Evidence map›Paper›PMID 27193844›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2016

Visualizing and Analyzing Branching Microtubule Nucleation Using Meiotic Xenopus Egg Extracts and TIRF Microscopy.

Matthew King, Sabine Petry

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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.

Matthew KingDepartment of Molecular Biology, Princeton University, Washington Road, Princeton, NJ, 08544, USA.
Sabine PetryDepartment of Molecular Biology, Princeton University, Washington Road, Princeton, NJ, 08544, USA. spetry@princeton.edu.

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
Building the Chromosome Segregation Machinery from ScratchDP2GM123493 · NIGMS · PRINCETON UNIVERSITY · PI PETRY, SABINE · 2016 to 2016
$2.4M
Role and Mechanism of Microtubule Nucleation within the Mitotic SpindleR00GM100013 · NIGMS · PRINCETON UNIVERSITY · PI PETRY, SABINE · 2013 to 2015
$745k
NIGMS NIH HHS DP2 GM123493NIGMS NIH HHS R00 GM100013NIGMS NIH HHS T32 GM007388
6 · The paper itself

Abstract

Mitotic and meiotic spindles consist primarily of microtubules, which originate from centrosomes and within the vicinity of chromatin. Indirect evidence suggested that microtubules also originate throughout the spindle, but the high microtubule density within the spindle precludes the direct observation of this phenomenon. By using meiotic Xenopus laevis egg extract and employing total internal reflection (TIRF) microscopy, microtubule nucleation from preexisting microtubules could be demonstrated and analyzed. Branching microtubule nucleation is an ideal mechanism to assemble and maintain a mitotic spindle, because microtubule numbers are amplified while preserving their polarity. Here, we describe the assays that made these findings possible and the experiments that helped identify the key molecular players involved.

Indexed as

MeiosisMicroscopy, ConfocalAnimalsCell DivisionCell NucleusGenes, ReporterMicrotubulesMitosisOocytesRecombinant Fusion ProteinsSpindle ApparatusStaining and LabelingXenopus laevisRecombinant Fusion ProteinsCell divisionCytoskeletonMeiotic spindleMicrotubuleMicrotubule nucleationMitotic spindleTIRF microscopyXenopus laevis egg extract

Identifiers

PMID27193844
PMCPMC5016078

What OpenQuestion holds

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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.