His primary scientific interests are in Internal medicine, Methylenetetrahydrofolate reductase, Endocrinology, Genotype and Homocysteine. The study incorporates disciplines such as Gastroenterology and Reductase in addition to Internal medicine. His Methylenetetrahydrofolate reductase research focuses on Thermolabile and how it connects with Allele frequency, Pregnancy and Mutation.
His research on Endocrinology frequently links to adjacent areas such as Inflammation. The Genotype study combines topics in areas such as Odds ratio and Risk factor. His Homocysteine research is multidisciplinary, incorporating perspectives in Case-control study, Genetics, Vitamin B12 and reductase.
The scientist’s investigation covers issues in Internal medicine, Genetics, Endocrinology, Molecular biology and Genotype. His work deals with themes such as Gastroenterology, Reductase and Immunology, which intersect with Internal medicine. Alexander S. Whitehead studies Vitamin which is a part of Endocrinology.
In his study, Acute-phase protein, Tumor necrosis factor alpha, Amyloidosis and Polymerase chain reaction is strongly linked to Serum amyloid A, which falls under the umbrella field of Molecular biology. His Genotype study also includes fields such as
Internal medicine, Homocysteine, Genotype, Endocrinology and Methylenetetrahydrofolate reductase are his primary areas of study. His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology, Reductase and Immunology. His Homocysteine study integrates concerns from other disciplines, such as Molecular biology, Formic acid, Dihydrofolate reductase and Risk factor.
His Genotype research incorporates themes from Offspring, Vitamin B12 and Allele. Alexander S. Whitehead interconnects Cystathionine beta synthase, Genetics and Polymorphism in the investigation of issues within Endocrinology. His Methylenetetrahydrofolate reductase research includes elements of Physiology and Cohort.
Alexander S. Whitehead focuses on Internal medicine, Genotype, Endocrinology, Maintenance dose and Gastroenterology. His studies in Genotype integrate themes in fields like Cobalamin, Homocysteine, Immunology and B vitamins. His Homocysteine research includes themes of Transcobalamins, Cyanocobalamin, Vitamin B12 and Transcobalamin.
Endocrinology and Allele are commonly linked in his work. His Allele study is related to the wider topic of Genetics. His work is dedicated to discovering how Gastroenterology, Odds ratio are connected with Cancer, Epidermoid carcinoma, Methylenetetrahydrofolate reductase, Skin cancer and Calcitriol receptor and other disciplines.
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Serum amyloid A, the major vertebrate acute-phase reactant.
Clarissa M. Uhlar;Alexander S. Whitehead.
FEBS Journal (1999)
The major acute phase reactants: C-reactive protein, serum amyloid P component and serum amyloid A protein
Diana M. Steel;Alexander S. Whitehead.
Immunology Today (1994)
Regulation of serum amyloid A protein expression during the acute-phase response
Liselotte E. Jensen;Alexander S. Whitehead.
Biochemical Journal (1998)
Thermolabile variant of 5, 10-methylenetetrahydrofolate reductaseassociated with low red-cell folates: implications for folate intake recommendations
Anne M Molloy;Sean Daly;James L Mills;Peadar N Kirke.
The Lancet (1997)
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
A S Whitehead;P Gallagher;J L Mills;P N Kirke.
QJM: An International Journal of Medicine (1995)
The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
D.L. Harmon;J.V. Woodside;J.W.G. Yarnell;D. McMaster.
QJM: An International Journal of Medicine (1996)
The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations
Derval J Gaughan;Leo A.J Kluijtmans;Sandrine Barbaux;Dorothy McMaster.
The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother
Denis C. Shields;Peadar N. Kirke;James L. Mills;Dorothy Ramsbottom.
American Journal of Human Genetics (1999)
Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations
Dawn L. Harmon;Denis C. Shields;Jayne V. Woodside;Dorothy McMaster.
Genetic Epidemiology (1999)
Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults.
Leo A. J. Kluijtmans;Ian S. Young;Colin A. Boreham;Liam Murray.
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