Evidence map›Paper›PMID 31509475›Full record

ArticleMolecular biology of the cell2019

Cytotoxicity of 1-deoxysphingolipid unraveled by genome-wide genetic screens and lipidomics in

A Galih Haribowo, J Thomas Hannich, Agnès H Michel, Márton Megyeri, Maya Schuldiner, Benoît Kornmann, Howard Riezman

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Demyelination in hereditary sensory neuropathy type-1C.Annals of clinical and translational neurology · 2020
    Article
  11. 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

7 authors.

A Galih HaribowoNCCR Chemical Biology and Department of Biochemistry, University of Geneva, 1211 Geneva, Switzerland.
J Thomas HannichNCCR Chemical Biology and Department of Biochemistry, University of Geneva, 1211 Geneva, Switzerland.
Agnès H MichelDepartment of Biochemistry, University of Oxford, OX1 3QU Oxford, United Kingdom.
Márton MegyeriDepartment of Molecular Genetics, Weizmann Institute of Science, 76100 Rehovot, Israel.
Maya SchuldinerDepartment of Molecular Genetics, Weizmann Institute of Science, 76100 Rehovot, Israel.
Benoît KornmannDepartment of Biochemistry, University of Oxford, OX1 3QU Oxford, United Kingdom.
Howard RiezmanNCCR Chemical Biology and Department of Biochemistry, University of Geneva, 1211 Geneva, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary sensory and autonomic neuropathy (HSAN) types IA and IC (IA/C) are caused by elevated levels of an atypical class of lipid named 1-deoxysphingolipid (DoxSL). How elevated levels of DoxSL perturb the physiology of the cell and how the perturbations lead to HSAN IA/C are largely unknown. In this study, we show that C

Indexed as

ActinsCeramidesHereditary Sensory and Autonomic NeuropathiesLipid MetabolismLipidomicsLipidsMitochondriaSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSphingolipids1-deoxysphingolipidActinsCeramidesdihydroceramideLipidsSaccharomyces cerevisiae ProteinsSphingolipids

Identifiers

PMID31509475
PMCPMC6789163

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.