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  • Search Condition : Filter (MeSH = Mitochondrial Proteins / genetics)
Species Resource Title
Human and Animal Cells HeLa(RCB0007) Direct Analysis of Mitochondrial Damage Caused by Misfolded/Destabilized Proteins.
C.elegans tm6212 , tm3586 , tm5171 , tm4919 Hypoxia-induced mitochondrial stress granules.
C.elegans tm4525 , tm4919 ATFS-1 counteracts mitochondrial DNA damage by promoting repair over transcription.
DNA material Genome Network Project Human cDNA Clone , IRAL001D22 (HGY080494) , IRAL011I06 (HGY084598) , IRAL003F10 (HGY081330) , IRAK013M01 (HGX005489) , IRAL004J02 (HGY081818) , IRAL007P17 (HGY083177) , IRAK013K21 (HGX005461) Protein N-myristoylation plays a critical role in the mitochondrial localization of human mitochondrial complex I accessory subunit NDUFB7.
C.elegans tm4919 Effect of the mitochondrial unfolded protein response on hypoxic death and mitochondrial protein aggregation.
C.elegans tm1108 Identification of Novel Therapeutic Targets for Polyglutamine Diseases That Target Mitochondrial Fragmentation.
C.elegans tm4525 , tm4803 , tm3165 Mitochondrial protein import determines lifespan through metabolic reprogramming and de novo serine biosynthesis.
C.elegans tmC5 Allele-specific mitochondrial stress induced by Multiple Mitochondrial Dysfunctions Syndrome 1 pathogenic mutations modeled in Caenorhabditis elegans.
DNA material pMAMtracker-Luc (RDB19895) , pMAMtracker-Green (RDB19896) Novel reporters of mitochondria-associated membranes (MAM), MAMtrackers, demonstrate MAM disruption as a common pathological feature in amyotrophic lateral sclerosis.
Drosophila DGRC#108479 , DGRC#101249 A Drosophila model of the neurological symptoms in Mpv17-related diseases.
Pathogenic eukaryotic microorganisms Aspergillus tubingensis IFM 65578 (= WU-2223L) Overexpression of the gene encoding alternative oxidase for enhanced glucose consumption in oxalic acid producing Aspergillus niger expressing oxaloacetate hydrolase gene.
Human and Animal Cells , Drosophila K562(RCB0027) PGAM5 interacts with Bcl-rambo and regulates apoptosis and mitophagy.
Human and Animal Cells HeLa Mammalian HEMK1 methylates glutamine residue of the GGQ motif of mitochondrial release factors.
DNA material pMXs-IP-HA-Parkin (RDB19764) , pMXs-IP-GFP-Omp25 (RDB19786) Parkin mediates proteasome-dependent protein degradation and rupture of the outer mitochondrial membrane.
Mice RBRC06294 LPL/AQP7/GPD2 promotes glycerol metabolism under hypoxia and prevents cardiac dysfunction during ischemia.
Drosophila DGRC#112001 Vmp1, Vps13D, and Marf/Mfn2 function in a conserved pathway to regulate mitochondria and ER contact in development and disease.
Human and Animal Cells HeLa.S3(RCB1525) Mito-FUNCAT-FACS reveals cellular heterogeneity in mitochondrial translation.
Human and Animal Cells COS-1(RCB0143) γ-Mangostin from Garcinia mangostana pericarps as a dual agonist that activates Both PPARα and PPARδ.
Human and Animal Cells Atg5^(+/+)MEF(RCB2710) , Atg5^(-/-)MEF(RCB2711) Parkin and PINK1 function in a vesicular trafficking pathway regulating mitochondrial quality control.
Human and Animal Cells PC-12(RCB0009) Newly developed Mg2+-selective fluorescent probe enables visualization of Mg2+ dynamics in mitochondria.