نتایج جستجو برای: hexosaminidase a

تعداد نتایج: 13431949  

Journal: :Journal of clinical pathology 1976
M McCormack

Hexosaminidase, alpha-mannosidase, beta-galactosidase, beta-glucuronidase, and arylsulphatase A were measured inperitoneal and pleural effusions from patients with benign, malignant, and inflammatory disorders. Compared with the benign transudates, all enzyme activities were moderately elevated in malignant effusions and markedly elevated in inflammatory effusions. The assay of hexosaminidase a...

2017
Vykuntaraju K. Gowda Raghavendraswami Amoghimath Varun M. Srinivasan Maya Bhat

Sandhoff disease is a neurodegenerative disease caused due to deficiency of hexosaminidase (HEX) A and B. A 1-year-old male child presented with regression of milestones, exaggerated startle response, decreased vision, and seizures from 6 months of age. The child had coarse facies without hepatosplenomegaly. Serum levels of β hexosaminidase total (A + B) were low. Genetic testing for Sandhoff d...

Journal: :European journal of biochemistry 1977
B Geiger B U Von Specht R Arnon

Human hexosaminidase A was covalently bound to soluble poly(N-vinylpyrrolidone), and the effect of this binding on the enzyme inactivation by various procedures was investigated. Whereas the polymer-bound hexosaminidase underwent inactivation to the same extent as the free enzyme, when exposed to heat or acidic pH, the conjugation to polymer appeared to protect the enzyme towards proteolysis. T...

2012
Atsuko SAKURAI Natsu YAMAGUCHI Kei SONOYAMA

We investigated Candida albicans-induced mast cell degranulation in vitro and in vivo. Cell wall fraction but not culture supernatant and cell membrane fraction prepared from hyphally grown C. albicans induced β-hexosaminidase release in RBL-2H3 cells. Cell wall mannan and soluble β-glucan fractions also induced β-hexosaminidase release. Histological examination of mouse forestomach showed that...

Journal: :Revista Brasileira De Oftalmologia 2023

RESUMO A doença de Tay-Sachs é um distúrbio neurodegenerativo autossômico recessivo, o qual envolve metabolismo dos lipídios, levando ao acúmulo gangliosídeos nos tecidos, devido à deficiência da enzima hexosaminidase A. Esse depósito progressivo resulta em perda função neurológica e, quando acomete as células ganglionares mácula, causa achado típico doença, a “mácula cereja”. patologia diagnos...

Journal: :The Biochemical journal 2011
Tian Liu Haitao Zhang Fengyi Liu Lei Chen Xu Shen Qing Yang

Chitinolytic β-N-acetyl-D-hexosaminidase is a branch of the GH20 (glycoside hydrolase family 20) β-N-acetyl-D-hexosaminidases that is only distributed in insects and micro-organisms, and is therefore a potential target for the action of insecticides. PUGNAc [O-(2-acetamido-2-deoxy-D-glucopyransylidene)-amino-N-phenylcarbamate] was initially identified as an inhibitor against GH20 β-N-acetyl-D-h...

Journal: :Acta Biochimica Polonica 1999

Journal: :Annals of Indian Academy of Neurology 2006

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