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Plos One
|
June 19, 2015
The Transcriptional Effects of PCB118 and PCB153 on the Liver, Adipose Tissue, Muscle and Colon of Mice: Highlighting of Glut4 and Lipin1 as Main Target Genes for PCB Induced Metabolic Disorders
Aurélia Mesnier, Serge Champion, Laurence Louis, et al.
Research and Practice in Thrombosis and Haemostasis
|
February 2, 2026
Selection and optimization strategy for Rap1-targeting single-domain antibodies as platelet activation markers
Marie-Christine Alessi, Maxime Moulard, Daniele Boulay-Moine, et al.
Plos One
|
November 13, 2012
The plasminogen activation system modulates differently adipogenesis and myogenesis of embryonic stem cells
Ola Hadadeh, Emilie Barruet, Franck Peiretti, et al.
Journal of Physiology and Biochemistry
|
February 23, 2024
Sialic acids cleavage induced by elastin-derived peptides impairs the interaction between insulin and its receptor in adipocytes 3T3-L1
Alexandre Guillot, Kevin Toussaint, Lucrece Ebersold, et al.
Orphanet Journal of Rare Diseases
|
May 8, 2015
CMTX1 patients' cells present genomic instability corrected by CamKII inhibitors
Saleh Mones, Burkhardt Gess, Benoit Bordignon, et al.
Journal of Medicinal Chemistry
|
April 3, 2020
Insights into PPARγ Phosphorylation and Its Inhibition Mechanism
Roberta Montanari, Davide Capelli, Keiko Yamamoto, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
January 10, 2022
Involvement of Multiple Variants of Soluble CD146 in Systemic Sclerosis: Identification of a Novel Profibrotic Factor
Marie Nollet, Richard Bachelier, Ahmad Joshkon, et al.
Cardiovascular Research
|
May 13, 2016
Soluble CD146 boosts therapeutic effect of endothelial progenitors through proteolytic processing of short CD146 isoform
Jimmy Stalin, Karim Harhouri, Lucas Hubert, et al.
Plos Genetics
|
January 19, 2021
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant
Pierre-Emmanuel Morange, Franck Peiretti, Lenaick Gourhant, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 1, 2021
GATA1 pathogenic variants disrupt MYH10 silencing during megakaryopoiesis
Paul Saultier, Sandrine Cabantous, Michel Puceat, et al.
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of 7
Search research articles
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Showing results (51-60 of 65) with videos related to
Sort By:
Page
of 7
Plos One
|
June 19, 2015
The Transcriptional Effects of PCB118 and PCB153 on the Liver, Adipose Tissue, Muscle and Colon of Mice: Highlighting of Glut4 and Lipin1 as Main Target Genes for PCB Induced Metabolic Disorders
Aurélia Mesnier, Serge Champion, Laurence Louis, et al.
Research and Practice in Thrombosis and Haemostasis
|
February 2, 2026
Selection and optimization strategy for Rap1-targeting single-domain antibodies as platelet activation markers
Marie-Christine Alessi, Maxime Moulard, Daniele Boulay-Moine, et al.
Plos One
|
November 13, 2012
The plasminogen activation system modulates differently adipogenesis and myogenesis of embryonic stem cells
Ola Hadadeh, Emilie Barruet, Franck Peiretti, et al.
Journal of Physiology and Biochemistry
|
February 23, 2024
Sialic acids cleavage induced by elastin-derived peptides impairs the interaction between insulin and its receptor in adipocytes 3T3-L1
Alexandre Guillot, Kevin Toussaint, Lucrece Ebersold, et al.
Orphanet Journal of Rare Diseases
|
May 8, 2015
CMTX1 patients' cells present genomic instability corrected by CamKII inhibitors
Saleh Mones, Burkhardt Gess, Benoit Bordignon, et al.
Journal of Medicinal Chemistry
|
April 3, 2020
Insights into PPARγ Phosphorylation and Its Inhibition Mechanism
Roberta Montanari, Davide Capelli, Keiko Yamamoto, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
January 10, 2022
Involvement of Multiple Variants of Soluble CD146 in Systemic Sclerosis: Identification of a Novel Profibrotic Factor
Marie Nollet, Richard Bachelier, Ahmad Joshkon, et al.
Cardiovascular Research
|
May 13, 2016
Soluble CD146 boosts therapeutic effect of endothelial progenitors through proteolytic processing of short CD146 isoform
Jimmy Stalin, Karim Harhouri, Lucas Hubert, et al.
Plos Genetics
|
January 19, 2021
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant
Pierre-Emmanuel Morange, Franck Peiretti, Lenaick Gourhant, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 1, 2021
GATA1 pathogenic variants disrupt MYH10 silencing during megakaryopoiesis
Paul Saultier, Sandrine Cabantous, Michel Puceat, et al.
Page
of 7