Evidence map›Paper›PMID 30530496›Full record

ReviewThe Journal of biological chemistry2019

Fatty acid recognition in the Frizzled receptor family.

Aaron H Nile, Rami N Hannoush

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. 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

2 authors at 2 institutions in 2 countries.

Aaron H NileFrom the Department of Early Discovery Biochemistry, Genentech, South San Francisco, California 94080.ORCID 0000-0002-7370-8769
Rami N HannoushFrom the Department of Early Discovery Biochemistry, Genentech, South San Francisco, California 94080 hannoush.rami@gene.com.
Center for Discovery · USGene Therapy Laboratory · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wnt signaling regulates physiological processes ranging from cell differentiation to bone formation. Dysregulation of Wnt signaling is linked to several human ailments, including colorectal, pancreatic, and breast cancers. As such, modulation of this pathway has been an attractive strategy for therapeutic development of anticancer agents. Since the discovery of Wnt proteins more than 35 years ago, research efforts continue to focus on understanding the biochemistry of their molecular interactions and their biological functions. Wnt is a secreted glycoprotein covalently modified with a

Indexed as

Multigene FamilyAnimalsBinding SitesCrystallography, X-RayFatty AcidsFrizzled ReceptorsHumansModels, MolecularSignal TransductionFatty AcidsFrizzled Receptorsbindingcancercell signalingcysteine-rich domain (CRD)dimerizationfatty acidfrizzled (FZD)glycoproteinG protein–coupled receptor (GPCR)lipid-binding proteinlipid–protein interactionstem cellsWnt signaling

Identifiers

PMID30530496
PMCPMC6333880
OpenAlexW2904104853

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.