Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Esther Arribas-González"'
Autor:
Eva Díaz-Guerra, Elena P. Moreno-Jiménez, Itziar de Rojas, César Rodríguez, Eva Rodríguez-Traver, Esther Arribas-González, María Orera, Isabel Hernández, Agustín Ruiz, Carlos Vicario
Publikováno v:
Stem Cell Research, Vol 39, Iss , Pp - (2019)
Genetic polymorphism of apolipoprotein E (APOE) confers differential susceptibility to late-onset Alzheimer's disease (LOAD). The ε3 allele of APOE, the most common isoform, does not represent a risk factor for LOAD. In contrast, the ε4 allele is t
Externí odkaz:
https://doaj.org/article/8e2f1789e21148eebc02e9b45ee6d12f
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:
Carlos Vicario, César Rodríguez, Isabel Hernández, Eva Rodríguez-Traver, Itziar de Rojas, Elena P. Moreno-Jiménez, Eva Díaz-Guerra, Agustín Ruiz, Esther Arribas-González, María Orera
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Stem Cell Research, Vol 39, Iss, Pp-(2019)
instname
Stem Cell Research, Vol 39, Iss, Pp-(2019)
Genetic polymorphism of apolipoprotein E (APOE) confers differential susceptibility to late-onset Alzheimer's disease (LOAD). The ε3 allele of APOE, the most common isoform, does not represent a risk factor for LOAD. In contrast, the ε4 allele is t
E3 ubiquitin ligases LNX1 and LNX2 are major regulators of the presynaptic glycine transporter GlyT2
Autor:
Esther Arribas-González, Carmen Aragón, J. de Juan-Sanz, Beatriz López-Corcuera, A. de la Rocha-Muñoz, Enrique Núñez
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9, pp.14944. ⟨10.1038/s41598-019-51301-x⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
instname
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9, pp.14944. ⟨10.1038/s41598-019-51301-x⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
The neuronal glycine transporter GlyT2 is an essential regulator of glycinergic neurotransmission that recaptures glycine in presynaptic terminals to facilitate transmitter packaging in synaptic vesicles. Alterations in GlyT2 expression or activity r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e84d69394f75b9f699017ea50e6d1f7
http://hdl.handle.net/10261/214510
http://hdl.handle.net/10261/214510
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Hyperekplexia or startle disease is a dysfunction of inhibitory glycinergic neurotransmission characterized by an exaggerated startle in response to trivial tactile or acoustic stimuli. Although rare, this disorder can have serious consequences, incl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dcf6bc72985d980cebab7a4ba710a7b
http://hdl.handle.net/10261/214911
http://hdl.handle.net/10261/214911
Ubiquitin ligase LNX1 is a major regulator of glycine recapture by the presynaptic transporter GlyT2
Autor:
Carmen Aragón, Jaime de Juan-Sanz, Beatriz López-Corcuera, Enrique Núñez, Esther Arribas-González
The neuronal glycine transporter GlyT2 is an essential regulator of glycinergic neurotransmission that recaptures glycine in presynaptic terminals to facilitate quantal transmitter packaging in synaptic vesicles. Alterations in GlyT2 expression or ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a309c3f1dbf291a00281f3a2c460de3e
Autor:
Ana M. Mata, Esther Arribas-González, Daniel Marcos, Francisco Zafra, Isaac Corbacho, María Berrocal, Carmen Aragón, Ignacio Ibáñez, Enrique Núñez, Jaime de Juan-Sanz, Beatriz López-Corcuera
Publikováno v:
Journal of Biological Chemistry. 289:34308-34324
Fast inhibitory glycinergic transmission occurs in spinal cord, brainstem, and retina to modulate the processing of motor and sensory information. After synaptic vesicle fusion, glycine is recovered back to the presynaptic terminal by the neuronal gl
Autor:
Ignacio Ibáñez, Cecilio Giménez, Carmen Aragón, Rhys H. Thomas, Francisco Zafra, Esther Arribas-González, Seo-Kyung Chung, Jaime Martínez-Villarreal, Beatriz López-Corcuera, Esperanza Jiménez, Julián Nevado, Lourdes R. Desviat, Jaime de Juan-Sanz, Gonzalo Perez-Siles, Robert J. Harvey, Pablo Lapunzina, Enrique Núñez, Maya Topf, Enrique Fernández-Sánchez, Noemí García-Tardón, Valeria Romanelli, Victoria M. James, Mark I. Rees
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Hyperekplexia or startle disease is characterized by an exaggerated startle response, evoked by tactile or auditory stimuli, producing hypertonia and apnea episodes. Although rare, this orphan disorder can have serious consequences, including sudden
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
"This research was originally published in Journal of Biological Chemistry. Esther Arribas-González, Jaime de Juan-Sanz, Carmen Aragón, and Beatriz López-Corcuera. Molecular Basis of the Dominant Negative Effect of a Glycine Transporter 2 Mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cac01c9c624634a8600892edf5b9e7c
http://hdl.handle.net/10486/679218
http://hdl.handle.net/10486/679218
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