Fibroblast growth factor receptors (FGFRs) and FGF ligands are highly expressed in the
developing kidney and lower urinary tract. Several classic studies showed many effects of …

Fibroblast growth factor receptors (Fgfrs) consist of four signaling family members and one
nonsignaling “decoy” receptor, Fgfr-like 1 (Fgfrl1), all of which are expressed in the …

Objective To retrospectively study prenatal ultrasound images of patients with
craniosynostosis to determine the extent to which prenatal diagnosis is possible. Method …

This study aimed to explore the spatio-temporal expression patterns of congenital anomalies
of kidney and urinary tract (CAKUT) candidate genes, Fibroblast Growth Factor Receptor 1 …

Fibroblast growth factor receptors (Fgfrs) are expressed in the ureteric bud and metanephric
mesenchyme of the developing kidney. Furthermore, in vitro and in vivo studies have shown …

The association between ear and kidney anomalies has long been recognized. However,
little is known about the underlying mechanisms. In the last two decades, embryonic …

This study aimed to explore how Dab1 gene functional silencing influences the spatial and
temporal expression patterns of fibroblast growth factor receptor 1 (FGFR1), fibroblast …

Gastroschisis (GS) is a full-thickness abdominal wall defect with prolapse of the bowel and
sporadically other viscera. The abdominal wall itself may close around the viscera …

Antley-Bixler syndrome (ABS)—consisting of ABS type 1 (skeletal only) and ABS type 2,
associated with cytochrome 450 mutations and P450 oxidoreductase deficiency (PORD …

Apert syndrome is a genetic disorder of autosomal dominant transmission. It is characterized
by craniofacial malformations that cause craniosynostosis, hypoplasia of the middle third of …