Evidence map›Paper›PMID 33396746›Full record

ArticleInternational journal of molecular sciences2020

Novel Insights into Selected Disease-Causing Mutations within the

Bożena Szulc, Yelyzaveta Zadorozhna, Mariusz Olczak, Wojciech Wiertelak, Dorota Maszczak-Seneczko

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Bożena SzulcFaculty of Biotechnology, University of Wroclaw, 14A F. Joliot-Curie St., 50-383 Wroclaw, Poland.
Yelyzaveta ZadorozhnaFaculty of Biotechnology, University of Wroclaw, 14A F. Joliot-Curie St., 50-383 Wroclaw, Poland.
Mariusz OlczakFaculty of Biotechnology, University of Wroclaw, 14A F. Joliot-Curie St., 50-383 Wroclaw, Poland.ORCID 0000-0001-8629-6364
Wojciech WiertelakFaculty of Biotechnology, University of Wroclaw, 14A F. Joliot-Curie St., 50-383 Wroclaw, Poland.ORCID 0000-0002-6716-0696
Dorota Maszczak-SeneczkoFaculty of Biotechnology, University of Wroclaw, 14A F. Joliot-Curie St., 50-383 Wroclaw, Poland.ORCID 0000-0002-5112-7920
University of Wrocław · PL

Funding

Narodowe Centrum Nauki 2016/21/B/NZ5/00144
6 · The paper itself

Abstract

Congenital disorders of glycosylation (CDG) are a group of rare genetic and metabolic diseases caused by alterations in glycosylation pathways. Five patients bearing CDG-causing mutations in the

Indexed as

MutationCell MembraneChromatography, High Pressure LiquidCRISPR-Cas SystemsCytidine MonophosphateFlow CytometryGene Knockdown TechniquesGenetic Association StudiesGenetic Predisposition to DiseaseGlycoconjugatesGlycosylationHEK293 CellsHumansLectinsNucleotide Transport ProteinsOrganic Anion TransportersCytidine MonophosphateGlycoconjugatesLectinsNucleotide Transport ProteinsOrganic Anion Transporterssialic acid transport proteinsSLC35A1 protein, humanSymportersCMP-sialic acid transportercongenital disorder of glycosylationglycolipidGolgi apparatuslectinmutationN-glycanO-glycanprotein dimerizationsialylation

Identifiers

PMID33396746
PMCPMC7795627
OpenAlexW3115938723

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.