Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vincent Agrapart"'
Autor:
Aurelie Nguyen Dinh Cat, Brigitte Escoubet, Vincent Agrapart, Violaine Griol-Charhbili, Trenton Schoeb, Wenguang Feng, Edgar Jaimes, David G Warnock, Frederic Jaisser
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e33743 (2012)
Fabry disease is an X-linked disorder of glycosphingolipid metabolism that results in progressive accumulation of neutral glycosphingolipids, (predominately globotriaosylceramide; GL-3) in lysosomes, as well as other cellular compartments and the ext
Externí odkaz:
https://doaj.org/article/bea0ae7dd6704052befae85e8921d938
Autor:
Paolo Renzi, Angelo Zinellu, Irene Guarino, Ciriaco Carru, Andrea Fortuna, Flavia Franconi, Rafael Morales, Giovanni Vanni Frajese, Stefano Vella, Gabriele Campana, Giuseppe Seghieri, Serafina Salvati, Antonella Di Biase, Santi Mario Spampinato, Alberto Loizzo, Gabriella Galietta, Stefano Loizzo, Giovanni Ghirlanda, Stefania Carta, Vincent Agrapart, Anna Capasso
Previously, we showed that our post-natal handling model induces pro-opiomelanocortin-derived (POMC) endogenous systems alterations in male mice at weaning. These alterations last up to adult age, and are at the basis of adult hormonal and metabolic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6af17d37d60386db7a432268da2cba0b
http://hdl.handle.net/11580/15744
http://hdl.handle.net/11580/15744
Autor:
Sabina Luchetti, Giovanni Vanni Frajese, Koen Bossers, Rafael Morales, Dick F. Swaab, Vincent Agrapart, Saskia Van de Bilt
Publikováno v:
Neurobiology of aging, 32(11), 1964-1976. Elsevier Inc.
Neurobiology of Aging, 32, 1964-1976. Elsevier B.V.
Neurobiology of Aging, 32, 1964-1976. Elsevier B.V.
Expression of the genes for enzymes involved in neurosteroid biosynthesis was studied in human prefrontal cortex (PFC) in the course of Alzheimer's disease (AD) (n = 49). Quantitative RT-PCR (qPCR) revealed that mRNA levels of diazepam binding inhibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761cf46cb43b4457264a90b6e14f0e7c
https://pubmed.ncbi.nlm.nih.gov/20045216
https://pubmed.ncbi.nlm.nih.gov/20045216
Autor:
Vincent Agrapart, Frederic Jaisser, Wenguang Feng, Brigitte Escoubet, Violaine Griol-Charhbili, Aurelie Nguyen Dinh Cat, David G. Warnock, Trenton R. Schoeb, Edgar A. Jaimes
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 5, p e33743 (2012)
PLoS ONE, Vol 7, Iss 5, p e33743 (2012)
Fabry disease is an X-linked disorder of glycosphingolipid metabolism that results in progressive accumulation of neutral glycosphingolipids, (predominately globotriaosylceramide; GL-3) in lysosomes, as well as other cellular compartments and the ext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d85eda39be2bd1a1a365f671c4f6c41
https://doi.org/10.1371/journal.pone.0033743
https://doi.org/10.1371/journal.pone.0033743