Zobrazeno 1 - 10
of 26
pro vyhledávání: '"L.E. Figuera-Villanueva"'
Akademický článek
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Autor:
José Francisco Muñoz-Valle, Jorge Ramón Padilla-Gutiérrez, Yeminia Valle, Ilian Janet García-González, L.E. Figuera-Villanueva, Nory Omayra Dávalos-Rodríguez, Emmanuel Valdés-Alvarado, Angélica Valdez-Haro, Héctor Enrique Flores-Salinas, Elena Sandoval-Pinto
Publikováno v:
Disease Markers, Vol 2015 (2015)
Disease Markers
Disease Markers
Background. Acute coronary syndrome (ACS) has an important impact in public health with high morbidity and mortality. Prothrombotic and proinflammatory states are involved in the pathogenesis of the disease. Plasminogen activator inhibitor-1 (PAI-1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2ab36030c80c4941c9ca721fffca0a4
https://doi.org/10.1155/2015/460974
https://doi.org/10.1155/2015/460974
Akademický článek
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Autor:
Lizeth Martínez-Jacobo, Kame A Galán-Huerta, Yadira X. Perez-Paramo, J.A. Nastasi-Catanese, Rocio Ortiz-Lopez, Martha M Rangel-Sosa, L.E. Figuera-Villanueva, Augusto Rojas-Martinez, Carlos Córdova-Fletes, Ana María Rivas-Estilla, I.A. González-Ramos, L. Arnaud-López
Publikováno v:
Clinical genetics. 93(6)
Splicing-related gene mutations might affect the expression of a single gene or multiple genes and cause clinically heterogeneous diseases. With the advent of next-generation sequencing, several splicing gene mutations have been exposed, yet most maj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba7327d0a22f68f98a7fcd7fd16e2b1c
https://pubmed.ncbi.nlm.nih.gov/29437235
https://pubmed.ncbi.nlm.nih.gov/29437235
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Mary Fafutis-Morris, L.E. Figuera-Villanueva, Anabell Alvarado-Navarro, José Francisco Muñoz-Valle, Alvaro J. Tovar-Cuevas, Margarita Montoya-Buelna, Jorge Ramón Padilla-Gutiérrez, Yeminia Valle
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2013 (2013)
BioMed Research International, Vol 2013 (2013)
Background. Leprosy is a debilitating infectious disease of human skin and nerves. Genetics factors of the host play an important role in the disease susceptibility. Toll-interacting protein (TOLLIP) is an inhibitory adaptor protein within the toll-l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2445f0512bac0523bb1f6f2c8c6a78f8
https://doi.org/10.1155/2013/459169
https://doi.org/10.1155/2013/459169
Autor:
A M Puebla-Prez, M R Flores-Marquez, G M Zniga-Gonzlez, Martha Patricia Gallegos-Arreola, R. Troyo-Sanroman, L.E. Figuera-Villanueva, G Morgn-Villela
Publikováno v:
ResearcherID
Scopus-Elsevier
Scopus-Elsevier
CYP1A1 is a gene involved in the high aryl hydrocarbon hydroxylase -inducible phenotype, which is a genetically-determined variation among individuals that has been associated with lung cancer risk. More specifically, CYP1A1 *2B and *4 polymorphisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8724e13ce578762a978f9485fd833b1
https://doi.org/10.5301/jbm.2008.379
https://doi.org/10.5301/jbm.2008.379
Autor:
M.P. Gallegos-Arreola, L.E. Figuera-Villanueva, R. Troyo-Sanroman, G. Morgán-Villela, A.M. Puebla-Pérez, M.R. Flores-Marquez, G.M. Zúñiga-González
Publikováno v:
The International Journal of Biological Markers. 23:24-30
Background CYP1A1 is a gene involved in the high aryl hydrocarbon hydroxylase -inducible phenotype, which is a genetically-determined variation among individuals that has been associated with lung cancer risk. More specifically, CYP1A1*2B and *4 poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96f2c22fb41a6bcaf5137ce4f4cf9dd3
https://doi.org/10.1177/172460080802300104
https://doi.org/10.1177/172460080802300104
Autor:
A. Stephens, D. García-Cruz, M.G. Lopez-Cardona, José Elías García-Ortiz, L.E. Figuera-Villanueva, L.X. Rodriguez-Rojas, M O García-Cruz, José Sánchez-Corona, F. Larios-Arceo, Alfredo Feria-Velasco, Nory Omayra Dávalos
Publikováno v:
ResearcherID
Myhre syndrome is a rare disorder characterized by low birthweight, short stature, mental retardation, facial dysmorphism (blepharophimosis, midfacial hypoplasia, prognathism), heart anomalies, muscle hypertrophy, decreased joint mobility and deafnes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9532058f0955a40c4129e097392200bd
https://doi.org/10.1097/00019605-200404000-00007
https://doi.org/10.1097/00019605-200404000-00007
Autor:
Jorge Ramón Padilla-Gutiérrez, Yeminia Valle, Fernando Rivas, L.E. Figuera-Villanueva, Nory Omayra Dávalos-Rodríguez, José Francisco Muñoz-Valle, Ilian Janet García-González, Héctor Enrique Flores-Salinas, Bianca Ethel Gutiérrez-Amavizca
Publikováno v:
BioMed Research International, Vol 2014 (2014)
BioMed Research International
BioMed Research International
Immunologic and inflammatory processes are involved in the pathogenesis of acute coronary syndrome (ACS) and type 2 diabetes mellitus (DM2). Human leukocyte antigen-G (HLA-G) is a negative regulator of the immune response. This study evaluates the 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca63b68b6a4abc09a9f84cf97d2c1a1c
https://doaj.org/article/ab9ff35dc2014450a58c4dfc84f240f3
https://doaj.org/article/ab9ff35dc2014450a58c4dfc84f240f3