نتایج جستجو برای: arsb gene

تعداد نتایج: 1141400  

Journal: :The Journal of nutritional biochemistry 2012
Sumit Bhattacharyya Joanne K Tobacman

The common food additive kappa-carrageenan (κ-CGN) is a sulfated polysaccharide that resembles chondroitin-4-sulfate (C4S) and dermatan sulfate (DS). All have a sulfate group on C4 of a glycoside (galactose for CGN and N-acetylgalactosamine for C4S), and the sulfate-bearing glycoside is linked in a β-1,4-configuration to an unsulfated, six-carbon sugar (galactose for CGN, glucuronate for C4S an...

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...

2017
Sumit Bhattacharyya Leo Feferman Joanne K. Tobacman

The chondroitin sulfatases N-acetylgalactosamine-4-sulfatase (ARSB) and galactosamine-N-acetyl-6-sulfatase (GALNS) remove either the 4-sulfate group at the non-reducing end of chondroitin 4-sulfate (C4S) and dermatan sulfate, or the 6-sulfate group of chondroitin 6-sulfate, chondroitin 4,6-disulfate (chondroitin sulfate E), or keratan sulfate. In human prostate cancer tissues, the ARSB activity...

2016
Gustavo Adolfo Giraldo Paola Ayala-Ramírez Juan Carlos Prieto Reggie García-Robles Johanna Carolina Acosta

INTRODUCTION Maroteaux-Lamy syndrome, or mucopolysaccharidosis (MPS) type VI, is an autosomal recessive lysosomal storage disease caused by a deficient activity of the enzyme arylsulfatase B (ARSB), required to degrade dermatan sulfate. The onset and progression of the disease vary, producing a spectrum of clinical presentation. So far, 133 mutations have been reported. The aim of this study is...

Journal: :Journal of Hazardous Materials 2021

Novel hyper-resistant bacteria were isolated from the Crven Dol mine (Allchar, North Macedonia), arsenic-rich extreme environment. Bacteria recovered a secondary mineral mixture, an alteration of hydrothermal realgar rich in arsenates (pharmacolite, hornesite, and talmessite). The sample was dark part at 28 m depth. Three bacterial strains consortium for their capacity to survive exposure 32 g/...

Journal: :Biochimica et biophysica acta 1990
B P Rosen C M Hsu C E Karkaria P Kaur J B Owolabi L S Tisa

An anion-translocating ATPase has been identified as the product of the arsenical resistance operon of resistance plasmid R773. When expressed in Escherichia coli this ATP-driven oxyanion pump catalyzes extrusion of the oxyanions arsenite, antimonite and arsenate. Maintenance of a low intracellular concentration of oxyanion produces resistance to the toxic agents. The pump is composed of two po...

Journal: :Case Reports in Clinical Medicine 2022

The lysosomal storage disorders are a group of diseases that typified by an accumulation waste products in the lysosomes. Mucopolysaccharidoses due to diverse enzyme deficiencies. Ms HT was 2 years and 5 months old when she presented our metabolic bone clinic with clinical features were suggestive genetic syndrome associated disease. urine GAG spot test positive. MPS screen identified reduction...

Journal: :Nanoscale 2015
Chao Deng Sen Zhang Yongxin Wu

Both high safety and low cost give aqueous rechargeable sodium-ion batteries (ARSB) the opportunity for application in stationary energy storage, but the low operating potential of the existing cathode materials limits its energy density. Here, we introduce a hydrothermal-assisted strategy to prepare the Na7V4(P2O7)4(PO4)/C nanorod and employ it as a novel high-property cathode material for ARS...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید