Zobrazeno 1 - 10
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pro vyhledávání: '"Don Clarke"'
Akademický článek
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Autor:
Bhatnagar, M. K., Kothari, K. L.
Publikováno v:
Current Science, 1966 Aug . 35(16), 417-417.
Externí odkaz:
https://www.jstor.org/stable/24215609
Publikováno v:
Ethnobotany of the Himalayas ISBN: 9783030574079
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c493c6dd66e3858d5a2ce4719b162bb4
https://doi.org/10.1007/978-3-030-57408-6_237
https://doi.org/10.1007/978-3-030-57408-6_237
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Yewande Pearse, Don Clarke, Shih-hsin Kan, Steven Q. Le, Valentina Sanghez, Anna Luzzi, Ivy Pham, Lina R. Nih, Jonathan D. Cooper, Patricia I. Dickson, Michelina Iacovino
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 27, Iss , Pp 452-463 (2022)
Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB) is a recessive genetic disorder that severely affects the brain due to a deficiency in the enzyme α-N-acetylglucosaminidase (NAGLU), leading to intra-lysosomal accumulation of partially de
Externí odkaz:
https://doaj.org/article/776a0875754d4cc8976309f509235d55
The chloroform extract of Swertia cordata (G. Don) roots was subjected to column chromatography, afforded two (one new and one known) xanthones. Both the compounds were isolated for the first time from S. cordata. The structures of the isolated compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7b93222009ef67da9ccd8367bf061b0
Autor:
Don Clarke, Yewande Pearse, Shih-hsin Kan, Steven Q. Le, Valentina Sanghez, Jonathan D. Cooper, Patricia I. Dickson, Michelina Iacovino
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 10, Iss , Pp 113-127 (2018)
Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB [MPS IIIB]) is a lysosomal storage disorder primarily affecting the brain that is caused by a deficiency in the enzyme α-N-acetylglucosaminidase (NAGLU), leading to intralysosomal accumulat
Externí odkaz:
https://doaj.org/article/a51965c026fa4337a9814a580dc89e80
Autor:
Steven Q. Le, Shih-hsin Kan, Don Clarke, Valentina Sanghez, Martin Egeland, Kristen N. Vondrak, Terence M. Doherty, Moin U. Vera, Michelina Iacovino, Jonathan D. Cooper, Mark S. Sands, Patricia I. Dickson
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 8, Iss C, Pp 42-51 (2018)
Antibodies against recombinant proteins can significantly reduce their effectiveness in unanticipated ways. We evaluated the humoral response of mice with the lysosomal storage disease mucopolysaccharidosis type I treated with weekly intravenous reco
Externí odkaz:
https://doaj.org/article/458c35de4ec1464eb7de993788d68d45
Autor:
Valentina Sanghez, Anna Luzzi, Don Clarke, Dustin Kee, Steven Beuder, Danielle Rux, Mitsujiro Osawa, Joaquín Madrenas, Tsui-Fen Chou, Michael Kyba, Michelina Iacovino
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186818 (2017)
Hemogenic endothelium (HE) undergoes endothelial-to-hematopoietic transition (EHT) to generate blood, a process that requires progressive down-regulation of endothelial genes and induction of hematopoietic ones. Previously, we have shown that the tra
Externí odkaz:
https://doaj.org/article/cbbdf91f80c6484ea0168b76418e3943
Autor:
Yewande Pearse, Don Clarke, Shih-hsin Kan, Steven Q. Le, Valentina Sanghez, Anna Luzzi, Ivy Pham, Lina R. Nih, Jonathan D. Cooper, Patricia I. Dickson, Michelina Iacovino
Sanfilippo syndrome type B (Mucopolysaccharidosis type IIIB or MPS IIIB) is a recessive genetic disorder that severely affects the brain due to a deficiency in the enzyme α-N-acetylglucosaminidase (NAGLU), leading to intralysosomal accumulation of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0291867037a3af9b333959e73610963a
https://doi.org/10.1101/2022.06.30.498131
https://doi.org/10.1101/2022.06.30.498131