Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rafael Guillermo Garzón Jaramillo"'
Autor:
María Alejandra Puentes-Tellez, Paula Andrea Lerma-Barbosa, Rafael Guillermo Garzón-Jaramillo, Diego A. Suarez, Angela J. Espejo-Mojica, Johana M. Guevara, Olga Yaneth Echeverri, Daniela Solano-Galarza, Alfredo Uribe-Ardila, Carlos J. Alméciga-Díaz
Publikováno v:
Heliyon, Vol 6, Iss 3, Pp e03635- (2020)
Lysosomal storage diseases (LSDs) are a group of about 50 inborn errors of metabolism characterized by the lysosomal accumulation of partially or non-degraded molecules due to mutations in proteins involved in the degradation of macromolecules, trans
Externí odkaz:
https://doaj.org/article/dc87a9a89f9d4088ab59aedf9db5ece1
Autor:
Lucas D. Pedroza-Camacho, Andrea Blanco-Vargas, Natalia Sánchez-Castro, Lucía A. Díaz-Ariza, Raúl A. Poutou-Piñales, Lina M. Rodríguez-Gacha, Aura M. Pedroza-Rodríguez, Rafael Guillermo Garzón-Jaramillo, Claudia M. Rivera-Hoyos
Publikováno v:
Heliyon
Heliyon, Vol 6, Iss 10, Pp e05218-(2020)
Heliyon, Vol 6, Iss 10, Pp e05218-(2020)
Different genus of bacteria has been reported with the capacity to solubilize phosphorus from phosphate rock (PR). Pseudomonas sp., (A18) and Serratia sp., (C7) isolated from soils at the “Departamento de Boyacá” Colombia, where Allium cepa is c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc044934b6dcbe48ef04f62f19b129f
http://europepmc.org/articles/PMC7566105
http://europepmc.org/articles/PMC7566105
Autor:
Eliana Benincore-Flórez, Diego Suárez, Carlos J. Alméciga-Díaz, Angela J. Espejo-Mojica, Olga Yaneth Echeverri-Peña, Andres Felipe Leal, Daniela Solano-Galarza, Rafael Guillermo Garzón Jaramillo
GM2 gangliosidosis are a group of pathologies characterized by GM2 ganglioside accumulation into the lysosome due to mutations on the genes encoding for the β-hexosaminidases subunits or the GM2 activator protein. Three GM2 gangliosidosis have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::612f956bc22b729008cbb07b3a63edc3
https://doi.org/10.20944/preprints202007.0137.v1
https://doi.org/10.20944/preprints202007.0137.v1
Autor:
Carlos J. Alméciga-Díaz, Diego Suárez, Olga Yaneth Echeverri-Peña, Andres Felipe Leal, Daniela Solano-Galarza, Eliana Benincore-Flórez, Angela J. Espejo-Mojica, Rafael Guillermo Garzón Jaramillo
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 6213, p 6213 (2020)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
GM2 gangliosidoses are a group of pathologies characterized by GM2 ganglioside accumulation into the lysosome due to mutations on the genes encoding for the β-hexosaminidases subunits or the GM2 activator protein. Three GM2 gangliosidoses have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edda2b55fdd0dd615967ef1f3e447746
https://pubmed.ncbi.nlm.nih.gov/32867370
https://pubmed.ncbi.nlm.nih.gov/32867370
Autor:
Olga Yaneth Echeverri, María Alejandra Puentes-Tellez, Alfredo Uribe-Ardila, Carlos J. Alméciga-Díaz, Diego Suárez, Angela J. Espejo-Mojica, Daniela Solano-Galarza, Johana Guevara, Rafael Guillermo Garzón-Jaramillo, Paula Andrea Lerma-Barbosa
Publikováno v:
Heliyon, Vol 6, Iss 3, Pp e03635-(2020)
Heliyon
Heliyon
Lysosomal storage diseases (LSDs) are a group of about 50 inborn errors of metabolism characterized by the lysosomal accumulation of partially or non-degraded molecules due to mutations in proteins involved in the degradation of macromolecules, trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a43348bc11f2e33a21a0158776de2b8
http://www.sciencedirect.com/science/article/pii/S2405844020304801
http://www.sciencedirect.com/science/article/pii/S2405844020304801
Autor:
Daniela Solano-Galarzaa, María Alejandra Puentes-Tellez, Carlos J. Alméciga-Díaz, Diego Suárez, Angela J. Espejo-Mojica, Rafael Guillermo Garzón-Jaramillo, Johana Guevara, Alfredo Uribe-Ardila, Olga Yaneth Echeverri, Paula Andrea Lerma-Barbosa
Publikováno v:
Molecular Genetics and Metabolism. 132:S88
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3e1e1e09dbd62073e69cb0808d0b0d6
https://doi.org/10.1016/j.ymgme.2020.12.211
https://doi.org/10.1016/j.ymgme.2020.12.211