Evidence map›Paper›PMID 35887289›Full record

ArticleInternational journal of molecular sciences2022

Targeted-Deletion of a Tiny Sequence via Prime Editing to Restore SMN Expression.

Miaojin Zhou, Shuqing Tang, Nannan Duan, Mi Xie, Zhuo Li, Mai Feng, Lingqian Wu, Zhiqing Hu, Desheng Liang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Prime Editing: An Overview.Methods in molecular biology (Clifton, N.J.) · 2027
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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

9 authors at 1 institution in 1 country.

Miaojin ZhouCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.ORCID 0000-0002-6636-6000
Shuqing TangCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Nannan DuanCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Mi XieCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Zhuo LiCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Mai FengCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Lingqian WuCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Zhiqing HuCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Desheng LiangCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Central South University · CN

Funding

China Postdoctoral Science Foundation 2020TQ0362National Natural Science Foundation of China 81902150National Natural Science Foundation of China 81970829National Natural Science Foundation of China 82101957Natural Science Foundation of Hunan Province 2021JJ30895Natural Science Foundation of Hunan Province 2021JJ40806Science and Technology Innovation Program of Hunan Province 2019SK1014
6 · The paper itself

Abstract

Spinal muscular atrophy (SMA) is a devastating autosomal recessive motor neuron disease associated with mutations in the survival motor neuron 1 (

Indexed as

Muscular Atrophy, SpinalRNA SplicingAlternative SplicingExonsHumansIntronsSurvival of Motor Neuron 1 ProteinSurvival of Motor Neuron 1 Proteinendoplasmic reticulum stressinduced pluripotent stem cellsintronic splicing silencer-N1motor neuronsprime editingspinal muscular atrophysurvival motor neuron gene 2targeted-deletion

Identifiers

PMID35887289
PMCPMC9317564
OpenAlexW4285798022

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.