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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person FRS3 (also known as FRS2beta) is predominantly expressed in ...

Class:IdSummation:1268222
_displayNameFRS3 (also known as FRS2beta) is predominantly expressed in ...
_timestamp2014-12-03 20:41:54
created[InstanceEdit:1268223] Rothfels, K, 2011-05-09
modified[InstanceEdit:1295635] Rothfels, K, 2011-05-17
[InstanceEdit:1549598] Rothfels, K, 2011-08-30
[InstanceEdit:5654383] Rothfels, Karen, 2014-12-03
textFRS3 (also known as FRS2beta) is predominantly expressed in the developing and adult neuroepithelium. As is the case for FRS2 (also known as FRS2alpha), binding of FRS3 to FGFR may be constitutive and/or independent of receptor activation. Elements of the downstream signaling mediated by the two FRS family members appear to be at least partially conserved, as FRS3 is phosphorylated upon FGF stimulation, binds PPTN11/SHP2 and GRB2 and results in ERK activation. Moreover, expression of FRS3 in FRS2-/- MEFs restores ERK activation.
(summation)[Reaction:5654571] Activated FGFR1 binds FRS3 [Homo sapiens]
[Reaction:5654603] Activated FGFR2 binds FRS3 [Homo sapiens]
[Reaction:5654623] Activated FGFR3 binds FRS3 [Homo sapiens]
[Reaction:5654651] Activated FGFR4 binds FRS3 [Homo sapiens]
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