1 and 5;Smedley;Neoplasia,1999

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3. Clinical outcomes of myeloid/lymphoid neoplasms with fibroblast growth factor receptor-1 (FGFR1) rearrangement;Hematology;2018-02-28

4. Pediatric 8p11 eosinophilic myeloproliferative syndrome (EMS): A case report and review of the literature;Pediatric Blood & Cancer;2016-11-03

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