Evidence map›Paper›PMID 38612397›Full record

ArticleInternational journal of molecular sciences2024

Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines.

Silvana Pileggi, Elisa A Colombo, Silvia Ancona, Roberto Quadri, Clara Bernardelli, Patrizia Colapietro, Michela Taiana, Laura Fontana, Monica Miozzo, Elena Lesma and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

11 authors at 1 institution in 1 country.

Silvana PileggiMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.ORCID 0000-0002-4306-9476
Elisa A ColomboMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.ORCID 0000-0001-9062-3188
Silvia AnconaPharmacology, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.ORCID 0000-0003-1999-129X
Roberto QuadriDepartment of Biosciences, Università degli Studi di Milano, 20133 Milan, Italy.
Clara BernardelliPharmacology, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.ORCID 0000-0002-3813-9038
Patrizia ColapietroMedical Genetics, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, 20122 Milan, Italy.
Michela TaianaDino Ferrari Centre, Neuroscience Section, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, 20122 Milan, Italy.
Laura FontanaMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.ORCID 0000-0001-9517-6997
Monica MiozzoMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.
Elena LesmaPharmacology, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.ORCID 0000-0002-9096-713X
Silvia M SirchiaMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milan, Italy.ORCID 0000-0002-6106-3721
University of Milan · IT

Funding

University of Milan Grant PSR2018_DIP_013_LINEA 2_2018_SIRCHIA
6 · The paper itself

Abstract

Beckwith-Wiedemann Syndrome (BWS) is an imprinting disorder characterized by overgrowth, stemming from various genetic and epigenetic changes. This study delves into the role of

Indexed as

Beckwith-Wiedemann SyndromeNeoplasmsAutophagyCell LineGlycogen Synthase Kinase 3HumansReceptor, IGF Type 2Glycogen Synthase Kinase 3IGF2R protein, humanReceptor, IGF Type 2autophagyBeckwith–Wiedemann Syndrome (BWS)IGF2IGF2RimprintingWNT pathway

Identifiers

PMID38612397
PMCPMC11011696
OpenAlexW4393082924

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.