Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Isabelle Caille"'
Autor:
Salima Messaoudi, Ada Allam, Julie Stoufflet, Theo Paillard, Anaïs Le Ven, Coralie Fouquet, Mohamed Doulazmi, Alain Trembleau, Isabelle Caille
Publikováno v:
eLife, Vol 12 (2024)
The fragile X syndrome (FXS) represents the most prevalent form of inherited intellectual disability and is the first monogenic cause of autism spectrum disorder. FXS results from the absence of the RNA-binding protein FMRP (fragile X messenger ribon
Externí odkaz:
https://doaj.org/article/13fa9b263153445990b54ed25e7201d9
Autor:
Julie Stoufflet, Isabelle Caillé
Publikováno v:
Cells, Vol 11, Iss 21, p 3384 (2022)
The primary cilium (PC) is a microtubule-based tiny sensory organelle emanating from the centrosome and protruding from the surface of most eukaryotic cells, including neurons. The extremely severe phenotypes of ciliopathies have suggested their para
Externí odkaz:
https://doaj.org/article/3a5a975f957944f8b3a6bcc960aba014
Autor:
Sabiha Abekhoukh, H. Bahar Sahin, Mauro Grossi, Samantha Zongaro, Thomas Maurin, Irene Madrigal, Daniele Kazue-Sugioka, Annick Raas-Rothschild, Mohamed Doulazmi, Pilar Carrera, Andrea Stachon, Steven Scherer, Maria Rita Drula Do Nascimento, Alain Trembleau, Ignacio Arroyo, Peter Szatmari, Isabel M. Smith, Montserrat Milà, Adam C. Smith, Angela Giangrande, Isabelle Caillé, Barbara Bardoni
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 4, Pp 463-474 (2017)
Cytoplasmic FMRP interacting protein 1 (CYFIP1) is a candidate gene for intellectual disability (ID), autism, schizophrenia and epilepsy. It is a member of a family of proteins that is highly conserved during evolution, sharing high homology with its
Externí odkaz:
https://doaj.org/article/b879a391863543d5b04344b33425077a
Autor:
Marie Néant-Fery, Eléonore Pérès, Carole Nasrallah, Monica Kessner, Simona Gribaudo, Charles Greer, Anne Didier, Alain Trembleau, Isabelle Caillé
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e40133 (2012)
Local protein synthesis in dendrites contributes to the synaptic modifications underlying learning and memory. The mRNA encoding the α subunit of the calcium/calmodulin dependent Kinase II (CaMKIIα) is dendritically localized and locally translated
Externí odkaz:
https://doaj.org/article/8d674c8098e045b586d3dd5ffe6098eb