FGF-3 is a member of the fibroblast growth factor family.

It is linked to a mutation in the fibroblast growth factor receptor-3.

Many growth factors are ignored including my favourite, basic fibroblast growth factor.

It can be associated with missense mutations in fibroblast growth factor receptor-3.

The other drug is a protein called FGF-1, for fibroblast growth factor.

Fibroblast growth factor 11 also known as FGF11 is a human gene.

Fibroblast growth factor 15 is a protein in mouse encoded by the Fgf15 gene.

RPL6 has been shown to interact with Basic fibroblast growth factor.

The following syndromes are associated with fibroblast growth factor receptors:

Fgf8 is also known as Fibroblast Growth Factor 8.

They had first mixed the fibrin with fibroblast growth factor, a substance that encourages cells to grow.

Fibroblast growth factor signaling during early vertebrate development.

Fibroblast growth factors comprise the largest family of growth factor ligands at 23 members.

There is some evidence that development involves Sonic hedgehog and Fibroblast growth factor 8.

Apert syndrome is caused by mutations in a gene called fibroblast growth factor receptor 2.

Regulation of cerebral cortical size and neuron number by fibroblast growth factors: implications for autism.

Pfeiffer syndrome is strongly associated with mutations of Fibroblast growth factor receptor 1 and 2.

They have additionally been suggested as regulators for fibroblast growth factor and bone morphogenic protein signaling.

This protein is indirectly involved in the non-cell autonomous inhibitory effect on fibroblast growth factor two signaling.

This particular family member binds both acidic and basic fibroblast growth factors and is involved in limb induction.

FGF15/19 refers to two orthologous fibroblast growth factors which share 50% aminoacid identity and have similar functions.

The sensitivity of Fibroblast Growth Factor 23 measurements in tumor induced osteomalacia.

These cells do not respond to androgens, glucocorticoids, or epidermal or fibroblast growth factors.

Achondroplasia is caused by a change in the DNA for fibroblast growth factor receptor 3.

Cysteine-rich fibroblast growth factor receptor is also implicated in neuronal growth and differentiation.