Alexandra Benchoua
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Explore the profile of Alexandra Benchoua including associated specialties, affiliations and a list of published articles.
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33
Citations
691
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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.
Willis C, Calvaruso M, Angeloni D, Baatout S, Benchoua A, Bereiter-Hahn J, et al.
NPJ Microgravity
. 2024 May;
10(1):50.
PMID: 38693246
Periodically, the European Space Agency (ESA) updates scientific roadmaps in consultation with the scientific community. The ESA SciSpacE Science Community White Paper (SSCWP) 9, "Biology in Space and Analogue Environments",...
3.
Cochet M, Piumi F, Gorna K, Berry N, Gonzalez G, Danckaert A, et al.
Vet Res
. 2024 Mar;
55(1):32.
PMID: 38493182
Outbreaks of West Nile virus (WNV) occur periodically, affecting both human and equine populations. There are no vaccines for humans, and those commercialised for horses do not have sufficient coverage....
4.
Davis T, Tabury K, Zhu S, Angeloni D, Baatout S, Benchoua A, et al.
NPJ Microgravity
. 2024 Feb;
10(1):16.
PMID: 38341423
Progress in mechanobiology allowed us to better understand the important role of mechanical forces in the regulation of biological processes. Space research in the field of life sciences clearly showed...
5.
Cialdai F, Brown A, Baumann C, Angeloni D, Baatout S, Benchoua A, et al.
NPJ Microgravity
. 2023 Oct;
9(1):84.
PMID: 37865644
The present white paper concerns the indications and recommendations of the SciSpacE Science Community to make progress in filling the gaps of knowledge that prevent us from answering the question:...
6.
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...
7.
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...
8.
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...
9.
Bergamelli M, Martin H, Aubert Y, Mansuy J, Marcellin M, Burlet-Schiltz O, et al.
Viruses
. 2022 Sep;
14(9).
PMID: 36146834
Although placental small extracellular vesicles (sEVs) are extensively studied in the context of pregnancy, little is known about their role during viral congenital infection, especially at the beginning of pregnancy....
10.
Benchoua A, Lasbareilles M, Tournois J
Cells
. 2021 Dec;
10(12).
PMID: 34943799
One of the major obstacles to the identification of therapeutic interventions for central nervous system disorders has been the difficulty in studying the step-by-step progression of diseases in neuronal networks...