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

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Electronic Gene Ontology annotations created by ARBA machine learning models

Development of noradrenergic neurons in the zebrafish hindbrain requires BMP, FGF8, and the homeodomain protein soulless/Phox2a.

Induction and differentiation of the zebrafish heart requires fibroblast growth factor 8 (fgf8/acerebellar).

Sef is a feedback-induced antagonist of Ras/MAPK-mediated FGF signalling.

Wnt1 and wnt10b function redundantly at the zebrafish midbrain-hindbrain boundary.

The role of the zebrafish nodal-related genes squint and cyclops in patterning of mesendoderm.

vhnf1 and Fgf signals synergize to specify rhombomere identity in the zebrafish hindbrain.

Genetic analysis of the roles of Hh, FGF8, and nodal signaling during catecholaminergic system development in the zebrafish brain.

Engrailed and Fgf8 act synergistically to maintain the boundary between diencephalon and mesencephalon.

Interplay between FGF, one-eyed pinhead, and T-box transcription factors during zebrafish posterior development.

Fgf signalling is required for formation of cartilage in the head.

Isthmus-to-midbrain transformation in the absence of midbrain-hindbrain organizer activity.

Nodal and Fgf pathways interact through a positive regulatory loop and synergize to maintain mesodermal cell populations.

Early requirement for fgf8 function during hindbrain pattern formation in zebrafish.

A direct role for Fgf but not Wnt in otic placode induction.

Fgf signalling controls the dorsoventral patterning of the zebrafish embryo.

Genetic interactions underlying otic placode induction and formation.

Hedgehog and Fgf signaling pathways regulate the development of tphR-expressing serotonergic raphe neurons in zebrafish embryos.

vhnf1 integrates global RA patterning and local FGF signals to direct posterior hindbrain development in zebrafish.

Pax8 and Pax2a function synergistically in otic specification, downstream of the Foxi1 and Dlx3b transcription factors.

Endocytosis controls spreading and effective signaling range of Fgf8 protein.

An essential role for Fgfs in endodermal pouch formation influences later craniofacial skeletal patterning.

Differentiation of the vertebrate retina is coordinated by an FGF signaling center.

Roles for fgf8 signaling in left-right patterning of the visceral organs and craniofacial skeleton.

Fgf8 drives myogenic progression of a novel lateral fast muscle fibre population in zebrafish.

Fgf signals from a novel signaling center determine axial patterning of the prospective neural retina.

Fgf19 regulated by Hh signaling is required for zebrafish forebrain development.

Differentiation of cerebellar cell identities in absence of Fgf signalling in zebrafish Otx morphants.

Zebrafish endoderm formation is regulated by combinatorial Nodal, FGF and BMP signalling.

Mutation of the atrophin2 gene in the zebrafish disrupts signaling by fibroblast growth factor during development of the inner ear.

FGF signaling is required for {beta}-catenin-mediated induction of the zebrafish organizer.

Noggin1 and Follistatin-like2 function redundantly to Chordin to antagonize BMP activity.

Genomic organization, alternative splicing, and multiple regulatory regions of the zebrafish fgf8 gene.

Fgf signaling negatively regulates Nodal-dependent endoderm induction in zebrafish.

Specification of epibranchial placodes in zebrafish.

Fgf-dependent otic induction requires competence provided by Foxi1 and Dlx3b.

Fgf8 haploinsufficiency results in distinct craniofacial defects in adult zebrafish.

Changes in retinoic acid signaling alter otic patterning.

REREa/Atrophin-2 interacts with histone deacetylase and Fgf8 signaling to regulate multiple processes of zebrafish development.

Early developmental specification of the thyroid gland depends on han-expressing surrounding tissue and on FGF signals.

Reiterative roles for FGF signaling in the establishment of size and proportion of the zebrafish heart.

FGF-dependent left-right asymmetry patterning in zebrafish is mediated by Ier2 and Fibp1.

Distinct phases of cardiomyocyte differentiation regulate growth of the zebrafish heart.

Fgf4 is required for left-right patterning of visceral organs in zebrafish.

Dynamic coupling of pattern formation and morphogenesis in the developing vertebrate retina.

Identification of early requirements for preplacodal ectoderm and sensory organ development.

Fgf signaling controls pharyngeal taste bud formation through miR-200 and Delta-Notch activity.

Midbrain-hindbrain boundary patterning and morphogenesis are regulated by diverse grainy head-like 2-dependent pathways.

Fgf22 regulated by Fgf3/Fgf8 signaling is required for zebrafish midbrain development.

Differential roles for 3-OSTs in the regulation of cilia length and motility.

Mesodermal Fgf10b cooperates with other fibroblast growth factors during induction of otic and epibranchial placodes in zebrafish.

Tbx1 controls the morphogenesis of pharyngeal pouch epithelia through mesodermal Wnt11r and Fgf8a.

An Fgf-Shh signaling hierarchy regulates early specification of the zebrafish skull.

Comparison of molecular marker expression in early zebrafish brain development following chronic ethanol or morpholino treatment.

Metalloproteinase Adamts16 Is Required for Proper Closure of the Optic Fissure.

Fgf-driven Tbx protein activities directly induce myf5 and myod to initiate zebrafish myogenesis.

Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain.

Fgf8 is mutated in zebrafish acerebellar (ace) mutants and is required for maintenance of midbrain-hindbrain boundary development and somitogenesis.

Duplication and divergence of fgf8 functions in teleost development and evolution.

Evolution of developmental regulation in the vertebrate FgfD subfamily.

Cis-regulation and chromosomal rearrangement of the fgf8 locus after the teleost/tetrapod split.

Genomic regulatory blocks encompass multiple neighboring genes and maintain conserved synteny in vertebrates.

Overlapping and distinct functions provided by fgf17, a new zebrafish member of the Fgf8/17/18 subgroup of Fgfs.

Fibroblast growth factor signaling is required for early somatic gonad development in zebrafish.