Evidence map›Paper›PMID 10655525›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Aberrant development of motor axons and neuromuscular synapses in erbB2-deficient mice.

W Lin, H B Sanchez, T Deerinck, J K Morris, M Ellisman, K F Lee

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 186 citations in OpenAlex.

  1. Pooled it
  2. ImmatureProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. ImmaturebioRxiv : the preprint server for biology · 2025
    Article
  6. Review
  7. Article
  8. NMJ-related diseases beyond the congenital myasthenic syndromes.Frontiers in cell and developmental biology · 2023
    Review
  9. Review
  10. Peripheral glia diversity.Journal of anatomy · 2022
    Review
  11. Review
  12. Review
  13. Article
  14. Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse.Biological reviews of the Cambridge Philosophical Society · 2021
    Review
  15. Review
  16. Neuromuscular Development and Disease: Learning FromFrontiers in cell and developmental biology · 2021
    Review
  17. Review
  18. Review
  19. Article
  20. Review

18 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

6 authors at 1 institution in 1 country.

W LinThe Salk Institute, La Jolla, CA 92037, USA.
H B Sanchez
T Deerinck
J K Morris
M Ellisman
K F Lee
Salk Institute for Biological Studies · US

Funding

VOLUMETRIC CONTOUR-BASED SURFACE RECONSTRUCTIONP41RR004050 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PASQUALE, ELENA B · 1989 to 2011
$28.0M
Viral VectorsP01AG010435 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TUSZYNSKI, MARK H. · 1991 to 2014
$20.9M
Salk Institute Cancer Training GrantT32CA009370 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Diana Clare Hargreaves, Jan Karlseder · 1986 to 2026
$8.6M
GENETIC ANALYSIS OF ERBB2 IN MAMMALIAN DEVELOPMENTR01HD034534 · NICHD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LEE, KUO-FEN · 1996 to 2011
$4.3M
DYNAMICS OF MEMBRANE ORGANIZATION AT NODES OF RANVIERR01NS014718 · NINDS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI ELLISMAN, MARK H · 1986 to 2005
$1.4M
NEUREGULINS AND ERBB2 AND CARDIAC DEVELOPMENTF32HL009756 · NHLBI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI MORRIS, JACQUELINE K · 1997 to 1999
–
NCI NIH HHS CA09370NCI NIH HHS T32 CA009370NCRR NIH HHS P41 RR004050NHLBI NIH HHS F32 HL009756NHLBI NIH HHS HL09756NIA NIH HHS P01 AG010435NICHD NIH HHS HD34534NICHD NIH HHS R01 HD034534NINDS NIH HHS R01 NS014718
6 · The paper itself

Abstract

Receptor tyrosine kinase erbB2, which is activated by neuregulin, is expressed in Schwann and muscle cells in the developing neuromuscular junction (NMJ). In vitro studies have shown that neuregulin promotes the survival and migration of Schwann cells and stimulates acetylcholine receptor gene transcription in cultured muscle cells. These findings suggest an important role for erbB2 in the development of the NMJ. Here we examine erbB2-deficient mice to determine whether erbB2 is required for NMJ development in vivo. Our analysis shows that there are pre- and postsynaptic defects of developing NMJ in erbB2-deficient embryos. The presynaptic defects include defasciculation and degeneration of the motor nerves, and an absence of Schwann cells. The postsynaptic defect features an impairment of junctional folds at the neuromuscular synapse in the mutants. These results demonstrate that erbB2 is essential for in vivo development of the NMJ.

Indexed as

Gene Expression Regulation, DevelopmentalGenes, erbB-2AnimalsAxonsCell MovementDiaphragmEmbryonic and Fetal DevelopmentErb-b2 Receptor Tyrosine KinasesIn Situ Hybridization, FluorescenceIntercostal MusclesMiceMice, KnockoutMice, Neurologic MutantsMorphogenesisMotor NeuronsMuscle ProteinsErb-b2 Receptor Tyrosine KinasesMuscle ProteinsNerve Tissue ProteinsNeuregulinsReceptors, Cholinergic

Identifiers

PMID10655525
PMCPMC15603
OpenAlexW2039431039

What OpenQuestion holds

Textmetadata
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.