Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr's disease) (Q85025921)

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scientific article published on 14 September 2010

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English	Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr's disease)	scientific article published on 14 September 2010

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20838928%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr's disease) (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20838928%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

basal ganglia calcification

1 reference

based on heuristic

inferred from title

3

object named as

Mayana Zatz

1 reference

Europe PubMed Central

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13 February 2020

author name string

Roberta R Lemos

1

1 reference

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13 February 2020

Danyllo F Oliveira

2

1 reference

Europe PubMed Central

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13 February 2020

João R M Oliveira

4

1 reference

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13 February 2020

publication date

14 September 2010

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13 February 2020

Journal of Molecular Neuroscience

1 reference

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13 February 2020

43

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13 February 2020

3

1 reference

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13 February 2020

333-336

1 reference

Europe PubMed Central

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13 February 2020

https://scigraph.springernature.com/pub.10.1007/s12031-010-9445-7

0 references

MGEA6 is tumor-specific overexpressed and frequently recognized by patient-serum antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MGEA6 multigene family has an active locus on 14q and at least nine pseudogenes on different chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PMUT: a web-based tool for the annotation of pathological mutations on proteins.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant dystonia-plus with cerebral calcifications

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

What is and what is not 'Fahr's disease'.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

cTAGE: a cutaneous T cell lymphoma associated antigen family with tumor-specific splicing

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identical twins with Idiopathic Basal Ganglia Calcification ("Fahr's Disease") presenting with a remarkably similar pattern of neuroimaging findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease")

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting the effects of amino acid substitutions on protein function

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of deleterious non-synonymous single nucleotide polymorphisms using sequence-derived information

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family

1 reference

https://pubmed.ncbi.nlm.nih.gov/20838928

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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