Evidence map›Paper›PMID 30635372›Full record

ArticleJournal of the American Society of Nephrology : JASN2019

New Insights into the Mechanism of NO

Laura Lagostena, Giovanni Zifarelli, Alessandra Picollo

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. 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 2 institutions in 3 countries.

Laura LagostenaDulbecco Telethon Laboratory, Istituto di Biofisica, Consiglio Nazionale delle Ricerche, Genova, Italy; and.
Giovanni ZifarelliDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK giovanni.zifarelli@dpag.ox.ac.uk apicollo@dti.telethon.it.
Alessandra PicolloDulbecco Telethon Laboratory, Istituto di Biofisica, Consiglio Nazionale delle Ricerche, Genova, Italy; and giovanni.zifarelli@dpag.ox.ac.uk apicollo@dti.telethon.it.
Dulbecco Telethon Institute · ITUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe mechanism of anion selectivity in the human kidney chloride channels ClC-Ka and ClC-Kb is unknown. However, it has been thought to be very similar to that of other channels and antiporters of the CLC protein family, and to rely on anions interacting with a conserved Ser residue (Ser

methodsTo investigate the role of several residues in anion selectivity of ClC-Ka, we created mutations that resulted in amino acid substitutions in these residues. We also used electrophysiologic techniques to assess the properties of the mutants.

resultsMutations in ClC-Ka that change Ser

conclusions ClC-Ka's mechanism of anion selectivity is largely independent of Ser

Indexed as

Amino Acid SubstitutionAnimalsBinding SitesCell Cycle ProteinsChloride ChannelsHumansKidneyModels, MolecularMutationPatch-Clamp TechniquesProteinsReference ValuesSignal TransductionXenopus laevisCell Cycle ProteinsChloride ChannelsCLC-1 channelNBL1 protein, humanProteinsBartter-s syndromeelectrophysiologyion channelion transportkidney tubule

Identifiers

PMID30635372
PMCPMC6362620
OpenAlexW2909573743

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.