نتایج جستجو برای: mucopolysaccharides

تعداد نتایج: 701  

Journal: :Arthritis & Rheumatism 1960

Journal: :International Journal of Clinical Biochemistry and Research 2023

Mucopolysaccharidosis is a lysosomal storage disorder, caused due to deficiency of enzymes required for the breakdown Mucopolysaccharides. These undegraded Mucopolysaccharides accumulate in various tissues and cause characteristic features like neurological deficit, impaired motor function, developmental delay, hearing loss, behavioral problems, corneal clouding, glaucoma, respiratory distress,...

Journal: :Cancer research 1974
J Kuroda S Saito N Seno S Nagase K Anno

Mucopolysaccharides were extracted by Pronase diges tion from two types of rat tumor tissues: MC sarcoma in duced in Donryu rats by s.c. injection of methylcholanthrene and a solid tumor developed by s.c. transplantation of AH-109A cells into the animals. The mucopolysaccharides were fractionated by anion-exchange chromatography and characterized by chemical analysis, electrophoresis, infrared ...

Journal: :Circulation research 1970
J T Judd B C Wexler

Myocardial necrosis was produced in rats by administering isoproterenol, and the increase in hexosamine-containing materials in the injured myocardium was investigated. Total hexosamine, galactosamine, neutral sugars, and uronic acids were determined on various fractions isolated from the hearts. Mucopolysaccharides were precipitated as the cetyl pyridinium chloride complex and fractionated acc...

Journal: :Journal of Biological Chemistry 1941

Journal: :The Journal of clinical investigation 1961
G P KERBY S M TAYLOR N M LANGLEY

Acid mucopolysaccharides of human plasma have been observed ( 1 ) to vary as do acute phase reactants, i.e., to increase nonspecifically in any inflammatory state. The euglobulin fraction itself with which the acid mucopolysaccharides were associated increased also in such circumstances. On later comparing levels of acid mucopolysaccharides in samples of serum and plasma drawn simultaneously, i...

Journal: :Clinica chimica acta; international journal of clinical chemistry 2006
Angelique J A Kooper Pim M W Janssens Akosua N J A de Groot Maria L F Liebrand-van Sambeek Catharina J M G van den Berg Gita B Tan-Sindhunata Paul P van den Berg Emilia K Bijlsma Arie P T Smits Ron A Wevers

BACKGROUND At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lysosomal storage diseases. The study proposes a diagnostic flowchart for prenatal diagnosis of non-immune hydrops fetalis. METHODS This study contains a series of 75 non-immune hydrops fetalis pregnancies. Mucopolysaccharides, oligosaccharides, neuraminic acid and 21 lysosomal enzymes were measure...

Journal: :Infection and immunity 1979
T J Fitzgerald R C Johnson

Treponema pallidum (Nichols strain) exhibited mucopolysaccharidase activity. Acidic mucopolysaccharides were broken down more rapidly by viable treponemes than by heat-inactivated treponemes or membrane filtrates of treponemal suspensions. Ouchterlony immunodiffusion demonstrated the occurrence of antibodies to the hyaluronidase-like enzyme within syphilitic sera. After intratesticular inoculat...

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