Jonathan A. Britto

Bone grafts and biomaterials substitutes for bone defect repair: A review

TGF-??1, FGF-2, and Receptor mRNA Expression in Suture Mesenchyme and Dura versus Underlying Brain in Fusing and Nonfusing Mouse Cranial Sutures

Netrin and Netrin Receptor Expression in the Embryonic Mammalian Nervous System Suggests Roles in Retinal, Striatal, Nigral, and Cerebellar Development

Sox9 Modulates Proliferation and Expression of Osteogenic Markers of Adipose-Derived Stem Cells (ASC)

The FGF family: biology, pathophysiology and therapy

C. elegans: des neurones et des gènes

Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome

Bad bones, absent smell, selfish testes: The pleiotropic consequences of human FGF receptor mutations

PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase

Reaching a Genetic and Molecular Understanding of Skeletal Development

Taking it to the max: The genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology

Abnormal wound healing: keloids

The control of human mesenchymal cell differentiation using nanoscale symmetry and disorder

Cellular signaling by fibroblast growth factor receptors

Extracellular Matrix Degradation and Remodeling in Development and Disease

FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease

Developmental regulation of the growth plate

Mesodermal expression of Fgfr2 is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome

Fibroblast growth factor signalling: from development to cancer

A tense situation: forcing tumour progression

Effects of FGF-2 on metaphyseal fracture repair in rabbit tibiae

Hypoxia-inducible factors promote breast cancer stem cell specification and maintenance in response to hypoxia or cytotoxic chemotherapy

FGF9 regulates early hypertrophic chondrocyte differentiation and skeletal vascularization in the developing stylopod

Mammalian homologs of seven in absentia regulate DCC via the ubiquitin–proteasome pathway

Hypertrophic Scarring and Keloids: Pathomechanisms and Current and Emerging Treatment Strategies

FGF18 is required for normal cell proliferation and differentiation during osteogenesis and chondrogenesis

Deleted in Colorectal Cancer (DCC) Encodes a Netrin Receptor

Placenta Growth Factor and Vascular Endothelial Growth Factor are Co-Expressed During Early Embryonic Development

FGF signaling in the developing endochondral skeleton

The Fibroblast Growth Factor signaling pathway

Natriuretic Peptides, Their Receptors, and Cyclic Guanosine Monophosphate-Dependent Signaling Functions

Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

Function of IRE1 alpha in the placenta is essential for placental development and embryonic viability

Wound Healing: A Cellular Perspective

Netrin-G1: a Novel Glycosyl Phosphatidylinositol-Linked Mammalian Netrin That Is Functionally Divergent from Classical Netrins

The Molecular Biology of Axon Guidance

Functions of Cell Surface Heparan Sulfate Proteoglycans

Differential Expression of Fibroblast Growth Factor Receptors in Human Digital Development Suggests Common Pathogenesis in Complex Acrosyndactyly and Craniosynostosis

Negative autoregulation of fibroblast growth factor receptor 2 expression characterizing cranial development in cases of Apert (P253R mutation) and Pfeiffer (C278F mutation) syndromes and suggesting a basis for differences in their cranial phenotypes

From Genotype to Phenotype: The Differential Expression of FGF, FGFR, and TGFβ Genes Characterizes Human Cranioskeletal Development and Reflects Clinical Presentation in FGFR Syndromes

Differential Expression of Fibroblast Growth Factor Receptors in Human Digital Development Suggests Common Pathogenesis in Complex Acrosyndactyly and Craniosynostosis

FIBROBLAST GROWTH FACTOR RECEPTORS ARE EXPRESSED IN CRANIOSYNOSTOTIC SUTURES

Toward Pathogenesis of Apert Cleft Palate: FGF, FGFR, and TGFβ Genes Are Differentially Expressed in Sequential Stages of Human Palatal Shelf Fusion

Cloning of the mouse homologue of the deleted in colorectal cancer gene (mDCC) and its expression in the developing mouse embryo.

Aggressive keloid scarring of the Caucasian wrist and palm