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

PubMed publication ID

19632744

1 reference