Evidence map›Paper›PMID 34717671›Full record

ReviewJournal of translational medicine2021

Gene therapy for cystic fibrosis: new tools for precision medicine.

Jin-A Lee, Alex Cho, Elena N Huang, Yiming Xu, Henry Quach, Jim Hu, Amy P Wong

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
–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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  11. The ageing of people living with cystic fibrosis: what to expect now?European respiratory review : an official journal of the European Respiratory Society · 2024
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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

7 authors.

Jin-A LeeProgram in Developmental and Stem Cell Biology, Hospital for Sick Children, 686 Bay Street, PGCRL 16-9420, Toronto, ON, M5G0A4, Canada.
Alex Cho *Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
Elena N Huang *Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
Yiming XuDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
Henry QuachDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
Jim HuDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
Amy P WongProgram in Developmental and Stem Cell Biology, Hospital for Sick Children, 686 Bay Street, PGCRL 16-9420, Toronto, ON, M5G0A4, Canada. apwong@sickkids.ca.ORCID 0000-0002-9580-1980

Funding

CFREF Medicine by Design MbDNI-2020-03SickKids Foundation - CIHR IHDCYH NI20-1070
6 · The paper itself

Abstract

The discovery of the Cystic fibrosis (CF) gene in 1989 has paved the way for incredible progress in treating the disease such that the mean survival age of individuals living with CF is now ~58 years in Canada. Recent developments in gene targeting tools and new cell and animal models have re-ignited the search for a permanent genetic cure for all CF. In this review, we highlight some of the more recent gene therapy approaches as well as new models that will provide insight into personalized therapies for CF.

Indexed as

Cystic FibrosisAnimalsCystic Fibrosis Transmembrane Conductance RegulatorGenetic TherapyHumansMiddle AgedMutationPrecision MedicineCystic Fibrosis Transmembrane Conductance RegulatorAlternative chloride channelsCFTRCystic fibrosisLungOrganoidsPrecision medicineStem cellsTMEM16A

Identifiers

PMID34717671
PMCPMC8556969

What Socratic 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 Socratic graph.