Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Nancy Martínez-Rodríguez"'
Autor:
Teresa Juárez-Cedillo, Nancy Martínez-Rodríguez, Gilberto Vargas-Alarcon, Enrique Juárez-Cedillo, Antonio Valle-Medina, Osvaldo Garrido-Acosta, Alfredo Ramirez
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
ObjectiveEvidence supports the important role of neuroinflammation in some types of dementia. This study aimed to evaluate the effect of epistasis of gene cytokines such as interleukin (IL)-α, IL-6, tumor necrosis factor (TNFα), and interferon-gamm
Externí odkaz:
https://doaj.org/article/a63cc33d025e47bdaa2763cefe98b228
Autor:
Elizabeth Ruiz-Sánchez, Janet Jiménez-Genchi, Yessica M. Alcántara-Flores, Carlos J. Castañeda-González, Carlos L. Aviña-Cervantes, Petra Yescas, María del Socorro González-Valadez, Nancy Martínez-Rodríguez, Antonio Ríos-Ortiz, Martha González-González, María E. López-Navarro, Patricia Rojas
Publikováno v:
BMC Psychiatry, Vol 21, Iss 1, Pp 1-13 (2021)
Abstract Background Cognitive functions represent useful endophenotypes to identify the association between genetic variants and schizophrenia. In this sense, the NR4A2 gene has been implicated in schizophrenia and cognition in different animal model
Externí odkaz:
https://doaj.org/article/1114cc9207a44e3fad93c8798f515ccb
Autor:
Teresa Juárez‐Cedillo, Gilberto Vargas‐Alarcón, Nancy Martínez‐Rodríguez, Enrique Juárez‐Cedillo, José Manuel Fragoso, Jorge Escobedo‐de‐la‐Peña
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 9, Pp n/a-n/a (2019)
Abstract Frailty is a geriatric syndrome, characterized by a loss in functional reserve with an increase in morbidity and mortality. There are no reports that link the genetic polymorphisms between interleukin 10 (IL10) and frailty; for this reason,
Externí odkaz:
https://doaj.org/article/d80180372fca424e867cc3ea44618572
Autor:
Nancy Martínez-Rodríguez, Carlos Posadas-Romero, Teresa Villarreal-Molina, Maite Vallejo, Leonardo Del-Valle-Mondragón, Julian Ramírez-Bello, Adan Valladares, Miguel Cruz-López, Gilberto Vargas-Alarcón
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e65700 (2013)
AimTo explore the role of the ACE gene polymorphisms in the risk of essential hypertension in Mexican Mestizo individuals and evaluate the correlation between these polymorphisms and the serum ACE levels.MethodsNine ACE gene polymorphisms were genoty
Externí odkaz:
https://doaj.org/article/0a5d12fde52242d78cbe5851b4c58f65
Autor:
Teresa Juárez-Cedillo, Nancy Martínez-Rodríguez, José Manuel Fragoso, Valentin Islas-Pérez, Amara lópez-Martínez, Antonio Valle-Medina
Publikováno v:
Molecular Neurobiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36a8bc509b7390ec581b73105f632fa5
https://doi.org/10.1007/s12035-023-03367-y
https://doi.org/10.1007/s12035-023-03367-y
Autor:
Nancy Martínez-Rodríguez, Jose M. Fragosos, Gilberto Vargas-Alarcón, Evangelina González-Figueroa, Teresa Juárez-Cedillo, Osvaldo Garrido-Acosta
Publikováno v:
Metabolic Brain Disease. 36:1223-1229
There is an inconsistent finding about the relationship of catechol-O-methyltransferase (COMT) with dementia susceptibility, as well as with cognitive impairment. To substantiate this, we examined COMT genotype effects in certain cognitive domains in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4c09f537ec175d96238b0250b22e381
https://doi.org/10.1007/s11011-021-00740-5
https://doi.org/10.1007/s11011-021-00740-5
Autor:
Enrique Calvo-Páramo, Gilberto Vargas-Alarcón, Consuelo Romero, Viviana Reyes-Martinez, Ana María Santos, Catalina Villota-Eraso, Juan C. Rueda, Luz Mabel Ávila-Portillo, Diana Padilla, Nancy Martínez-Rodríguez, Ruben Burgos-Vargas, Guisselle-Nathalia Muñoz, Francy Cuervo, John Londoño, Sofia Arias-Correal, Santiago Bernal-Macías, Juan F. Medina
Publikováno v:
RMD Open
RMD Open, Vol 6, Iss 2 (2020)
RMD Open, Vol 6, Iss 2 (2020)
ObjectiveTo determine the association between endoplasmic reticulum aminopeptidase (ERAP)1 and ERAP2 single-nucleotide polymorphisms (SNPs) and human leukocyte antigens (HLA)-B27+ or HLA-B15+ patients with spondyloarthritis (SpA).Methods104 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e43d1fe59abc9e8918ac197df2615401
http://europepmc.org/articles/PMC7525252
http://europepmc.org/articles/PMC7525252
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Gilberto Vargas-Alarcón, José Manuel Fragoso, Teresa Juárez-Cedillo, Nancy Martínez-Rodríguez, Enrique Juarez-Cedillo, Jorge Escobedo-de-la-Peña
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 9, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Frailty is a geriatric syndrome, characterized by a loss in functional reserve with an increase in morbidity and mortality. There are no reports that link the genetic polymorphisms between interleukin 10 (IL10) and frailty; for this reason, our objec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fbf1ed3e0471365fa425a48e5ca99a9
https://doaj.org/article/d80180372fca424e867cc3ea44618572
https://doaj.org/article/d80180372fca424e867cc3ea44618572