Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Raquel Gordo-Gilart"'
Autor:
Bernardo Frider, Amalia Castillo, Raquel Gordo-Gilart, Andrés Bruno, Marcelo Amante, Luis Alvarez, Verónica Mathet
Publikováno v:
Annals of Hepatology, Vol 14, Iss 5, Pp 745-751 (2015)
Introduction. Progressive familial intrahepatic cholestasis type 3 (PFIC-3) is a severe liver disorder associated with inherited dysfunction of multidrug resistance protein 3 (MDR3/ABCB4), which functions as a phospholipid floppase, translocating pho
Externí odkaz:
https://doaj.org/article/55e78ab0a46f4361ab5210d9411349cf
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0150098 (2016)
Multidrug resistance protein 3 (MDR3, ABCB4) is a hepatocellular membrane protein that mediates biliary secretion of phosphatidylcholine. Null mutations in ABCB4 gene give rise to severe early-onset cholestatic liver disease. We have previously shown
Externí odkaz:
https://doaj.org/article/e767ed31b5294b62b8bce7b3ffbcf785
Autor:
C. Díaz, Sara Andueza, Loreto Hierro, Carola López, Raquel Gordo-Gilart, Luis Alvarez, Paloma Jara, Gema Muñoz-Bartolo
Publikováno v:
Liver International. 36:258-267
Background & Aims Monoallelic defects in ABCB4, which encodes the canalicular floppase for phosphatidylcholine MDR3, have been encountered in association with a variety of hepatobiliary disorders, particularly in adult subjects. In this study, we exa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66cde2f7f742e7ddd9c1ea4379f3d578
https://doi.org/10.1111/liv.12910
https://doi.org/10.1111/liv.12910
Autor:
Luis Alvarez, Daniel D'Agostino, Sara Andueza, Raquel Gordo-Gilart, Pilar Martínez-Fernández, Paloma Jara, Loreto Hierro
Publikováno v:
Gut. 64:147-155
Objective Progressive familial intrahepatic cholestasis type 3 (PFIC3) is a potentially lethal autosomal recessive liver disease associated with mutations in ABCB4 , the gene encoding the canalicular translocator of phosphatidylcholine MDR3. While so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e8b8f31397f253a01d7d6fc9948e3e4
https://doi.org/10.1136/gutjnl-2014-306896
https://doi.org/10.1136/gutjnl-2014-306896
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0150098 (2016)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS ONE
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS ONE
Multidrug resistance protein 3 (MDR3, ABCB4) is a hepatocellular membrane protein that mediates biliary secretion of phosphatidylcholine. Null mutations in ABCB4 gene give rise to severe early-onset cholestatic liver disease. We have previously shown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cfda31a08bd22865a2ee6c7a25eef14
http://europepmc.org/articles/PMC4764328?pdf=render
http://europepmc.org/articles/PMC4764328?pdf=render
Autor:
Veronica Lidia Mathet, Luis Alvarez, Amalia Inés Castillo, Marcelo Amante, Bernardo Frider, Raquel Gordo-Gilart, Andrés Bruno
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Annals of Hepatology, Vol 14, Iss 5, Pp 745-751 (2015)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Annals of Hepatology, Vol 14, Iss 5, Pp 745-751 (2015)
Introduction. Progressive familial intrahepatic cholestasis type 3 (PFIC-3) is a severe liver disorder associated with inherited dysfunction of multidrug resistance protein 3 (MDR3/ABCB4), which functions as a phospholipid floppase, translocating pho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a5f0d15c536d4b3a034c3b41a1243f
https://annalsofhepatology.publisherspanel.com/resources/html/article/details?id=127509&language=en
https://annalsofhepatology.publisherspanel.com/resources/html/article/details?id=127509&language=en
