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LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity

Mitochondrion(2020)10.1016/j.mito.2020.01.004Source: DataRank Database

LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity is a research paper published in Mitochondrion (2020). On theSindex it has a DataRank of 0. It has been cited 28 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access28 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (1 grants)Impact (FWCI 0.00)OA: greenTopics (29)IDs (PubMed, OpenAlex)SDGs (2)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (5)

Daniel Brezavar,Jennifer Hanson,Austin Larson ORCID,Penelope E. Bonnen ORCID,Arnaud Besse

Live enrichment

PubMed:23304386 OpenAlex:https://openalex.org/W31923470

National Institutes of Health

Grant: 1F32NS008372-01

REGULATION OF THE CYTOSKELETON IN AXONS AND DENDRITES

FWCI

0.00

Citation Percentile

0.0%

greenLicense: Elsevier TDM

journalhttp://new.medigraphic.com/cgi-bin/resumenI.cgi?IDREVISTA=85&IDARTICULO=29417&IDPUBLICACION=3204

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8628847

publisherhttps://api.elsevier.com/content/article/PII:S1567724919302089?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1567724919302089?httpAccept=text/plain

https://doi.org/10.1016/j.mito.2020.01.004

Fields of Study

Infectious Disease Case Reports and TreatmentsAbdominal vascular conditions and treatmentsPediatric Urology and Nephrology Studies0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

MedicineAbscessXanthogranulomatous pyelonephritisRadiologyGeneral surgerySurgeryInternal medicineKidneyNephrectomyInfant, NewbornMitophagyHemeOxidative PhosphorylationMitochondriaElectron TransportMitochondrial ProteinsATP-Dependent ProteasesMitochondrial EncephalomyopathiesSeizuresProteolysisHumansFemaleMolecular Chaperones

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Gender equality