Evidence map›Paper›PMID 39039299›Full record

ArticleEMBO reports2024

Fam134c and Fam134b shape axonal endoplasmic reticulum architecture in vivo.

Francescopaolo Iavarone, Marta Zaninello, Michela Perrone, Mariagrazia Monaco, Esther Barth, Felix Gaedke, Maria Teresa Pizzo, Giorgia Di Lorenzo, Vincenzo Desiderio, Eduardo Sommella and 7 more

Abstract read
In one paragraph

Article in EMBO reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
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

17 authors.

Francescopaolo Iavarone *Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy. f.iavarone@tigem.it.ORCID 0000-0002-8855-1848
Marta Zaninello *Institute for Genetics, Faculty of Mathematics and Natural Sciences, University of Cologne, Cologne, Germany.ORCID 0009-0002-6009-0901
Michela PerroneDepartment of Experimental Medicine, Division of Pharmacology, University of Campania "L. Vanvitelli", Naples, Italy.ORCID 0000-0002-3284-9944
Mariagrazia MonacoTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.ORCID 0009-0008-9637-7174
Esther BarthInstitute for Genetics, Faculty of Mathematics and Natural Sciences, University of Cologne, Cologne, Germany.
Felix GaedkeCologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, Cologne, Germany.ORCID 0000-0002-7744-4940
Maria Teresa PizzoTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.
Giorgia Di LorenzoTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.ORCID 0000-0001-8659-5268
Vincenzo DesiderioDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Via L. Armanni 5, 80138, Naples, Italy.ORCID 0000-0003-1819-6083
Eduardo SommellaDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, Fisciano, SA, 84084, Italy.
Fabrizio MerciaiDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, Fisciano, SA, 84084, Italy.
Emanuela SalviatiDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, Fisciano, SA, 84084, Italy.
Pietro CampigliaDepartment of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, Fisciano, SA, 84084, Italy.
Livio LuongoDepartment of Experimental Medicine, Division of Pharmacology, University of Campania "L. Vanvitelli", Naples, Italy.
Elvira De LeonibusTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy. deleonibus@tigem.it.ORCID 0000-0003-0220-2864
Elena RugarliInstitute for Genetics, Faculty of Mathematics and Natural Sciences, University of Cologne, Cologne, Germany. elena.rugarli@uni-koeln.de.ORCID 0000-0002-5782-1067
Carmine SettembreTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy. settembre@tigem.it.ORCID 0000-0002-5829-8589

Funding

EC | European Research Council (ERC) ERC-101045285-AUTOSELECTFondazione Telethon (FT) GSA21F005Ministero della Salute (Italy Ministry of Health) PNRR-MAD-2022-12376672
6 · The paper itself

Abstract

Endoplasmic reticulum (ER) remodeling is vital for cellular organization. ER-phagy, a selective autophagy targeting ER, plays an important role in maintaining ER morphology and function. The FAM134 protein family, including FAM134A, FAM134B, and FAM134C, mediates ER-phagy. While FAM134B mutations are linked to hereditary sensory and autonomic neuropathy in humans, the physiological role of the other FAM134 proteins remains unknown. To address this, we investigate the roles of FAM134 proteins using single and combined knockouts (KOs) in mice. Single KOs in young mice show no major phenotypes; however, combined Fam134b and Fam134c deletion (Fam134b/c

Indexed as

AxonsEndoplasmic ReticulumMembrane ProteinsAnimalsHumansMiceMice, KnockoutFam134b protein, mouseMembrane ProteinsAxonEndoplasmic ReticulumFAM134BFAM134C

Identifiers

PMID39039299
PMCPMC11316074

What OpenQuestion holds

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Registered trials

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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.