Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ana I. Moreno-Manuel"'
Autor:
Álvaro Macías, Andrés González-Guerra, Ana I. Moreno-Manuel, Francisco M. Cruz, Lilian K. Gutiérrez, Nieves García-Quintáns, Marta Roche-Molina, Francisco Bermúdez-Jiménez, Vicente Andrés, María Linarejos Vera-Pedrosa, Isabel Martínez-Carrascoso, Juan A. Bernal, José Jalife
We thank C. Galán-Arriola (from CNIC) for help in the graphical illustration of the manuscript; M. Fernández-Tenorio (from the University of Bern) for valuable guidance in the experimental details of calcium dynamics in permeabilized cells; and H.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6096e8ff26ee527e2006ee3c0a5665a8
https://hdl.handle.net/20.500.12105/15257
https://hdl.handle.net/20.500.12105/15257
Autor:
Nieves García-Quintáns, Marta Roche-Molina, Isabel Martínez-Carrascoso, Alvaro Macias, Ana I. Moreno-Manuel, Lilian K. Gutiérrez, Andrés González-Guerra, José Jalife, Vicente Andrés, Francisco Bermúdez-Jiménez, Francisco Cruz, Juan A. Bernal, María Linarejos Vera-Pedrosa
Publikováno v:
Circulation Research. 129
Background: Andersen-Tawil syndrome type 1 (ATS1), caused by trafficking deficient mutations in the gene KCNJ2 coding the inward rectifier K + channel Kir2.1, is associated with life-threatening arrhythmias, which in some patients resemble catecholam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c86aa932511bdbc05766b3b2d18001c
https://doi.org/10.1161/res.129.suppl_1.p356
https://doi.org/10.1161/res.129.suppl_1.p356
Autor:
Francisco Bermúdez-Jiménez, Marta Roche-Molina, Lilian K. Gutiérrez, Isabel Martínez-Carrascoso, José Jalife, Nieves García-Quintáns, Alvaro Macias, Juan A. Bernal, Andrés González-Guerra, Vicente Andrés, María Linarejos Vera-Pedrosa, Ana I. Moreno-Manuel, Francisco Cruz
Andersen-Tawil Syndrome (ATS) is associated with life threatening arrhythmias of unknown mechanism. We report on a mouse model carrying the trafficking-deficient mutant Kir2.1Δ314-315. The mouse recapitulates the electrophysiological phenotype of ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5421fcc83fab0a28d1b5d72cc4656855
https://doi.org/10.1101/2021.06.17.448833
https://doi.org/10.1101/2021.06.17.448833
Autor:
Alvaro Macias, Andrés González-Guerra, Ana I. Moreno-Manuel, Francisco M. Cruz, Nieves García-Quintáns, Lilian K. Gutiérrez, Marta Roche-Molina, Francisco Bermúdez-Jiménez, María L. Vera-Pedrosa, Isabel Martínez-Carrascoso, Juan A. Bernal, Jose Jalife
Publikováno v:
Heart Rhythm. 18:S473-S474
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73fe309e7ab03899dfd4d97f3727f49a
https://doi.org/10.1016/j.hrthm.2021.07.015
https://doi.org/10.1016/j.hrthm.2021.07.015
Autor:
Juan A. Bernal, Lilian K. Gutiérrez, Nieves García-Quintáns, Francisco Bermúdez-Jiménez, Marta Roche-Molina, Alvaro Macias, Ana I. Moreno-Manuel, María Linarejos Vera-Pedrosa, Francisco Cruz, Isabel Martínez-Carrascoso, Andrés González-Guerra, José Jalife
Publikováno v:
Heart Rhythm. 18:S35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c000ee0765721c2ecbf5a810a82b98a3
https://doi.org/10.1016/j.hrthm.2021.06.103
https://doi.org/10.1016/j.hrthm.2021.06.103
Autor:
María Linarejos Vera-Pedrosa, Ana I. Moreno-Manuel, Luis Tercedor, Miguel A. Alvarez, Francisco Bermúdez, Lilian Gutiérrez Espinosa de los Monteros, Juan Jiménez Jáimez
Publikováno v:
Journal of the American College of Cardiology. 75:469
Short QT Syndrome (SQTS) is a very rare cardiac channelopathy that leads to an abbreviated QTc interval and sudden cardiac death (SCD). It is a genetically heterogeneous entity, with only 25 % of cases identified as having a pathogenic mutation in ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f8d9bf63e69129987cfe68e8c98110
https://doi.org/10.1016/s0735-1097(20)31096-2
https://doi.org/10.1016/s0735-1097(20)31096-2