Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II.
about
Human METTL20 methylates lysine residues adjacent to the recognition loop of the electron transfer flavoprotein in mitochondriaGlutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patientsMolecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II--and identification of glycine substitution for valine-157 in the sequence of the precursor, producing an unstableGenetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weaknessMolecular studies on primary lipoprotein lipase (LPL) deficiency. One base deletion (G916) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript.Organic acidurias: a review. Part 2.Mammalian mitochondrial beta-oxidation.Binding of the human "electron transferring flavoprotein" (ETF) to the medium chain acyl-CoA dehydrogenase (MCAD) involves an arginine and histidine residue.A novel ETFDH mutation in an adult patient with late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.Molecular study of electron transfer flavoprotein alpha-subunit deficiency in two Japanese children with different phenotypes of glutaric acidemia type II.
P2860
Q24300752-108912D3-67DF-4BCE-AD44-F5DB774B028CQ24564728-CEE3847D-95DB-47AA-B625-2708DE650457Q24678683-18E94583-3770-41BB-9590-833C56839330Q35585085-0768CC3E-FE40-4175-B1D7-A84A36BB137CQ35597975-86680500-13A8-4C2D-8428-25FB3B2B0CF1Q37463522-9F4E90DE-D03E-4D85-84F6-88BC584A2BDBQ41280085-BC96E5BC-C776-4995-A432-82915D11E7B8Q44704030-3EDCCD77-8881-40CE-A027-70213EA19B4FQ48339565-66CCEF99-50A5-4720-91BC-8BC5A602C476Q51693814-870DDE82-EABB-4244-9B6E-26F420187C0F
P2860
Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II.
description
1986 nî lūn-bûn
@nan
1986 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@ast
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@en
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@nl
type
label
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@ast
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@en
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@nl
prefLabel
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@ast
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@en
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@nl
P2093
P2860
P356
P1476
Biosynthesis of electron trans ...... in glutaric aciduria type II.
@en
P2093
P2860
P304
P356
10.1172/JCI112691
P407
P577
1986-10-01T00:00:00Z