Annie Michaud
Overview
Explore the profile of Annie Michaud including associated specialties, affiliations and a list of published articles.
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Articles
29
Citations
743
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Recent Articles
1.
Gubler M, Gribouval O, Antignac C, Michaud A, Corvol P
Bull Acad Natl Med
. 2015 Aug;
198(2):339-48.
PMID: 26263708
Renal tubular dysgenesis is a severe disease characterized by the absence of differentiated proximal tubules, leading to fetal anuria and persistent oligohydramnios. The absence of amniotic fluid results in a...
2.
Michaud A, Acharya K, Masuyer G, Quenechdu N, Gribouval O, Moriniere V, et al.
Hum Mol Genet
. 2013 Oct;
23(6):1479-91.
PMID: 24163131
Renal tubular dysgenesis (RTD) is a recessive autosomal disease characterized most often by perinatal death. It is due to the inactivation of any of the major genes of the renin-angiotensin...
3.
Marc Y, Gao J, Balavoine F, Michaud A, Roques B, Llorens-Cortes C
Hypertension
. 2012 Jun;
60(2):411-8.
PMID: 22710644
Brain renin-angiotensin system hyperactivity has been implicated in the development and maintenance of hypertension. We reported previously in the brain that aminopeptidase A and aminopeptidase N are involved in the...
4.
Charrier E, Cordeiro P, Cordeau M, Dardari R, Michaud A, Harnois M, et al.
Cell Immunol
. 2012 May;
276(1-2):114-21.
PMID: 22578600
Plasmacytoid dendritic cells (PDCs) from human umbilical cord blood (UCB) produce lower amounts of IFN-α upon TLR stimulation compared with adult counterparts. This difference may play a role in the...
5.
Gribouval O, Moriniere V, Pawtowski A, Arrondel C, Sallinen S, Saloranta C, et al.
Hum Mutat
. 2011 Nov;
33(2):316-26.
PMID: 22095942
Autosomal recessive renal tubular dysgenesis (RTD) is a severe disorder of renal tubular development characterized by early onset and persistent fetal anuria leading to oligohydramnios and the Potter sequence, associated...
6.
Koch A, Mathivet T, Larrivee B, Tong R, Kowalski J, Pibouin-Fragner L, et al.
Dev Cell
. 2011 Jan;
20(1):33-46.
PMID: 21238923
Robo4 is an endothelial cell-specific member of the Roundabout axon guidance receptor family. To identify Robo4 binding partners, we performed a protein-protein interaction screen with the Robo4 extracellular domain. We...
7.
Michaud A, Bur D, Gribouval O, Muller L, Iturrioz X, Clemessy M, et al.
Hum Mol Genet
. 2010 Nov;
20(2):301-11.
PMID: 21036942
Renal tubular dysgenesis (RTD) is a recessive autosomal disease characterized by persistent fetal anuria and perinatal death. During the systematic screening of mutations of the different genes of the renin-angiotensin...
8.
Doucet M, Dube A, Joanisse D, Debigare R, Michaud A, Pare M, et al.
Thorax
. 2010 Oct;
65(11):963-70.
PMID: 20965933
Background: Factors involved in the regulation of muscle mass in chronic obstructive pulmonary disease (COPD) are still poorly understood. Comparing the signalisation involved in muscle mass regulation between two muscles...
9.
Michaud A, Dardari R, Charrier E, Cordeiro P, Herblot S, Duval M
J Immunother
. 2010 Apr;
33(4):382-90.
PMID: 20386468
Lymphoid differentiation and activation critically depend on cytokine stimulation and the interleukin-7 (IL-7) signaling in particular. Although it has been demonstrated that IL-7 may play a role in natural killer...
10.
Debigare R, Maltais F, Cote C, Michaud A, Caron M, Mofarrahi M, et al.
COPD
. 2008 Apr;
5(2):75-84.
PMID: 18415806
Peripheral muscle wasting is a feature of chronic obstructive pulmonary disease (COPD). Potent therapeutic strategies are needed to improve peripheral muscle mass in these patients. We hypothesized that the evaluation...