(Q36438687)

14 August 2017

No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort (English)

1 reference

amyotrophic lateral sclerosis

14 August 2017

0 references

1 reference

2

Stefania Corti

1 reference

14 August 2017

Daniela Galimberti

8

0 references

Giacomo P Comi

Giacomo P Comi

17

0 references

Elio Scarpini

Elio Scarpini

13

0 references

Gabriele Siciliano

Gabriele Siciliano

10

0 references

Nereo Bresolin

Nereo Bresolin

16

0 references

Chiara Fenoglio

5

Chiara Fenoglio

1 reference

14 August 2017

15

Bryan J Traynor

1 reference

14 August 2017

6

Serena Ghezzi

1 reference

14 August 2017

7

Michela Ranieri

1 reference

14 August 2017

9

Michelangelo Mancuso

1 reference

14 August 2017

Roberto Del Bo

1

1 reference

14 August 2017

Domenico Santoro

3

1 reference

14 August 2017

Isabella Ghione

4

1 reference

14 August 2017

Chiara Briani

11

1 reference

14 August 2017

Luigi Murri

12

1 reference

14 August 2017

Jennifer C Schymick

14

1 reference

14 August 2017

25 July 2009

1 reference

14 August 2017

Neurobiology of Aging

1 reference

14 August 2017

32

1 reference

14 August 2017

6

1 reference

14 August 2017

1157-1158

1 reference

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Novel exon 1 progranulin gene variant in Alzheimer's disease.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

ALS and FTLD: two faces of TDP-43 proteinopathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Gene expression study on peripheral blood identifies progranulin mutations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Progranulin: normal function and role in neurodegeneration

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Genetics of sporadic amyotrophic lateral sclerosis.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Progranulin in frontotemporal lobar degeneration and neuroinflammation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Haploview: analysis and visualization of LD and haplotype maps

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Progranulin (PGRN) expression in ALS: an immunohistochemical study.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Progranulin variability has no major role in Parkinson disease genetic etiology

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Genetics. The elusive ALS genes

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511779

Absence of angiogenic genes modification in Italian ALS patients

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19632744

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19632744

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEUROBIOLAGING.2009.06.006

1 reference

14 August 2017

1 reference

14 August 2017

1 reference