Results 111 to 120 of about 1,823 (170)
Exploring the causal relationship between gut microbiota, circulating metabolites, immune cells, and inflammation-related proteins and coronary artery calcification: A multi-omics Mendelian randomization study. [PDF]
Medicine (Baltimore)Ma L, Xiao M, Cai S, Ding Y.
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A multidomain hydrolase from the thermophile Thermanaeromonas toyohensis degrades high molecular mass forms of polyhydroxybutyrate. [PDF]
Protein SciQuirk S +5 more
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An enantioselective formal synthesis of thienamycin. [PDF]
Tetrahedron LettBreunig JL, Lin YC, Pierce JG.
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Acute gamma hydroxybutyrate toxicity.
The California journal of emergency medicine, 2001 openaire +3 more sources
Importance of oligo-( R )-3-hydroxybutyrates to S. lividans KcsA channel structure and function
Molecular BioSystems, 2010 Rosetta N Reusch
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Applied Microbiology and Biotechnology, 2009
4-Hydroxybutyrate (4HB) was produced by Aeromonas hydrophila 4AK4, Escherichia coli S17-1, or Pseudomonas putida KT2442 harboring 1,3-propanediol dehydrogenase gene dhaT and aldehyde dehydrogenase gene aldD from P. putida KT2442 which are capable of transforming 1,4-butanediol (1,4-BD) to 4HB.
Lei, Zhang +3 more
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4-Hydroxybutyrate (4HB) was produced by Aeromonas hydrophila 4AK4, Escherichia coli S17-1, or Pseudomonas putida KT2442 harboring 1,3-propanediol dehydrogenase gene dhaT and aldehyde dehydrogenase gene aldD from P. putida KT2442 which are capable of transforming 1,4-butanediol (1,4-BD) to 4HB.
Lei, Zhang +3 more
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Brain and Development, 1994
The clinical findings in six patients from three families with 4-hydroxybutyric aciduria are described. The onset of disease was in early infancy in all cases. All infants presented with severe global delay and severe hypotonia, and all patients had seizure disorder.
Z, Rahbeeni +9 more
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The clinical findings in six patients from three families with 4-hydroxybutyric aciduria are described. The onset of disease was in early infancy in all cases. All infants presented with severe global delay and severe hypotonia, and all patients had seizure disorder.
Z, Rahbeeni +9 more
openaire +2 more sources
BioEssays, 1984
AbstractRecent work has led to the discovery of six patients with 4‐hydroxybutyric acid‐uria, a severe hereditary human pathology characterized by the accumulation of a compound of known neuropharmacologic activity in body fluids. The enzymatic deficiency has been localized to succinic semialdehyde dehydrogenase, one of two enzymes involved in the ...
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AbstractRecent work has led to the discovery of six patients with 4‐hydroxybutyric acid‐uria, a severe hereditary human pathology characterized by the accumulation of a compound of known neuropharmacologic activity in body fluids. The enzymatic deficiency has been localized to succinic semialdehyde dehydrogenase, one of two enzymes involved in the ...
openaire +1 more source