(Q45010782)

English

Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is associated with osteoporotic vertebral fractures, but is a weak predictor of BMD.

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scholarly article

1 reference

Europe PubMed Central

8 December 2017

Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is associated with osteoporotic vertebral fractures, but is a weak predictor of BMD. (English)

1 reference

Europe PubMed Central

8 December 2017

0 references

author name string

Morten M Villadsen

1

1 reference

Europe PubMed Central

8 December 2017

Mathias H Bünger

2

1 reference

Europe PubMed Central

8 December 2017

Mette Carstens

3

1 reference

Europe PubMed Central

8 December 2017

Liselotte Stenkjaer

4

1 reference

Europe PubMed Central

8 December 2017

Bente L Langdahl

5

1 reference

Europe PubMed Central

8 December 2017

language of work or name

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publication date

6 August 2004

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Europe PubMed Central

8 December 2017

Osteoporosis International

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Europe PubMed Central

8 December 2017

16

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Europe PubMed Central

8 December 2017

4

1 reference

Europe PubMed Central

8 December 2017

411-416

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Europe PubMed Central

8 December 2017

https://scigraph.springernature.com/pub.10.1007/s00198-004-1704-4

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The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of a common allelic polymorphism (C677T) in the methylene tetrahydrofolate reductase gene with a reduced risk of osteoporotic fractures. A case control study in Danish postmenopausal women.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic defects as important factors for moderate hyperhomocysteinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficacy of wheat germ lectin-precipitated alkaline phosphatase in serum as an estimator of bone mineralization rate: comparison to serum total alkaline phosphatase and serum bone Gla-protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic determinants of bone mass in adults. A twin study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radioimmunoassay of the carboxyterminal propeptide of human type I procollagen

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of methylenetetrahydrofolate reductase (MTHFR) polymorphism with bone mineral density in postmenopausal Japanese women

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Universal standardization for dual x-ray absorptiometry: patient and phantom cross-calibration results

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radioimmunoassay for the pyridinoline cross-linked carboxy-terminal telopeptide of type I collagen: a new serum marker of bone collagen degradation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene on homocysteine levels in elderly men and women from the British regional heart study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma homocysteine, methylenetetrahydrofolate reductase mutation and carotid damage in elderly healthy women.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relations between diurnal variations in serum osteocalcin, cortisol, parathyroid hormone, and ionized calcium in normal individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased plasma homocysteine after menopause

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An Sp1 binding site polymorphism in the COLIA1 gene predicts osteoporotic fractures in both men and women

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for McKusick's hypothesis of deficient collagen cross-linking in patients with homocystinuria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common methylenetetrahydrofolate reductase (C677T) polymorphism is associated with low bone mineral density and increased fracture incidence after menopause: longitudinal data from the Danish osteoporosis prevention study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15300362

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00198-004-1704-4

1 reference

Europe PubMed Central

8 December 2017

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0 references

1 reference

Europe PubMed Central

8 December 2017

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