Evidence map›Paper›PMID 26433683›Full record

ReviewCellular and molecular life sciences : CMLS2016

The endoplasmic reticulum: structure, function and response to cellular signaling.

Dianne S Schwarz, Michael D Blower

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 791 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
791citing papers in PubMed, 2 pooled it
–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

791 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  16. SIEVEseq: unified differential expression, variability, and skewness analyses using RNA-Seq data.DNA research : an international journal for rapid publication of reports on genes and genomes · 2026
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731 more citing papers are in PubMed but not listed here.

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

2 authors.

Dianne S SchwarzDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Michael D BlowerDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, 02114, USA. blower@molbio.mgh.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endoplasmic reticulum (ER) is a large, dynamic structure that serves many roles in the cell including calcium storage, protein synthesis and lipid metabolism. The diverse functions of the ER are performed by distinct domains; consisting of tubules, sheets and the nuclear envelope. Several proteins that contribute to the overall architecture and dynamics of the ER have been identified, but many questions remain as to how the ER changes shape in response to cellular cues, cell type, cell cycle state and during development of the organism. Here we discuss what is known about the dynamics of the ER, what questions remain, and how coordinated responses add to the layers of regulation in this dynamic organelle.

Indexed as

AnimalsCalciumEndoplasmic ReticulumFertilizationHumansLipid MetabolismMitosisProtein BiosynthesisProtein FoldingProteinsSignal TransductionUnfolded Protein ResponseCalciumProteinsFertilizationInterphaseMitosisOrganizationPhosphorylationUnfolded protein response

Identifiers

PMID26433683
PMCPMC4700099

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.