Zobrazeno 1 - 10
of 43
pro vyhledávání: '"J. L. Stirling"'
Autor:
Egidia Costanzi, Sofia Stinchi, A. Orlacchio, A.R. Menghini, Antonio Orlacchio, J. L. Stirling, Tommaso Beccari
Publikováno v:
Mammalian Genome. 9:869-873
Mouse lysosomal alpha-d-mannosidase (EC 3.2.1.24) is an enzyme involved in the catabolism of N-linked glycoproteins. The gene is differentially expressed in mouse tissues, and the highest level of mRNA is found in the epididymis. The expression of ma
Autor:
Carmen Bertoni, Su-Chen Li, M. G. Appolloni, J. L. Stirling, Yu-Teh Li, Tommaso Beccari, A. Orlacchio
Publikováno v:
Mammalian Genome. 8:90-93
The GM2 activator protein is an essential component for the degradation of GM2 ganglioside by hexosaminidase A in vivo. Mutations in the human gene coding for the GM2 activator protein cause the AB variant of GM2-gangliosidosis, a condition that is c
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1243:489-495
In HL-60 cells the most abundant isoenzymes of beta-N-acetyl-hexosaminidase are A (alpha beta) and S (alpha alpha). Sub-cellular fractionation of HL-60 cells by differential centrifugation showed that both A and S forms were present in the lysosomal
Autor:
Winston Hutchinson, Luana Cassandra Breitenbach Barroso Coelho, Achamma Koshy, J. L. Stirling, Donald Robinson
Publikováno v:
Applied Biochemistry and Biotechnology. 32:171-185
Analysis was made of the nature of interactions between β-N-acetylhexosaminidase and affinity chromatography gels made by coupling 2-acetamido-N-(6-aminohexanoyl)-2-deoxy-β-D-glucopyranosylamine (ANAG) to CNBr-Sepharose columns. This showed that al
Autor:
D, Robinson, J L, Stirling
Publikováno v:
Advances in genetics. 44
Publikováno v:
Biochimica et biophysica acta. 1536(2-3)
Mutations in the PKD1 gene are responsible for 85% of cases of autosomal dominant polycystic kidney disease (ADPKD). This gene encodes a large membrane associated glycoprotein, polycystin-1, which is predicted to contain a number of extracellular pro
Beta-mannosidase is an exoglycosidase involved in the degradation of N-linked oligosaccharides moieties of glycoproteins. Lack of beta-mannosidase activity leads to the lysosomal disorder beta-mannosidosis (MIM 248510). We have isolated and sequenced
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::229e41b144fcec926a5adda9645ed615
http://hdl.handle.net/11391/161948
http://hdl.handle.net/11391/161948
Autor:
Brunella Tancini, Aldo Orlacchio, Cristina Cavalieri, J. L. Stirling, Carla Emiliani, Simona Mencarelli
It is believed that the lysosomal glycohydrolase beta-N-acetylhexosaminidase plays a part in several important processes of reproduction and it has been postulated that this enzyme is subject to hormonal regulation. During pregnancy, activity levels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42b106e82e00b4be74bef3ec56ee34c8
http://hdl.handle.net/11391/161908
http://hdl.handle.net/11391/161908
Autor:
Sabata Martino, Antonio Tabilio, Aldo Orlacchio, Franca Falzetti, J. L. Stirling, Carla Emiliani
beta-N-Acetylhexosaminidase isoenzymes, and the distribution of the alpha- and beta-subunits forming the enzyme in a representative series of fresh leukaemic cells and in established leukaemic cell lines, were obtained by using a combination of DEAE-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c91449e80fa1235bbd61435350af210
http://hdl.handle.net/11391/161898
http://hdl.handle.net/11391/161898
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 7(9)