Paper · 1618138

Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification.

Isaacs HV and 2 others. Development, 1992. Cited by 288 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification. Papers, record 1618138. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/1618138

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification.; PubMed
Journal: Development; PubMed
Year: 1992; PubMed
Publication types: Journal Article; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/1618138/; PubMed
DOI: https://doi.org/10.1242/dev.114.3.711; PubMed
The journal: https://conductscience.org/library/journal-index/8701744; PubMed
Citations, by iCite: 288; iCite
Relative citation ratio, by iCite: 5.18; iCite
Revised in PubMed: 2022-02-15; PubMed

Authors3

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename
1	Isaacs HV	H V
2	Tannahill D	D
3	Slack JM	J M

Source PubMed

Topics12

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
Embryonic Induction	Major topic
Fibroblast Growth Factors	Major topic
Mesoderm	Major topic
Amino Acid Sequence
Animals
Base Sequence
Blotting, Southern
Female
Genetic Techniques
Molecular Probe Techniques
Molecular Sequence Data
Xenopus laevis

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References0

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

None in this release.

Cited by56

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 288 citations.

PMID	Title	Journal	Year	In Papers	Source
38,637,565	Xbra modulates the activity of linker region phosphorylated Smad1 during Xenopus development.	Sci Rep	2024	https://conductscience.org/library/papers/38637565	PubMed
37,597,164	The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains.	Dev Dyn	2023	https://conductscience.org/library/papers/37597164	PubMed
37,281,879	Determination, induction and pattern formation in early amphibian embryos.	Dev Growth Differ	1996	https://conductscience.org/library/papers/37281879	PubMed
37,281,644	A Drosophila receptor-type tyrosine kinase (DFR1) acts as a fibroblast growth factor receptor in Xenopus embryos.	Dev Growth Differ	1996	https://conductscience.org/library/papers/37281644	PubMed
37,281,476	Bone morphogenetic protein acts as a ventral mesoderm modifier in early Xenopus embryos.	Dev Growth Differ	1995	https://conductscience.org/library/papers/37281476	PubMed
34,440,915	Functional Roles of FGF Signaling in Early Development of Vertebrate Embryos.	Cells	2021	https://conductscience.org/library/papers/34440915	PubMed
33,369,095	Xenopus leads the way: Frogs as a pioneering model to understand the human brain.	Genesis	2021	https://conductscience.org/library/papers/33369095	PubMed
28,600,394	TGF-β Family Signaling in Early Vertebrate Development.	Cold Spring Harb Perspect Biol	2018	https://conductscience.org/library/papers/28600394	PubMed
27,499,864	Distinct patterns of endosulfatase gene expression during Xenopus laevis limb development and regeneration.	Regeneration (Oxf)	2015	https://conductscience.org/library/papers/27499864	PubMed
25,681,501	Sulf1 has ligand-dependent effects on canonical and non-canonical Wnt signalling.	J Cell Sci	2015	https://conductscience.org/library/papers/25681501	PubMed

1 to 10 of 56

See all 56 cited by

Genes3

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes	Source
FGF2	2,247	PubTator's text mining	https://conductscience.org/library/genes/2247	NCBI Gene
FGF4	2,249	PubTator's text mining	https://conductscience.org/library/genes/2249	NCBI Gene
FGF6	2,251	PubTator's text mining	https://conductscience.org/library/genes/2251	NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data10

The data bank entries PubMed's record names. Trial numbers are under Trials.

Data bank	Accession	Source
GENBANK	L12697	GENBANK
GENBANK	L12698	GENBANK
GENBANK	L12699	GENBANK
GENBANK	L12700	GENBANK
GENBANK	L12701	GENBANK
GENBANK	L12702	GENBANK
GENBANK	L12703	GENBANK
GENBANK	X62593	GENBANK
GENBANK	X62619	GENBANK
GENBANK	X62620	GENBANK

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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