Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Adriana Alexandra Ibarra Rodríguez"'
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:
Omer Campo Nieto, Winston Rojas Montoya, Claudio Bravi, Constanza Elena Duque Vélez, Adriana Alexandra Ibarra Rodríguez, Gabriel Bedoya Berrío, Andrés Ruiz Linares
Publikováno v:
Iatreia, Vol 23, Iss 4-S (2010)
En las poblaciones humanas de Colombia existe una limitada diversidad de linajes maternos, representada por los haplogrupos amerindios A, B, C y D; un aporte materno africano restringido a algunas áreas y una muy baja contribución materna europea.
Externí odkaz:
https://doaj.org/article/4cbe08ef6522495fb492daa97d83e5f6
Autor:
Martha Eugenia Martínez Barbosa, Oscar Dario Palacio Salas, Yeny Cecilia Posada Posada, Adriana Alexandra Ibarra Rodríguez, Tomás Restrepo Álvarez
Publikováno v:
Iatreia, Vol 23, Iss 4-S (2010)
Los alelos nulos, las nuevas variantes alélicas y la observación de tres alelos en algunos marcadores genéticos; son los hallazgos más comunes en la genotipificación durante el analisis de STRs. Los Alelos nulos (Allele Dropout/Null Allele): son
Externí odkaz:
https://doaj.org/article/f4034a8ea8944924855ce8fe68d53984
Autor:
Martha Eugenia Martínez Barbosa, Oscar Darío Palacio Salas, Yeny Cecilia Posada Posada, Adriana Alexandra Ibarra Rodríguez, Tomás Restrepo Álvarez
Publikováno v:
Iatreia, Vol 23, Iss 4-S (2010)
Los alelos nulos, las nuevas variantes alélicas y la observación de tres alelos en algunos marcadores genéticos; son los hallazgos más comunes en la genotipificación durante el analisis de STRs. Los Alelos nulos (Allele Dropout/Null Allele): son
Externí odkaz:
https://doaj.org/article/d5afe903fa62468f8f0302b1f1f2bfeb
Autor:
Ana Karina Zambrano, Santiago Cadena-Ullauri, Patricia Guevara-Ramírez, Viviana A. Ruiz-Pozo, Rafael Tamayo-Trujillo, Elius Paz-Cruz, Adriana Alexandra Ibarra-Rodríguez, Nieves Doménech
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
Hypertension is one of the primary risk factors associated with cardiovascular diseases (CVDs). It is a condition that affects people worldwide, and its prevalence is increasing due to several factors, such as lack of physical activity, population ag
Externí odkaz:
https://doaj.org/article/50d2cedc6b944ef683bce837561a9d22
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
Autor:
Ilaria Boschi, Juan E. Ruiz Gomez, Gloria C. Vicuña Giraldo, Mishel M. Stephenson Ojea, Juan Pablo Acierno, J. Carlos Álvarez Merino, Ulises Toscanini, A. Gaviria, Ana María López-Parra, Ferran Casals, Santiago Cobos Navarrete, Laura Catelli, Mariana Herrera Piñero, Gulbanu K. Zorba, Lourdes Prieto Solla, Manuel López Soto, Esperanza González-Moya, Gian Carlo Iannacone, Carlos Vullo, M. Aler, Gabriela Berardi, Jane Valdivia Olarte, Adriana Alexandra Ibarra Rodríguez, Thomas J. Parsons, Y. Posada, Carola Romanini, Zlatan Bajunovic, Marco D. García King, Walter Ruben Bozzo, Maria Alessandra Marrucci, Carlos Baeza-Richer, Manuel Velázquez Miranda, Aikaterini Papaioannou, Francesc Calafell, Victor G. Saragoni, Maria João Porto
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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The Spanish and Portuguese-Speaking Working Group of the International Society for Forensic Genetics (GHEP-ISFG) has organized a second collaborative exercise on a simulated case of Disaster Victim Identification (DVI), with the participation of eigh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa641c87266f0ee761c60c4dc7543a32
https://doi.org/10.1016/j.fsigen.2021.102527
https://doi.org/10.1016/j.fsigen.2021.102527
Autor:
Santiago Cadena-Ullauri, Patricia Guevara-Ramirez, Viviana Ruiz-Pozo, Rafael Tamayo-Trujillo, Elius Paz-Cruz, Tatiana Sánchez Insuasty, Nieves Doménech, Adriana Alexandra Ibarra-Rodríguez, Ana Karina Zambrano
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
IntroductionGenomic screening is an informative and helpful tool for the clinical management of inherited conditions such as cardiac diseases. Cardiac-inherited diseases are a group of disorders affecting the heart, its system, function, and vasculat
Externí odkaz:
https://doaj.org/article/8b6abfdf9e0a4c699e840409b6cb3be8