Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Gemma, Gou"'
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S76-S77 (2023)
Externí odkaz:
https://doaj.org/article/2d67951efd844f2e9107ea5a59d3ab99
Autor:
Murat Kilinc, Vineet Arora, Thomas K Creson, Camilo Rojas, Aliza A Le, Julie Lauterborn, Brent Wilkinson, Nicolas Hartel, Nicholas Graham, Adrian Reich, Gemma Gou, Yoichi Araki, Àlex Bayés, Marcelo Coba, Gary Lynch, Courtney A Miller, Gavin Rumbaugh
Publikováno v:
eLife, Vol 11 (2022)
Loss-of-function variants in SYNGAP1 cause a developmental encephalopathy defined by cognitive impairment, autistic features, and epilepsy. SYNGAP1 splicing leads to expression of distinct functional protein isoforms. Splicing imparts multiple cellul
Externí odkaz:
https://doaj.org/article/b2d529b24e8e40d98531dc9a6b1666ca
Autor:
Àlex Bayés, Mark O. Collins, Rita Reig-Viader, Gemma Gou, David Goulding, Abril Izquierdo, Jyoti S. Choudhary, Richard D. Emes, Seth G. N. Grant
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-15 (2017)
Systematic analysis of the zebrafish synapse proteome has been lacking. Here the authors characterize the ultrastructure of zebrafish synapse and compare the proteomes of postsynaptic density in zebrafish and mice, offering a resource for future stud
Externí odkaz:
https://doaj.org/article/cd29502cc77e4a8c9f3d4ffe5972b000
Publikováno v:
PeerJ, Vol 7, p e6372 (2019)
Colorectal cancer (CRC), also known as colon cancer, is the third most common form of cancer worldwide in men and the second in women and is characterized by several genetic alterations, among them the expression of several genes. 1,2-dimethylhydrazi
Externí odkaz:
https://doaj.org/article/80fbd43f6563491dbcec63a9cc055712
Autor:
David Ramos-Vicente, Jie Ji, Esther Gratacòs-Batlle, Gemma Gou, Rita Reig-Viader, Javier Luís, Demian Burguera, Enrique Navas-Perez, Jordi García-Fernández, Pablo Fuentes-Prior, Hector Escriva, Nerea Roher, David Soto, Àlex Bayés
Publikováno v:
eLife, Vol 7 (2018)
Glutamate receptors are divided in two unrelated families: ionotropic (iGluR), driving synaptic transmission, and metabotropic (mGluR), which modulate synaptic strength. The present classification of GluRs is based on vertebrate proteins and has rema
Externí odkaz:
https://doaj.org/article/d66856ff2ccc4b5886e1c1a585dda8d3
Autor:
Murat Kilinc, Vineet Arora, Thomas K Creson, Camilo Rojas, Aliza A Le, Julie Lauterborn, Brent Wilkinson, Nicolas Hartel, Nicholas Graham, Adrian Reich, Gemma Gou, Yoichi Araki, Àlex Bayés, Marcelo Coba, Gary Lynch, Courtney A Miller, Gavin Rumbaugh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2632c3ea572bd76f5bc9d445cec22daf
https://doi.org/10.7554/elife.75707.sa2
https://doi.org/10.7554/elife.75707.sa2
Autor:
Murat Kilinc, Vineet Arora, Thomas K Creson, Camilo Rojas, Aliza A Le, Julie Lauterborn, Brent Wilkinson, Nicolas Hartel, Nicholas Graham, Adrian Reich, Gemma Gou, Yoichi Araki, Àlex Bayés, Marcelo Coba, Gary Lynch, Courtney A Miller, Gavin Rumbaugh
SummaryLoss-of-function variants in SYNAGP1 cause a developmental encephalopathy defined by cognitive impairment, autistic features, and epilepsy. SYNGAP1 splicing leads to expression of distinct functional protein isoforms. Splicing imparts multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efb18f076d5c40f09c226078126faafd
https://doi.org/10.1101/2021.12.05.471306
https://doi.org/10.1101/2021.12.05.471306
Autor:
Murat, Kilinc, Vineet, Arora, Thomas K, Creson, Camilo, Rojas, Aliza A, Le, Julie, Lauterborn, Brent, Wilkinson, Nicolas, Hartel, Nicholas, Graham, Adrian, Reich, Gemma, Gou, Yoichi, Araki, Àlex, Bayés, Marcelo, Coba, Gary, Lynch, Courtney A, Miller, Gavin, Rumbaugh
Publikováno v:
eLife. 11
Loss-of-function variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f5dbee7add81c55648ff7db937942db8
https://pubmed.ncbi.nlm.nih.gov/36285208
https://pubmed.ncbi.nlm.nih.gov/36285208
Autor:
Gemma Gou, Courtney A. Miller, Murat Kilinc, Nicholas A. Graham, Sabyasachi Maity, Gavin Rumbaugh, Yoichi Araki, Adrian Reich, Brent Wilkinson, Nicolas G. Hartel, Julie C. Lauterborn, Camilo Rojas, Aliza A. Le, Thomas K. Creson, Marcelo P. Coba, Gary Lynch, Àlex Bayés
SummarySynGAP-α1 is a splice variant of the neurodevelopmental disorder risk gene, SYNGAP1/Syngap1. α1 encodes the C-terminal PDZ binding motif (PBM) that promotes liquid-liquid phase separation, a candidate process for postsynaptic density organiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ada8ed2e72f883ce1258bce0819fb451
Autor:
Richard L. Huganir, Cristian de Quintana-Schmidt, Murat Kilinc, Àlex Bayés, Gavin Rumbaugh, Yoichi Araki, Elena Serrano, Adriana Roca-Fernandez, Gemma Gou, Rita Reig-Viader
Publikováno v:
JOURNAL OF NEUROCHEMISTRY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Journal of Neurochemistry
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Journal of Neurochemistry
The SynGAP protein is a major regulator of synapse biology and neural circuit function. Genetic variants linked to epilepsy and intellectual disability disrupt synaptic function and neural excitability. SynGAP has been involved in multiple signaling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce595b3b2a242e0e4502585523caa953