Evidence map›Paper›PMID 31888107›Full record

ArticleInternational journal of molecular sciences2019

Mitochondrial Dynamics of Proximal Tubular Epithelial Cells in Nephropathic Cystinosis.

Domenico De Rasmo, Anna Signorile, Ester De Leo, Elena V Polishchuk, Anna Ferretta, Roberto Raso, Silvia Russo, Roman Polishchuk, Francesco Emma, Francesco Bellomo

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Cystinosis and Cellular Energy Failure: Mitochondria at the Crossroads.International journal of molecular sciences · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Frontiers in immunology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Renal and Extra Renal Manifestations in Adult Zebrafish Model of Cystinosis.International journal of molecular sciences · 2021
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Bone Disease in Nephropathic Cystinosis: Beyond Renal Osteodystrophy.International journal of molecular sciences · 2020
    Review
  19. 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

10 authors at 4 institutions in 1 country.

Domenico De RasmoInstitute of Biomembranes, Bioenergetics and Molecular Biotechnology (IBIOM), National Research Council (CNR), 70124 Bari, Italy.
Anna SignorileDepartment of Basic Medical Sciences, Neurosciences and Sense Organs, University of Bari "Aldo Moro", 70124 Bari, Italy.
Ester De LeoRenal Diseases Research Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital-IRCCS, 00146 Rome, Italy.
Elena V PolishchukTelethon Institute of Genetics and Medicine, 80078 Pozzuoli, Italy.
Anna FerrettaInstitute of Biomembranes, Bioenergetics and Molecular Biotechnology (IBIOM), National Research Council (CNR), 70124 Bari, Italy.ORCID 0000-0003-2279-9557
Roberto RasoRenal Diseases Research Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital-IRCCS, 00146 Rome, Italy.
Silvia RussoDepartment of Basic Medical Sciences, Neurosciences and Sense Organs, University of Bari "Aldo Moro", 70124 Bari, Italy.
Roman PolishchukTelethon Institute of Genetics and Medicine, 80078 Pozzuoli, Italy.
Francesco EmmaDivision of Nephrology, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital-IRCCS, 00165 Rome, Italy.ORCID 0000-0002-0383-3468
Francesco BellomoRenal Diseases Research Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital-IRCCS, 00146 Rome, Italy.ORCID 0000-0003-2912-8764
Bambino Gesù Children's Hospital · ITInstitute of Biomembranes, Bioenergetics and Molecular Biotechnologies · ITTelethon Institute Of Genetics And Medicine · ITUniversity of Bari Aldo Moro · IT

Funding

Cystinosis Research Foundation CRFF-2017-001Ministero della Salute Ricerca Corrente
6 · The paper itself

Abstract

Nephropathic cystinosis is a rare lysosomal storage disorder caused by mutations in

Indexed as

Amino Acid Transport Systems, NeutralCells, CulturedCysteamineCystinosisEpithelial CellsGTP PhosphohydrolasesHumansKidney Tubules, ProximalMembrane ProteinsMitochondriaMitochondrial DynamicsMitochondrial ProteinsUbiquitinationUbiquitin-Protein LigasesAmino Acid Transport Systems, NeutralCTNS protein, humanCysteamineFIS1 protein, humanGTP PhosphohydrolasesMembrane ProteinsMFN2 protein, humanMitochondrial ProteinsOPA1 protein, humanparkin proteinUbiquitin-Protein LigasescysteamineFanconi syndromemitochondrial cristaemitochondrial dynamicsmitochondrial fissionmitochondrial fusionnephropathic cystinosis

Identifiers

PMID31888107
PMCPMC6982165
OpenAlexW2997380075

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.