Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maria Fernanda Martinez-Reza"'
Autor:
Judith Thomas, Maria Fernanda Martinez-Reza, Manja Thorwirth, Yvette Zarb, Karl-Klaus Conzelmann, Stefanie M. Hauck, Sofia Grade, Magdalena Götz
Publikováno v:
Science advances. 8(23)
Transplantation is a clinically relevant approach for brain repair, but much remains to be understood about influences of the disease environment on transplant connectivity. To explore the effect of amyloid pathology in Alzheimer’s disease (AD) and
Autor:
Giulia Santoni, Lukas van den Heuvel, Bianca A. Silva, Simone Astori, Hendrik Heiser, Carmen Sandi, Maria Fernanda Martinez-Reza, Johannes Gräff, Allison M. Burns
Publikováno v:
Nature Neuroscience
Fear and trauma generate some of the longest-lived memories. Despite the corresponding need to understand how such memories can be attenuated, the underlying brain circuits remain unknown. Here, combining viral tracing, neuronal activity mapping, fib
Autor:
William B. Dobyns, Maria Fernanda Martinez-Reza, Jamel Chelly, Tessa van Dijk, Lydie Burglen, Martin W. Breuss, Gregory M. Cooper, Stefano Lise, Nadia Bahi-Buisson, Norine Voisin, Usha Kini, Linlea Armstrong, Nicholas J. Cowan, Stéphanie Valence, Andrea Wenninger-Weinzierl, Thomas A. Leonard, Frank Baas, Lukas Landler, Ennio Del Giudice, Jonathan A. Bernstein, Ghayda Mirzaa, Guoling Tian, Kimberly A. Aldinger, Bregje W.M. van Bon, Alexandre Reymond, Tyler Mark Pierson, Giuseppina Vitiello, Ratna Tripathy, Thomas Gstrein, Gaetano Terrone, Alex R. Paciorkowski, Maria Christina Sergaki, Alessandra D'Amico, Susan M. Hiatt, Ines Leca, Janneke Weiss, Ellyn Farrelly, Alistair T. Pagnamenta, Jenny C. Taylor, Nicola Brunetti-Pierri, David A. Keays
Publikováno v:
Neuron, 100, 6, pp. 1354
Neuron, vol 100, iss 6
Neuron, 100, 1354
Neuron, 100(6), 1354
Neuron, vol 100, iss 6
Neuron, 100, 1354
Neuron, 100(6), 1354
Corpus callosum malformations are associated with a broad range of neurodevelopmental diseases. We report that de novo mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations (MCC-CH-CM) in the abs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65f44f6e382cd93a35303ff90caf884b
https://doi.org/10.1016/j.neuron.2018.10.044
https://doi.org/10.1016/j.neuron.2018.10.044