Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Peter F. Daniel"'
Publikováno v:
Glycobiology. 4:551-566
Previously, alpha-mannosidases were classified as enzymes that process newly formed N-glycans or degrade mature glycoproteins. In this review, we suggest that two endoplasmic reticulum (ER) alpha-mannosidases, previously assigned processing roles, ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b48ab2ed9e47b91622458fdc70659cd7
https://doi.org/10.1093/glycob/4.5.551
https://doi.org/10.1093/glycob/4.5.551
Publikováno v:
Biochemical Journal. 286:47-53
The digestion of radiolabelled natural oligosaccharide substrates by human liver neutral alpha-mannosidase has been studied by h.p.l.c. and h.p.t.l.c. The high-mannose oligosaccharides Man9GlcNAc and Man8GlcNAc are hydrolysed by the enzyme by two dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52ec28aa137ac1cf1e6eb60e5e8a4634
https://doi.org/10.1042/bj2860047
https://doi.org/10.1042/bj2860047
Publikováno v:
Journal of Biological Chemistry. 267:9706-9712
A novel lysosomal alpha-mannosidase, with unique substrate specificity, has been partially purified from human spleen by chromatography through concanavalin A-Sepharose, DEAE-Sephadex, and Sephacryl S-300. This enzyme can catalyze the hydrolysis of o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a458b8f8f6b02e41d7f9ec6fcd11ae8
https://doi.org/10.1016/s0021-9258(19)50148-x
https://doi.org/10.1016/s0021-9258(19)50148-x
Autor:
Christopher D. Warren, B.G. Winchester, S. al Daher, Peter F. Daniel, Roger W. Jeanloz, R. DeGasperi
Publikováno v:
Journal of Biological Chemistry. 266:16556-16563
Lysosomal alpha-mannosidases were partially purified from bovine and feline liver and employed to digest a large number of oligosaccharides with structures corresponding to the oligomannosyl parts of complex, hybrid, and high-mannose glycans. The inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2f93b09701acfb0c30c92fbd0ac5187
https://doi.org/10.1016/s0021-9258(18)55337-0
https://doi.org/10.1016/s0021-9258(18)55337-0
Publikováno v:
Journal of Lipid Research, Vol 32, Iss 1, Pp 157-164 (1991)
Previous studies from our laboratory have shown that male C57BL/6J mice excrete into the urine multilamellar lysosomal bodies that contain specific neutral glycosphingolipids. These mice excrete approximately 20-30% of their kidney glycolipids each d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3c8757c37981417b71425f938a92f3f
https://doi.org/10.1016/s0022-2275(20)42254-0
https://doi.org/10.1016/s0022-2275(20)42254-0
Autor:
Peter F. Daniel, Steven Lane, Rose-Mary Boustany, David W. Johnson, Kinuko Suzuki, Wei-Hua Qian, Alyson Cook, Susanne Speier
Publikováno v:
American journal of medical genetics. 57(2)
The role of subunit-9 of mitochondrial ATP synthase in Batten disease was defined by characterizing the expression of genes encoding this protein in human tissues. Two genetically distinct neuronal ceroid-lipofuscinoses (NCL) comprise Batten disease:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e88b0b22fcb172499243bdc95c6e88d
https://pubmed.ncbi.nlm.nih.gov/7668362
https://pubmed.ncbi.nlm.nih.gov/7668362
Autor:
Gerald T. Keusch, Sonja K. Gross, Munir Mobassaleh, Robert H. McCluer, Srinivasa S. Raghavan, Peter F. Daniel, K. A. Balasubramanian, Mary Jacewicz
Publikováno v:
The Journal of infectious diseases. 169(3)
Shiga toxin recognizes a galactose-alpha 1-->4-galactose terminal glycolipid, globotriaosylceramide (Gb3), in sensitive mammalian cells and is translocated by endocytosis to the cytoplasm, where it blocks protein synthesis. To determine if Gb3 is bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::511b09ee1830f6d12627171d2ffe5854
https://pubmed.ncbi.nlm.nih.gov/8158025
https://pubmed.ncbi.nlm.nih.gov/8158025
Publikováno v:
Glycobiology. 2(4)
Normal human fibroblasts and fibroblasts from a patient with alpha-mannosidosis were grown in the presence or absence of 100 microM swainsonine for 7 days. Accumulated oligosaccharides were isolated and analysed by high performance liquid chromatogra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f051d8b95a353cae59bbd8c52e69aa
https://pubmed.ncbi.nlm.nih.gov/1421754
https://pubmed.ncbi.nlm.nih.gov/1421754
Publikováno v:
American journal of medical genetics. 42(4)
In agreement with reports from other laboratories, we have shown that patients with the juvenile or late infantile forms of neuronal ceroid-lipofuscinosis (NCL) have greatly increased levels (5-fold to 20-fold) of dolichyl pyrophosphoryl oligosacchar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d8f9986b67e0ff76bbe9ced93b92d6
https://pubmed.ncbi.nlm.nih.gov/1609840
https://pubmed.ncbi.nlm.nih.gov/1609840
Autor:
Peter F. Daniel, S al Daher, R De Gasperi, Bryan Winchester, Nicholas A. Hall, Christopher D. Warren
The specificity of human liver lysosomal alpha-mannosidase (EC 3.2.1.24) towards a series of oligosaccharide substrates derived from high-mannose, complex and hybrid asparagine-linked glycans and from the storage products in alpha-mannosidosis was in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e67eb370c1a6454a699165665c9d5f5
https://europepmc.org/articles/PMC1151307/
https://europepmc.org/articles/PMC1151307/
