Zobrazeno 1 - 4
of 4
pro vyhledávání: '"MESH : alpha-Glucosidases"'
Autor:
Véronique Roig-Zamboni, Beatrice Cobucci-Ponzano, Roberta Iacono, Maria Carmina Ferrara, Stanley Germany, Yves Bourne, Giancarlo Parenti, Marco Moracci, Gerlind Sulzenbacher
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2017, 8, pp.1111. ⟨10.1038/s41467-017-01263-3⟩
'Nature Communications ', vol: 8, pages: 1111-1-1111-10 (2017)
Nature Communications, Nature Publishing Group, 2017, 8, pp.1111. 〈10.1038/s41467-017-01263-3〉
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Nature Communications, Nature Publishing Group, 2017, ⟨10.1038/s41467-017-01263-3⟩
Nature communications 8 (2017). doi:10.1038/s41467-017-01263-3
info:cnr-pdr/source/autori:Roig-Zamboni V.; Cobucci-Ponzano B.; Iacono R.; Ferrara M.C.; Germany S.; Bourne Y.; Parenti G.; Moracci M.; Sulzenbacher G./titolo:Structure of human lysosomal acid alpha-glucosidase-A guide for the treatment of Pompe disease/doi:10.1038%2Fs41467-017-01263-3/rivista:Nature communications/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:8
Nature Communications, 2017, ⟨10.1038/s41467-017-01263-3⟩
Nature Communications, 2017, 8, pp.1111. ⟨10.1038/s41467-017-01263-3⟩
Nature Communications, Nature Publishing Group, 2017, 8, pp.1111. ⟨10.1038/s41467-017-01263-3⟩
'Nature Communications ', vol: 8, pages: 1111-1-1111-10 (2017)
Nature Communications, Nature Publishing Group, 2017, 8, pp.1111. 〈10.1038/s41467-017-01263-3〉
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Nature Communications, Nature Publishing Group, 2017, ⟨10.1038/s41467-017-01263-3⟩
Nature communications 8 (2017). doi:10.1038/s41467-017-01263-3
info:cnr-pdr/source/autori:Roig-Zamboni V.; Cobucci-Ponzano B.; Iacono R.; Ferrara M.C.; Germany S.; Bourne Y.; Parenti G.; Moracci M.; Sulzenbacher G./titolo:Structure of human lysosomal acid alpha-glucosidase-A guide for the treatment of Pompe disease/doi:10.1038%2Fs41467-017-01263-3/rivista:Nature communications/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:8
Nature Communications, 2017, ⟨10.1038/s41467-017-01263-3⟩
Nature Communications, 2017, 8, pp.1111. ⟨10.1038/s41467-017-01263-3⟩
Pompe disease, a rare lysosomal storage disease caused by deficiency of the lysosomal acid α-glucosidase (GAA), is characterized by glycogen accumulation, triggering severe secondary cellular damage and resulting in progressive motor handicap and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c82ffd7ffc81e6e645698e18bb52b05
https://hal.archives-ouvertes.fr/hal-01802847/file/s41467-017-01263-3.pdf
https://hal.archives-ouvertes.fr/hal-01802847/file/s41467-017-01263-3.pdf
Autor:
Yves Blériot, Dominic S. Alonzi, A. Waldo Saville, Alexander C. Weymouth-Wilson, Francis Xavier Wilson, Sarah F. Jenkinson, Atsushi Kato, Daniel Best, George W. J. Fleet, Shinpei Nakagawa, Takahito Kunimatsu, Terry D. Butters, Caroline Norez, R. Fernando Martínez, Frédéric Becq, James Mui
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (15), pp.7380-97. ⟨10.1021/jo4005487⟩
Journal of Organic Chemistry, American Chemical Society, 2013, 78, pp.7380-7397. ⟨10.1021/jo4005487⟩
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (15), pp.7380-97. ⟨10.1021/jo4005487⟩
Journal of Organic Chemistry, American Chemical Society, 2013, 78, pp.7380-7397. ⟨10.1021/jo4005487⟩
International audience; The Ho crossed aldol condensation provides access to a series of carbon branched iminosugars as exemplified by the synthesis of enantiomeric pairs of isoDMDP, isoDGDP, and isoDAB, allowing comparison of their biological activi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::301ecae9d8c35550ab07037e70bb827d
https://hal.archives-ouvertes.fr/hal-00990546
https://hal.archives-ouvertes.fr/hal-00990546
Autor:
Leonardo Salviati, Claude Desnuelle
Publikováno v:
Current Opinion in Neurology
Current Opinion in Neurology, Lippincott, Williams & Wilkins, 2011, 24 (5), pp.443-8. ⟨10.1097/WCO.0b013e32834a1e00⟩
Current Opinion in Neurology, Lippincott, Williams & Wilkins, 2011, 24 (5), pp.443-8. ⟨10.1097/WCO.0b013e32834a1e00⟩
International audience; PURPOSE OF REVIEW: The first reports published in 2010 on enzyme replacement therapy in late-onset Pompe disease (LOPD) allow us now to stand back and adapt the strategies. In the meantime, substantial progress has been made i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22aaf055b101ec3c1d9b7d484d95f6cc
https://hal.archives-ouvertes.fr/hal-00756605
https://hal.archives-ouvertes.fr/hal-00756605
Publikováno v:
Journal of Insect Physiology
Journal of Insect Physiology, Elsevier, 2003, 49 (1), pp.11-24. ⟨10.1016/S0022-1910(02)00222-6⟩
Journal of Insect Physiology, Elsevier, 2003, 49 (1), pp.11-24. ⟨10.1016/S0022-1910(02)00222-6⟩
International audience; Transmission electron micrographs of the pea aphid midgut revealed that its anterior region has cells with an apical complex network of lamellae (apical lamellae) instead of the usual regularly-arranged microvilli. These apica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3b7c10540de8427a73c79a5278e0786
https://hal.archives-ouvertes.fr/hal-00402183
https://hal.archives-ouvertes.fr/hal-00402183