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Details on Person Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes

Class:IdLiteratureReference:1637891
_displayNameFrequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
_timestamp2011-10-05 18:33:26
author[Person:1614151] Pollock, PM
[Person:1614693] Gartside, MG
[Person:1614685] Dejeza, LC
[Person:1614715] Powell, MA
[Person:1614704] Mallon, MA
[Person:1614051] Davies, H
[Person:111044] Mohammadi, M
[Person:1614071] Futreal, PA
[Person:1614179] Stratton, MR
[Person:69411] Trent, JM
[Person:1614694] Goodfellow, PJ
created[InstanceEdit:1637892] Rothfels, K, 2011-10-05
journalOncogene
pages7158-62
pubMedIdentifier17525745
titleFrequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
volume26
year2007
(literatureReference)[EntityWithAccessionedSequence:1637889] FGFR2c A315T [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:1637895] FGFR2 C383R mutant [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:1637900] FGFR2 K660E [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:1637908] FGFR2 L764Hfs*4 [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:1637910] FGFR2 N549K [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:1637924] FGFR2b S373C [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:1637931] FGFR2b Y376C [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2029866] p-8Y-FGFR2b S376C [plasma membrane] [Homo sapiens]
[Complex:2029923] FGFR2b S373C mutant dimer [plasma membrane] [Homo sapiens]
[Complex:2029924] FGFR2b Y376C mutant dimer [plasma membrane] [Homo sapiens]
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No pathways have been reviewed or authored by Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes (1637891)