Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Armas Cayarga A"'
Autor:
Madhuparna Nandi, Mitterrand Muamba Moyo, Sakina Orkhis, Jeanne Masunga Faida Mobulakani, Marc-André Limoges, Fjolla Rexhepi, Marian Mayhue, Anny Armas Cayarga, Gisela Cofino Marrero, Subburaj Ilangumaran, Alfredo Menendez, Sheela Ramanathan
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Interleukin-15, produced by hematopoietic and parenchymal cells, maintains immune cell homeostasis and facilitates activation of lymphoid and myeloid cell subsets. IL-15 interacts with the ligand-binding receptor chain IL-15Rα during biosynthesis, a
Externí odkaz:
https://doaj.org/article/9d34f11efbbe4603ac7f330ed52290e6
Autor:
Armas Cayarga, Anny, Perea Hernández, Yenitse, González González, Yaimé J., Figueredo Lago, Juan E., Valdivia Álvarez, Irinia Y., Gómez Cordero, Ivonne, Santos Hernández, Niurka, Vega Sánchez, Héctor, La Rosa Hernández, Deyanira, Martínez Pérez, Ernesto L.
Publikováno v:
In Biologicals March 2019 58:22-27
Akademický článek
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Autor:
Juan Emilio Figueredo Lago, Anny Armas Cayarga, Yaimé Josefina González González, Teresa Collazo Mesa
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-7 (2017)
Abstract Background Mutation scanning methods in Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene may not distinguish between a Cystic Fibrosis (CF) causing mutation and a benign variant. We have developed a simple and fast method for
Externí odkaz:
https://doaj.org/article/521025bca7524bbfa47f49e89ab8e90b
Autor:
Alicia Molina Kautzman, Jeanne Masunga Faida Mobulakani, Gisela Marrero Cofino, Akouavi Julite Irmine Quenum, Anny Armas Cayarga, Claude Asselin, Louis‐Charles Fortier, Subburaj Ilangumaran, Alfredo Menendez, Sheela Ramanathan
Publikováno v:
The Anatomical Record. 306:1111-1130
Inflammatory bowel diseases (IBDs) are characterized by abnormal, non-antigen specific chronic inflammation of unknown etiology. Genome-wide association studies show that many IBD genetic susceptibility loci map to immune function genes and compellin
Autor:
Idania Gonzalez-Perez, Yaimé Josefina González González, Ariel Vina-Rodriguez, Anny Armas Cayarga, Rosa Lydia Solís
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical, Vol 37, Iss 1, Pp 25-27 (2004)
Forty voluntary blood donors from two different blood banks in Havana, Cuba, who were repeatedly reactive on the routine screening of antibodies to hepatitis C virus, by Umelisa HCV test, were analyzed for the presence of HCV RNA using a nested PCR a
Externí odkaz:
https://doaj.org/article/5c81be4c5d1f42899102009f43affb00
Autor:
Figueredo Lago, Juan Emilio1 juan.figueredo@cie.cu, Armas Cayarga, Anny1, González González, Yaimé Josefina1, Collazo Mesa, Teresa2
Publikováno v:
BMC Medical Genetics. 5/25/2017, Vol. 18, p1-7. 7p.
Autor:
Figueredo-Lago, Juan E.1 juan.figueredo@cie.cu, Armas-Cayarga, Anny1, González-González, Yaimé J.1, Collazo-Mesa, Teresa2, de la Rosa, Iria García1, Perea-Hernández, Yenitse1, Santos-González, Elvia N.2
Publikováno v:
Biotecnologia Aplicada. 2015, Vol. 32 Issue 4, p4301-4306. 6p.
Autor:
Ivonne Gómez Cordero, Héctor Vega Sánchez, Ernesto L. Martínez Pérez, Niurka Santos Hernández, Yenitse Perea Hernández, Irinia Y. Valdivia Álvarez, Juan Emilio Figueredo Lago, Anny Armas Cayarga, Deyanira La Rosa Hernández, Yaimé Josefina González González
Publikováno v:
Biologicals : journal of the International Association of Biological Standardization. 58
Detection of hepatitis B virus (HBV) DNA is particularly important for detection of early acute and of occult HBV infection. On the other hand, HBV DNA detection and quantification are essential to diagnose and treat chronic HBV infection. In this st
Autor:
Yaimé Josefina González González, Anny Armas Cayarga, Teresa Collazo Mesa, Juan Emilio Figueredo Lago
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-7 (2017)
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-7 (2017)
Background Mutation scanning methods in Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene may not distinguish between a Cystic Fibrosis (CF) causing mutation and a benign variant. We have developed a simple and fast method for scanning