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Paper · 40723922

Genetic Diversity in the Suppressyn Gene Sequence: From Polymorphisms to Loss-of-Function Mutations.

Sugimoto J and 4 others. Biomolecules, 2025. Cited by 2 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Genetic Diversity in the Suppressyn Gene Sequence: From Polymorphisms to Loss-of-Function Mutations. Papers, record 40723922. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/40723922

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Paper

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

Title
Genetic Diversity in the Suppressyn Gene Sequence: From Polymorphisms to Loss-of-Function Mutations.
PubMed
Journal
Biomolecules
PubMed
Year
2025
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural
PubMed
Citations, by iCite
2
iCite
Revised in PubMed
2026-05-27
PubMed

Authors5

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

OrderAuthorForenameKindORCID iD
1Sugimoto JJun
2Schust DJDanny Jhttps://orcid.org/0000-0003-4561-7808
3Nagamatsu TTakeshi
4Jinno YYoshihiro
5Kudo YYoshikihttps://orcid.org/0000-0001-6542-3408

Source PubMed

Topics8

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

MeSH termMajor
Loss of Function MutationMajor topic
Polymorphism, GeneticMajor topic
Genetic VariationMajor topic
Humans
Female
Pregnancy
Placenta
Trophoblasts

Source PubMed

Grants5

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 bySource
1R01HD094937The National Institutes of HealthR01HD094937PubMedNIH RePORTER
JP17K11238JSPS KAKENHIPubMedPubMed
JP20K09644JSPS KAKENHIPubMedPubMed
JP25462567JSPS KAKENHIPubMedPubMed
1R21A1145071The National Institutes of HealthPubMedPubMed

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.

References30

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

OrderPMIDTitleJournalYearIn PapersSource
119,321,927Syncytin-1 and glial cells missing a: hypoxia-induced deregulated gene expression along with disordered cell fusion in primary term human trophoblasts.Gynecol Obstet Invest2009https://conductscience.org/library/papers/19321927PubMed
235,859,055How trophoblasts fuse: an in-depth look into placental syncytiotrophoblast formation.Cell Mol Life Sci2022https://conductscience.org/library/papers/35859055PubMed
335,357,919The complete sequence of a human genome.Science2022https://conductscience.org/library/papers/35357919PubMed
439,078,391Conserved cysteine residues in Kaposi's sarcoma herpesvirus ORF34 are necessary for viral production and viral pre-initiation complex formation.J Virol2024https://conductscience.org/library/papers/39078391PubMed
526,432,243Human genomics: The end of the start for population sequencing.Nature2015https://conductscience.org/library/papers/26432243PubMed
621,493,955Reduced expression of both syncytin 1 and syncytin 2 correlates with severity of preeclampsia.Reprod Sci2011https://conductscience.org/library/papers/21493955PubMed
719,795,446Beneficial and detrimental effects of human endogenous retroviruses.Int J Cancer2010https://conductscience.org/library/papers/19795446PubMed
834,125,187Cell dynamics in human villous trophoblast.Hum Reprod Update2021https://conductscience.org/library/papers/34125187PubMed
935,954,303Endogenous Retroviruses and Placental Evolution, Development, and Diversity.Cells2022https://conductscience.org/library/papers/35954303PubMed
1018,215,254Human endogenous retrovirus-FRD envelope protein (syncytin 2) expression in normal and trisomy 21-affected placenta.Retrovirology2008https://conductscience.org/library/papers/18215254PubMed

Cited by2

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 2 citations.

PMIDTitleJournalYearIn PapersSource
42,352,360Beyond Genetic Conservation: The Baton Pass Model of Essential Biological Functions.Biomolecules2026https://conductscience.org/library/papers/42352360PubMed
41,184,406Variations in blood levels of the anti-fusogenic endogenous retroviral protein suppressyn are associated with fetal growth outcome in preeclampsia.Sci Rep2025https://conductscience.org/library/papers/41184406PubMed

Genes1

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

GeneNCBI Gene IDLinked byIn Genes
ERVH48-190,625PubTator's text mininghttps://conductscience.org/library/genes/90625

Source NCBI Gene

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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The record and each of its lists are JSON, twenty rows a page. No key.

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