نتایج جستجو برای: arylsulfatase b

تعداد نتایج: 899802  

Journal: :Investigative ophthalmology & visual science 1986
L E Stramm R J Desnick M E Haskins G D Aguirre

Feline mucopolysaccharidosis VI (MPS VI) is a recessively inherited lysosomal storage disease resulting from a deficiency of arylsulfatase B (ASB). Previous histopathologic findings have indicated that the disease is expressed morphologically in non-pigmented retinal pigment epithelial cells (RPE) in the posterior pole and superior equatorial regions by the accumulation of vacuolated inclusions...

2003
R. STAHN K. - P. MAIER K. HANNIG

A combination of differential centrifugation and carrier-free continuous electrophoresis is introduced as a new method for the isolation of animal cell organelles . Various buffers were systematically checked in order to find the system which preserves the organelles and gives as well a good separation in the free-flow electrophoresis apparatus. Triethanolamine-acetate buffer (10 mm), pH 7 .4 w...

2017
Magdalena Zaborowska Jan Kucharski Jadwiga Wyszkowska

This study analysed the effectiveness of innovative (basalt meal, brown algae extract) and conventional (barley straw) substances which hypothetically alleviate the inhibiting effect of Cd2+ on biochemical properties of soil, with particular regard to the activity of arylsulfatase. An analysis of their potential was carried out based on the activity of arylsulfatase and the number of Pseudomona...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1980
J Houglum J K Pai V Atrache D E Sok C J Sih

Perfusion of cat paws with compound 48/80 released two slow reacting substances (SRSs) which were isolated and characterized as 5-hydroxy-6-S-cysteinylglycyl-7,9,11,14-icosatetraenoic acid (SRS I) and 5-hydroxy-6-S-cysteinyl-7,9,11,14-icosatetraeonic acid (SRS II) on the basis of chemical degradations, amino acid analyses, spectroscopic and enzymic experiments, and comparison with synthetic sam...

2013
Marion M Brands Marianne Hoogeveen-Westerveld Marian A Kroos Willemieke Nobel George J Ruijter Lale Özkan Iris Plug Daniel Grinberg Lluïsa Vilageliu Dicky J Halley Ans T van der Ploeg Arnold J Reuser

BACKGROUND Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome; MPS VI) is an autosomal recessive lysosomal storage disorder in which deficiency of N-acetylgalactosamine 4-sulfatase (arylsulfatase B; ARSB) leads to the storage of glycosaminoglycans (GAGs) in connective tissue. The genotype-phenotype correlation has been addressed in several publications but the picture is not complete. Since...

Journal: :Applied and environmental microbiology 1977
J W Fitzgerald J R George

Arylsulfatase was released almost completely from intact cells of Pseudomonas C12B after osmotic shock or after treatment with lysozyme. These results suggest that the enzyme is cell wall associated in this soil isolate.

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