FgfR2IIIa-F, FgfR2IIIb-R
Primer Detail
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Name
FgfR2IIIa-F, FgfR2IIIb-R
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Primer 1 Sequence
CCCATCCTCCAAGCTGGACTGCCT
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Primer 2 Sequence
CTGTTTGGGCAGGACAGTGAGCCA
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ID
MGI:6402449
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Region Covered
exons 7-8
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Synonyms
R2-IIIb primers
Fgfr2
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fibroblast growth factor receptor 2
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J:72517
Hajihosseini MK, et al., A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3855-60
J:144432
Hajihosseini MK, et al., Evidence that Fgf10 contributes to the skeletal and visceral defects of an apert syndrome mouse model. Dev Dyn. 2009 Feb;238(2):376-85
J:150712
Yaguchi Y, et al., Fibroblast growth factor (FGF) gene expression in the developing cerebellum suggests multiple roles for FGF signaling during cerebellar morphogenesis and development. Dev Dyn. 2009 Jun 19;238(8):2058-2072