Remy Bordonne
Montpellier, France
Last Updated: 09/26/2026
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Found 16 publications
B-cell immune deficiency in twin sisters expands the phenotype of MOPDI.
Journal: Clinical genetics
Published: February 26, 2024
Deficiency of the minor spliceosome component U4atac snRNA secondarily results in ciliary defects in human and zebrafish.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: February 21, 2023
Mutations in the non-coding RNU4ATAC gene affect the homeostasis and function of the Integrator complex.
Journal: Nucleic acids research
Published: March 15, 2022
Identification and structural analysis of the Schizosaccharomyces pombe SMN complex.
Journal: Nucleic acids research
Published: January 13, 2021
Splicing efficiency of minor introns in a mouse model of SMA predominantly depends on their branchpoint sequence and can involve the contribution of major spliceosome components.
Journal: RNA (New York, N.Y.)
Published: November 09, 2020
Splicing Defects of the Profilin Gene Alter Actin Dynamics in an S. pombe SMN Mutant.
Journal: iScience
Published: April 03, 2019
A new cis-acting motif is required for the axonal SMN-dependent Anxa2 mRNA localization.
Journal: RNA (New York, N.Y.)
Published: January 24, 2017
Disruption of snRNP biogenesis factors Tgs1 and pICln induces phenotypes that mirror aspects of SMN-Gemins complex perturbation in Drosophila, providing new insights into spinal muscular atrophy.
Journal: Neurobiology of disease
Published: October 26, 2015
Genetic Interactions between the Members of the SMN-Gemins Complex in Drosophila.
Journal: PloS one
Published: April 01, 2015
Last Updated: 09/26/2026