Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Aura M. Ramírez"'
Autor:
Henry A. Cordoba-Ruiz, Dennis J. Díaz-Rincón, Carlos J. Alméciga-Díaz, Fredy Ruiz, Sergio Diaz, Juan Camilo Losada, Carolina Cardona, Raúl A. Poutou-Piñales, Patricia Landázuri, Alexander Rodríguez-López, Angela J. Espejo-Mojica, Natalia Pimentel, Aura M. Ramírez, Luis Alejandro Barrera-Avellaneda
Publikováno v:
Biotechnology and Applied Biochemistry. 65:655-664
Hunter syndrome (Mucopolysaccharidosis II, MPS II) is an X-linked lysosomal storage disease produced by the deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS). Currently, MPS II patients are mainly treated with enzyme replacement therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::106843fa99545f2ae6480e3a339c3eef
https://doi.org/10.1002/bab.1660
https://doi.org/10.1002/bab.1660
Publikováno v:
mBio, Vol 15, Iss 4 (2024)
ABSTRACTWe previously demonstrated that mutation of sarA in Staphylococcus aureus limits biofilm formation, cytotoxicity for osteoblasts and osteoclasts, and virulence in osteomyelitis, and that all of these phenotypes can be attributed to the increa
Externí odkaz:
https://doaj.org/article/3ccebaa7a23c4c8cae222edb8ef3cfc2
Autor:
Laura Beltran, Camilo Andres Patarroyo, Adelina P Meléndez, Andrea Ardila, Oscar F. Sánchez, Carlos J. Alméciga-Díaz, Alexander Rodríguez-López, Aura M. Ramírez
Publikováno v:
European Journal of Pharmaceutical Sciences. 109:48-55
Phenylketonuria (PKU) is an autosomal recessive disorder caused by a defective phenylalanine hydroxylase (PAH), which catalyzes the hydroxylation of l -phenylalanine ( l -Phe) to l -tyrosine ( l -Tyr) in presence of the cofactor tetrahydrobiopterin (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e5be9faf6f7ba11c2f3fec02e292205
https://doi.org/10.1016/j.ejps.2017.07.033
https://doi.org/10.1016/j.ejps.2017.07.033
Publikováno v:
Virulence, Vol 14, Iss 1 (2023)
ABSTRACTWe previously demonstrated that MgrA, SarA, SarR, SarS, SarZ, and Rot bind at least three of the four promoters associated with genes encoding primary extracellular proteases in Staphylococcus aureus (Aur, ScpA, SspA/SspB, SplA-F). We also sh
Externí odkaz:
https://doaj.org/article/d1bcb2343cc645f088045915c1d8530b
Autor:
Natalia, Pimentel, Alexander, Rodríguez-Lopez, Sergio, Díaz, Juan C, Losada, Dennis J, Díaz-Rincón, Carolina, Cardona, Ángela J, Espejo-Mojica, Aura M, Ramírez, Fredy, Ruiz, Patricia, Landázuri, Raúl A, Poutou-Piñales, Henry A, Cordoba-Ruiz, Carlos J, Alméciga-Díaz, Luis A, Barrera-Avellaneda
Publikováno v:
Biotechnology and applied biochemistry. 65(5)
Hunter syndrome (Mucopolysaccharidosis II, MPS II) is an X-linked lysosomal storage disease produced by the deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS). Currently, MPS II patients are mainly treated with enzyme replacement therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f6ef464ec7aa7e6638e5d0709dd7597
https://pubmed.ncbi.nlm.nih.gov/29633336
https://pubmed.ncbi.nlm.nih.gov/29633336
Autor:
Alexander Rodríguez-López, Carlos J. Alméciga-Díaz, Jhonnathan Sánchez, Angela J. Espejo-Mojica, Luis A. Barrera, Dennis Diaz, Andrea Pardo, Luisa Pimentel, Jefferson Moreno, Aura M. Ramírez, Laura Beltran
Publikováno v:
Scientific Reports
Mucopolysaccharidosis IV A (MPS IV A, Morquio A disease) is a lysosomal storage disease (LSD) produced by mutations on N-acetylgalactosamine-6-sulfate sulfatase (GALNS). Recently an enzyme replacement therapy (ERT) for this disease was approved using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17121291660efbd9e8088aef45b10ae6
Autor:
Laura Beltran, Alexander Rodríguez-López, Jhonnathan Sánchez, Camilo Losada, Carlos J. Almeciga, Angela J. Espejo-Mojica, Dennis Diaz, Luis A. Barrera, Aura M. Ramírez, Natalia Pimentel
Publikováno v:
Molecular Genetics and Metabolism. 117:S17-S18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::729fed73e04b3d1dcfcb47992fc42a3b
https://doi.org/10.1016/j.ymgme.2015.12.170
https://doi.org/10.1016/j.ymgme.2015.12.170
Autor:
Joseph S. Rom, Karen E. Beenken, Aura M. Ramirez, Christopher M. Walker, Ethan J. Echols, Mark S. Smeltzer
Publikováno v:
Virulence, Vol 12, Iss 1, Pp 584-600 (2021)
Using the USA300, methicillin-resistant Staphylococcus aureus strain LAC, we previously examined the impact of regulatory mutations implicated in biofilm formation on protease production and virulence in a murine sepsis model. Here we examined the im
Externí odkaz:
https://doaj.org/article/667e5f226bad44028b6c87c5ff2ede7b
Autor:
Karen E. Beenken, Mara J. Campbell, Aura M. Ramirez, Karrar Alghazali, Christopher M. Walker, Bailey Jackson, Christopher Griffin, William King, Shawn E. Bourdo, Rebecca Rifkin, Silke Hecht, Daniel G. Meeker, David E. Anderson, Alexandru S. Biris, Mark S. Smeltzer
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract We previously reported the development of an osteogenic bone filler scaffold consisting of degradable polyurethane, hydroxyapatite, and decellularized bovine bone particles. The current study was aimed at evaluating the use of this scaffold
Externí odkaz:
https://doaj.org/article/499612545c514ba09349c6d9e0ce2907
Autor:
Aura M. Ramirez, Karen E. Beenken, Stephanie D. Byrum, Alan J. Tackett, Lindsey N. Shaw, Brittney D. Gimza, Mark S. Smeltzer
Publikováno v:
Virulence, Vol 11, Iss 1, Pp 1738-1762 (2020)
Using DNA affinity chromatography we demonstrate that the S. aureus regulatory proteins MgrA, Rot, SarA, and SarS bind DNA baits derived from the promoter regions associated with the genes encoding aureolysin, ScpAB, SspABC, and SplA-F. Three of four
Externí odkaz:
https://doaj.org/article/40cc6068c73e432795025640766a5025