Blue Native electrophoresis to study mitochondrial and other protein complexes.
about
SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumorsCytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assemblyMutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial diseaseMutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial diseaseMutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and fliesIdentification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunitsETHE1 mutations are specific to ethylmalonic encephalopathyThe mitochondrial fission protein hFis1 requires the endoplasmic reticulum gateway to induce apoptosisCmc1p is a conserved mitochondrial twin CX9C protein involved in cytochrome c oxidase biogenesis.SURF1 deficiency causes demyelinating Charcot-Marie-Tooth diseaseNDUFA2 complex I mutation leads to Leigh diseaseThe essentials of protein import in the degenerate mitochondrion of Entamoeba histolyticamTERF2 regulates oxidative phosphorylation by modulating mtDNA transcriptionMice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency.Cytochrome c oxidase is required for the assembly/stability of respiratory complex I in mouse fibroblastsRapid purification and mass spectrometric characterization of mitochondrial NADH dehydrogenase (Complex I) from rodent brain and a dopaminergic neuronal cell line.LYRM7/MZM1L is a UQCRFS1 chaperone involved in the last steps of mitochondrial Complex III assembly in human cells.Interaction between the oxa1 and rmp1 genes modulates respiratory complex assembly and life span in Podospora anserina.Mass spectrometric identification of proteins in complex post-genomic projects. Soluble proteins of the metabolically versatile, denitrifying 'Aromatoleum' sp. strain EbN1.Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants.The peripheral membrane subunits of the SAM complex function codependently in mitochondrial outer membrane biogenesisNovel role of ATPase subunit C targeting peptides beyond mitochondrial protein import.Targeting of the cytosolic poly(A) binding protein PABPC1 to mitochondria causes mitochondrial translation inhibitionExpression of the yeast NADH dehydrogenase Ndi1 in Drosophila confers increased lifespan independently of dietary restriction.Separation and identification of HSP-associated protein complexes from pancreatic cancer cell lines using 2D CN/SDS-PAGE coupled with mass spectrometry.A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple familiesExome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy.Mitochondrial ATP synthase: architecture, function and pathology.High-fat diet decreases activity of the oxidative phosphorylation complexes and causes nonalcoholic steatohepatitis in mice.The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.Nongradient blue native gel analysis of serum proteins and in-gel detection of serum esterase activities.Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy.A detergent-free strategy for the reconstitution of active enzyme complexes from native biological membranes into nanoscale discsCommon and Novel TMEM70 Mutations in a Cohort of Italian Patients with Mitochondrial EncephalocardiomyopathyREXO2 is an oligoribonuclease active in human mitochondria.A mutation in C2orf64 causes impaired cytochrome c oxidase assembly and mitochondrial cardiomyopathyPioglitazone leads to an inactivation and disassembly of complex I of the mitochondrial respiratory chainMitochondrial aminopeptidase deletion increases chronological lifespan and oxidative stress resistance while decreasing respiratory metabolism in S. cerevisiaeMTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention.
P2860
Q24296457-D8B2BD48-EB3B-4FAF-8221-5D4CFB6EB576Q24299292-BEB5087B-F0F0-4E99-BC25-5D0B442AEF47Q24302215-63A77A7C-6AB4-4CCA-BF46-B454218EBC29Q24313044-029639BC-BE5B-48D3-AEC2-BB66A43DEEC5Q24338706-FD4659B8-5E27-4A0D-ADCA-63A566B5213CQ24338844-84325932-859C-40A0-A90F-45D2924C9874Q24655953-0343C288-2983-4E07-A68C-7A86A3917F6AQ24673883-FE40A822-DD2D-43F1-A176-C7AD9CDAFEA3Q27937872-5A1B1A8C-024B-49DF-8328-ABDB7F6D0857Q28118095-5448EC1C-7BAF-4A40-8921-2A77855552D9Q28282142-A05B521F-0B68-4472-9930-495E5A8A6BD9Q28473253-286DCA9D-C162-4328-B47A-60713FD26E0DQ28512464-BB9E169D-D107-422E-9609-011D3636E0D1Q28512560-DC2B84B5-D071-4AA5-975D-E72D1C541DC0Q28585444-B8BCCEC0-B79D-46D9-99A8-EACA6FD05D71Q31135400-59967E35-82F2-42D7-A6BD-EEEEC01EA22EQ32884553-3FF2742E-AE01-4C30-B006-13A01FBDF951Q33209001-8DF69B1F-F97D-410D-96DB-9B646DB3A398Q33249185-7458A2E5-1C14-4518-B265-D7667EDE7F23Q33252661-B351231D-9455-4E80-8BBC-147B1C39B5F0Q33304765-7DC4D2B1-1843-49AC-9D68-A480F92E4316Q33571588-678D6967-EF0B-4950-BC6F-D4AFB198D133Q33922370-D050AA80-42CC-468F-8E7C-42BE3D54D145Q33927197-906F6EAA-BFAE-4DB4-9344-61FDA1C52E58Q34057985-5E328D42-6C53-408C-A57D-5A38C500C999Q34162933-8568875A-0D56-4B54-A148-28C41FD87E14Q34163172-F7C38E32-4245-40A0-AF89-E6727BF1450DQ34203277-72477E63-6646-40A7-B977-AF8AF0E6EA47Q34211463-112E899B-C2C2-4932-8BD3-223524232CAEQ34424185-04E3AAA0-88DA-40B6-87EA-F900F944C818Q34489613-73896A9A-A98F-471B-8A43-9296EF033D83Q34556725-1D6AAA7D-D05A-49B1-93AC-7B21C6F155C6Q34614921-6D70F770-1C84-4BCA-A7FD-907D126C1BC6Q34714812-20815213-846F-4040-9299-5CA8CC0AB5F7Q34734718-6568B7C5-5C69-4EB4-A40C-3F5C370C7EE3Q34760646-65ECBD53-128C-46D3-862B-490A30933B01Q34768367-7BADE21E-82BA-463E-BF33-7B107B050B43Q34893444-04BA4833-63B2-4395-9642-55A6B1373A72Q35015111-4FC95886-4E4F-4D44-A98A-712827871CABQ35234097-11487D14-DB21-48CF-AF87-F9809A1786DC
P2860
Blue Native electrophoresis to study mitochondrial and other protein complexes.
description
2002 nî lūn-bûn
@nan
2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@ast
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@en
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@nl
type
label
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@ast
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@en
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@nl
prefLabel
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@ast
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@en
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@nl
P1433
P1476
Blue Native electrophoresis to study mitochondrial and other protein complexes.
@en
P2093
Leo G J Nijtmans
Nadine S Henderson
P304
P356
10.1016/S1046-2023(02)00038-5
P50
P577
2002-04-01T00:00:00Z