APC2 controls dendrite development by promoting microtubule dynamics

Autor: Kahn, Olga I, Schätzle, Philipp, van de Willige, Dieudonnée, Tas, Roderick P, Lindhout, Feline W, Portegies, Sybren, Kapitein, Lukas C, Hoogenraad, Casper C, Sub Cell Biology, Celbiologie

Publikováno v: Nature Communications, 9. Nature Publishing Group
Nature Communications
Nature Communications, 9(1):2773. Nature Publishing Group
Nature Communications, Vol 9, Iss 1, Pp 1-17 (2018)

Mixed polarity microtubule organization is the signature characteristic of vertebrate dendrites. Oppositely oriented microtubules form the basis for selective cargo trafficking in neurons, however the mechanisms that establish and maintain this organ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4adb0d27dd0888dfc9f7bb5a9624697
https://dspace.library.uu.nl/handle/1874/374799

Forward motility is essential for trypanosome infection in the tsetse fly

Autor: Rotureau, Brice, Ooi, Cher-Pheng, Huet, Diego, Perrot, Sylvie, Bastin, Philippe

Publikováno v: Cellular Microbiology
Cellular Microbiology, 2014, 16 (3), pp.425-433. ⟨10.1111/cmi.12230⟩
Cellular Microbiology, Wiley, 2014, 16 (3), pp.425-433. ⟨10.1111/cmi.12230⟩

International audience; African trypanosomes are flagellated protozoan parasites transmitted by the bite of tsetse flies and responsible for sleeping sickness in humans. Their complex development in the tsetse digestive tract requires several differe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d1f49d2dcb4e21d5ae4e41f82f59dd80
https://pubmed.ncbi.nlm.nih.gov/24134537

Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11)

Autor: Pio D'Adamo, Francesca Donaudy, Paolo Gasparini, Elio Marciano, Angela D'Eustacchio, Annamaria Franzè, Maria Vittoria Cubellis, Monica Errichiello, Claudio Saulino, Gennaro Auletta, Pasquale Giannini, Francesca Di Leva, Alfredo Ciccodicola

Publikováno v: Audiology & neuro-otology
11 (2006): 157–164. doi:10.1159/000091199
info:cnr-pdr/source/autori:Di Leva F.; D'Adamo P.; Cubellis M.V.; D'Eustacchio A.; Errichiello M.; Saulino C.; Auletta G.; Giannini P.; Donaudy F.; Ciccodicola A.; Gasparini P.; Franze A.; Marciano E./titolo:Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11)/doi:10.1159%2F000091199/rivista:Audiology & neuro-otology (Print)/anno:2006/pagina_da:157/pagina_a:164/intervallo_pagine:157–164/volume:11

We ascertained a large Italian family with an autosomal dominant form of non-syndromic sensorineural hearing loss with vestibular involvement. A genome-wide scan found linkage to locus DFNA11. Sequencing of the MYO7A gene in the linked region identif

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02e2d0ed9aca0764453b06095a2578fd
http://hdl.handle.net/11588/364791

Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping

Autor: Bartoloni, L., Blouin, J. -L C., Sainsbury, A. J., Gos, A., Morris, M. A., Affara, N. A., Delozier-Blanchet, C. D., Stylianos Antonarakis

Publikováno v: Scopus-Elsevier
Cytogenetics and Cell Genetics, Vol. 84, No 3-4 (1999) pp. 188-189

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::250ae40fce79260dc717b570d58821d6
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033049623&partnerID=MN8TOARS