Evidence map›Paper›PMID 40950402›Full record

ArticleFrontiers in cell and developmental biology2025

A human Angelman Syndrome class II pluripotent stem cell line with fluorescent paternal

Gautami R Kelkar, Samantha R Stuppy, Dilara Sen, Z Begum Yagci, Linna Han, Lexi Land, Jessica K Hartman, Albert J Keung

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Gautami R Kelkar *Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.
Samantha R Stuppy *Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.
Dilara SenDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.
Z Begum YagciDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.
Linna HanDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.
Lexi LandCell Microsystems, Durham, NC, United States.
Jessica K HartmanCell Microsystems, Durham, NC, United States.
Albert J KeungDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Angelman Syndrome (AS) is characterized in large part by the loss of functional UBE3A protein in mature neurons. A majority of AS etiologies is linked to deletion of the maternal copy of the Methods: Previously derived induced Pluripotent Stem Cells (iPSCs) with a Class II large deletion at the Results: The reporter is successfully integrated into the genome and reports paternal Discussion: This human-cell-based model can be used to screen novel therapeutic candidates, facilitate tracking of

Indexed as

Angelman Syndromecerebral organoidsfluorescent reporterhiPSCimprintingneurodevelopmenttherapeutic screeningUBE3A reactivation

Identifiers

PMID40950402
PMCPMC12426290

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.