Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Juan C. de Karam"'
Autor:
Mario Mellado, Juan C. de Karam, Félix M. Goñi, Rosa Ana Lacalle, Ibai Artetxe, Jesús Sot, Ana M. Rojas, Laura Martínez-Muñoz, Rosa M. Peregil, Santos Mañes
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Type I phosphatidylinositol 4-phosphate 5-kinases (PIP5KIs; α, β, and γ) are a family of isoenzymes that produce phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2] using phosphatidylinositol 4-phosphate as substrate. Their structural homology with
Autor:
Tatiane P. Sudbrack, María E. Lanio, Carlos Alvarez, Uris Ros, Juan C. de Karam, Diana Martinez, Daylin Diaz, Rosangela Itri, Pedro A. Valiente, Shirley Schreier, Lohans Pedrera, Fabiola Pazos, Eduardo Maffud Cilli
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
The sea anemone Stichodactyla helianthus produces two pore-forming proteins, sticholysins I and II (St I and St II). Despite their high identity (93%), these toxins exhibit differences in hemolytic activity that can be related to those found in their
Autor:
María Teresa Echeverría Arnedo, Mónica Ramos, Paulino Gómez-Puertas, Jan-Jaap Wesselink, Sebastián Menao, Beatriz Puisac, Juan Pié, Ignacio Gimenez, Fausto G. Hegardt, Angeles Pié, Juan C. de Karam, María Concepción Gil-Rodríguez, Feliciano J. Ramos, Núria Casals, María Esperanza Teresa-Rodrigo
Publikováno v:
Molecular Biology Reports; Vol 39
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
The genes HMGCS2 and HMGCL encode the two main enzymes for ketone-body synthesis, mitochondrial HMG-CoA synthase and HMG-CoA lyase. Here, we identify and describe possible splice variants of these genes in human tissues. We detected an alternative tr
Autor:
Eduardo López-Viñas, Beatriz Puisac, Antonio Baldellou, Fausto G. Hegardt, Matthew A. Deardorff, Jesús Legarreta, Juan C. de Karam, Ian D. Krantz, Juan Pié, Milagros Ciero, Inés Bueno, María Concepción Gil-Rodríguez, María Teresa Echeverría Arnedo, Encarnación Rubio, Feliciano J. Ramos, Ana Losada, Paulino Gómez-Puertas, Núria Casals, María Pilar Ribate, Mª Teresa Calvo, José L. Olivares
Cornelia de Lange syndrome (CdLS) manifests facial dysmorphic features, growth and cognitive impairment, and limb malformations. Mutations in three genes (NIPBL, SMC1A, and SMC3) of the cohesin complex and its regulators have been found in affected p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2441c0ea76af1bde9e629e8d71925d29
https://europepmc.org/articles/PMC2923429/
https://europepmc.org/articles/PMC2923429/