Valerie Risson
Overview
Explore the profile of Valerie Risson including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
511
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Recent Articles
1.
Halegua T, Risson V, Carras J, Rouyer M, Coudert L, Jacquier A, et al.
Nat Commun
. 2025 Jan;
16(1):397.
PMID: 39755699
Prime Editing can rewrite genes in living cells by allowing point mutations, deletions, or insertion of small DNA sequences with high precision. However, its safe and efficient delivery into human...
2.
Mouradian S, Cicciarello D, Lacoste N, Risson V, Berretta F, Le Grand F, et al.
Nucleic Acids Res
. 2024 Feb;
52(7):3667-3681.
PMID: 38321961
The Wnt/β-Catenin pathway plays a key role in cell fate determination during development and in adult tissue regeneration by stem cells. These processes involve profound gene expression and epigenome remodeling...
3.
Jacquier A, Theuriet J, Fontaine F, Mosbach V, Lacoste N, Ribault S, et al.
Brain
. 2022 Dec;
146(8):3470-3483.
PMID: 36454683
Distal hereditary motor neuropathy represents a group of motor inherited neuropathies leading to distal weakness. We report a family of two brothers and a sister affected by distal hereditary motor...
4.
Jacquier A, Risson V, Simonet T, Roussange F, Lacoste N, Ribault S, et al.
Acta Neuropathol
. 2022 Aug;
144(4):707-731.
PMID: 35948834
Congenital myasthenic syndromes (CMS) are predominantly characterized by muscle weakness and fatigability and can be caused by a variety of mutations in genes required for neuromuscular junction formation and maintenance....
5.
Jacquier A, Ribault S, Mendes M, Lacoste N, Risson V, Carras J, et al.
Hum Mutat
. 2022 Jul;
43(12):1898-1908.
PMID: 35904125
MORC2 gene encodes a ubiquitously expressed nuclear protein involved in chromatin remodeling, DNA repair, and transcriptional regulation. Heterozygous mutations in MORC2 gene have been associated with a spectrum of disorders...
6.
Pucci S, Bolchi C, Bavo F, Pallavicini M, De Palma C, Renzi M, et al.
Pharmacol Res
. 2021 Nov;
175:105959.
PMID: 34756924
Glioblastomas (GBMs), the most frequent brain tumours, are highly invasive and their prognosis is still poor despite the use of combination treatment. MG624 is a 4-oxystilbene derivative that is active...
7.
Ghasemizadeh A, Christin E, Guiraud A, Couturier N, Abitbol M, Risson V, et al.
Elife
. 2021 Aug;
10.
PMID: 34448452
Skeletal muscles are composed of hundreds of multinucleated muscle fibers (myofibers) whose myonuclei are regularly positioned all along the myofiber's periphery except the few ones clustered underneath the neuromuscular junction...
8.
Jacquier A, Risson V, Schaeffer L
J Vis Exp
. 2019 Jan;
(143).
PMID: 30663652
Neurodegeneration of spinal motoneurons (MNs) is implicated in a large spectrum of neurological disorders including amyotrophic lateral sclerosis, Charcot-Marie-Tooth disease, and spinal muscular atrophy, which are all associated with muscular...
9.
Mangeot P, Risson V, Fusil F, Marnef A, Laurent E, Blin J, et al.
Nat Commun
. 2019 Jan;
10(1):45.
PMID: 30604748
Programmable nucleases have enabled rapid and accessible genome engineering in eukaryotic cells and living organisms. However, their delivery into target cells can be technically challenging when working with primary cells...
10.
Vernay A, Therreau L, Blot B, Risson V, Dirrig-Grosch S, Waegaert R, et al.
Hum Mol Genet
. 2016 Jun;
25(15):3341-3360.
PMID: 27329763
Mutations in the charged multivesicular body protein 2B (CHMP2B) are associated with frontotemporal dementia (FTD), amyotrophic lateral sclerosis (ALS), and with a mixed ALS-FTD syndrome. To model this syndrome, we...