FGFR1 Oncogene Partner 2

Known as: FGFR1OP2, Fibroblast Growth Factor Receptor 1 Oncogene Partner 2 
FGFR1 oncogene partner 2 (253 aa, ~29 kDa) is encoded by the human FGFR1OP2 gene. This protein may be involved in wound responses.
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2013
01220042013

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Hematological malignancies with FGFR1 abnormality (8p11 myeloproliferative syndrome; EMS) are rare atypical stem cell disorders… (More)
  • figure 1
  • figure 2
Is this relevant?
2013
2013
Background:A strong, consistent association between childhood irradiation and subsequent thyroid cancer provides an excellent… (More)
  • figure 1
  • table 1
  • figure 2
  • table 2
Is this relevant?
2012
2012
BACKGROUND A previous study on the genetic association between single nucleotide polymorphisms in FGFR1OP2/wit3.0 and the long… (More)
  • table 1
  • table 2
  • table 3
  • table 3
  • figure 1
Is this relevant?
2011
2011
The KG-1a cell line is developed from a human stem cell myeloproliferative neoplasm as the result of intragenic disruption and a… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2010
2010
Wounds created in the oral cavity heal rapidly and leave minimal scarring. We have examined a role of a previously isolated cDNA… (More)
  • figure 1
  • table 1
  • table 2
  • figure 2
  • figure 3
Is this relevant?
2010
2010
Wound closure and infection control are the primary goal of wound management. A variety of disinfectants and antimicrobial agents… (More)
Is this relevant?
2009
2009
Hematological malignancies associated with FGFR1 rearrangements (8p11-chromosome eighth-myeloproliferative syndrome (EMS) are… (More)
  • table 1
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
Review
2009
Review
2009
The serine/threonine protein phosphatases are targeted to specific subcellular locations and substrates in part via interactions… (More)
Is this relevant?
2006
2006
The 8p11 myeloproliferative syndrome (EMS) is associated with translocations that disrupt the FGFR1 gene. To date, 8 fusion… (More)
Is this relevant?
2004
2004
The 8p11 myeloproliferative syndrome (EMS) is an aggressive hematological malignancy caused by the fusion of diverse partner… (More)
Is this relevant?