Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Automatic assignment of GO terms using logical inference, based on on inter-ontology links
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
The surface ectoderm is essential for nephric duct formation in intermediate mesoderm.
Cerberus-like is a secreted BMP and nodal antagonist not essential for mouse development.
BMP4 rescues a non-cell-autonomous function of Msx1 in tooth development.
Altered growth responses of pulmonary artery smooth muscle cells from patients with primary pulmonary hypertension to transforming growth factor-beta(1) and bone morphogenetic proteins.
Bone morphogenetic proteins promote development of fetal pancreas epithelial colonies containing insulin-positive cells.
Functional analysis of bone morphogenetic protein type II receptor mutations underlying primary pulmonary hypertension.
BMPs and BMP receptors in mouse metanephric development: in vivo and in vitro studies.
Sonic hedgehog regulates proliferation and differentiation of mesenchymal cells in the mouse metanephric kidney.
Bone morphogenetic protein 2/4 signaling regulates early thymocyte differentiation.
Evidence that bone morphogenetic protein 4 has multiple biological functions during kidney and urinary tract development.
Endogenous TGF-beta signaling suppresses maturation of osteoblastic mesenchymal cells.
FLRG, member of the follistatin family, a new player in hematopoiesis.
Effect of bone morphogenetic proteins-4, -5 and -6 on DNA synthesis and expression of bone-related proteins in cultured human periodontal ligament cells.
Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression.
Bone morphogenetic protein-4 inhibitor gremlin is overexpressed in idiopathic pulmonary fibrosis.
Antagonistic effects of bone morphogenetic protein-4 and -7 on renal mesangial cell proliferation induced by aldosterone through MAPK activation.
Repulsive guidance molecule RGMa alters utilization of bone morphogenetic protein (BMP) type II receptors by BMP2 and BMP4.
BMP4 induces HO-1 via a Smad-independent, p38MAPK-dependent pathway in pulmonary artery myocytes.
Noncanonical Wnt-4 signaling enhances bone regeneration of mesenchymal stem cells in craniofacial defects through activation of p38 MAPK.
Immunohistochemical analysis of Sonic hedgehog signalling in normal human urinary tract development.
Regulation of bone morphogenetic protein signalling in human pulmonary vascular development.
Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.
SIX2 and BMP4 mutations associate with anomalous kidney development.
Hemojuvelin regulates hepcidin expression via a selective subset of BMP ligands and receptors independently of neogenin.
Targeting of bone morphogenetic protein growth factor complexes to fibrillin.
BMP-2/4 and BMP-6/7 differentially utilize cell surface receptors to induce osteoblastic differentiation of human bone marrow-derived mesenchymal stem cells.
Involvement of FGF and BMP family proteins and VEGF in early human kidney development.
SMAD proteins control DROSHA-mediated microRNA maturation.
BMPER is an endothelial cell regulator and controls bone morphogenetic protein-4-dependent angiogenesis.
GDF3 is a BMP inhibitor that can activate Nodal signaling only at very high doses.
Agrin binds BMP2, BMP4 and TGFbeta1.
Endogenous Wnt/beta-catenin signaling is required for cardiac differentiation in human embryonic stem cells.
BMP-mediated inhibition of FGF signaling promotes cardiomyocyte differentiation of anterior heart field progenitors.
DIP2 disco-interacting protein 2 homolog A (Drosophila) is a candidate receptor for follistatin-related protein/follistatin-like 1--analysis of their binding with TGF-β superfamily proteins.
WFIKKN1 and WFIKKN2 bind growth factors TGFβ1, BMP2 and BMP4 but do not inhibit their signalling activity.
Monocytic cells derived from human embryonic stem cells and fetal liver share common differentiation pathways and homeostatic functions.
Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment.
Inhibition of microRNA-302 (miR-302) by bone morphogenetic protein 4 (BMP4) facilitates the BMP signaling pathway.
Rnf165/Ark2C enhances BMP-Smad signaling to mediate motor axon extension.
MicroRNA-363 negatively regulates the left ventricular determining transcription factor HAND1 in human embryonic stem cell-derived cardiomyocytes.
The formation and function of the cardiac conduction system.
Bone morphogenetic protein 4 regulates microRNAs miR-494 and miR-126-5p in control of endothelial cell function in angiogenesis.
Novel regulators of bone formation: molecular clones and activities.
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling.
A mammalian serine/threonine kinase receptor specifically binds BMP-2 and BMP-4.
The daf-4 gene encodes a bone morphogenetic protein receptor controlling C. elegans dauer larva development.
Evidence from normal expression and targeted misexpression that bone morphogenetic protein (Bmp-4) plays a role in mouse embryonic lung morphogenesis.
The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4.
Bone morphogenetic proteins (BMPs) as regulators of dorsal forebrain development.
Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes.
FAM20C phosphorylates FAM20C substrates
BMP4 is required in the anterior heart field and its derivatives for endocardial cushion remodeling, outflow tract septation, and semilunar valve development.
Lack of evidence that fibrillin1 regulates bone morphogenetic protein 4 activity in kidney or lung.