ConductScience.org, home
Papers
API referenceFor AI assistants

Paper · 41597181

Single-Cell RNA-Seq Reveals Conserved Cellular Communication Mechanisms Governing Ocular Lineage Specification from Human iPS Cells.

Howard L and 10 others. Cells, 2026. Cited by 0 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Download JSON
Cite this record

ConductScience Library. Single-Cell RNA-Seq Reveals Conserved Cellular Communication Mechanisms Governing Ocular Lineage Specification from Human iPS Cells. Papers, record 41597181. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41597181

On this page

Paper

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

Title
Single-Cell RNA-Seq Reveals Conserved Cellular Communication Mechanisms Governing Ocular Lineage Specification from Human iPS Cells.
PubMed
Journal
Cells
PubMed
Year
2026
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
0
iCite
Revised in PubMed
2026-07-01
PubMed

Authors11

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

OrderAuthorForenameKindORCID iD
1Howard LLaurahttps://orcid.org/0000-0002-5751-6185
2Ishikawa YYuki
3Kamuro RReihttps://orcid.org/0000-0002-0628-904X
4Katayama TTomohiko
5Bains KKKiranjit Khttps://orcid.org/0000-0001-6617-5768
6Hill MJMatthew J
7Blake DJDerek Jhttps://orcid.org/0000-0002-5005-4731
8Park SJSung-Joonhttps://orcid.org/0000-0002-1774-9590
9Hayashi RRyuheihttps://orcid.org/0000-0002-4699-8617
10Quantock AJAndrew J

1 to 10 of 11Source PubMed

See all 11 authors

Topics11

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

MeSH termMajor
Induced Pluripotent Stem CellsMajor topic
Cell LineageMajor topic
Cell CommunicationMajor topic
Single-Cell AnalysisMajor topic
EyeMajor topic
RNA-SeqMajor topic
Humans
Cell Differentiation
Signal Transduction
Single-Cell Gene Expression Analysis
Transcriptome

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
BB/S015981/1, BB/R021244/1, BB/X000966/1BBSRCPubMed
20H03842, 23H03060Japan Society for the Promotion of Science (JSPS)PubMed
JPMJFR210WJapan Science and Technology Agency (JST)PubMed

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.

References98

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

OrderPMIDTitleJournalYearIn PapersSource
125,670,788Activin/Nodal signalling in stem cells.Development2015https://conductscience.org/library/papers/25670788PubMed
215,705,857BMP4-dependent expression of Xenopus Grainyhead-like 1 is essential for epidermal differentiation.Development2005https://conductscience.org/library/papers/15705857PubMed
337,671,011Single-cell sequencing of individual retinal organoids reveals determinants of cell-fate heterogeneity.Cell Rep Methods2023https://conductscience.org/library/papers/37671011PubMed
432,133,359FGF Signaling Pathway: A Key Regulator of Stem Cell Pluripotency.Front Cell Dev Biol2020https://conductscience.org/library/papers/32133359PubMed
519,279,133Activin/Nodal signalling maintains pluripotency by controlling Nanog expression.Development2009https://conductscience.org/library/papers/19279133PubMed
621,150,893A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly.Eur J Hum Genet2011https://conductscience.org/library/papers/21150893PubMed
734,463,252TGFβ signalling is required to maintain pluripotency of human naïve pluripotent stem cells.Elife2021https://conductscience.org/library/papers/34463252PubMed
831,796,115Genetics and functions of the retinoic acid pathway, with special emphasis on the eye.Hum Genomics2019https://conductscience.org/library/papers/31796115PubMed
930,322,383Identification of influential proteins in the classical retinoic acid signaling pathway.Theor Biol Med Model2018https://conductscience.org/library/papers/30322383PubMed
1027,650,846Reconstructed cell fate-regulatory programs in stem cells reveal hierarchies and key factors of neurogenesis.Genome Res2016https://conductscience.org/library/papers/27650846PubMed

1 to 10 of 98

See all 98 references

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.

None in this release.

Genes2

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

GeneNCBI Gene IDLinked byIn GenesSource
BMP1649PubTator's text mininghttps://conductscience.org/library/genes/649NCBI Gene
INHBE83,729PubTator's text mininghttps://conductscience.org/library/genes/83729NCBI 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.

For software

Read this paper from software.

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

GET https://conductscience.org/api/papers/v1/41597181

GET https://conductscience.org/api/papers/v1/41597181/references?page=2

API referenceFor AI assistants