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Paper · 38637565

Xbra modulates the activity of linker region phosphorylated Smad1 during Xenopus development.

Kumar S and 6 others. Sci Rep, 2024. Cited by 6 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Xbra modulates the activity of linker region phosphorylated Smad1 during Xenopus development. Papers, record 38637565. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/38637565

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Paper

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

Title
Xbra modulates the activity of linker region phosphorylated Smad1 during Xenopus development.
PubMed
Journal
Sci Rep
PubMed
Year
2024
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
6
iCite
Relative citation ratio, by iCite
0.8, provisional
iCite
Revised in PubMed
2024-04-25
PubMed

Authors7

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

OrderAuthorForenameKindORCID iD
1Kumar SSantosh
2Umair ZZobia
3Kumar VVijay
4Goutam RSRavi Shankar
5Park SSoochul
6Lee UUnjoo
7Kim JJaebong

Source PubMed

Topics8

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

MeSH termMajor
Mitogen-Activated Protein KinasesMajor topic
Signal TransductionMajor topic
Animals
Nervous System
Phosphorylation
Smad1 Protein
Xenopus laevis
Xenopus Proteins

Source PubMed

Grants3

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.

Grant, as the record writes itAgencyCountryNIH projectStated by
2018M3C7A1056285National Research Foundation of KoreaPubMed
2021R1A4A1027355National Research Foundation of KoreaPubMed
2021M3H9A1097557National Research Foundation of KoreaPubMed

Source PubMed

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.

References42

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

OrderPMIDTitleJournalYearIn PapersSource
19,442,883Formation and function of Spemann's organizer.Annu Rev Cell Dev Biol1997https://conductscience.org/library/papers/9442883PubMed
29,507,084BMP-2/-4 and Wnt-8 cooperatively pattern the Xenopus mesoderm.Mech Dev1998https://conductscience.org/library/papers/9507084PubMed
321,857,938Direct response elements of BMP within the PV.1A promoter are essential for its transcriptional regulation during early Xenopus development.PLoS One2011https://conductscience.org/library/papers/21857938PubMed
411,880,340eFGF is required for activation of XmyoD expression in the myogenic cell lineage of Xenopus laevis.Development2002https://conductscience.org/library/papers/11880340PubMed
512,809,600Mechanisms of TGF-beta signaling from cell membrane to the nucleus.Cell2003https://conductscience.org/library/papers/12809600PubMed
611,112,331FGF signaling restricts the primary blood islands to ventral mesoderm.Dev Biol2000https://conductscience.org/library/papers/11112331PubMed
730,061,699Xbra and Smad-1 cooperate to activate the transcription of neural repressor ventx1.1 in Xenopus embryos.Sci Rep2018https://conductscience.org/library/papers/30061699PubMed
825,373,906The tumor suppressor Smad4/DPC4 is regulated by phosphorylations that integrate FGF, Wnt, and TGF-β signaling.Cell Rep2014https://conductscience.org/library/papers/25373906PubMed
93,479,265Synergistic induction of mesoderm by FGF and TGF-beta and the identification of an mRNA coding for FGF in the early Xenopus embryo.Cell1987https://conductscience.org/library/papers/3479265PubMed
1015,829,520Transgenic zebrafish reveal stage-specific roles for Bmp signaling in ventral and posterior mesoderm development.Development2005https://conductscience.org/library/papers/15829520PubMed

1 to 10 of 42

See all 42 references

Cited by3

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 6 citations.

PMIDTitleJournalYearIn PapersSource
42,371,315BMP/Ventx1.1 axis modulates the multiciliogenesis in the early Xenopus epidermis.Genes Genomics2026https://conductscience.org/library/papers/42371315PubMed
40,370,638Artesunate disrupts germ layer formation by inhibiting BMP signaling pathway.Anim Cells Syst (Seoul)2025https://conductscience.org/library/papers/40370638PubMed
40,208,485Perillic acid disrupts the specification of germ layers by upregulating the FGF/MAPK pathway.Genes Genomics2025https://conductscience.org/library/papers/40208485PubMed

Genes0

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

None in this release.

Drugs0

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

None in this release.

Data0

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

None in this release.

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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