Soluble and microsomal forms of NADH-cytochrome beta 5 reductase from human placenta. Similarity with NADH-methemoglobin reductase from human erythrocytes.
about
Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.Advances in hereditary red cell enzyme anomalies.Development and validation of a spectrophotometric assay for measuring the activity of NADH: cytochrome b5 reductase in human tumour cells.Interaction between cytochrome b5 and hemoglobin: involvement of beta 66 (E10) and beta 95 (FG2) lysyl residues of hemoglobin.NADH cytochrome b5 reductase activity in lymphoid cell lines. Expression of the defect in epstein Barr virus transformed lymphoblastoid cell lines from patients with recessive congenital methemoglobinemiaMembrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency.NADH-methemoglobin reductase activity in the erythrocytes of newborn and adult mammals.Direct enzyme titration curve of NADH: cytochrome b5 reductase by combined isoelectric focusing/electrophoresis. Interactions between enzyme and cytochrome b5.Transcriptional and translational mechanisms of cytochrome b5 reductase isoenzyme generation in humans.Heterogeneity of the rat NADH-cytochrome-b5-reductase transcripts resulting from multiple alternative first exons.An interpretation of human diaphorase isozymes in terms of three gene loci DIA1, DIA2 and DIA3.Homozygous NADH-methemoglobin reductase and aspartylglucosaminidase deficiencies in a moderately retarded Sicilian child.Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases.Prenatal diagnosis of recessive congenital methaemoglobinaemia type II: novel mutation in the NADH-cytochrome b5 reductase gene leading to stop codon read-through.
P2860
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P2860
Soluble and microsomal forms of NADH-cytochrome beta 5 reductase from human placenta. Similarity with NADH-methemoglobin reductase from human erythrocytes.
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
1977年论文
@zh
1977年论文
@zh-cn
name
Soluble and microsomal forms o ...... ctase from human erythrocytes.
@en
type
label
Soluble and microsomal forms o ...... ctase from human erythrocytes.
@en
prefLabel
Soluble and microsomal forms o ...... ctase from human erythrocytes.
@en
P2093
P1476
Soluble and microsomal forms o ...... ctase from human erythrocytes.
@en
P2093
P356
10.1016/0005-2744(77)90136-X
P577
1977-03-01T00:00:00Z