Identification and characterization of an inhibitory fibroblast growth factor receptor 2 (FGFR2) molecule, up-regulated in an Apert Syndrome mouse model

Critical Role of FLRT1 Phosphorylation in the Interdependent Regulation of FLRT1 Function and FGF Receptor Signalling

(2010) Lee M. Wheldon et al.   PLoS One

N-Glycosylation Regulates Fibroblast Growth Factor Receptor/EGL-15 Activity inCaenorhabditis elegans in Vivo

(2009) Urszula M. Polanska et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The FGF family: biology, pathophysiology and therapy

(2009) Andrew Beenken et al.   NATURE REVIEWS DRUG DISCOVERY

Klotho

(2009) Makoto Kuro-o   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Evidence that Fgf10 contributes to the skeletal and visceral defects of an apert syndrome mouse model

(2008) Mohammad K. Hajihosseini et al.   DEVELOPMENTAL DYNAMICS

Rare mutations ofFGFR2causing apert syndrome: identification of the first partial gene deletion, and anAluelement insertion from a new subfamily

(2008) Elena G. Bochukova et al.   HUMAN MUTATION