Evidence map›Paper›PMID 35413967›Full record

ArticleScientific reports2022

Systemic bis-phosphinic acid derivative restores chloride transport in Cystic Fibrosis mice.

Mélanie Faria da Cunha, Iwona Pranke, Ali Sassi, Christiane Schreiweis, Stéphanie Moriceau, Dragana Vidovic, Aurélie Hatton, Mariane Sylvia Carlon, Geordie Creste, Farouk Berhal and 11 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Keratin 8 is a scaffolding and regulatory protein of ERAD complexes.Cellular and molecular life sciences : CMLS · 2022
    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

21 authors at 9 institutions in 3 countries.

Mélanie Faria da CunhaINSERM U1151, équipe 11, Paris, France.
Iwona Pranke *INSERM U1151, équipe 11, Paris, France.
Ali Sassi *INSERM U1151, équipe 11, Paris, France.
Christiane SchreiweisINSERM U1151, équipe 8, Paris, France.
Stéphanie MoriceauINSERM U1151, équipe 8, Paris, France.
Dragana VidovicMolecular Virology and Gene Therapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Aurélie HattonINSERM U1151, équipe 11, Paris, France.
Mariane Sylvia CarlonMolecular Virology and Gene Therapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Geordie CresteUniversité de Paris, Paris, France.
Farouk BerhalUniversité de Paris, Paris, France.
Guillaume PrestatUniversité de Paris, Paris, France.
Romain FreundUniversité de Paris, Paris, France.
Norbert OdolczykInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Jean Philippe JaisUnité de Biostatistiques, Assistance Publique Hôpitaux de Paris, Paris, France.
Christine Gravier-PelletierUniversité de Paris, Paris, France.
Piotr ZielenkiewiczInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Vincent JullienLaboratoire de Bactériologie-Virologie-Hygiène, Hôpital Avicenne, Bobigny, France.
Alexandre HinzpeterINSERM U1151, équipe 11, Paris, France.
Franck OuryUniversité de Paris, Paris, France.
Aleksander EdelmanINSERM U1151, équipe 11, Paris, France.
Isabelle Sermet-GaudelusINSERM U1151, équipe 11, Paris, France. isabelle.sermet@aphp.fr.
Inserm · FRUniversité Paris Cité · FRInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PLKU Leuven · BELaboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques · FRAssistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FRHôpital Avicenne · FRHôpital Necker-Enfants Malades · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the Cystic Fibrosis Transmembrane Conductance Regulator gene (CFTR) are responsible for Cystic Fibrosis (CF). The most common CF-causing mutation is the deletion of the 508th amino-acid of CFTR (F508del), leading to dysregulation of the epithelial fluid transport in the airway's epithelium and the production of a thickened mucus favoring chronic bacterial colonization, sustained inflammation and ultimately respiratory failure. c407 is a bis-phosphinic acid derivative which corrects CFTR dysfunction in epithelial cells carrying the F508del mutation. This study aimed to investigate c407 in vivo activity in the F508del Cftr

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorAnimalsChloridesIon TransportMiceMutationPhosphinic AcidsChloridesCystic Fibrosis Transmembrane Conductance RegulatorPhosphinic Acids

Identifiers

PMID35413967
PMCPMC9005718
OpenAlexW4223456754

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.