Johann Soret
Overview
Explore the profile of Johann Soret including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
553
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0
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Recent Articles
1.
Jacquier V, Prevot M, Gostan T, Bordonne R, Benkhelifa-Ziyyat S, Barkats M, et al.
RNA
. 2021 Dec;
28(3):303-319.
PMID: 34893560
Spinal muscular atrophy (SMA) is a devastating neurodegenerative disease caused by reduced amounts of the ubiquitously expressed Survival of Motor Neuron (SMN) protein. In agreement with its crucial role in...
2.
Antoine M, Patrick K, Soret J, Duc P, Rage F, Cacciottolo R, et al.
iScience
. 2020 Jan;
23(1):100809.
PMID: 31927482
Spinal muscular atrophy (SMA) is a devastating motor neuron disorder caused by mutations in the survival motor neuron (SMN) gene. It remains unclear how SMN deficiency leads to the loss...
3.
Rihan K, Antoine E, Maurin T, Bardoni B, Bordonne R, Soret J, et al.
RNA
. 2017 Mar;
23(6):899-909.
PMID: 28258160
Spinal muscular atrophy (SMA) is caused by mutations and/or deletions of the survival motor neuron gene (). Besides its function in the biogenesis of spliceosomal snRNPs, SMN might possess a...
4.
Barbarossa A, Antoine E, Neel H, Gostan T, Soret J, Bordonne R
Mol Cell Biol
. 2013 Dec;
34(4):595-605.
PMID: 24298023
During the early steps of snRNP biogenesis, the survival motor neuron (SMN) complex acts together with the methylosome, an entity formed by the pICln protein, WD45, and the PRMT5 methyltransferase....
5.
Rage F, Boulisfane N, Rihan K, Neel H, Gostan T, Bertrand E, et al.
RNA
. 2013 Oct;
19(12):1755-66.
PMID: 24152552
Spinal muscular atrophy is a neuromuscular disease resulting from mutations in the SMN1 gene, which encodes the survival motor neuron (SMN) protein. SMN is part of a large complex that...
6.
Piazzon N, Schlotter F, Lefebvre S, Dodre M, Mereau A, Soret J, et al.
Nucleic Acids Res
. 2012 Dec;
41(2):1255-72.
PMID: 23221635
Spinal muscular atrophy is a severe motor neuron disease caused by reduced levels of the ubiquitous Survival of MotoNeurons (SMN) protein. SMN is part of a complex that is essential...
7.
Boulisfane N, Choleza M, Rage F, Neel H, Soret J, Bordonne R
Hum Mol Genet
. 2010 Nov;
20(4):641-8.
PMID: 21098506
The survival of motor neuron (SMN) protein is essential for cytoplasmic assembly of spliceosomal snRNPs. Although the normal proportion of endogenous snRNAs is unevenly altered in spinal muscular atrophy (SMA)...
8.
Campion Y, Neel H, Gostan T, Soret J, Bordonne R
EMBO J
. 2010 Apr;
29(11):1817-29.
PMID: 20400941
Spinal muscular atrophy results from deletions or mutations in the survival of motor neuron (SMN1) gene. The SMN protein has an essential role in the biogenesis of spliceosomal snRNPs, but...
9.
Tournier I, Vezain M, Martins A, Charbonnier F, Baert-Desurmont S, Olschwang S, et al.
Hum Mutat
. 2008 Jun;
29(12):1412-24.
PMID: 18561205
Numerous unclassified variants (UVs) have been found in the mismatch repair genes MLH1 and MSH2 involved in hereditary nonpolyposis colorectal cancer (HNPCC or Lynch syndrome). Some of these variants may...
10.
Girard C, Verheggen C, Neel H, Cammas A, Vagner S, Soret J, et al.
J Biol Chem
. 2007 Nov;
283(4):2060-9.
PMID: 18039666
Tgs1 is the hypermethylase responsible for m(3)G cap formation of U small nuclear RNAs (U snRNAs) and small nucleolar RNAs (snoRNAs). In vertebrates, hypermethylation of snRNAs occurs in the cytoplasm,...