Evidence map›Paper›PMID 29735527›Full record

ArticleThe Journal of biological chemistry2018

Nuclear PTEN deficiency causes microcephaly with decreased neuronal soma size and increased seizure susceptibility.

Atsushi Igarashi, Kie Itoh, Tatsuya Yamada, Yoshihiro Adachi, Takashi Kato, Daisuke Murata, Hiromi Sesaki, Miho Iijima

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Editorial: Neuroinflammation and cognitive impairment.Frontiers in aging neuroscience · 2024
    Article
  6. Review
  7. The HECT family of E3 ubiquitin ligases and PTEN.Seminars in cancer biology · 2022
    Review
  8. Mitochondria inter-organelle relationships in cancer protein aggregation.Frontiers in cell and developmental biology · 2022
    Review
  9. Generating a new mouse model for nuclear PTEN deficiency by a single K13R mutation.Genes to cells : devoted to molecular & cellular mechanisms · 2021
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Nuclear PTEN and p53 suppress stress-induced liver cancer through distinct mechanisms.Biochemical and biophysical research communications · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. PTEN Nuclear Functions.Cold Spring Harbor perspectives in medicine · 2020
    Review
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.

Atsushi IgarashiFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Kie ItohFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Tatsuya YamadaFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Yoshihiro AdachiFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Takashi KatoFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Daisuke MurataFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Hiromi SesakiFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Miho IijimaFrom the Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205 miijima@jhmi.edu.

Funding

Lipid Signaling in ChemotaxisR01GM084015 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI IIJIMA, MIHO · 2009 to 2019
$2.9M
Mitochondrial Quality Control by Drp1R01GM123266 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI SESAKI, HIROMI · 2018 to 2021
$1.4M
NIGMS NIH HHS R01 GM084015NIGMS NIH HHS R01 GM123266
6 · The paper itself

Abstract

Defects in phosphatase and tensin homolog (PTEN) are associated with neurological disorders and tumors. PTEN functions at two primary intracellular locations: the plasma membrane and the nucleus. At the membrane, PTEN functions as a phosphatidylinositol (3,4,5)-trisphosphate phosphatase and suppresses PI 3-kinase signaling that drives cell growth and tumorigenesis. However, the

Indexed as

CRISPR-Cas SystemsAmino Acid SubstitutionAnimalsBrainCell NucleusCell SizeFemaleGene EditingMaleMiceMicrocephalyMutationNeuronsPhosphatidylinositol 3-KinasesPTEN PhosphohydrolaseSeizuresPhosphatidylinositol 3-KinasesPTEN PhosphohydrolasePten protein, mousebraincell signalinggenome editinglipid signalingmousemouse geneticsnucleusphosphatase and tensin homolog (PTEN)phosphatidylinositide 3-kinase (PI 3-kinase)PIP3 signaling

Identifiers

PMID29735527
PMCPMC6005449

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.