Sam Bryce-Smith
Overview
Explore the profile of Sam Bryce-Smith including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
167
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0
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Recent Articles
1.
Brown A, Wilkins O, Keuss M, Hill S, Zanovello M, Lee W, et al.
Nature
. 2024 Jun;
631(8020):E7.
PMID: 38890465
No abstract available.
2.
Bryce-Smith S, Brown A, Mehta P, Mattedi F, Mikheenko A, Barattucci S, et al.
bioRxiv
. 2024 Feb;
PMID: 38313254
Nuclear depletion and cytoplasmic aggregation of the RNA-binding protein TDP-43 is the hallmark of ALS, occurring in over 97% of cases. A key consequence of TDP-43 nuclear loss is the...
3.
Bryce-Smith S, Burri D, Gazzara M, Herrmann C, Danecka W, Fitzsimmons C, et al.
RNA
. 2023 Oct;
29(12):1839-1855.
PMID: 37816550
The tremendous rate with which data is generated and analysis methods emerge makes it increasingly difficult to keep track of their domain of applicability, assumptions, limitations, and consequently, of the...
4.
Bryce-Smith S, Burri D, Gazzara M, Herrmann C, Danecka W, Fitzsimmons C, et al.
bioRxiv
. 2023 Jul;
PMID: 37425672
The tremendous rate with which data is generated and analysis methods emerge makes it increasingly difficult to keep track of their domain of applicability, assumptions, and limitations and consequently, of...
5.
Devoy A, Price G, De Giorgio F, Bunton-Stasyshyn R, Thompson D, Gasco S, et al.
iScience
. 2022 Mar;
25(4):103999.
PMID: 35296030
[This corrects the article DOI: 10.1016/j.isci.2021.103463.].
6.
Brown A, Wilkins O, Keuss M, Hill S, Zanovello M, Lee W, et al.
Nature
. 2022 Feb;
603(7899):131-137.
PMID: 35197628
Variants of UNC13A, a critical gene for synapse function, increase the risk of amyotrophic lateral sclerosis and frontotemporal dementia, two related neurodegenerative diseases defined by mislocalization of the RNA-binding protein...
7.
Devoy A, Price G, De Giorgio F, Bunton-Stasyshyn R, Thompson D, Gasco S, et al.
iScience
. 2022 Jan;
24(12):103463.
PMID: 34988393
Amyotrophic lateral sclerosis/frontotemporal dementia (ALS/FTD) is a fatal neurodegenerative disorder, and continued innovation is needed for improved understanding and for developing therapeutics. We have created next-generation knockin mouse models, by...