E-LIB Suche - Ergebnisse für: Smith, Bradley N.

1

Identification of a novel interaction of FUS and syntaphili..:

Salam, Shaakir ; Tacconelli, Sara ; Smith, Bradley N....
Scientific Reports. 11 (2021) 1 - p. , 2021

Link: https://doi.org/10.1038/..

2

SCFD1 expression quantitative trait loci in amyotrophic lat..:

Iacoangeli, Alfredo ; Fogh, Isabella ; Selvackadunco, Sashika...
Brain Communications. 3 (2021) 4 - p. , 2021

Link: https://doi.org/10.1093/..

3

A recessive S174X mutation in Optineurin causes amyotrophic..:

Gotkine, Marc ; de Majo, Martina ; Wong, Chun Hao...
Neurobiology of Aging. 106 (2021) - p. 1-6 , 2021

Link: https://doi.org/10.1016/..

4

CYLD is a causative gene for frontotemporal dementia – amyo..:

Kwok, John B ; Blair, Ian P ; Atkin, Julie D...
Brain. 143 (2020) 3 - p. 783-799 , 2020

Link: https://doi.org/10.1093/..

5

C9orf72 poly GA RAN-translated protein plays a key role in ..:

Lee, Youn-Bok ; Baskaran, Pranetha ; Gomez-Deza, Jorge...
Human Molecular Genetics. 30 (2020) 3-4 - p. 318-320 , 2020

Link: https://doi.org/10.1093/..

6

Publisher Correction: Exome sequencing in amyotrophic later..:

ALSGENS Consortium ; Farhan, Sali M. K. ; Howrigan, Daniel P....
Nature Neuroscience. 23 (2019) 2 - p. 295-295 , 2019

Link: https://doi.org/10.1038/..

7

Exome sequencing in amyotrophic lateral sclerosis implicate..:

ALSGENS Consortium ; Farhan, Sali M. K. ; Howrigan, Daniel P....
Nature Neuroscience. 22 (2019) 12 - p. 1966-1974 , 2019

Link: https://doi.org/10.1038/..

8

Striking phenotypic variation in a family with the P506S UB..:

Gkazi, Soragia Athina ; Troakes, Claire ; Topp, Simon...
Neurobiology of Aging. 73 (2019) - p. 229.e5-229.e9 , 2019

Link: https://doi.org/10.1016/..

9

RRM adjacent TARDBP mutations disrupt RNA binding and enhan..:

Chen, Han-Jou ; Topp, Simon D ; Hui, Ho Sang...
Brain. 142 (2019) 12 - p. 3753-3770 , 2019

Link: https://doi.org/10.1093/..

10

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene:

Nicolas, Aude ; Kenna, Kevin P. ; Renton, Alan E....
Neuron. 97 (2018) 6 - p. 1267-1288 , 2018

Link: https://doi.org/10.1016/..

11

ALS-associated missense and nonsense TBK1 mutations can bot..:

de Majo, Martina ; Topp, Simon D. ; Smith, Bradley N....
Neurobiology of Aging. 71 (2018) - p. 266.e1-266.e10 , 2018

Link: https://doi.org/10.1016/..

12

C9orf72 poly GA RAN-translated protein plays a key role in ..:

Lee, Youn-Bok ; Baskaran, Pranetha ; Gomez-Deza, Jorge...
Human Molecular Genetics. 26 (2017) 24 - p. 4765-4777 , 2017

Link: https://doi.org/10.1093/..

13

Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal T..:

Thomas-Jinu, Swapna ; Gordon, Patricia M. ; Fielding, Triona...
Neuron. 94 (2017) 2 - p. 322-336.e5 , 2017

Link: https://doi.org/10.1016/..

14

C9ORF72 and UBQLN2 mutations are causes of amyotrophic late..:

Scotter, Emma L. ; Smyth, Leon ; Bailey, James W.T....
Neurobiology of Aging. 49 (2017) - p. 214.e1-214.e5 , 2017

Link: https://doi.org/10.1016/..

15

Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal T..:

Thomas-Jinu, Swapna ; Gordon, Patricia M. ; Fielding, Triona...
Neuron. 94 (2017) 4 - p. 931 , 2017

Link: https://doi.org/10.1016/..