entity

Complex_I

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about Complex_I: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.

2Connections
1Hypotheses
1Analyses
1Outgoing
1Incoming

Wiki Pages (20)

Knowledge base pages for this entity

Personalized Treatment Plan — Atypical Parkinsonism (CBS/PSP)

therapeutic · 15794 words

Progressive Supranuclear Palsy (PSP)

disease · 12907 words

Corticobasal Syndrome (CBS)

disease · 11374 words

Parkinson's Disease

disease · 8807 words

CBS/PSP Supplements Guide

therapeutic · 6929 words

Outgoing (1)

TargetRelationTypeStr
mitochondrial_respirationcatalyzespathway0.50

Incoming (1)

SourceRelationTypeStr
MT-ND1component_ofgene0.50

Targeting Hypotheses (1)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
CRISPR-Mediated Mitochondrial Genome Editing for Complex I D 0.491 neurodegeneration CRISPR-based therapeutic approaches for

Mentioning Analyses (1)

Scientific analyses that reference this entity

CRISPR-based therapeutic approaches for neurodegenerative diseases

neurodegeneration | 2026-04-03 | 14 hypotheses Top: 0.622

Related Papers (7)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
Whole mitochondrial genome sequencing in individuals with Leber hereditary optic [PMID:40969215] Srilekha S, Ambika S, Hemavathy N, Vidhy Front Neurol 2025 0
Exploring rare mitochondrial DNA in Leber hereditary optic neuropathy. [PMID:41080639] Cao S, Liu Y, Sun M, Zhang Y, Sun Y et a Adv Ophthalmol Pract Res 2025 0
Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Ins [PMID:39578757] Chkioua L, Amri Y, Sahli C, Nasri T, Mil BMC Genomics 2024 0
Leber's hereditary optic neuropathy: Current approaches and future perspectives [PMID:34454075] Mohana Devi S, Abishek Kumar B, Mahalaxm Mitochondrion 2021 0
Mitochondrial DNA-Associated Leigh Syndrome Spectrum. [PMID:20301352] Adam MP, Bick S, Mirzaa GM, Pagon RA, Wa 1993 0
Leber Hereditary Optic Neuropathy. [PMID:20301353] Adam MP, Bick S, Mirzaa GM, Pagon RA, Wa 1993 0
Primary Mitochondrial Disorders Overview. [PMID:20301403] Adam MP, Bick S, Mirzaa GM, Pagon RA, Wa 1993 0