Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Nave, K.A"'
Publikováno v:
In Journal of Comparative Pathology January 2020 174:151-151
Publikováno v:
Aktuelle Neurologie; 20240101, Issue: Preprints
Publikováno v:
Aktuelle Neurologie; 20240101, Issue: Preprints
Autor:
Leitzen, E., Raddatz, B., Jin, W., Ulrich, R., Goebbels, S., Nave, K.A., Baumgärtner, W., Hansmann, F.
Publikováno v:
In Journal of Comparative Pathology January 2018 158:101-101
Autor:
Nobbio L. 1, 2, Gherardi G. 1, Vigo T. 1, Passalacqua M. 2, 3, Melloni E. 2, Abbruzzese M. 1, 4, Mancardi G. 1, Nave K.A. 5, Schenone A. 1
Publikováno v:
European journal of neuroscience
23 (2006): 1445–1452.
info:cnr-pdr/source/autori:Nobbio L. 1,2, Gherardi G. 1, Vigo T. 1,2, Passalacqua M. 2,3, Melloni E. 2,3, Abbruzzese M. 1,4, Mancardi G. 1,2, Nave K.A. 5, Schenone A. 1,2/titolo:Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease/doi:/rivista:European journal of neuroscience (Print)/anno:2006/pagina_da:1445/pagina_a:1452/intervallo_pagine:1445–1452/volume:23
23 (2006): 1445–1452.
info:cnr-pdr/source/autori:Nobbio L. 1,2, Gherardi G. 1, Vigo T. 1,2, Passalacqua M. 2,3, Melloni E. 2,3, Abbruzzese M. 1,4, Mancardi G. 1,2, Nave K.A. 5, Schenone A. 1,2/titolo:Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease/doi:/rivista:European journal of neuroscience (Print)/anno:2006/pagina_da:1445/pagina_a:1452/intervallo_pagine:1445–1452/volume:23
Clinical progression in hereditary and acquired demyelinating disorders of both the central and peripheral nervous system is mainly due to a time-dependent axonal impairment. We established 90-day dorsal root ganglia (DRG) cultures from a rat model o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::b07e790bcc0e04f21c9d8fc3f54d5984
https://publications.cnr.it/doc/10232
https://publications.cnr.it/doc/10232
Autor:
Vigo T. 1, 2, Nobbio L. 1, Hummelen P.V 3, Abbruzzese M. 1, 4, Mancardi G. 1, Verpoorten N. 5, Verhoeven K. 5, Sereda M.W. 6, Nave K.A. 6, Timmerman V. 5, Schenone A.1
Publikováno v:
Molecular and cellular neurosciences
28 (2005): 703–714.
info:cnr-pdr/source/autori:Vigo T. 1,2, Nobbio L. 1,2, Hummelen P.V 3, Abbruzzese M. 1,4, Mancardi G. 1,2, Verpoorten N. 5, Verhoeven K. 5, Sereda M.W. 6, Nave K.A. 6, Timmerman V. 5, Schenone A.1,2/titolo:Experimental Charcot-Marie-Tooth type 1A: A cDNA microarrays analysis/doi:/rivista:Molecular and cellular neurosciences (Print)/anno:2005/pagina_da:703/pagina_a:714/intervallo_pagine:703–714/volume:28
28 (2005): 703–714.
info:cnr-pdr/source/autori:Vigo T. 1,2, Nobbio L. 1,2, Hummelen P.V 3, Abbruzzese M. 1,4, Mancardi G. 1,2, Verpoorten N. 5, Verhoeven K. 5, Sereda M.W. 6, Nave K.A. 6, Timmerman V. 5, Schenone A.1,2/titolo:Experimental Charcot-Marie-Tooth type 1A: A cDNA microarrays analysis/doi:/rivista:Molecular and cellular neurosciences (Print)/anno:2005/pagina_da:703/pagina_a:714/intervallo_pagine:703–714/volume:28
To reveal the spectrum of genes that are modulated in Charcot-Marie-Tooth neuropathy type 1A (CMT1A), which is due to overexpression of the gene coding for the peripheral myelin protein 22 (pmp22), we performed a cDNA microarray experiment with cDNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::8d05d85b126e8fc566152618d0e4953b
https://publications.cnr.it/doc/10182
https://publications.cnr.it/doc/10182
Akademický článek
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Akademický článek
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Autor:
Stassart, R.M.1,2 stassart@em.mpg.de, Nave, K.A.1
Publikováno v:
Experimental Neurology. Jul2015, Vol. 269, p90-92. 3p.
Publikováno v:
In New BIOTECHNOLOGY April 2010 27 Supplement 1:S58-S58