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Details on Person Syndromic craniosynostosis: from history to hydrogen bonds

Class:IdLiteratureReference:2046359
_displayNameSyndromic craniosynostosis: from history to hydrogen bonds
_timestamp2012-01-11 19:11:02
author[Person:190975] Cunningham, ML
[Person:190976] Seto, ML
[Person:2046335] Ratisoontorn, C
[Person:2046331] Heike, CL
[Person:2046334] Hing, AV
created[InstanceEdit:2046358] Rothfels, K, 2012-01-11
journalOrthod Craniofac Res
pages67-81
pubMedIdentifier17552943
titleSyndromic craniosynostosis: from history to hydrogen bonds
volume10
year2007
(literatureReference)[Pathway:1226099] Signaling by FGFR in disease [Homo sapiens]
[Pathway:1839122] Signaling by activated point mutants of FGFR1 [Homo sapiens]
[Pathway:1839124] FGFR1 mutant receptor activation [Homo sapiens]
[Pathway:1839126] FGFR2 mutant receptor activation [Homo sapiens]
[Reaction:2033479] Dimerization of FGFR2 point mutants with enhanced kinase activity [Homo sapiens]
[Reaction:2033490] Autocatalytic phosphorylation of FGFR2 point mutants with enhanced kinase activity [Homo sapiens]
[Pathway:2033519] Activated point mutants of FGFR2 [Homo sapiens]
[Pathway:5655253] Signaling by FGFR2 in disease [Homo sapiens]
[Pathway:5655302] Signaling by FGFR1 in disease [Homo sapiens]
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