(Q35811238)

10 August 2017

FUS and TDP43 genetic variability in FTD and CBS (English)

1 reference

10 August 2017

Christopher M Morris

5

0 references

John Anthony Hardy

10

object named as

John Hardy

1 reference

10 August 2017

12

Parastoo Momeni

1 reference

10 August 2017

11

Jordan Grafman

1 reference

10 August 2017

2

Raffaele Ferrari

1 reference

10 August 2017

1

Edward D Huey

1 reference

10 August 2017

Jorge H Moreno

3

1 reference

10 August 2017

Christopher Jensen

4

1 reference

10 August 2017

Felix Potocnik

6

1 reference

10 August 2017

Rajesh N Kalaria

7

1 reference

10 August 2017

Michael Tierney

8

1 reference

10 August 2017

Eric M Wassermann

9

1 reference

10 August 2017

language of work or name

1 reference

23 September 2011

1 reference

10 August 2017

Neurobiology of Aging

1 reference

10 August 2017

33

1 reference

10 August 2017

5

1 reference

10 August 2017

1016.e9-17

1 reference

Frontotemporal dementia: from Mendelian genetics towards genome wide association studies

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

The multiple phenotypes of corticobasal syndrome and corticobasal degeneration: implications for further study

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

FTD and ALS: a tale of two diseases

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Mutations in FUS cause FALS and SALS in French and French Canadian populations

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Genetic contribution of FUS to frontotemporal lobar degeneration

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Genetic Variability in CHMP2B and Frontotemporal Dementia

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489700

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.

15 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21943958

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

TDP-43 gene analysis in frontotemporal lobar degeneration

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21943958

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

No association of TDP-43 with sporadic frontotemporal dementia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21943958

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEUROBIOLAGING.2011.08.004

1 reference

10 August 2017

1 reference

10 August 2017

1 reference