Evidence map›Paper›PMID 30026687›Full record

ArticleFrontiers in molecular neuroscience2018

The F238L Point Mutation in the Cannabinoid Type 1 Receptor Enhances Basal Endocytosis via Lipid Rafts.

Melanie Wickert, Keri L Hildick, Gemma L Baillie, Ruth Jelinek, Alejandro Aparisi Rey, Krisztina Monory, Miriam Schneider, Ruth A Ross, Jeremy M Henley, Beat Lutz

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2018. 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
1.9field-weighted citation impact, top 15% of its field
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, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Neurobiology of cannabinoid receptor signaling
.Dialogues in clinical neuroscience · 2020
    Review
  10. Article
  11. 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

10 authors at 5 institutions in 3 countries.

Melanie WickertInstitute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Keri L HildickSchool of Biochemistry, University of Bristol, Bristol, United Kingdom.
Gemma L BaillieFaculty of Medicine, University of Toronto, Toronto, ON, Canada.
Ruth JelinekInstitute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Alejandro Aparisi ReyInstitute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Krisztina MonoryInstitute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Miriam SchneiderInstitute of Psychopharmacology, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Ruth A RossFaculty of Medicine, University of Toronto, Toronto, ON, Canada.
Jeremy M HenleySchool of Biochemistry, University of Bristol, Bristol, United Kingdom.
Beat LutzInstitute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
University Medical Center of the Johannes Gutenberg University Mainz · DEJohannes Gutenberg University Mainz · DEUniversity of Bristol · GBUniversity of Toronto · CAUniversity Hospital Heidelberg · DE

Funding

Biotechnology and Biological Sciences Research Council BB/F00723X/1Biotechnology and Biological Sciences Research Council BB/K014358/1Medical Research Council MR/L003791/1
6 · The paper itself

Abstract

Defining functional domains and amino acid residues in G protein coupled receptors (GPCRs) represent an important way to improve rational drug design for this major class of drug targets. The cannabinoid type 1 (CB1) receptor is one of the most abundant GPCRs in the central nervous system and is involved in many physiological and pathophysiological processes. Interestingly, cannabinoid type 1 receptor with a phenylalanine 238 to leucine mutation (CB1F238L) has been already linked to a number of both

Indexed as

axonal polarizationCB1endocytosislipid raftpoint mutation

Identifiers

PMID30026687
PMCPMC6041392
OpenAlexW2807934856

What OpenQuestion 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 OpenQuestion graph.