نتایج جستجو برای: hexosaminidase a

تعداد نتایج: 13431949  

2007
Masayuki YOSHIKAWA Seikou NAKAMURA Yasuyo KATO Koudai MATSUHIRA Hisashi MATSUDA

active saponin constituents from Camellia (C.) sinensis (Theaceae), we have reported the isolation and structure elucidation of theasaponins A1—A5, C1, E1—E13, F1—F3, G1, G2, and H1, 2—6) assamsaponins A—I, and camelliasaponins B1 and C1 9) from the seeds of Japanese C. sinensis (L.) O. KUNTZE and Sri Lankan C. sinensis L. var. assamica PERRE, and foliatheasaponins I—V from the leaves of Japane...

Journal: :Investigative ophthalmology & visual science 2009
Michelle L McDonald Yanru Wang Shivaram Selvam Tamako Nakamura Robert H Chow Joel E Schechter Samuel C Yiu Austin K Mircheff

PURPOSE Lacrimal immunohistopathology has diverse clinical presentations, suggesting that inflammatory mediators exert diverse influences. Chronic exposure to agonistic acetylcholine receptor autoantibodies has been studied previously; the present work addressed mediators that signal through other G protein-coupled receptors. METHODS Acinus-like structures and reconstituted acinar epithelial ...

Journal: :The Journal of pharmacology and experimental therapeutics 2002
Grant R Stenton Osamu Nohara René E Déry Harissios Vliagoftis Mark Gilchrist Ankur Johri John L Wallace Morley D Hollenberg Redwan Moqbel A Dean Befus

Because thrombin-induced inflammation is partially mast cell-dependent and involves proteinase-activated receptors (PARs), we hypothesized that mast cells express PAR and can be stimulated with PAR-activating peptides (PAR-AP). We demonstrated that rat peritoneal mast cells expressed PAR-1 and PAR-2 mRNA, and that PAR-2AP (tc-LIGRLO-NH(2), 1 microm) induced 64.2 +/- 4.4% specific beta-hexosamin...

ژورنال: ارمغان دانش 2019

Background and aim: Tachyx is a rare autosomal recessive and neurological disorder caused by glycosfenolipid accumulation (GM2 ganglioside) in cell lysosomes. The accumulation of GM2 ganglioside is due to the mutation in the beta-hexose aminase gene (HEXA), which reduces the activity and deficiency of the HEXA enzyme. The aim of this study was to report 2 cases of T.Sax disease.   Case report:...

2015
Z.K. Timur S. Akyildiz Demir C. Marsching R. Sandhoff V. Seyrantepe

Tay–Sachs disease is a severe lysosomal storage disorder caused by mutations in the HEXA gene coding for α subunit of lysosomal β-Hexosaminidase A enzyme, which converts GM2 to GM3 ganglioside. HexA−/− mice, depleted of the β-Hexosaminidase A iso-enzyme, remain asymptomatic up to 1 year of age because of a metabolic bypass by neuraminidase(s). These enzymes remove a sialic acid residue converti...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran narjes jafari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran habibeh nejad biglari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran sayena jabbeh dari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran farzad ahmad abadi 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad-reza alaee 4. department of pediatric endocrinology, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, jafari n, nejad biglari h, jabbeh dari s, ahmad abadi f, alaee mr, nemati h, saket s, tonekaboni sh, taghdiri mm, ghofrani m. gm2-gangliosidosis (sandhoff and tay sachs disease): diagnosis and neuroimaging findings (an iranian pediatric case series) iran j child neurol. 2014 summer;8(3): 55-60.   abstract objective gm2-gangliosidosis disease is a rare aut...

Journal: :Journal of cell science 1998
S R da Costa F A Yarber L Zhang M Sonee S F Hamm-Alvarez

Stimulation of lacrimal acini with secretagogues such as carbachol initiates movement and fusion of acinar secretory vesicles with the apical plasma membrane, resulting in release of protein into the nascent tear fluid. Using rabbit lacrimal acini reconstituted in vitro from isolated cells, we have investigated the organization of the apical cytoskeleton and its role in stimulated secretion. Co...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید