Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Karl-F Bergeron"'
Autor:
Karl-F Bergeron, Tatiana Cardinal, Aboubacrine M Touré, Mélanie Béland, Diana L Raiwet, David W Silversides, Nicolas Pilon
Publikováno v:
PLoS Genetics, Vol 11, Iss 3, p e1005093 (2015)
Neural crest cells (NCC) are a transient migratory cell population that generates diverse cell types such as neurons and glia of the enteric nervous system (ENS). Via an insertional mutation screen for loci affecting NCC development in mice, we ident
Externí odkaz:
https://doaj.org/article/08c074bf0c304468956a50af33a16676
Autor:
Julia V. Burnier, Vahé Nerguizian, Catherine Mounier, Ixchel Ocampo, Luz-María Sánchez, Thupten Tsering, Paula G. Font de Rubinat, Ion Stiharu, Rubén R. López, Anas Alazzam, Sergio Camacho-León, Karl-F. Bergeron
Publikováno v:
Langmuir : the ACS journal of surfaces and colloids. 37(28)
Liposomes encapsulate different substances ranging from drugs to genes. Control over the average size and size distribution of these nanoparticles is vital for biomedical applications since these characteristics determine to a high degree where lipos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfb4157f1f168452e2e0bd2a92bab905
https://pubmed.ncbi.nlm.nih.gov/34232664
https://pubmed.ncbi.nlm.nih.gov/34232664
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 330, p 330 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 330, p 330 (2021)
Obesity is an important aspect of the metabolic syndrome and is often associated with chronic inflammation. In this context, inflammation of organs participating in energy homeostasis (such as liver, adipose tissue, muscle and pancreas) leads to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9024db2e257a398419bffaef0cc8428b
http://europepmc.org/articles/PMC7795523
http://europepmc.org/articles/PMC7795523
Publikováno v:
Gene
ApoD is a 25 to 30 kDa glycosylated protein, member of the lipocalin superfamily. As a transporter of several small hydrophobic molecules, its known biological functions are mostly associated to lipid metabolism and neuroprotection. ApoD is a multi-l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df13b56eb284eaf4258a51fe7dbf487d
https://pubmed.ncbi.nlm.nih.gov/32554047
https://pubmed.ncbi.nlm.nih.gov/32554047
Autor:
Denis R. Joanisse, Pascale Mauriège, Catherine Mounier, Frederik Desmarais, Jean Bergeron, Eric Rassart, Simon Biron, Karl-F. Bergeron, Michel Lacaille, Isabelle Lemieux
Publikováno v:
Endocrine. 61:248-257
Apolipoprotein D (ApoD) is a lipocalin participating in lipid transport. It binds to a variety of ligands, with a higher affinity for arachidonic acid, and is thought to have a diverse array of functions. We investigated a potential role for ApoD in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e8786acaa1763b1522fd18b35bce105
https://doi.org/10.1007/s12020-018-1621-5
https://doi.org/10.1007/s12020-018-1621-5
Autor:
Mohamed Amine Lounis, Karl-F. Bergeron, James M. Ntambi, Catherine Mounier, Maggie S. Burhans
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 313:E710-E720
Stearoyl-CoA desaturase-1 (SCD1) is a key player in lipid metabolism. SCD1 catalyzes the synthesis of monounsaturated fatty acids (MUFA). MUFA are then incorporated into triacylglycerols and phospholipids. Previous studies have shown that Scd1 defici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c10eaa9cda669c3a3397ad71c1897876
https://doi.org/10.1152/ajpendo.00151.2017
https://doi.org/10.1152/ajpendo.00151.2017
The causes of the obesity crisis and its comorbidities have been at the center of intensive research for decades. Throughout this time, numerous mechanisms have been found to cause or modulate the progression of these pathologies. Together, they pain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71a7639e4baf6bb7a4d88dfbc039f1ac
https://doi.org/10.1016/b978-0-12-819404-1.00011-7
https://doi.org/10.1016/b978-0-12-819404-1.00011-7
Autor:
Guillaume Fyfe-Desmarais, Catherine Mounier, Karl-F. Bergeron, Vincent Hervé, Frederik Desmarais, Eric Rassart, Morgane Perrotte, Charles Ramassamy, Gaetan Ravaut
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 8
International Journal of Molecular Sciences, Vol 22, Iss 4118, p 4118 (2021)
Volume 22
Issue 8
International Journal of Molecular Sciences, Vol 22, Iss 4118, p 4118 (2021)
Apolipoprotein D (ApoD) is a secreted lipocalin associated with neuroprotection and lipid metabolism. In rodent, the bulk of its expression occurs in the central nervous system. Despite this, ApoD has profound effects in peripheral tissues, indicatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354d08146107851203920c06cb0e105a
https://doi.org/10.3390/ijms22084118
https://doi.org/10.3390/ijms22084118
Autor:
Julia V. Burnier, Vahé Nerguizian, Luz-María Sánchez, Anas Alazzam, Ion Stiharu, Rubén R. López, Paula G. Font de Rubinat, Karl-F. Bergeron, Catherine Mounier, Thupten Tsering
Publikováno v:
Colloids and Surfaces B: Biointerfaces. 198:111447
Liposomes are versatile particles used in the biomedical field as drug delivery systems (DDS). Liposome production using micromixers have shown to yield nanoparticles for DDS in a single step with a controllable size by changing flow conditions. None
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5207ffdcf24a54c12629f7e949bfc742
https://doi.org/10.1016/j.colsurfb.2020.111447
https://doi.org/10.1016/j.colsurfb.2020.111447
Autor:
Sabri Ahmed Rial, Mohamed Amine Lounis, Jessica C. Ralston, Catherine Mounier, Simon Lalonde, David M. Mutch, Karl-F. Bergeron
Publikováno v:
Lipids. 52:129-150
Berardinelli-Seip congenital lipodystrophy (BSCL) is an autosomal recessive disorder. The more severe form, designated BSCL2, arises due to mutations in the BSCL2 gene. Patients with BSCL2, as well as Bscl2 −/− mice, have a near total absence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe6a00f733dfb9a1be2ca362c2aad70
https://doi.org/10.1007/s11745-016-4210-5
https://doi.org/10.1007/s11745-016-4210-5