Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility. (Q46322206)

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English	Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

18846434

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

title

Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility (English)

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stated in

Europe PubMed Central

PubMed publication ID

18846434

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

main subject

sperm motility

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inferred from title

author

Handan Ankarali

series ordinal

4

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Europe PubMed Central

PubMed publication ID

18846434

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

author name string

Aysen Gunel-Ozcan

series ordinal

1

1 reference

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Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

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15 January 2020

M Murad Basar

series ordinal

2

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Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

Ucler Kisa

series ordinal

3

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stated in

Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

publication date

10 October 2008

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Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

published in

Molecular Biology Reports

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stated in

Europe PubMed Central

PubMed publication ID

18846434

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

volume

36

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Europe PubMed Central

PubMed publication ID

18846434

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

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15 January 2020

issue

7

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Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

page(s)

1709-1714

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Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

cites work

Physiology of iron transport and the hemochromatosis gene.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS11033-008-9372-7

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21 January 2018

The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

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Crossref

reference URL

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21 January 2018

Relationships of testicular iron and ferritin concentrations with testicular weight and sperm production in boars

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Crossref

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21 January 2018

Uncommon mutations and polymorphisms in the hemochromatosis gene

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of HFE mutations among Turkish blood donors according to transferrin saturation: genotype screening for hereditary hemochromatosis among voluntary blood donors in Turkey.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms of iron accumulation in hereditary hemochromatosis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global prevalence of putative haemochromatosis mutations

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the hemochromatosis mutations C282Y and H63D in infertile men

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for hemochromatosis in Turkey

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HFE H63D mutation frequency shows an increase in Turkish women with breast cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HFE mutations and Alzheimer's disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The impact of hemochromatosis mutations and transferrin genotype on gonadotropin serum levels in infertile men.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities in estrogen, androgen, and insulin metabolism in idiopathic hemochromatosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemochromatosis genotypes and risk of 31 disease endpoints: meta-analyses including 66,000 cases and 226,000 controls

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The significance of haemochromatosis gene mutations in the general population: implications for screening

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypogonadism in hereditary hemochromatosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Association Between H63D Mutations in HFE and Amyotrophic Lateral Sclerosis in a Dutch Population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemochromatosis: understanding the mechanism of disease and implications for diagnosis and patient management following the recent cloning of novel genes involved in iron metabolism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human platelets express hemochromatosis protein (HFE) and transferrin receptor 2

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HFE mutations, iron deficiency and overload in 10,500 blood donors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predictive value of abnormal sperm morphology in in vitro fertilization

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationships between serum hormone levels and semen quality among men from an infertility clinic

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18846434

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S11033-008-9372-7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

PubMed publication ID

18846434

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18846434

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18846434%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 January 2020

ResearchGate publication ID

23310720

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