Evidence map›Paper›PMID 34948052›Full record

ArticleInternational journal of molecular sciences2021

Impaired Retromer Function in Niemann-Pick Type C Disease Is Dependent on Intracellular Cholesterol Accumulation.

Kristina Dominko, Ana Rastija, Sandra Sobocanec, Lea Vidatic, Sarah Meglaj, Andrea Lovincic Babic, Birgit Hutter-Paier, Alessio-Vittorio Colombo, Stefan F Lichtenthaler, Sabina Tahirovic and 1 more

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.5field-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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Endo-lysosomal dysfunction and neuronal-glial crosstalk in Niemann-Pick type C disease.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  3. The ancestral type of the R-RAS protein has oncogenic potential.Cellular & molecular biology letters · 2024
    Article
  4. Adenosine ACurrent issues in molecular biology · 2023
    Article
  5. Article
  6. Review
  7. 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 4 institutions in 3 countries.

Kristina DominkoLaboratory for Neurodegenerative Disease Research, Division of Molecular Medicine, Ruder Boskovic Institute, 10000 Zagreb, Croatia.
Ana RastijaLaboratory for Neurodegenerative Disease Research, Division of Molecular Medicine, Ruder Boskovic Institute, 10000 Zagreb, Croatia.
Sandra SobocanecLaboratory for Mitochondrial Bioenergetics and Diabetes, Division of Molecular Medicine, Ruder Boskovic Institute, 10000 Zagreb, Croatia.ORCID 0000-0001-8915-6009
Lea VidaticLaboratory for Neurodegenerative Disease Research, Division of Molecular Medicine, Ruder Boskovic Institute, 10000 Zagreb, Croatia.
Sarah MeglajDivision of Biology, Faculty of Science, University of Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0001-5143-7913
Andrea Lovincic BabicDivision of Biology, Faculty of Science, University of Zagreb, 10000 Zagreb, Croatia.
Birgit Hutter-PaierQPS Austria GmbH, 8074 Grambach, Austria.
Alessio-Vittorio ColomboGerman Center for Neurodegenerative Diseases (DZNE), 81377 Munich, Germany.
Stefan F LichtenthalerGerman Center for Neurodegenerative Diseases (DZNE), 81377 Munich, Germany.ORCID 0000-0003-2211-2575
Sabina TahirovicGerman Center for Neurodegenerative Diseases (DZNE), 81377 Munich, Germany.ORCID 0000-0003-4403-9559
Silva HecimovicLaboratory for Neurodegenerative Disease Research, Division of Molecular Medicine, Ruder Boskovic Institute, 10000 Zagreb, Croatia.ORCID 0000-0001-6077-433X
Ruđer Bošković Institute · HRGerman Center for Neurodegenerative Diseases · DEUniversity of Zagreb · HRQPS (Austria) · AT

Funding

Alzheimer's Association Grant through the AD Strategic Fund ADSF-21-831226-CCroatian Science Foundation IP-2016-06-2799Deutsche Forschungsgemeinschaft EXC 2145 SyNergy- ID 390857198
6 · The paper itself

Abstract

Niemann-Pick type C disease (NPC) is a rare inherited neurodegenerative disorder characterized by an accumulation of intracellular cholesterol within late endosomes and lysosomes due to NPC1 or NPC2 dysfunction. In this work, we tested the hypothesis that retromer impairment may be involved in the pathogenesis of NPC and may contribute to increased amyloidogenic processing of APP and enhanced BACE1-mediated proteolysis observed in NPC disease. Using

Indexed as

Loss of Function MutationAnimalsCells, CulturedCHO CellsCholesterolCricetulusDisease Models, AnimalFemaleHumansMaleMembrane Transport ProteinsMiceNeuronsNiemann-Pick C1 ProteinNiemann-Pick Disease, Type CPrimary Cell CultureCholesterolMembrane Transport ProteinsNiemann-Pick C1 ProteinNpc1 protein, mouseReceptors, LDLSorl1 protein, mouseVesicular Transport ProteinsVps26 protein, mouseVps35 protein, mousecholesterol homeostasisendolysosomal pathwayneurodegenerationneurodegenerative diseasesNPC1rare diseasesretromer

Identifiers

PMID34948052
PMCPMC8705785
OpenAlexW4200307148

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.