Zobrazeno 1 - 10
of 267
pro vyhledávání: '"M. Fasolini"'
Akademický článek
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Autor:
Alessandro Nodari, Angelo Quattrini, Stefano C. Previtali, L Wrabetz, Giorgia Dina, M.L Feltri, Ulrike Mayer, M. Fasolini
Publikováno v:
Molecular and Cellular Neuroscience. 23:210-218
Defects in laminins or laminin receptors are responsible for various neuromuscular disorders, including peripheral neuropathies. Interactions between Schwann cells and their basal lamina are fundamental to peripheral nerve development and successful
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da71779e24a5974d728e91448227f2fe
https://doi.org/10.1016/s1044-7431(03)00014-9
https://doi.org/10.1016/s1044-7431(03)00014-9
Akademický článek
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Publikováno v:
Annals of the New York Academy of Sciences. 883
We have previously shown that increased dosage of the mouse protein zero gene (Mpz) causes a dysmyelinating neuropathy in transgenic (Tg80) mice. To ask whether the dysmyelination is dose dependent, we inbred one of the Tg80 lines and compared the re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a22c1d76b5620a2b8c9667ac92448e0
https://pubmed.ncbi.nlm.nih.gov/10586254
https://pubmed.ncbi.nlm.nih.gov/10586254
Publikováno v:
Annals of the New York Academy of Sciences. 883
Normal peripheral nerve myelination depends on Schwann cell-basal lamina interactions. An important component of Schwann cell basal lamina is laminin--predominantly laminins 2 and 4. Mutations in the alpha 2 chain common to these two isoforms are ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab55cca17b94e0bb5bb8cb739c335fda
https://pubmed.ncbi.nlm.nih.gov/10586237
https://pubmed.ncbi.nlm.nih.gov/10586237
Autor:
Khouzani, Mohammad Shiravi1 (AUTHOR) mshiravi433@gmail.com, Kandasamy, Krishnaveni2 (AUTHOR)
Publikováno v:
Jentashapir Journal of Cellular & Molecular Biology. May2024, Vol. 15 Issue 2, p1-10. 10p.
Autor:
P Fratta, Ml. Feltri, K Toyka, Albee Messing, M D'antonio, G Dati, Angelo Quattrini, M Fasolini, J Zielasek, Lawrence Wrabetz
Publikováno v:
Journal of the Peripheral Nervous System. 6:58-59
Charcot-Marie-Tooth 1B neuropathy (CMT1B), Dejerine-Sottas syndrome (DSS) and Congenital Hypomyelination are each associated with mutations in MPZ, encoding P0 glycoprotein, the major structural protein of peripheral nerve myelin. To explore whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fc669e668cde260933cf40ce3b90ca9
https://doi.org/10.1046/j.1529-8027.2001.01007-53.x
https://doi.org/10.1046/j.1529-8027.2001.01007-53.x
Autor:
Wigerinck, Stijn1,2 (AUTHOR), Gregory, Adriana V3 (AUTHOR), Smith, Byron H4 (AUTHOR), Iliuta, Ioan-Andrei5 (AUTHOR), Hanna, Christian1,6 (AUTHOR), Chedid, Maroun1 (AUTHOR), Kaidbay, Hasan-Daniel N1 (AUTHOR), Senum, Sarah R1,7 (AUTHOR), Shukoor, Shebaz1 (AUTHOR), Harris, Peter C1,7 (AUTHOR), Torres, Vicente E1 (AUTHOR), Kline, Timothy L3 (AUTHOR), Chebib, Fouad T5 (AUTHOR) chebib.fouad@mayo.edu
Publikováno v:
Clinical Kidney Journal. Oct2023, Vol. 16 Issue 10, p1691-1700. 10p.
Autor:
Caroli, Anna1 (AUTHOR) anna.caroli@marionegri.it, Kline, Timothy L.2 (AUTHOR) kline.timothy@mayo.edu
Publikováno v:
Journal of Clinical Medicine. Aug2023, Vol. 12 Issue 15, p5133. 26p.
Autor:
Liu, Jie1 (AUTHOR), Mallick, Shubhadip1 (AUTHOR), Xie, Yusheng1 (AUTHOR), Grassin, Corentin2 (AUTHOR), Lucas, Belén1 (AUTHOR), Schölermann, Beate1 (AUTHOR), Pahl, Axel1,3 (AUTHOR), Scheel, Rebecca4 (AUTHOR), Strohmann, Carsten4 (AUTHOR), Protzel, Christoph5 (AUTHOR), Berg, Thorsten5 (AUTHOR), Merten, Christian2 (AUTHOR), Ziegler, Slava1 (AUTHOR), Waldmann, Herbert1,6 (AUTHOR) Herbert.waldmann@mpi-dortmund.mpg.de
Publikováno v:
Angewandte Chemie. 5/15/2023, Vol. 135 Issue 21, p1-8. 8p.