Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Santiago Figueroa Perez"'
Autor:
Stuart J. Pocock, Alexander R. Lyon, Daniel M. Bloomfield, Amany El-Gazayerly, Claudio Gimpelewicz, Faiez Zannad, Piotr Ponikowski, Warren Sherman, Fady I. Malik, Wendy Gattis Stough, Marco Metra, Anna Baczynska, Krishna Prasad, Karsten Bruins Slot, Caroline Boulton, Jose Lopez-Sendon, Pieter A. de Graeff, Maureen Cronin, Ian Laws, Isabelle Richard-Lordereau, Benoit Tyl, Karl Swedberg, Stefan D. Anker, Salim Janmohamed, Gerasimos Filippatos, Martin R. Cowie, Lothar Roessig, Heidi Janssen, Santiago Figueroa Perez, Martin Lefkowitz, Pieter A. Doevendans, Marc A. Pfeffer, Giuseppe M.C. Rosano, Narimon Honarpour, Maria Borentain, Albert M. Kim, Maria Angeles Alonso Garcia, John J.V. McMurray, Dominik Lautsch
Publikováno v:
European Journal of Heart Failure. 19:718-727
Despite the availability of a number of different classes of therapeutic agents with proven efficacy in heart failure, the clinical course of heart failure patients is characterized by a reduction in life expectancy, a progressive decline in health-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8f01ad99121884291aec9c2fad3ab50
https://doi.org/10.1002/ejhf.809
https://doi.org/10.1002/ejhf.809
Publikováno v:
Carbohydrate Research. 328:95-102
A highly convergent synthetic approach was developed to obtain α-galactosyl cerebroside O-(α- d -galactopyranosyl)-2-hexacosylamino- d -ribo-1,3,4-octadecantriol, which has previously been demonstrated to have immunostimulatory activity. Known 4,6-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64d5481dfc79849c348ce16b706edd7a
https://doi.org/10.1016/s0008-6215(00)00092-6
https://doi.org/10.1016/s0008-6215(00)00092-6
Publikováno v:
Journal of Carbohydrate Chemistry. 17:835-850
5-Azido-3-oxa-l-pentanol was prepared from 2-(2-chloroethoxy)ethanol and used as a spacer in the chemical synthesis of the trisaccharide β-D-Gal-(1→4)-[α-L-Fuc-(1→3)]-GlcNAc and the tetrasaccharide α-L-Fuc-α-(1→2)-β-D-Gal-(1→4)-[α-L-Fuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5abc58239b35c1090af0b22caa231ea4
https://doi.org/10.1080/07328309808007459
https://doi.org/10.1080/07328309808007459
Publikováno v:
Glycoconjugate Journal. 15:251-263
Clusters of di-, tri-, and tetra-antennary α-D-mannopyranosides were synthesized in good yields based on the coupling of amine-bearing mono- or trisaccharide {Man α(1→6)[Man α(1→3)]Man} haptens to poly-isocyanate or -isothiocyanate tethering c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f83bdc228299bdd1352fde50b34696cb
https://doi.org/10.1023/a:1006945028547
https://doi.org/10.1023/a:1006945028547
Autor:
Thomas Heinemann, Santiago Figueroa-Perez, Barbara Schnieders, Sven Nätzker, Richard R. Schmidt, Gerhild van Echten-Deckert, Konrad Sandhoff
Publikováno v:
Biological Chemistry. 383
Intracellular phosphorylation of cis-4-methylsphingosine was previously shown to result in a metabolically stable compound that accumulates in Swiss 3T3 fibroblasts and mimics the mitogenic effect induced by the short-lived sphingosine metabolite, sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aacab9854a72586e6b57dcb92fe17e6b
https://doi.org/10.1515/bc.2002.212
https://doi.org/10.1515/bc.2002.212
Publikováno v:
ChemInform. 32
A highly convergent synthetic approach was developed to obtain α-galactosyl cerebroside O-(α- d -galactopyranosyl)-2-hexacosylamino- d -ribo-1,3,4-octadecantriol, which has previously been demonstrated to have immunostimulatory activity. Known 4,6-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae5425f4532554e07a6895b5e318f101
https://doi.org/10.1002/chin.200101222
https://doi.org/10.1002/chin.200101222