about
Glutathione in Cellular Redox Homeostasis: Association with the Excitatory Amino Acid Carrier 1 (EAAC1)Heritability of glutathione and related metabolites in stored red blood cells.The redox basis of epigenetic modifications: from mechanisms to functional consequences.Unveiling the roles of the glutathione redox system in vivo by analyzing genetically modified mice.Emerging regulatory paradigms in glutathione metabolism.5-Oxoprolinuria in Heterozygous Patients for 5-Oxoprolinase (OPLAH) Missense ChangesSerum γ-Glutamyl Transferase Is Inversely Associated with Bone Mineral Density Independently of Alcohol Consumption.Vitamin B-6 restriction tends to reduce the red blood cell glutathione synthesis rate without affecting red blood cell or plasma glutathione concentrations in healthy men and women.Impaired glutathione synthesis in neurodegeneration.Glutathione dysregulation and the etiology and progression of human diseases.Acetaminophen toxicity and 5-oxoproline (pyroglutamic acid): a tale of two cycles, one an ATP-depleting futile cycle and the other a useful cycle.Acquired 5-oxoproline acidemia successfully treated with N-acetylcysteine.Gamma-glutamyl transferase: the silent partner?The pathogenesis of cystinosis: mechanisms beyond cystine accumulation.Role of glutathione in immunity and inflammation in the lung.What is the clinical significance of 5-oxoproline (pyroglutamic acid) in high anion gap metabolic acidosis following paracetamol (acetaminophen) exposure?Rare hereditary red blood cell enzymopathies associated with hemolytic anemia - pathophysiology, clinical aspects, and laboratory diagnosis.Discovery of a widespread prokaryotic 5-oxoprolinase that was hiding in plain sight.Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD)Defective GSS causes Glutathione synthetase deficiency (GSS deficiency)5-Oxoprolinase deficiency: report of the first human OPLAH mutation.Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency.D-Galactose Causes Motor Coordination Impairment, and Histological and Biochemical Changes in the Cerebellum of Rats.A case of severe glutathione synthetase deficiency with novel GSS mutations.Glutathione is a low-affinity substrate of the human sodium-dependent dicarboxylate transporter.UPLC-MS metabolic profiling of second trimester amniotic fluid and maternal urine and comparison with NMR spectral profiling for the identification of pregnancy disorder biomarkersNew insights into the genetics of 5-oxoprolinase deficiency and further evidence that it is a benign biochemical condition
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մարտին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Inborn errors in the metabolism of glutathione
@ast
Inborn errors in the metabolism of glutathione
@en
Inborn errors in the metabolism of glutathione
@en-gb
Inborn errors in the metabolism of glutathione
@nl
type
label
Inborn errors in the metabolism of glutathione
@ast
Inborn errors in the metabolism of glutathione
@en
Inborn errors in the metabolism of glutathione
@en-gb
Inborn errors in the metabolism of glutathione
@nl
prefLabel
Inborn errors in the metabolism of glutathione
@ast
Inborn errors in the metabolism of glutathione
@en
Inborn errors in the metabolism of glutathione
@en-gb
Inborn errors in the metabolism of glutathione
@nl
P2860
P356
P1476
Inborn errors in the metabolism of glutathione
@en
P2093
Agne Larsson
Ellinor Ristoff
P2860
P2888
P356
10.1186/1750-1172-2-16
P407
P5008
P577
2007-03-30T00:00:00Z
P5875
P6179
1002274888