Results 81 to 90 of about 1,946 (125)

Arylsulfatase B activities and glycosaminoglycan levels in retrovirally transduced mucopolysaccharidosis type VI cells. Prospects for gene therapy. [PDF]

J Clin Invest, 1996
Fillat C, Simonaro CM, Yeyati PL, Abkowitz JL, Haskins ME, Schuchman EH.   +5 more
europepmc   +1 more source

Normal MPS excretion, but dermatan sulphaturia, combined with a mild Maroteaux-Lamy phenotype. [PDF]

J Med Genet, 1991
Tønnesen T, Gregersen HN, Güttler F.
europepmc   +1 more source

The small leucine-rich repeat proteoglycan biglycan binds to alpha-dystroglycan and is upregulated in dystrophic muscle. [PDF]

J Cell Biol, 2000
Bowe MA, Mendis DB, Fallon JR.
europepmc   +1 more source

Multiple sulfatase deficiency: catalytically inactive sulfatases are expressed from retrovirally introduced sulfatase cDNAs. [PDF]

Proc Natl Acad Sci U S A, 1992
Rommerskirch W, von Figura K.
europepmc   +1 more source

An insight into the biochemistry of inborn errors of metabolism for a clinical neurologist.

Ann Indian Acad Neurol, 2008
Christopher R, Sankaran BP.
europepmc   +1 more source

Specificity Studies of Bacterial Sulfatases by Means of Structurally Defined Sulfated Oligosaccharides Isolated from Shark Cartilage Chondroitin Sulfate D

FEBS Journal, 1996
Kazuyuki Sugahara
exaly   +2 more sources

Abstract 538: Inhibition of progression of malignant melanomas in B16F10 murine model by mecombinant N-acetylgalactosamine-4-Sulfatase (arylsulfatase B)

Cancer Research, 2023
Introduction: Lower expression and activity of N-acetylgalactosamine-4-sulfatase (Arylsulfatase B; ARSB) were inversely associated with increased invasiveness in seven human melanoma cell lines (Oncotarget 2017, 8(3):4169-4180).
J. Tobacman, I. O-Sullivan, S. Bhattacharyya   +2 more
semanticscholar   +1 more source

Interactions of CFTR and Arylsulfatase B (ARSB; N-acetylgalactosamine-4-sulfatase) in Prostate Carcinoma

International Journal of Molecular Sciences
Defective CFTR (cystic fibrosis transmembrane conductance regulator) is pathognomonic for cystic fibrosis (CF), which is characterized by an accumulation of tenacious secretions in pulmonary airways, as well as by abnormal ductal secretions in other ...
S. Bhattacharyya, J. Tobacman
semanticscholar   +1 more source