Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Iris Grigg"'
Autor:
Mohiuddin Mohiuddin, Zlatko Marusic, Mirna Anicic, Van Dijck Anke, Elisa Cappuyns, Rizzuti Ludovico, Alessandro Vitriolo, Gal Hacohen Kleiman, Iris Grigg, Giuseppe Testa, Illana Gozes, R. Frank Kooy, Christopher E. Pearson
Many neurodevelopmental disorders, including autism, are caused by de novo mutations, that might arise as early as in the parental germline, during embryonic, fetal development, or as late as post-natal aging. Intra-tissue mutation-load variations co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b146813d0e3cbd27f84e21ad2979dc0
https://doi.org/10.1101/2022.06.21.496616
https://doi.org/10.1101/2022.06.21.496616
Autor:
Iris Grigg, Oxana Kapitansky, Illana Gozes, Gidon Karmon, R.F. Kooy, Michael Gershovits, Adva Hadar, Yanina Ivashko-Pachima, Johannes Attems, Korenkova, David Gurwitz, Carmen Laura Sayas
Publikováno v:
Molecular psychiatry
Molecular Psychiatry
Molecular Psychiatry
With Alzheimer’s disease (AD) exhibiting reduced ability of neural stem cell renewal, we hypothesized that de novo mutations controlling embryonic development, in the form of brain somatic mutations instigate the disease. A leading gene presenting
Autor:
Iris Grigg, Vlasta Korenková, Zlatko Marušić, Olga Touloumi, Roza Lagoudaki, Nikolaos Grigoriadis, Anke Van Dijck, Mirna Aničić, R. Frank Kooy, Jurica Vuković, Tom Aharon Hait, Illana Gozes, Yanina Ivashko-Pachima
Publikováno v:
Translational Psychiatry
Translational psychiatry
Translational Psychiatry, Vol 10, Iss 1, Pp 1-10 (2020)
Translational psychiatry
Translational Psychiatry, Vol 10, Iss 1, Pp 1-10 (2020)
Given our recent discovery of somatic mutations in autism spectrum disorder (ASD)/intellectual disability (ID) genes in postmortem aged Alzheimer’s disease brains correlating with increasing tauopathy, it is important to decipher if tauopathy is un
Autor:
Andy Y. L. Gao, Illana Gozes, Iris Grigg, Gidon Karmon, Albert Le, Vlasta Korenková, Shlomo Sragovich, Gal Hacohen-Kleiman, Metsada Pasmanik-Chor, R. Anne McKinney
Publikováno v:
Journal of Clinical Investigation. 128:4956-4969
Previous findings showed that in mice, complete knockout of activity-dependent neuroprotective protein (ADNP) abolishes brain formation, while haploinsufficiency (Adnp+/–) causes cognitive impairments. We hypothesized that mutations in ADNP lead to
Autor:
Illana Gozes, Gidon Karmon, Elisa Cappuyns, Eliezer Giladi, Iris Grigg, Yankel Gabet, A Van Dijck, Michal Eger, R F Kooy, Metsada Pasmanik-Chor, Gal Hacohen-Kleiman, S Bedrosian-Sermone, O Elpeleg
Publikováno v:
Translational Psychiatry. 7:e1166-e1166
A major flaw in autism spectrum disorder (ASD) management is late diagnosis. Activity-dependent neuroprotective protein (ADNP) is a most frequent de novo mutated ASD-related gene. Functionally, ADNP protects nerve cells against electrical blockade. I
Autor:
Grigg, Iris, Ivashko-Pachima, Yanina, Hait, Tom Aharon, Korenková, Vlasta, Touloumi, Olga, Lagoudaki, Roza, Van Dijck, Anke, Marusic, Zlatko, Anicic, Mirna, Vukovic, Jurica, Kooy, R. Frank, Grigoriadis, Nikolaos, Gozes, Illana
Publikováno v:
Translational Psychiatry; 7/13/2020, Vol. 10 Issue 1, p1-10, 10p