Laure Chatrousse
Overview
Explore the profile of Laure Chatrousse including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
131
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Recent Articles
1.
Thibaudeau A, Schmitt K, Francois L, Chatrousse L, Hoffmann D, Cousin L, et al.
Transl Psychiatry
. 2024 Jun;
14(1):249.
PMID: 38858349
Phelan-McDermid syndrome (PMDS) arises from mutations in the terminal region of chromosome 22q13, impacting the SHANK3 gene. The resulting deficiency of the postsynaptic density scaffolding protein SHANK3 is associated with...
2.
Chatrousse L, Poullion T, El-Kassar L, Giraud-Triboult K, Boissart C, Sanatine P, et al.
Stem Cell Res
. 2023 Sep;
72:103209.
PMID: 37769384
Phelan-McDermid syndrome (PMS) is a rare genetic disease characterized by a global developmental delay with autism spectrum disorder. PMS is caused by loss of function mutations in the SHANK3 gene...
3.
Boissart C, Lasbareilles M, Tournois J, Chatrousse L, Poullion T, Benchoua A
Front Pharmacol
. 2023 Jul;
14:1152180.
PMID: 37435497
Alteration in the development, maturation, and projection of dopaminergic neurons has been proposed to be associated with several neurological and psychiatric disorders. Therefore, understanding the signals modulating the genesis of...
4.
Boissart C, Chatrousse L, Poullion T, El-Kassar L, Giraud-Triboult K, Benchoua A
Stem Cell Res
. 2023 Jun;
71:103144.
PMID: 37331109
Lesch-Nyhan disease (LND) is a X-linked genetic disease affecting boys characterized by complex neurological and neuropsychiatric symptoms. LND is caused by loss of function mutations in the HPRT1 gene leading...
5.
Ruillier V, Tournois J, Boissart C, Lasbareilles M, Mahe G, Chatrousse L, et al.
JCI Insight
. 2020 Jan;
5(4).
PMID: 31990683
Lesch-Nyhan disease (LND) is a rare monogenic disease caused by deficiency of the salvage pathway enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT). LND is characterized by severe neuropsychiatric symptoms that currently cannot be...
6.
Quartier A, Chatrousse L, Redin C, Keime C, Haumesser N, Maglott-Roth A, et al.
Biol Psychiatry
. 2018 Feb;
84(4):239-252.
PMID: 29428674
Background: Prenatal exposure to androgens during brain development in male individuals may participate to increase their susceptibility to develop neurodevelopmental disorders such as autism spectrum disorder (ASD) and intellectual disability....
7.
Ben MBarek K, Habeler W, Plancheron A, Jarraya M, Regent F, Terray A, et al.
Sci Transl Med
. 2017 Dec;
9(421).
PMID: 29263231
Replacing defective retinal pigment epithelial (RPE) cells with those derived from human embryonic stem cells (hESCs) or human-induced pluripotent stem cells (hiPSCs) is a potential strategy for treating retinal degenerative...
8.
Darville H, Poulet A, Rodet-Amsellem F, Chatrousse L, Pernelle J, Boissart C, et al.
EBioMedicine
. 2016 Jun;
9:293-305.
PMID: 27333044
Autism spectrum disorders affect millions of individuals worldwide, but their heterogeneity complicates therapeutic intervention that is essentially symptomatic. A versatile yet relevant model to rationally screen among hundreds of therapeutic...