Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse

Autor: Ung, D., Iacono, G, Méziane, H, Blanchard, E., Papon, M-A, Selten, M, van Rhijn, J-R, Montjean, R, Rucci, J, Martin, Stéphane, Fleet, A, Birling, M-C, Marouillat, S, Roepman, R, Selloum, M, Lux, A., Thépault, R-A, Hamel, P, Mittal, K, Vincent, J., Dorseuil, O, Stunnenberg, H, Billuart, P, Nadif Kasri, N, Hérault, Y., Laumonnier, F

Publikováno v: Molecular Psychiatry, 23, 1356-1367
Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2018, 23 (5), pp.1356-1367. ⟨10.1038/mp.2017.39⟩
Molecular Psychiatry, 23, 5, pp. 1356-1367
Molecular Psychiatry, 2018, 23 (5), pp.1356-1367. ⟨10.1038/mp.2017.39⟩

Contains fulltext : 193089.pdf (Publisher’s version ) (Open Access) Synapse development and neuronal activity represent fundamental processes for the establishment of cognitive function. Structural organization as well as signalling pathways from r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a94e226ccedc91361bf1d5a4b39bb344
https://hdl.handle.net/2066/197525

Identification of C12orf4 as a gene for autosomal recessive intellectual disability

Autor: Anju K Philips, Pinelli M, Ci, Bie, Mustonen A, Määttä T, Hh, Arts, Wu K, Roepman R, Js, Moilanen, Raza S, Varilo T, Scala G, Cocozza S, Gilissen C, Kl, Gassen, Järvelä I

Publikováno v: Clinical Genetics, 91, 1, pp. 100-105
Europe PubMed Central
Clinical Genetics, 91, 100-105
Clinical Genetics, 91(1), 100. Wiley-Blackwell

Contains fulltext : 169700.pdf (Publisher’s version ) (Closed access) Intellectual disability (ID) is a major health problem in our society. Genetic causes of ID remain unknown because of its vast heterogeneity. Here we report two Finnish families

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::018b7c0ed747049cc658a558594d7f84
https://hdl.handle.net/2066/169700

Functional analyses of Pericentrin and Syne-2 interaction in ciliogenesis

Autor: Falk, N.S., Kessler, K., Schramm, Sinja-Fee, Boldt, K., Becirovic, Elvir, Michalakis, Stylianos, Roepman, R., Brandstaetter, Johann Helmut, Giessl, A.

Publikováno v: Journal of Cell Science, 131, 16, pp.
Journal of Cell Science, 131,

Item does not contain fulltext

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a200804c6d4553df678cbcd41489a676
https://doi.org/10.1242/jcs.218487

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.