Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pablo Alonso-Torres"'
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63230 (2013)
The neuronal transporter GlyT2 is a polytopic, 12-transmembrane domain, plasma membrane glycoprotein involved in the removal and recycling of synaptic glycine from inhibitory synapses. Mutations in the human GlyT2 gene (SLC6A5) that cause deficient g
Externí odkaz:
https://doaj.org/article/c6947de83add45808a2750e0d9876d3f
Autor:
Carmen Aragón, Esperanza Jiménez, Lara Rodenstein, Francisco Zafra, Gonzalo Perez-Siles, Pablo Alonso-Torres, Enrique Núñez, Beatriz López-Corcuera
Publikováno v:
Traffic. 10:829-843
The neuronal glycine transporter GLYT2 belongs to the neurotransmitter:sodium:symporter (NSS) family and removes glycine from the synaptic cleft, thereby aiding the termination of the glycinergic signal and achieving the reloading of the presynaptic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::950951c825a2541649bf9efc618c3b3b
https://doi.org/10.1111/j.1600-0854.2009.00911.x
https://doi.org/10.1111/j.1600-0854.2009.00911.x
Publikováno v:
Journal of Neurochemistry. 105:2080-2090
The neuronal glycine transporter GLYT2 is a plasma membrane protein that removes the neurotransmitter glycine from the synaptic cleft, thereby aiding the pre-synaptic terminal reloading and the termination of the glycinergic signal. Missense mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fce4269415dbf0cb855cc5b390b69b5
https://doi.org/10.1111/j.1471-4159.2008.05292.x
https://doi.org/10.1111/j.1471-4159.2008.05292.x
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
PLoS ONE
PLoS ONE, Vol 8, Iss 5, p e63230 (2013)
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
PLoS ONE
PLoS ONE, Vol 8, Iss 5, p e63230 (2013)
The neuronal transporter GlyT2 is a polytopic, 12-transmembrane domain, plasma membrane glycoprotein involved in the removal and recycling of synaptic glycine from inhibitory synapses. Mutations in the human GlyT2 gene (SLC6A5) that cause deficient g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::984b144e2d78db5fc23046a223562e20
http://hdl.handle.net/10261/95622
http://hdl.handle.net/10261/95622
Publikováno v:
The Biochemical journal. 412(3)
The neuronal glycine transporter GLYT2 controls the availability of the neurotransmitter in glycinergic synapses, and the modulation of its function may influence synaptic transmission. The active transporter is located in membrane rafts and reaches
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::423e03d786996fa1f254b4b141e56cb9
https://pubmed.ncbi.nlm.nih.gov/18341477
https://pubmed.ncbi.nlm.nih.gov/18341477