Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Edwin Alexander Rodríguez-López"'
Autor:
Angela Johana Espejo Mojica, Angela Rocío Mosquera, Edwin Alexander Rodríguez-López, Dennis Johana Díaz, Laura Milena Betrán, Francy Liliana Hernández, Carlos Javier Alméciga Díaz, Luis Alejandro Barrera
Publikováno v:
Universitas Scientiarum, Vol 21, Iss 3, Pp 195-217 (2016)
β-hexosaminidases (Hex) are dimeric enzymes involved in the lysosomal degradation of glycolipids and glycans. They are formed by α- and/or β-subunits encoded byHEXA and HEXB genes, respectively. Mutations in these genes lead to Tay Sachs or Sandho
Externí odkaz:
https://doaj.org/article/c0b11ebbfff04d678c4c7e530980e457
Autor:
Angela María Alvarado-Fernández, Edwin Alexander Rodríguez-López, Angela Johana Espejo-Mojica, Angela Rocío Mosquera-Arévalo, Carlos Javier Alméciga-Díaz, Alba Alicia Trespalacios-Rangel
Publikováno v:
Cryobiology. 105:32-40
The methylotrophic yeast Komagataella phaffii, previously known as Pichia pastoris, has been reported as a host for producing human recombinant lysosomal enzymes intended for enzyme replacement therapy. K. phaffii has advantages such as easy genetic
Autor:
Johana María Guevara Morales, Edwin Alexander Rodríguez López, Olga Yaneth Echeverri Peña, Eugenia Espinosa García, Luis Alejandro Barrera A., Yeny M. Cuellar Fernández
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9bae711c53393e0a71389a07a8c48cf
https://doi.org/10.2307/j.ctv86dgfs.16
https://doi.org/10.2307/j.ctv86dgfs.16
Autor:
Edwin Alexander Rodríguez López, Eugenia Espinosa García, Johana María Guevara Morales, Luis Alejandro Barrera A., Olga Yaneth Echeverri Peña, Yeny M. Cuéllar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88c2dce014764ce865fc934b4bd317ad
https://doi.org/10.2307/j.ctv86dgfs.12
https://doi.org/10.2307/j.ctv86dgfs.12
Autor:
Edwin Alexander Rodríguez López, Eugenia Espinosa García, Johana María Guevara Morales, Luis Alejandro Barrera A., Olga Yaneth Echeverri Peña
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1096b1bf9fc369ab76993465dffe2666
https://doi.org/10.2307/j.ctv86dgfs.17
https://doi.org/10.2307/j.ctv86dgfs.17
Autor:
Juan Camilo Losada Díaz, Jacobo Cepeda del Castillo, Edwin Alexander Rodriguez-López, Carlos J. Alméciga-Díaz
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 1, p 232 (2019)
The mucopolysaccharidoses (MPS) are a group of 11 lysosomal storage diseases (LSDs) produced by mutations in the enzymes involved in the lysosomal catabolism of glycosaminoglycans. Most of the mutations affecting these enzymes may lead to changes in
Externí odkaz:
https://doaj.org/article/eda6ad79323745f799c240cc19a7408a