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

Nature genetics, 1995-05, Vol.10 (1), p.111-113

1995

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Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

The Lancet (British edition), 1995-10, Vol.346 (8982), p.1070-1071

1995

Volltextzugriff (PDF)

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

American journal of human genetics, 1996-01, Vol.58 (1), p.35-41

1996

Volltextzugriff (PDF)

In vitro dendritic cell infection by pseudotyped adenoviral vectors does not correlate with their in vivo immunogenicity

Virology (New York, N.Y.), 2005-02, Vol.332 (1), p.1-7

2005

Volltextzugriff (PDF)

Tpr Is Localized within the Nuclear Basket of the Pore Complex and Has a Role in Nuclear Protein Export

The Journal of cell biology, 2002-02, Vol.156 (4), p.617-630

2002

Volltextzugriff (PDF)

Methylenetetrahydrofolate Reductase Polymorphism, Plasma Folate, Homocysteine, and Risk of Myocardial Infarction in US Physicians

Circulation (New York, N.Y.), 1996-11, Vol.94 (10), p.2410-2416

1996

Volltextzugriff (PDF)

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

Mammalian genome, 1998-08, Vol.9 (8), p.652-656

1998

Volltextzugriff (PDF)

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency

American journal of human genetics, 1995-05, Vol.56 (5), p.1052-1059

1995

Volltextzugriff (PDF)

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1997-03, Vol.17 (3), p.569

1997

Volltextzugriff (PDF)

The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse chromosome 4

Mammalian genome, 1996-11, Vol.7 (11), p.864-865

1996

Volltextzugriff (PDF)

At-home genetic tests

American family physician, 2006-02, Vol.73 (3), p.540-541

2006

Volltextzugriff (PDF)

The curly-tail ( ct) mouse, an animal model of neural tube defects, displays altered homocysteine metabolism without folate responsiveness or a defect in Mthfr

Molecular genetics and metabolism, 2002-08, Vol.76 (4), p.297-304

2002

Volltextzugriff (PDF)

Molecular genetic analysis in mild hyperhomocysteinemia : A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk facotr for cardiovascular disease

American journal of human genetics, 1996, Vol.58 (1), p.35-41

1996

Volltextzugriff (PDF)

Carrier testing for spinal muscular atrophy

Genetics in medicine, 2010-10, Vol.12 (10), p.621-622

2010

Volltextzugriff (PDF)

Engineering of papain: selective alteration of substrate specificity by site-directed mutagenesis

Biochemistry (Easton), 1991-09, Vol.30 (37), p.8929-8936

1991

Volltextzugriff (PDF)

VITAMIN "A" AND THE COMMON COLD

Canadian Medical Association journal, 1931-10, Vol.25 (4), p.412-416

1931

Volltextzugriff (PDF)

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Methylenetetrahydrofolate Reductase
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Oxidoreductases Acting On Ch-Nh Group Donors - Genetics
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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

In vitro dendritic cell infection by pseudotyped adenoviral vectors does not correlate with their in vivo immunogenicity

Tpr Is Localized within the Nuclear Basket of the Pore Complex and Has a Role in Nuclear Protein Export

Methylenetetrahydrofolate Reductase Polymorphism, Plasma Folate, Homocysteine, and Risk of Myocardial Infarction in US Physicians

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease

The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse chromosome 4

At-home genetic tests

The curly-tail ( ct) mouse, an animal model of neural tube defects, displays altered homocysteine metabolism without folate responsiveness or a defect in Mthfr

Molecular genetic analysis in mild hyperhomocysteinemia : A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk facotr for cardiovascular disease

Carrier testing for spinal muscular atrophy

Engineering of papain: selective alteration of substrate specificity by site-directed mutagenesis

VITAMIN "A" AND THE COMMON COLD

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