Evidence map›Paper›PMID 35412287›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Dissection and Direct Imaging of Axonal Transport in Drosophila Segmental Nerves.

William M Saxton, Angeline Lim, Inna Djagaeva

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Neuronal signaling · 2023
    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

3 authors at 1 institution in 1 country.

William M SaxtonDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA, USA. bsaxton@ucsc.edu.
Angeline LimDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA, USA.
Inna DjagaevaDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA, USA.
University of California, Santa Cruz · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For neurons, especially those with long axons, the forceful transport of mitochondria, vesicles, and other cytoplasmic components by cytoskeletal motors is vital. Defects in cytoplasmic transport machinery cause a degradation of signaling capacity that is most severe for neurons with the longest axons. In humans, with motor axons up to a meter long, even a mild mutation in one copy of the gene that codes for kinesin-1, the primary anterograde axonal transport motor, can cause spastic paraplegia and other distal neuropathies.To address questions about the molecular mechanisms of organelle movement, we turned to Drosophila as a model system, because it offered rigorous genetic and molecular approaches to the identification and inhibition of specific elements of transport machinery. However, methods for direct observation of organelle transport were largely lacking. We describe here an approach that we developed for imaging the transport behaviors of specific organelles in the long motor axons of larvae. It is straightforward, the equipment is commonly available, and it provides a powerful tool for studying the contributions of specific proteins to organelle transport mechanisms.

Indexed as

Axonal TransportDrosophilaAnimalsAxonsKinesinsMicroscopy, FluorescenceNeuronsKinesinsAxonal organellesDrosophilaFast transportMitochondriaNeuropeptides

Identifiers

PMID35412287
OpenAlexW4225490842

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.