(Q35641365)

9 August 2017

title

A yeast functional screen predicts new candidate ALS disease genes (English)

1 reference

amyotrophic lateral sclerosis

9 August 2017

main subject

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based on heuristic

inferred from title

corrigendum / erratum

Correction for Couthouis et al., A yeast functional screen predicts new candidate ALS disease genes

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author

Dennis W. Dickson

23

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Mariely DeJesus-Hernandez

9 August 2017

4

Mariely DeJesus-Hernandez

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Fadia Ibrahim

Fadia Ibrahim

15

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Caroline Ingre

Caroline Ingre

20

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Julien Couthouis

Julien Couthouis

1

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Katie M. Williams

Kelly L Williams

18

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Jennifer A. Fifita

Jennifer A Solski

17

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Zissimos Mourelatos

Zissimos Mourelatos

40

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James Shorter

James Shorter

3

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John Q. Trojanowski

30

John Q Trojanowski

1 reference

9 August 2017

39

Rosa Rademakers

1 reference

9 August 2017

31

Albert Ludolph

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9 August 2017

32

Wim Robberecht

1 reference

9 August 2017

33

Peter M Andersen

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9 August 2017

36

Oliver D King

1 reference

9 August 2017

Neill R Graff-Radford

22

Neill R Graff-Radford

1 reference

9 August 2017

35

Ian P Blair

1 reference

9 August 2017

21

Kevin Boylan

1 reference

9 August 2017

25

Lauren Elman

1 reference

9 August 2017

Vivianna M Van Deerlin

38

Vivianna Van Deerlin

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9 August 2017

41

Aaron D Gitler

1 reference

9 August 2017

37

Nancy M Bonini

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9 August 2017

26

Leo McCluskey

1 reference

9 August 2017

13

Zamia Diaz

1 reference

9 August 2017

Michael P Hart

2

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9 August 2017

Renske Erion

5

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9 August 2017

Rachel Oristano

6

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9 August 2017

Annie X Liu

7

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9 August 2017

Daniel Ramos

8

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9 August 2017

Niti Jethava

9

1 reference

9 August 2017

Divya Hosangadi

10

1 reference

9 August 2017

James Epstein

11

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9 August 2017

Ashley Chiang

12

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9 August 2017

Tadashi Nakaya

14

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9 August 2017

Hyung-Jun Kim

16

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9 August 2017

Jelena Mojsilovic-Petrovic

19

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9 August 2017

Dana Clay-Falcone

24

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9 August 2017

Robert Greene

27

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9 August 2017

Robert G Kalb

28

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9 August 2017

Virginia M-Y Lee

29

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9 August 2017

Garth A Nicholson

34

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9 August 2017

language of work or name

English

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publication date

7 November 2011

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Proceedings of the National Academy of Sciences of the United States of America

9 August 2017

published in

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9 August 2017

volume

108

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9 August 2017

issue

52

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9 August 2017

page(s)

20881-20890

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The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span.

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

12 July 2018

1 reference

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RNA-binding proteins with prion-like domains in ALS and FTLD-U.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

A yeast model of FUS/TLS-dependent cytotoxicity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

A seeding reaction recapitulates intracellular formation of Sarkosyl-insoluble transactivation response element (TAR) DNA-binding protein-43 inclusions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Exome sequencing reveals VCP mutations as a cause of familial ALS

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Implications of the prion-related Q/N domains in TDP-43 and FUS.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Prion-like disorders: blurring the divide between transmissibility and infectivity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Ubiquilin modifies TDP-43 toxicity in a Drosophila model of amyotrophic lateral sclerosis (ALS).

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

A Drosophila model for TDP-43 proteinopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

The transcellular spread of cytosolic amyloids, prions, and prionoids

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Exome sequencing makes medical genomics a reality

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Exome sequencing identifies the cause of a mendelian disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

The TET family of proteins: functions and roles in disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Targeted capture and massively parallel sequencing of 12 human exomes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Recent advances in motor neuron disease.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

A systematic survey identifies prions and illuminates sequence features of prionogenic proteins

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Rethinking ALS: the FUS about TDP-43.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Rules for nuclear localization sequence recognition by karyopherin beta 2

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Mixtures of wild-type and a pathogenic (E22G) form of Abeta40 in vitro accumulate protofibrils, including amyloid pores.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Cooperative interaction of EWS with CREB-binding protein selectively activates hepatocyte nuclear factor 4-mediated transcription.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Acceleration of oligomerization, not fibrillization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: implications for pathogenesis and therapy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Neurodegenerative disease: amyloid pores from pathogenic mutations.

11 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease.

11 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis

11 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3248518

7 December 2018

Identifiers

DOI

10.1073/PNAS.1109434108

1 reference

9 August 2017

0 references

1 reference

9 August 2017

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