Evidence map›Paper›PMID 34203454›Full record

ArticleInternational journal of molecular sciences2021

Aberrant Alternative Splicing in U2af1/Tet2 Double Mutant Mice Contributes to Major Hematological Phenotypes.

Cristina Martínez-Valiente, Cristian Garcia-Ruiz, Beatriz Rosón, Alessandro Liquori, Elisa González-Romero, Raúl Fernández-González, Isabel Gómez-Redondo, José Cervera, Alfonso Gutiérrez-Adán, Alejandra Sanjuan-Pla

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Sex-BiasedCancer discovery · 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

10 authors at 2 institutions in 1 country.

Cristina Martínez-ValienteHematology Research Group, Instituto de Investigación Sanitaria La Fe, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Cristian Garcia-RuizHematology Research Group, Instituto de Investigación Sanitaria La Fe, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0003-2914-7914
Beatriz RosónHematology Research Group, Instituto de Investigación Sanitaria La Fe, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Alessandro LiquoriHematology Research Group, Instituto de Investigación Sanitaria La Fe, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0002-4842-5986
Elisa González-RomeroHematology Research Group, Instituto de Investigación Sanitaria La Fe, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Raúl Fernández-GonzálezAnimal Reproduction Department, INIA, Ctra. de La Coruña, km 7.5, 28040 Madrid, Spain.
Isabel Gómez-RedondoAnimal Reproduction Department, INIA, Ctra. de La Coruña, km 7.5, 28040 Madrid, Spain.ORCID 0000-0002-9319-7580
José CerveraHematology Service, Hospital Universitario y Politécnico La Fe, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.ORCID 0000-0001-8252-1106
Alfonso Gutiérrez-AdánAnimal Reproduction Department, INIA, Ctra. de La Coruña, km 7.5, 28040 Madrid, Spain.ORCID 0000-0001-9893-9179
Alejandra Sanjuan-PlaHematology Research Group, Instituto de Investigación Sanitaria La Fe, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Instituto de Investigación Sanitaria La Fe · ESHospital Universitari i Politècnic La Fe · ES

Funding

Ministerio de Economía, Industria y Competitividad, Gobierno de España SAF2017-82171-R
6 · The paper itself

Abstract

Mutations in splicing factors are recurrent somatic alterations identified in myelodysplastic syndromes (MDS) and they frequently coincide with mutations in epigenetic factors. About 25% of patients present concurrent mutations in such pathways, suggesting a cooperative role in the pathogenesis of MDS. We focused on the splicing factor U2AF1 involved in the recognition of the 3' splice site during pre-mRNA splicing. Using a CRISPR/Cas9 system, we created heterozygous mice with a carboxy-terminal truncated U2af1 allele (U2af1

Indexed as

Alternative SplicingAnimalsClustered Regularly Interspaced Short Palindromic RepeatsDioxygenasesDNA-Binding ProteinsMiceMyelodysplastic SyndromesProto-Oncogene ProteinsRNA Splicing FactorsSplicing Factor U2AFDioxygenasesDNA-Binding ProteinsProto-Oncogene ProteinsRNA Splicing FactorsSplicing Factor U2AFTet2 protein, mouseZrsr1 protein, mousealternative splicingmyelodysplastic syndromeTET2U2AF1

Identifiers

PMID34203454
PMCPMC8269301
OpenAlexW3175561120

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.