Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Eric Nelles"'
Autor:
Linda Jo Bone, Kenneth H. Fischbeck, Yi-Tian Xu, Eric Nelles, Klaus Willecke, Steven S. Scherer
Publikováno v:
Glia. 24:8-20
Mutations in the gene encoding the gap junction protein connexin32 (Cx32) cause X-linked Charcot-Marie-Tooth disease (CMTX), a common form of inherited demyelinating peripheral neuropathy. To learn more about the pathogenesis of CMTX, we examined the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56fc971461b43042f001471e50098e14
https://doi.org/10.1002/(sici)1098-1136(199809)24:1<8::aid-glia2>3.0.co
https://doi.org/10.1002/(sici)1098-1136(199809)24:1<8::aid-glia2>3.0.co
Publikováno v:
Current Biology. 8(5):299-302
Intercellular channels of gap junctions are formed in vertebrates by the protein family of connexins and allow direct exchange of ions, metabolites and second messenger molecules between apposed cells (reviewed in [1–3]). In the mouse, connexin40 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df22ff41d54e698da584c9c07d101dac
Autor:
Achim Temme, Albrecht Buchmann, Klaus Willecke, Heinz-Dieter Gabriel, Eric Nelles, Michael Schwarz
Publikováno v:
Current Biology. 7:713-716
Connexins are subunits of gap junction channels, which mediate the direct transfer of ions, second messenger molecules and other metabolites between contacting cells. Gap junctions are thought to be involved in tissue homeostasis, embryonic developme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf8db2f45d96decf6fe977dbab54a53b
https://doi.org/10.1016/s0960-9822(06)00302-2
https://doi.org/10.1016/s0960-9822(06)00302-2
Autor:
Dirk Jung, Christoph Butzler, Frank Stümpel, Achim Temme, Klaus Willecke, Ursula Dahl, Klaus V. Toyka, Rolf Dermietzel, Jürgen Zielasek, Heinz-Dieter Gabriel, Kurt Jungermann, Otto Traub, Eric Nelles
Publikováno v:
Proceedings of the National Academy of Sciences. 93:9565-9570
The gap junctional protein connexin32 is expressed in hepatocytes, exocrine pancreatic cells, Schwann cells, and other cell types. We have inactivated the connexin32 gene by homologous recombination in the mouse genome and have generated homozygous c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deeb10a4b0af4e3e6a1b75a5f6d1bdf3
https://doi.org/10.1073/pnas.93.18.9565
https://doi.org/10.1073/pnas.93.18.9565
Autor:
Klaus Willecke, Marjorie Fanjul, Paolo Meda, Susanne Suter, Marc Chanson, Domenico Bosco, Eric Nelles
Publikováno v:
The Journal of Cell Biology, Vol. 141, No 5 (1998) pp. 1267-75
The Journal of Cell Biology
The Journal of Cell Biology
To determine whether junctional communication between pancreatic acinar cells contributes to their secretory function in vivo, we have compared wild-type mice, which express the gap junctional proteins connexin32 (Cx32) and connexin26, to mice defici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e308526e8beb047f16de6d53d9c77f92
https://archive-ouverte.unige.ch/unige:27027
https://archive-ouverte.unige.ch/unige:27027
Autor:
Jürgen Zielasek, Melitta Schachner, Klaus Willecke, Patrizia Anzini, Dirk H.-H. Neuberg, Ueli Suter, Rudolf Martini, Klaus V. Toyka, Eric Nelles
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Mutations affecting the connexin 32 (Cx32) gene are associated with the X-linked form of the hereditary peripheral neuropathy Charcot–Marie–Tooth disease (CMTX). We show that Cx32-deficient mice develop a late-onset progressive peripheral neuropa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887b3763decd818de4ac309b4b29b629
https://pubmed.ncbi.nlm.nih.gov/9169515
https://pubmed.ncbi.nlm.nih.gov/9169515
Autor:
D. R. Beniac, R. A. Ridsdale, M. D. Luckevich, T. A. Tompkins, G. Harauz, J. Sedzik, S. Hjertén, E. Brekkan, P. Lundahl, Michael B. Tropak, John C. Roder, F. Giordano, B. Chang, A. M. La Ronde, A. Al-Sabbagh, M. Kretschmer, A. Asipu, G. E. Blair, B. Mak, M. A. Moscarello, R. Doucette, K. Gratto, V. Verge, J. Yeung, A. Nazarali, P. Murphy, P. Topilko, S. Schneider-Maunoury, T. Seitanidou, A. Baron-Van Evercooren, P. Charnay, M. J. Lee, A. Brennan, A. Tabernero, Z. Dong, A. Blanchard, G. Zoidl, K. R. Jessen, R. Mirsky, E. Couve, F. Cabello, J. Krsulovic, M. Roncagliolo, J. Li, E. L. Hertzberg, J. I. Nagy, Dirk H.-H. Neuberg, Patrizia Anzini, Eric Nelles, Klaus Willecke, Melitta Schachner, Rudolf Martini, Ueli Suter, R. Ankerhold, C. A. O. Stuermer, Karen J. Chandross, W. T. Norton, L. D. Hudson, R. I. Cohen, K. Asakura, S. F. Hunter, M. Rodriguez, Rashmi Bansal, Susan Winkler, S. E. Pfeiffer, Y. S. Oh., V. W. Yong, B. H. J. Juurlink, R. W. Griebel, R. M. Devon, A. Khorchid, G. Almazan, H.-N. Liu, G. W. Konat, Gu Jin, R. C. Wiggins, S. K. Thorburne, B. L. Bartnik, H. Marrif, L. Hertz, S. E. Jelinski, J. Y. Yager, M. R. Del Bigio, J. N. Kanfer, H. L. Weiner, P. A. Nelson, J. K. Dyer, J. Bourque, J. D. Steeves, Monika Labes, Arthur Roach, Parker L. Andersen, David J. Schreyer, J. L. Vanderluit, A. Peterson, W. Tetzlaff, C. O. Hanemann, A. Gabreëls-Festen, H. W. Mueller, L. A. Karchewski, V. M. K. Verge, M. Foldvari, M. R. Jaafari
Publikováno v:
Cell Biology and Pathology of Myelin ISBN: 9780306455957
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ccba320f138951e01d5cfe8aaa3194c
https://doi.org/10.1007/978-1-4615-5949-8_34
https://doi.org/10.1007/978-1-4615-5949-8_34
Autor:
Jan Van Keer, David Derthoo, Olivier Van Caenegem, Michel De Pauw, Eric Nellessen, Nathalie Duerinckx, Walter Droogne, Gábor Vörös, Bart Meyns, Ann Belmans, Stefan Janssens, Johan Van Cleemput, Johan Vanhaecke
Publikováno v:
Journal of Transplantation, Vol 2017 (2017)
In this 3-year, open-label, multicenter study, 57 maintenance heart transplant recipients (>1 year after transplant) with renal insufficiency (eGFR 30–60 mL/min/1.73 m2) were randomized to start everolimus with CNI withdrawal (N=29) or continue the
Externí odkaz:
https://doaj.org/article/e72bfb6a0bf14aae862ccfb3449e4fd1