Zobrazeno 1 - 10
of 733
pro vyhledávání: '"T. D. Butters"'
Autor:
I. U. Pismenetskaya, T. D. Butters
Publikováno v:
The Ukrainian Biochemical Journal, Vol 89, Iss 1, Pp 59-70 (2017)
To verify the idea that extracellular free oligosaccharides might be able to reflect the functional status of the endoplasmic reticulum (ER) and lysosomal-endosomal system, HPLC-profiles of serum-derived free oligosaccharides (FOS) in human healthy a
Externí odkaz:
https://doaj.org/article/c0e483c046844e178942ba2f3462dfe6
Autor:
I. U. Pismenetskaya, T. D. Butters
Publikováno v:
Regulatory Mechanisms in Biosystems, Vol 6, Iss 1, Pp 51-56 (2015)
Free oligosaccharides (FOS) are unbound structural analogs of glycans of glycoconjugates. There are several sources of them inside the cell: 1) multistep pathways of N-glycosylation, 2) the cell quality control and endoplastic reticulum-associated de
Externí odkaz:
https://doaj.org/article/3313fe1e3212497f8d609429e1bba239
Autor:
I. U. Pismenetskaya, T. D. Butters
Publikováno v:
The Ukrainian Biochemical Journal, Vol 86, Iss 6, Pp 5-17 (2014)
Metabolism of glycoproteins and glycolipids is accompanied by the appearance of unbound structural analogues of the carbohydrate portion of glycoconjugates or so called free oligosaccharides. There are their several sources inside the cell: 1) multis
Externí odkaz:
https://doaj.org/article/afddbcf904784f6d8d7aab6bd753c218
Autor:
I. U. Pismenetskaya, T. D. Butters
Publikováno v:
Regulatory Mechanisms in Biosystems, Vol 7, Iss 1, Pp 59–64-59–64 (2016)
Free oligosaccharides (FOS) are unbound to proteins or lipids structural analogs of their glycans. FOS appear as by-products of endoplasmic reticulum synthesis, cell control folding with endoplastic reticulum-associated degradation and lysosomal/endo
Externí odkaz:
https://doaj.org/article/d4113cba1296462aaf86474ba335ecb2
Publikováno v:
Біологічні студії, Vol 6, Iss 2, Pp 45-54 (2012)
The phenomenon of programmed apoptotic desialylation of cell glycans was described previously. However, the possibility of this process application to the sialylated glycolipids of membranes stayes unknown. Granulocytes of human peripherical blood we
Externí odkaz:
https://doaj.org/article/476d860cca1e43b79e9686b85d957cd2
Autor:
T D Butters, I U Pismenetskaya
Publikováno v:
Ukrainian Biochemical Journal, Vol 89, Iss 1, Pp 59-70 (2017)
To verify the idea that extracellular free oligosaccharides might be able to reflect the functional status of the endoplasmic reticulum (ER) and lysosomal-endosomal system, HPLC-profiles of serum-derived free oligosaccharides (FOS) in human healthy a
Autor:
T D Butters, Frances M. Platt, Gabriele Reinkensmeier, David Harvey, Ulrika Andersson, V Hunnam, David R. Wing, Brett Garner, Raymond A. Dwek
The functional importance of glycolipids has emphasized the need for more sensitive methods of detection, characterization, and quantification than has often been possible using traditional thin-layer chromatographic techniques. We describe the use o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5682e50dc8f9dfe75fe32117e36f446
https://ora.ox.ac.uk/objects/uuid:1c51f2c8-b6b5-45d3-b988-c1646963b2f9
https://ora.ox.ac.uk/objects/uuid:1c51f2c8-b6b5-45d3-b988-c1646963b2f9
Paediatric neurodegenerative diseases are frequently caused by inborn errors in glycosphingolipid (GSL) catabolism and are collectively termed the glycosphingolipidoses. GSL catabolism occurs in the lysosome and a defect in an enzyme involved in GSL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a896ec3949f6a0d7047cb29fbcfcaf5d
https://doi.org/10.1046/j.1365-2990.2002.00422.x
https://doi.org/10.1046/j.1365-2990.2002.00422.x
Publikováno v:
Біологічні студії, Vol 6, Iss 2, Pp 45-54 (2012)
The phenomenon of programmed apoptotic desialylation of cell glycans was described previously. However, the possibility of this process application to the sialylated glycolipids of membranes stayes unknown. Granulocytes of human peripherical blood we
Autor:
Frances M. Platt, Kieran Clarke, A B Kulkarni, Tanya Heare, David A. Priestman, Keith M. Channon, Nicholas J. Alp, Raymond A. Dwek, T D Butters, P Qasba
Publikováno v:
Europe PubMed Central
OBJECTIVE: Fabry disease results from alpha-gala-ctosidase A deficiency and is characterized by the lysosomal accumulation of globotriaosylceramide. Globotriaosylceramide storage predominantly affects endothelial cells, altering vascular wall morphol