Evidence map›Paper›PMID 18848778›Full record

ReviewTrends in cell biology2008

Ror receptor tyrosine kinases: orphans no more.

Jennifer L Green, Steven G Kuntz, Paul W Sternberg

Open access · greenAbstract readReview
In one paragraph

Review in Trends in cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

131 citing papers in PubMed, 249 citations in OpenAlex.

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  19. Crystal structure of the kringle domain of human receptor tyrosine kinase-like orphan receptor 1 (hROR1).Acta crystallographica. Section F, Structural biology communications · 2022
    Article
  20. Article

71 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

3 authors at 2 institutions in 1 country.

Jennifer L GreenDepartment of Developmental Biology, Stanford University School of Medicine, Beckman Center, B269, 279 Campus Drive, Stanford, CA 94305-5323, USA. jlgreen@stanford.edu
Steven G Kuntz
Paul W Sternberg
California Institute of Technology · USStanford University · US

Funding

PREDOCTORAL TRAINING IN BIOLOGY AND CHEMISTRYT32GM007616 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STERNBERG, PAUL WARREN · 1985 to 2019
$22.9M
Howard Hughes Medical InstituteNIGMS NIH HHS GM07616NIGMS NIH HHS T32 GM007616
6 · The paper itself

Abstract

Receptor tyrosine kinase-like orphan receptor (Ror) proteins are a conserved family of tyrosine kinase receptors that function in developmental processes including skeletal and neuronal development, cell movement and cell polarity. Although Ror proteins were originally named because the associated ligand and signaling pathway were unknown, recent studies in multiple species have now established that Ror proteins are Wnt receptors. Depending on the cellular context, Ror proteins can either activate or repress transcription of Wnt target genes and can modulate Wnt signaling by sequestering Wnt ligands. New evidence implicates Ror proteins in planar cell polarity, an alternative Wnt pathway. Here, we review the progress made in understanding these mysterious proteins and, in particular, we focus on their function as Wnt receptors.

Indexed as

AnimalsCaenorhabditis elegans ProteinsCell MovementCell PolarityHumansMAP Kinase Kinase 4PhylogenyProtein Structure, TertiaryReceptor Protein-Tyrosine KinasesReceptor Tyrosine Kinase-like Orphan ReceptorsWnt ProteinsCaenorhabditis elegans ProteinsCAM-1 protein, C elegansMAP Kinase Kinase 4Receptor Protein-Tyrosine KinasesReceptor Tyrosine Kinase-like Orphan ReceptorsWnt Proteins

Identifiers

PMID18848778
PMCPMC4672995
OpenAlexW1971237575

What OpenQuestion holds

Textmetadata
LicenceTDM
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.