The FGFRL1 Receptor Is Shed from Cell Membranes, Binds Fibroblast Growth Factors (FGFs), and Antagonizes FGF Signaling inXenopusEmbryos

RANK/RANKL: Regulators of Immune Responses and Bone Physiology

(2009) Andreas Leibbrandt et al.   Annals of the New York Academy of Sciences

Multiple congenital malformations of Wolf-Hirschhorn syndrome are recapitulated in Fgfrl1 null mice

(2009) C. Catela et al.   Disease Models & Mechanisms

The FGF family: biology, pathophysiology and therapy

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

Characterization of the first FGFRL1 mutation identified in a craniosynostosis patient

(2008) Thorsten Rieckmann et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions

(2008) Hannelie Engbers et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Pax3 regulation of FGF signaling affects the progression of embryonic progenitor cells into the myogenic program

(2008) M. Lagha et al.   GENES & DEVELOPMENT

Large-scale screening for novel low-affinity extracellular protein interactions

(2008) K. M. Bushell et al.   GENOME RESEARCH

The cell surface receptor FGFRL1 forms constitutive dimers that promote cell adhesion

(2007) Thorsten Rieckmann et al.   EXPERIMENTAL CELL RESEARCH