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Search results (28)

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myotrophic lateral sclerosis caused by TARDBP mutations: from genetics to TDP-43 proteinopathy.

Balendra R. et al, (2025), The Lancet. Neurology, 24, 456 - 470

xonal RNA localization is essential for long-term memory.

de Queiroz BR. et al, (2025), Nature communications, 16

Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A.

Brown A-L. et al, (2024), Nature, 631

Mis-spliced transcripts generate de novo proteins in TDP-43-related ALS/FTD.

Seddighi S. et al, (2024), Science translational medicine, 16

Transcriptome-wide RNA binding analysis of C9orf72 poly(PR) dipeptides.

Balendra R. et al, (2023), Life science alliance, 6

TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A.

Brown A-L. et al, (2022), Nature, 603, 131 - 137

Genome-wide RNA binding analysis ofC9orf72poly(PR) dipeptides

Balendra R. et al, (2022)

TDP-43 condensation properties specify its RNA-binding and regulatory repertoire.

Hallegger M. et al, (2021), Cell, 184, 4680 - 4696.e22

psiCLIP reveals dynamic RNA binding by DEAH-box helicases before and after exon ligation.

Strittmatter LM. et al, (2021), Nature communications, 12

TDP-43 condensation properties specify its RNA binding and regulation

Hallegger M. et al, (2021), FEBS OPEN BIO, 11, 17 - 18

PsiCLIP reveals dynamic RNA binding by DEAH-box helicases before and after exon ligation

Strittmatter L. et al, (2020)

Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.

Fratta P. et al, (2018), The EMBO journal, 37

High-Resolution RNA Maps Suggest Common Principles of Splicing and Polyadenylation Regulation by TDP-43.

Rot G. et al, (2017), Cell reports, 19, 1056 - 1067

The alternative splicing program of differentiated smooth muscle cells involves concerted non-productive splicing of post-transcriptional regulators.

Llorian M. et al, (2016), Nucleic acids research, 44, 8933 - 8950

Regulation of constitutive and alternative mRNA splicing across the human transcriptome by PRPF8 is determined by 5' splice site strength.

Wickramasinghe VO. et al, (2015), Genome biology, 16

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