A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes. (Q47383531)

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scientific article published on 15 November 2003

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English	A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes.	scientific article published on 15 November 2003

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

title

A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

main subject

risk factor

0 references

type 2 diabetes

1 reference

based on heuristic

inferred from title

diabetic retinopathy

1 reference

based on heuristic

inferred from title

proliferative diabetic retinopathy

1 reference

based on heuristic

inferred from title

author

Mojca Globocnik Petrovic

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

author name string

Borut Peterlin

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Jana Makuc

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Marko Hawlina

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Daniel Petrovic

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

publication date

15 November 2003

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

published in

Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

volume

48

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

issue

12

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

page(s)

646-649

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Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

cites work

Lysosomal iron accumulation in diabetic nephropathy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

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Evaluation of the iron status of a population

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk factors for progression to proliferative diabetic retinopathy in the EURODIAB Prospective Complications Study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

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The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

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Cross-talk between iron metabolism and diabetes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

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inferred from PubMed ID database lookup

Role of hemochromatosis C282Y and H63D mutations in HFE gene in development of type 2 diabetes and diabetic nephropathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changes in gene expression with iron loading and chelation in cardiac myocytes and non-myocytic fibroblasts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proliferative retinopathy in a patient with diabetes mellitus and idiopathic haemochromatosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid tightening of blood glucose control leads to transient deterioration of retinopathy in insulin dependent diabetes mellitus: the Oslo study

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morbidity risk in HFE associated hereditary hemochromatosis C282Y heterozygotes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of free iron on collagen synthesis, cell proliferation and MMP-2 expression in rat hepatic stellate cells

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

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HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

based on heuristic

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Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

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Outpatient insulin therapy in type 1 and type 2 diabetes mellitus: scientific review

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

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Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iron induces Bcl-2 expression in human dermal microvascular endothelial cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Wisconsin epidemiologic study of diabetic retinopathy. III. Prevalence and risk of diabetic retinopathy when age at diagnosis is 30 or more years

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of iron status

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening of Patients With Iron Overload to Identify Hemochromatosis and Porphyria Cutanea Tarda

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

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The appearance of retinopathy and progression to proliferative retinopathy: the WHO Multinational Study of Vascular Disease in Diabetes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14618419

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10038-003-0094-3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

PubMed publication ID

14618419

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14618419

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14618419%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

ResearchGate publication ID

226382819

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