Zobrazeno 1 - 4
of 4
pro vyhledávání: '"José Luis Laso-Bayas"'
Autor:
Santiago Cadena-Ullauri, Patricia Guevara-Ramírez, Viviana A. Ruiz-Pozo, Rafael Tamayo-Trujillo, Elius Paz-Cruz, Daniel Simancas-Racines, Rita Ibarra-Castillo, José Luis Laso-Bayas, Ana Karina Zambrano
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Ion channels, vital transmembrane protein complexes, regulate ion movement within cells. Germline variants in channel-encoding genes lead to channelopathies. The sodium channels in cardiac cells exhibit a structure of an alpha sub
Externí odkaz:
https://doaj.org/article/ccf41cb3d8374b2f8ae9a72656de2030
Autor:
Rafael Tamayo-Trujillo, Rita Ibarra-Castillo, José Luis Laso-Bayas, Patricia Guevara-Ramirez, Santiago Cadena-Ullauri, Elius Paz-Cruz, Viviana A. Ruiz-Pozo, Nieves Doménech, Adriana Alexandra Ibarra-Rodríguez, Ana Karina Zambrano
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
IntroductionLong QT syndrome (LQTS) is an autosomal dominant inherited cardiac condition characterized by a QT interval prolongation and risk of sudden death. There are 17 subtypes of this syndrome associated with genetic variants in 11 genes. The se
Externí odkaz:
https://doaj.org/article/116eda59f6564a36b99bc01589a51bdd
Autor:
Ana Karina Zambrano, Elius Paz-Cruz, Santiago Cadena-Ullauri, Patricia Guevara-Ramírez, Viviana A. Ruiz-Pozo, Rafael Tamayo-Trujillo, Rita Ibarra-Castillo, José Luis Laso-Bayas, Nieves Doménech, Adriana Alexandra Ibarra-Rodríguez, Ricardo Hidalgo
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionHearing loss is the most common sensory disability, and it is estimated that 50% of cases are caused by genetic factors. One of the genes associated with deafness is the eyes absent homolog 4 (EYA4) gene, a transcription factor related to
Externí odkaz:
https://doaj.org/article/9f472c019a894db4974659f3e03ad6e7
Autor:
Patricia Guevara-Ramírez, Santiago Cadena-Ullauri, Rita Ibarra-Castillo, José Luis Laso-Bayas, Elius Paz-Cruz, Rafael Tamayo-Trujillo, Viviana A. Ruiz-Pozo, Nieves Doménech, Adriana Alexandra Ibarra-Rodríguez, Ana Karina Zambrano
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
IntroductionCardiac laminopathies are caused by mutations in the LMNA gene and include a wide range of clinical manifestations involving electrical and mechanical changes in cardiomyocytes. In Ecuador, cardiovascular diseases were the primary cause o
Externí odkaz:
https://doaj.org/article/cac4cb09c8fb4d00b547dfa6272e001f