dc.contributor.author | BATTALOGLU, Esra | |
dc.contributor.author | NIEMANN, Axel | |
dc.contributor.author | KIRSCHNER, Janbernd | |
dc.contributor.author | STENDEL, Claudia | |
dc.contributor.author | ROOS, Andreas | |
dc.contributor.author | DECONINCK, Tine | |
dc.contributor.author | PEREIRA, Jorge | |
dc.contributor.author | CASTAGNER, Francois | |
dc.contributor.author | KORINTHENBERG, Rudolf | |
dc.contributor.author | KETELSEN, Uwe-Peter | |
dc.contributor.author | NICHOLSON, Garth | |
dc.contributor.author | OUVRIER, Robert | |
dc.contributor.author | SEEGER, Juergen | |
dc.contributor.author | DE JONGHE, Peter | |
dc.contributor.author | WEIS, Joachim | |
dc.contributor.author | KRUETTGEN, Alexander | |
dc.contributor.author | RUDNIK-SCHOENEBORN, Sabine | |
dc.contributor.author | BERGMANN, Carsten | |
dc.contributor.author | SUTER, Ueli | |
dc.contributor.author | ZERRES, Klaus | |
dc.contributor.author | TIMMERMAN, Vincent | |
dc.contributor.author | RELVAS, Joao B. | |
dc.contributor.author | SENDEREK, Jan | |
dc.contributor.author | Parman, Yesim | |
dc.date.accessioned | 2021-03-04T14:24:48Z | |
dc.date.available | 2021-03-04T14:24:48Z | |
dc.date.issued | 2007 | |
dc.identifier.citation | STENDEL C., ROOS A., DECONINCK T., PEREIRA J., CASTAGNER F., NIEMANN A., KIRSCHNER J., KORINTHENBERG R., KETELSEN U., BATTALOGLU E., et al., "Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4", AMERICAN JOURNAL OF HUMAN GENETICS, cilt.81, sa.1, ss.158-164, 2007 | |
dc.identifier.issn | 0002-9297 | |
dc.identifier.other | av_8165cdd6-4336-4cb6-a2fd-b30a5ec6d58e | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/88199 | |
dc.identifier.uri | https://doi.org/10.1086/518770 | |
dc.description.abstract | GTPases of the Rho subfamily are widely involved in the myelination of the vertebrate nervous system. Rho GTPase activity is temporally and spatially regulated by a set of specific guanine nucleotide exchange factors (GEFs). Here, we report that disruption of frabin/ FGD4, a GEF for the Rho GTPase cell- division cycle 42 (Cdc42), causes peripheral nerve demyelination in patients with autosomal recessive Charcot-Marie-Tooth ( CMT) neuropathy. These data, together with the ability of frabin to induce Cdc42- mediated cell-shape changes in transfected Schwann cells, suggest that Rho GTPase signaling is essential for proper myelination of the peripheral nervous system. | |
dc.language.iso | eng | |
dc.subject | Temel Bilimler | |
dc.subject | GENETİK VE HAYAT | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıbbi Genetik | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.title | Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4 | |
dc.type | Makale | |
dc.relation.journal | AMERICAN JOURNAL OF HUMAN GENETICS | |
dc.contributor.department | , , | |
dc.identifier.volume | 81 | |
dc.identifier.issue | 1 | |
dc.identifier.startpage | 158 | |
dc.identifier.endpage | 164 | |
dc.contributor.firstauthorID | 24574 | |