Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases. (Q50532074)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29518107 AND SRC:MED&resulttype=core&format=json

19 March 2020

title

Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases (English)

1 reference

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19 March 2020

main subject

cognitive dysfunction

1 reference

16

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19 March 2020

Veronica Tisato

1

1 reference

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19 March 2020

Giovanni Zuliani

2

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19 March 2020

Donato Gemmati

17

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19 March 2020

author name string

Marco Vigliano

3

1 reference

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19 March 2020

Giovanna Longo

4

1 reference

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19 March 2020

Eugenia Franchini

5

1 reference

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19 March 2020

Paola Secchiero

6

1 reference

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19 March 2020

Giorgio Zauli

7

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19 March 2020

Elvezia Maria Paraboschi

8

1 reference

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19 March 2020

Ajay Vikram Singh

9

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19 March 2020

Maria Luisa Serino

10

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19 March 2020

Beatrice Ortolani

11

1 reference

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19 March 2020

Amedeo Zurlo

12

1 reference

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19 March 2020

Cristina Bosi

13

1 reference

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19 March 2020

Antonio Greco

14

1 reference

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19 March 2020

Davide Seripa

15

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19 March 2020

language of work or name

English

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publication date

8 March 2018

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19 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29518107 AND SRC:MED&resulttype=core&format=json

19 March 2020

volume

13

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19 March 2020

issue

3

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19 March 2020

page(s)

e0193867

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Creative Commons Attribution 4.0 International

19 March 2020

copyright license

start time

8 March 2018

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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A novel mammalian iron-regulated protein involved in intracellular iron metabolism

16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome

16 June 2018

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16 June 2018

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Effects of transferrin genetic phenotypes on total iron-binding capacity

16 June 2018

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Prevalence of Alzheimer's disease and other dementias in an elderly urban population: Relationship with age, sex, and education

16 June 2018

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A histochemical study of iron, transferrin, and ferritin in Alzheimer's diseased brains

16 June 2018

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16 June 2018

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No Genetic Overlap Between Circulating Iron Levels and Alzheimer's Disease

14 August 2018

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Effect of APOE Genotype on Amyloid Deposition, Brain Volume, and Memory in Cognitively Normal Older Individuals.

14 August 2018

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Association of Cerebrospinal Fluid Ferritin Level With Preclinical Cognitive Decline in APOE-ε4 Carriers.

14 August 2018

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Serum Soluble Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand Levels in Older Subjects with Dementia and Mild Cognitive Impairment.

14 August 2018

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Determinants of iron accumulation in the normal aging brain

14 August 2018

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Oxidative stress and APO E polymorphisms in Alzheimer's disease and in mild cognitive impairment.

14 August 2018

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Association between HFE polymorphisms and susceptibility to Alzheimer’s disease: a meta-analysis of 22 studies including 4,365 cases and 8,652 controls

14 August 2018

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Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease

14 August 2018

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HFE H63D, C282Y and AGTR1 A1166C polymorphisms and brain white matter lesions in the aging brain

14 August 2018

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DNA-array of gene variants in venous leg ulcers: detection of prognostic indicators.

14 August 2018

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Changes of some oxidative stress markers in the serum of patients with mild cognitive impairment and Alzheimer's disease

14 August 2018

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CAT53 and HFE alleles in Alzheimer's disease: a putative protective role of the C282Y HFE mutation

14 August 2018

1 reference

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Lipid peroxidation and antioxidant enzyme activities in vascular and Alzheimer dementias.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Influence of gene polymorphisms in ulcer healing process after superficial venous surgery.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Prognostic role of factor XIII gene variants in nonhealing venous leg ulcers.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

The overlapping of local iron overload and HFE mutation in venous leg ulcer pathogenesis.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Factor XIII contrasts the effects of metalloproteinases in human dermal fibroblast cultured cells

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Transferrin C2 variant does confer a risk for Alzheimer's disease in caucasians.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Magnetic resonance imaging shows delayed ischemic striatal neurodegeneration

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Association study between late-onset Alzheimer's disease and the transferrin gene polymorphisms in Chinese

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Association of HFE mutations with neurodegeneration and oxidative stress in Alzheimer's disease and correlation with APOE

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

An iron-responsive element type II in the 5'-untranslated region of the Alzheimer's amyloid precursor protein transcript

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

The hemochromatosis gene affects the age of onset of sporadic Alzheimer's disease.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Plasma oxidative stress parameters in men and women with early stage Alzheimer type dementia

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Mutations in the hemochromatosis gene and the clinical outcome of multiple sclerosis

30 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843269

Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI

30 November 2018

1 reference

12 December 2020

The effect of transferrin polymorphisms on iron metabolism

1 reference

12 December 2020

The basal ganglia in haemochromatosis

1 reference

12 December 2020

The Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patients

1 reference

12 December 2020

Interaction of the H63D mutation in the hemochromatosis gene with the apolipoprotein E epsilon 4 allele modulates age at onset of Alzheimer's disease

1 reference

12 December 2020

Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension

1 reference

12 December 2020

Serum iron and matrix metalloproteinase-9 variations in limbs affected by chronic venous disease and venous leg ulcers

1 reference

12 December 2020

Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes?

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0193867

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29518107 AND SRC:MED&resulttype=core&format=json

19 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29518107 AND SRC:MED&resulttype=core&format=json

19 March 2020

PubMed publication ID

29518107

1 reference