3 results match your criteria 1289t

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Salegentibacter chungangensis sp. nov., isolated from a sea sand and emended description of the genus Salegentibacter.

Int J Syst Evol Microbiol 2014 May 29;64(Pt 5):1514-1519. Epub 2014 Jan 29.

Department of Microbiology, Chung-Ang University College of Medicine, Seoul, Republic of Korea.

A Gram-stain-negative, non-motile, rod-shaped, strictly aerobic bacterial strain, designated CAU 1289T, was isolated from a marine sand and its taxonomic position was investigated using a polyphasic approach. It grew optimally at pH 6.5 and 30 °C and in the presence of 3% (w/v) NaCl. Read More

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Genetic variations and haplotypes of the 5' regulatory region of CYP2C19 in South Indian population.

Drug Metab Pharmacokinet 2009 ;24(2):185-93

Pharmacogenomics laboratory, Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.

CYP2C19 is expressed polymorphically with about 21 variant alleles. Genotype-phenotype association studies of CYP2C19 have shown marked deviations, suggesting the presence of other variations in the intronic and 5' regulatory region affecting its expression. This study aims to identify the genetic polymorphisms and construction of haplotypes of variations in 5' regulatory region of CYP2C19 among the South Indian population. Read More

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November 2009

Mutation analysis in patients with N-acetylglutamate synthase deficiency.

Hum Mutat 2003 Jun;21(6):593-7

Universitätsklinikum Münster, Klinik und Poliklinik für Kinderheilkunde, Münster, Germany.

N-acetylglutamate synthase (NAGS) is the key enzyme for the regulation of the hepatic urea cycle and is also highly expressed in kidney and gut. The reaction product, N-acetylglutamate, is an allosteric activator of carbamylphosphate synthetase 1 in the liver, catalyzing the initial step of ammonia detoxification. NAGS deficiency is a rare inborn error of metabolism inherited as an autosomal recessive trait leading to hyperammonemia. Read More

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