Evidence map›Paper›PMID 11175774›Full record

ArticleNature genetics2001

Modifying with mitochondria.

K B Avraham

Abstract readComment
PubMed Publisher
In one paragraph

Article in Nature genetics, 2001. 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
–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

1 citing paper in PubMed.

  1. At the speed of sound: gene discovery in the auditory system.American journal of human genetics · 2001
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

K B AvrahamDepartment of Human Genetics and Molecular Medicine, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel. karena@post.tau.ac.il

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An elegant set of mouse crosses has been used to identify a mitochondrial variant that interacts with a nuclear locus on chromosome 10, Ahl, to modify age-related hearing loss. This discovery sets the stage for the identification of factors that modify expression levels and variability of human hearing impairments.

Indexed as

Age FactorsAnimalsCell NucleusCrosses, GeneticDeafnessMiceMice, Mutant StrainsMitochondriaMutationQuantitative Trait, Heritable

Identifiers

PMID11175774

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.