A. Whitehead

C. Thorn, A. Whitehead, 2002, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Pemetrexed alters folate phenotype and inflammatory profile in EA.hy 926 cells grown under low-folate conditions.

J. Arora, I. Blair, A. Whitehead, 2012, European journal of pharmacology.

The molecular basis for genetic deficiency of the second component of human complement.

T. Lint, P. Kilbridge, H. Colten, 1985, The New England journal of medicine.

Identification of novel members of the serum amyloid A protein superfamily as constitutive apolipoproteins of high density lipoprotein.

William Arbuthnot Sir Lane, J. Lélias, A. Whitehead, 1992, The Journal of biological chemistry.

Regulation of serum amyloid A protein expression during the acute-phase response.

A. Whitehead, L. Jensen, 1998, The Biochemical journal.

SAA 2 and SAA 1 Amyloid A Genes , Activation of the Human Acute Phase Serum the Cytokine-Driven Transcriptional Differential Glucocorticoid Enhancement of

C. Thorn, A. Whitehead, 2002 .

Use of the acute phase serum amyloid A2 (SAA2) gene promoter in the analysis of pro- and anti-inflammatory mediators: differential kinetics of SAA2 promoter induction by IL-1 beta and TNF-alpha compared to IL-6.

A. Steinkasserer, A. Whitehead, D. Steel, 1997, Journal of immunological methods.

The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypes.

L. Truedsson, P. Schneider, A. Whitehead, 1988, Human immunology.

DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex.

H. Colten, A. Whitehead, D. Woods, 1984, The New England journal of medicine.

A monoclonal antibody against human complement component C3: the production of C3 by human cells in vitro

W. Bodmer, Robert B Sim, A. Whitehead, 1981, European journal of immunology.

TGF‐β down‐regulates IL‐1α‐induced TLR2 expression in murine hepatocytes

C. Thorn, J. Inoue, H. Hayashi, 2004, Journal of leukocyte biology.

The mouse interleukin 1 receptor antagonist protein: gene structure and regulation in vitro.

A. Whitehead, M. Rits, C. Uhlar, 1994, Cytokine.

Molecular map of the murine S region.

J. Seidman, H. Colten, D. Chaplin, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Structure of the Mouse Serum Amyloid A 5 (Saa5) Gene: Relationship to Other Members of the Serum Amyloid A Family

A. Butler, A. Whitehead, 1997, Scandinavian journal of immunology.

Nucleotide sequence and expression of the human gene encoding apolipoprotein H (β2-glycoprotein I)

M. Peeples, A. Whitehead, D. Steel, 1991 .

DNA polymorphism of MHC III genes in inbred and wild mouse strains

H. Colten, A. Falus, E. Wakeland, 2004, Immunogenetics.

Resistance to Secondary Amyloidosis in A/J Mice is Not Significantly Associated with Allelic Variants Linked to the Serum Amyloid A Gene Cluster

A. Butler, A. Whitehead, A. Whitehead, 1994, Scandinavian journal of immunology.

Genome-wide association study confirms lung cancer susceptibility loci on chromosome 5p15 and 15q25 in an African-American population

Krista A. Zanetti, Xifeng, E. Gillanders, 2016 .

Linkage between the loci for autosomal dominant neuronal Charcot-Marie-Tooth neuropathy (CMT1) and serum amyloid P component (APCS) on human chromosome 1.

A. Whitehead, V. Ionasescu, C. Searby, 1988, Cytogenetics and cell genetics.

Generation of soluble recombinant human acute phase serum amyloid A2 (A-SAA2) protein and its use in development of an A-SAA specific ELISA.

S. Doyle, A. Whitehead, C. Kilty, 1996, Journal of immunological methods.

Expression and Regulation of Constitutive and Acute Phase Serum Amyloid A mRNAs in Hepatic and Non‐Hepatic Cell Lines

A. Whitehead, D. Steel, C. Uhlar, 1996, Scandinavian journal of immunology.

In vitro Evaluation of an Enhanced Human Serum Amyloid A (SAA2) Promoter‐Regulated Soluble TNF Receptor Fusion Protein for Anti‐Inflammatory Gene Therapy

C. Thorn, R. Munford, A. Whitehead, 2001, Scandinavian journal of immunology.

Pellino3, a Novel Member of the Pellino Protein Family, Promotes Activation of c-Jun and Elk-1 and May Act as a Scaffolding Protein

A. Whitehead, L. Jensen, 2003, The Journal of Immunology.

Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.

H. Colten, P. Schneider, A. Whitehead, 1986, The Journal of clinical investigation.

Vitamin B6 status, MTHFR and hyperhomocysteinaemia.

J. Yarnell, J. Woodside, I. Young, 1997, QJM : monthly journal of the Association of Physicians.

Localization of the human MHC-linked complement genes between HLA-B and HLA-DR by using HLA mutant cell lines.

H. Colten, R. Demars, A. Whitehead, 1985, Journal of immunology.

High frequency (71%) of cystathionine β‐synthase mutation G307S in Irish homocystinuria patients

D. McConnell, S. Tan, J. Kraus, 1995 .

Use of a cDNA clone for the fourth component of human complement (C4) for analysis of a genetic deficiency of C4 in guinea pig.

H. Colten, A. Markham, A. Whitehead, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Act as a Scaffolding Protein Family , Promotes Activation of c-Jun and Elk-1 Pellino 3 , a Novel Member of the Pellino Protein

A. Whitehead, L. Jensen, 2003 .

Tissue‐specific regulation of the human acute‐phase serum amyloid A genes, SAA1 and SAA2, by glucocorticoids in hepatic and epithelial cells

C. Thorn, A. Whitehead, Zhi-yong Lu, 2003, European journal of immunology.

Differential Glucocorticoid Enhancement of the Cytokine-Driven Transcriptional Activation of the Human Acute Phase Serum Amyloid A Genes, SAA1 and SAA2

C. Thorn, A. Whitehead, 2002, The Journal of Immunology.

Biosynthesis of human acute-phase serum amyloid A protein (A-SAA) in vitro: the roles of mRNA accumulation, poly(A) tail shortening and translational efficiency.

A. Whitehead, J. Rogers, D. Steel, 1993, The Biochemical journal.

Serum amyloid A transcription in Atlantic salmon (Salmo salar L.) hepatocytes is enhanced by stimulation with macrophage factors, recombinant human IL-1 beta, IL-6 and TNF alpha or bacterial lipopolysaccharide.

A. Whitehead, B. Robertsen, J. Jørgensen, 2000, Developmental and comparative immunology.

This information is current as Receptor Accessory Protein Involvement of a Soluble Form of the IL-1 IL-1 Signaling Cascade in Liver Cells and the

A. Whitehead, A. Mantovani, M. Muzio, 2000 .

Quantification of Plasma 8-Isoprostane by High-Performance Liquid Chromatography with Tandem Mass Spectrometry in a Case-Control Study of Lung Cancer

A. Vachani, Dongxiao Sun, J. Muscat, 2022, International Journal of Environmental Research and Public Health.

Family, Promotes Activation of c-Jun and Elk-1 Pellino3, a Novel Member of the Pellino Protein

A. Whitehead, L. Jensen, 2003 .

Journal Nutrition, Health and Ageing

A. Evans, F. Cambien, F. Kee, 2003 .

Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome.

G. Bruns, C. Shelley, A. Whitehead, 1989, Proceedings of the National Academy of Sciences of the United States of America.

The gene encoding the mouse serum amyloid A protein, apo-SAA5, maps to proximal chromosome 7

M. Seldin, A. Butler, A. Whitehead, 2004, Immunogenetics.

Amyloid precursors and amyloidosis in rheumatoid arthritis.

G. Cunnane, A. Whitehead, Gaye Cunnane, 1999, Bailliere's best practice & research. Clinical rheumatology.

A constitutively expressed serum amyloid A protein gene (SAA4) is closely linked to, and shares structural similarities with, an acute-phase serum amyloid A protein gene (SAA2).

A. Whitehead, G. Sellar, D. Steel, 1993, Genomics.

Structure, expression, and evolution of guinea pig serum amyloid P component and C-reactive protein.

P. Sharp, A. Whitehead, M. Rits, 1993, Journal of biochemistry.

Heterogeneous modulation of acute-phase-reactant mRNA levels by interleukin-1 beta and interleukin-6 in the human hepatoma cell line PLC/PRF/5.

A. Whitehead, D. Steel, 1991, The Biochemical journal.

Acute phase induction of mouse serum amyloid P component. Correlation with other parameters of inflammation.

A. Whitehead, K. Zahedi, 1989, Journal of immunology.

Mild folate deficiency induces a proatherosclerotic phenotype in endothelial cells.

I. Blair, A. Whitehead, K. S. Brown, 2006, Atherosclerosis.

BELFAST centenarians: A Case of Optimal Cardiovascular Risk?

F. Cambien, I. Young, G. Archbold, 2010 .

BELFAST centenarians: a case of optimised cardiovascular risk?

F. Cambien, I. Young, G. Archbold, 2010, Current pharmaceutical design.

IL-1 and IL-6 mediate increased production and synthesis by hepatocytes of acute-phase reactant mouse serum amyloid P-component (SAP)

N. Ku, A. Whitehead, K. Zahedi, 1990, Inflammation.

Regulation of mouse serum amyloid P gene expression by cytokines in vitro.

A. Whitehead, K. Zahedi, 1993, Biochimica et biophysica acta.

Mouse C-reactive protein. Generation of cDNA clones, structural analysis, and induction of mRNA during inflammation.

J. Lélias, A. Whitehead, M. Rits, 1990, The Biochemical journal.

The mouse C-reactive protein gene maps to distal chromosome 1 and, like its human counterpart, is closely linked to the serum amyloid P component gene

A. Whitehead, I. Yunis, 2004, Immunogenetics.

Characterization of the gene encoding mouse serum amyloid P component. Comparison with genes encoding other pentraxins.

A. Whitehead, M. Rits, 1989, The Biochemical journal.

Localization of four human serum amyloid A (SAA) protein superfamily genes to chromosome 11p: characterization of a fifth SAA-related gene sequence.

A. Whitehead, G. Sellar, 1993, Genomics.

Reply to PB Duell and MR Malinow

A. Evans, J. Yarnell, J. Woodside, 1999 .

Mouse IL-1 receptor antagonist protein. Molecular characterization, gene mapping, and expression of mRNA in vitro and in vivo.

M. Seldin, A. Whitehead, M. Rits, 1991, Journal of immunology.

Biosynthesis and postsynthetic processing of human C-reactive protein.

H. Colten, A. Whitehead, R. Kay, 1983, Journal of immunology.

Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1.

H. McNulty, L. Murray, C. Boreham, 2009, Clinical immunology.

Quantitation of metalloproteinase gene expression in rheumatoid and psoriatic arthritis synovial tissue distal and proximal to the cartilage-pannus junction.

B. Bresnihan, D. Kane, O. FitzGerald, 2004, The Journal of rheumatology.

Complementary DNA and derived amino acid sequence of the alpha subunit of human complement protein C8: evidence for the existence of a separate alpha subunit messenger RNA.

H. Colten, S. Ng, A. Rao, 1987, Biochemistry.

Isolation and sequence analysis of a cDNA clone encoding the fifth complement component.

H. Colten, R. Ogden, A. Whitehead, 1985, The Journal of biological chemistry.

Thiol and cardiovascular risk factor status in a male northern Irish population.

A. Evans, J. Yarnell, C. Cardwell, 2008, International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition.

Simplified Simultaneous Assay of Total Plasma Homocysteine and Methionine by HPLC and Pulsed Integrated Amperometry

J. Mills, A. Whitehead, D. Weir, 1998 .

Acute-phase serum amyloid A production by rheumatoid arthritis synovial tissue

Alexander S Whitehead, Oliver FitzGerald, B. Bresnihan, 2000, Arthritis research.

Serum amyloid A in the assessment of early inflammatory arthritis.

B. Bresnihan, D. Shields, O. FitzGerald, 2000, The Journal of rheumatology.

Posttranscriptional regulation of acute phase serum amyloid A2 expression by the 5'- and 3'-untranslated regions of its mRNA.

D. Longley, A. Whitehead, D. Steel, 1999, Journal of immunology.

Serum amyloid A, the major vertebrate acute-phase reactant.

A. Whitehead, C. Uhlar, C. Uhlar, 1999, European journal of biochemistry.

Genetic analysis of the thermolabile variant of 5, 10-methylenetetrahydrofolate reductase as a risk factor for ischemic stroke.

D. Coakley, D. Shields, I. Graham, 1999, Arteriosclerosis, thrombosis, and vascular biology.

Production and characterisation of a monoclonal antibody to progesterone.

V. Fantl, A. Whitehead, D. Y. Wang, 1981, Journal of steroid biochemistry.

Thermolabile variant of 5, 10-methylenetetrahydrofolate reductaseassociated with low red-cell folates: implications for folate intake recommendations

S. Daly, J. Mills, A. Whitehead, 1997, The Lancet.

Structure of the human sialophorin (CD43) gene. Identification of features atypical of genes encoding integral membrane proteins.

C. Shelley, A. Whitehead, E. Remold-O’Donnell, 1990, The Biochemical journal.

Organization, Structure and Expression of Pentraxin Genes

A. Whitehead, 1989 .

The human serum amyloid A protein (SAA) superfamily gene cluster: mapping to chromosome 11p15.1 by physical and genetic linkage analysis.

W. Bickmore, A. Whitehead, V. van Heyningen, 1994, Genomics.

Pretreatment Red Blood Cell Total Folate Concentration Is Associated With Response to Pemetrexed in Stage IV Nonsquamous Non–Small‐cell Lung Cancer

C. Langer, I. Blair, A. Vachani, 2017, Clinical lung cancer.

Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.

Krista A. Zanetti, E. Gillanders, S. Chanock, 2016, Lung cancer.

The human and mouse methylenetetrahydrofolate reductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene.

L. Kluijtmans, A. Whitehead, S. Barbaux, 2000, Gene.

Function and biological applications of catalytic nucleic acids.

A. Whitehead, D. J. Gaughan, D. Gaughan, 1999, Biochimica et biophysica acta.

The evolution of haematopoietic cytokine/receptor complexes.

D. Shields, A. Whitehead, D. Harmon, 1995, Cytokine.

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.

M. McDonnell, L. E. Mitchell, A. Whitehead, 2002, American journal of human genetics.

Efficient In Vitro Cleavage of Mouse Acute Phase Serum Amyloid A mRNA Mediated by a Synthetic Hammerhead Ribozyme

A. Whitehead, D. J. Gaughan, D. Gaughan, 1997, Scandinavian journal of immunology.

Phase I trial of UFT/leucovorin and irinotecan in patients with advanced cancer.

C. Thorn, D. Haller, P. O'dwyer, 2004, European journal of cancer.

Phase I clinical and pharmacogenetic trial of irinotecan and raltitrexed administered every 21 days to patients with cancer.

L. Kluijtmans, D. Haller, P. O'dwyer, 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The Reduced Folate Carrier (SLC19A1) c.80G>A Polymorphism is Associated with Red Cell Folate Concentrations Among Women

H. McNulty, J. Strain, L. Murray, 2009, Annals of human genetics.

Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11.

G. Bruns, F. Rosen, M. Cicardi, 1986, Proceedings of the National Academy of Sciences of the United States of America.

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations.

A. Evans, L. Kluijtmans, J. Yarnell, 2001, Atherosclerosis.

Fine mapping of the human pentraxin gene region on chromosome 1q23

M. Walsh, A. Whitehead, A. Divane, 2007, Immunogenetics.

Loss of function polymorphisms in NAT1 protect against spina bifida

L. E. Mitchell, A. Whitehead, L. Jensen, 2006, Human Genetics.

The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida.

L. E. Mitchell, A. Whitehead, L. Jensen, 2005, Birth defects research. Clinical and molecular teratology.

Molecular Biology of the Human and Mouse MHC Class III Genes: Phylogenetic Conservation, Genetics and Regulation of Expression

A. Whitehead, R. Sackstein, 1985, Immunological reviews.

Association of methylenetetrahydrofolate reductase polymorphism and the risk of squamous cell carcinoma in renal transplant patients.

D. Shields, G. Murphy, P. Dicker, 2007, Transplantation.

A common ABCC2 promoter polymorphism is not a determinant of the risk of spina bifida.

Caroline F Thorn, Laura E Mitchell, Alexander S Whitehead, 2004, Birth defects research. Part A, Clinical and molecular teratology.

Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations

A. Evans, D. Shields, J. Yarnell, 1999, Genetic epidemiology.

Effects of human recombinant growth hormone (rhGH) on inflammatory responses in patients undergoing abdominal aortic aneurysm repair

K. Mealy, L. O’Mahony, A. Whitehead, 1998, Intensive Care Medicine.

On meta‐ and mega‐analyses for gene–environment interactions

Jing Huang, Paul Scheet, Yong Chen, 2017, Genetic epidemiology.

The MTHFR C677T polymorphism is associated with depressive episodes in patients from Northern Ireland

S. Cooper, A. Evans, C. Mulholland, 2004, Journal of psychopharmacology.

Thermolabile MTHFR genotype and retinal vascular occlusive disease

M. Cahill, D. Shields, I. Graham, 2001, The British journal of ophthalmology.

Characterization of genomic and complementary DNA sequence of human C-reactive protein, and comparison with the complementary DNA sequence of serum amyloid P component.

J. Korenberg, A. Whitehead, P. Woo, 1985, The Journal of biological chemistry.

The MTHFR C677T polymorphism is associated with depressive episodes in patients from Northern Ireland

S. Cooper, A. Evans, C. Mulholland, 2004 .

The Xenopus laevis homologue of the 64-kDa subunit of cleavage stimulation factor.

A. Whitehead, S. Barbaux, G. Sellar, 1996, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

Postprandial factor VII metabolism: the effect of the R353Q and 10 bp polymorphisms

M. Gibney, E. Noone, H. Roche, 2000, British Journal of Nutrition.

Human serum amyloid P component. cDNA isolation, complete sequence of pre-serum amyloid P component, and localization of the gene to chromosome 1.

H. Colten, G. Bruns, A. Whitehead, 1985, The Journal of biological chemistry.

Pretranslational regulation of the synthesis of the third component of complement in human mononuclear phagocytes by the lipid A portion of lipopolysaccharide.

R. Strunk, F. S. Cole, A. Whitehead, 1985, The Journal of clinical investigation.

Homocysteine and Cerebral Infarction in Finnish Male Smokers

J. Virtamo, G. Smith, Y. Ben-Shlomo, 2003, Stroke.

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation.

A. Evans, R. Rozen, D. Shields, 1996, Circulation.

Homocysteine levels and disease duration independently correlate with coronary artery calcification in patients with systemic lupus erythematosus.

R. Cron, A. Cucchiara, A. Whitehead, 2006, Arthritis and rheumatism.

A common insertion/deletion polymorphism of the thymidylate synthase (TYMS) gene is a determinant of red blood cell folate and homocysteine concentrations

H. McNulty, J. Strain, L. Murray, 2005, Human Genetics.

Apolipoprotein E genotype and warfarin dosing among Caucasians and African Americans

C. Thorn, C. Brensinger, S. Kimmel, 2008, The Pharmacogenomics Journal.

Alcohol increases homocysteine and reduces B vitamin concentration in healthy male volunteers--a randomized, crossover intervention study.

L. Kluijtmans, J. Woodside, M. McKinley, 2008, QJM : monthly journal of the Association of Physicians.

Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy.

D. Fitzgerald, A. Whitehead, R. Murphy, 2000, Arteriosclerosis, thrombosis, and vascular biology.

Phase I C linical a nd P harmacogenetic T rial o f I rinotecan and R altitrexed A dministered E very 2 1 D ays t o P atients With C ancer

D. Haller, J. Stevenson, A. Whitehead, 2001 .

Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults.

H. McNulty, L. Kluijtmans, L. Murray, 2003, Blood.

The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia.

J. Yarnell, J. Woodside, I. Young, 1996, QJM : monthly journal of the Association of Physicians.

Correlate With Coronary Artery Calcification in Patients With Systemic Lupus Erythematosus

R. Cron, A. Cucchiara, A. Whitehead, 2006 .

Characterization of Two Distinct Serum Amyloid A Gene Products Defined by Their Complementary DNAs

J. Sipe, A. Whitehead, A. Cohen, 1986 .

Influence of the cystathionine β-synthase 844ins68 and methylenetetrahydrofolate reductase 677C>T polymorphisms on folate and homocysteine concentrations

A. Evans, J. Yarnell, J. Woodside, 2008, European Journal of Human Genetics.

Community-living nonagenarians in northern ireland have lower plasma homocysteine but similar methylenetetrahydrofolate reductase thermolabile genotype prevalence compared to 70-89-year-old subjects.

H. McNulty, J. Woodside, I. Young, 2000, Atherosclerosis.

Accurate and rapid "multiplex heteroduplexing" method for genotyping key enzymes involved in folate/homocysteine metabolism.

L. Kluijtmans, A. Whitehead, S. Barbaux, 2000, Clinical chemistry.

Development of a genotyping microarray for studying the role of gene-environment interactions in risk for lung cancer.

Chris P. Sarnowski, Mingyao Li, I. Blair, 2013, Journal of biomolecular techniques : JBT.

The human T locus and spina bifida risk

L. E. Mitchell, A. Whitehead, S. Barbaux, 2004, Human Genetics.

Characterization and acute phase modulation of canine apolipoprotein H (beta 2-glycoprotein I).

M. Peeples, A. Whitehead, G. Sellar, 1993, Biochemical and biophysical research communications.

Thermolabile methylenetetrahydrofolate reductase, homocysteine, and cardiovascular disease risk: the European Concerted Action Project.

S. Vollset, H. Blom, P. Ueland, 2003, The American journal of clinical nutrition.

The 5,10-methylenetetrahydrofolate reductase C677T polymorphism interacts with smoking to increase homocysteine.

H. McNulty, L. Kluijtmans, L. Murray, 2004, Atherosclerosis.

IRAK1b, a Novel Alternative Splice Variant of Interleukin-1 Receptor-associated Kinase (IRAK), Mediates Interleukin-1 Signaling and Has Prolonged Stability*

A. Whitehead, L. Jensen, 2001, The Journal of Biological Chemistry.

Isolation of human C-reactive protein complementary DNA and localization of the gene to chromosome 1.

H. Colten, G. Bruns, A. Markham, 1983, Science.

Genetic and biochemical determinants of serum concentrations of monocyte chemoattractant protein-1, a potential neural tube defect risk factor.

I. Blair, L. E. Mitchell, A. Whitehead, 2008, Birth defects research. Part A, Clinical and molecular teratology.

Parkinson's, Alzheimer's, and motor neurone disease

A. Whitehead, Y. Ben-Shlomo, G. Smith, 1996, BMJ.

Molecular characterization of the mouse mannose-binding proteins. The mannose-binding protein A but not C is an acute phase reactant.

J. Lélias, A. Whitehead, K. Sastry, 1991, Journal of immunology.

TGF-beta down-regulates IL-1alpha-induced TLR2 expression in murine hepatocytes.

C. Thorn, J. Inoue, H. Hayashi, 2004, Journal of leukocyte biology.

Age-dependent Lamin remodeling induces cardiac dysfunction via dysregulation of cardiac transcriptional programs

E. Lakatta, R. Bodmer, B. Ren, 2021 .

Ribozyme mediated cleavage of acute phase serum amyloid A (A‐SAA) mRNA in vitro

A. Whitehead, D. Steel, D. Gaughan, 1995, FEBS letters.

An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women

H. McNulty, L. Murray, C. Boreham, 2008, Human Genetics.

Nucleotide sequence and expression of the human gene encoding apolipoprotein H (beta 2-glycoprotein I).

M. Peeples, H. Mehdi, A. Whitehead, 1991, Gene.

Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus.

L. E. Mitchell, A. Whitehead, K. S. Brown, 2004, Birth defects research. Part A, Clinical and molecular teratology.

Organization of the region encompassing the human serum amyloid A (SAA) gene family on chromosome 11p15.1.

W. Bickmore, S. Boyle, A. Whitehead, 1994, Genomics.

Methylenetetrahydrofolate reductase genotypes and predisposition to atherothrombotic disease; evidence that all three MTHFR C677T genotypes confer different levels of risk.

L. Kluijtmans, A. Whitehead, 2001, European heart journal.

Cloning of human prealbumin complementary DNA. Localization of the gene to chromosome 18 and detection of a variant prealbumin allele in a family with familial amyloid polyneuropathy.

M. Skinner, G. Bruns, J. Sipe, 1984, Molecular biology & medicine.

Expression of a biologically active recombinant mouse IL-1 receptor antagonist and its use in vivo to modulate aspects of the acute phase response.

Robert B Sim, A. Whitehead, S. Grehan, 1997, Journal of immunology.

Characterization, Expression and Evolution of Mouse β2-Glycoprotein 1 (Apolipoprotein H)

A. Whitehead, G. Sellar, L. Seery, 1994 .

Acute-phase serum amyloid A production by rheumatoid arthritis synovial tissue

B. Bresnihan, O. FitzGerald, A. Whitehead, 2000, Arthritis research.

Characterization and Acute-Phase Modulation of Canine Apolipoprotein H (β2-Glycoprotein 1)

M. Peeples, A. Whitehead, G. Sellar, 1993 .

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.

D C Shields, A M Molloy, D. Shields, 1995, QJM : monthly journal of the Association of Physicians.

Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications

R. Corbally, A. Whitehead, D. Weir, 1999, Gut.

Whole-blood folate values in subjects with different methylenetetrahydrofolate reductase genotypes: differences between the radioassay and microbiological assays.

J. Mills, A. Whitehead, D. Weir, 1998, Clinical chemistry.

The transcobalamin (TCN2) 776C>G polymorphism affects homocysteine concentrations among subjects with low vitamin B12 status

J. Yarnell, J. Woodside, I. Young, 2010, European Journal of Clinical Nutrition.

Reduced frequency of the thermolabile methylenetetrahydrofolate reductase genotype in the elderly.

L. Kluijtmans, A. Whitehead, 1999, Atherosclerosis.

The human C-reactive protein gene (CRP) and serum amyloid P component gene (APCS) are located on the proximal long arm of chromosome 1

U. Francke, H. Colten, A. Whitehead, 1986, Immunogenetics.

ELAM-1/E-selectin promoter contains an inducible AP-1/CREB site and is not NF-κB-specific

A. Whitehead, L. Jensen, 2003 .

Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly

S. Scherer, L. Tsui, S. Antonarakis, 1998, Human Genetics.

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.

D. Shields, J. Mills, A. Whitehead, 1999, American journal of human genetics.

ELAM-1/E-selectin promoter contains an inducible AP-1/CREB site and is not NF-kappa B-specific.

A. Whitehead, L. Jensen, 2003, BioTechniques.

Thiol and cardiovascular risk factor status in a male northern Irish population.

J. Yarnell, C. Cardwell, J. Woodside, 2008, International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition.

Total homocysteine is not a determinant of arterial pulse wave velocity in young healthy adults.

P. Robson, H. McNulty, J. Strain, 2004, Atherosclerosis.

Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications

R. Corbally, A. Whitehead, D. Weir, 1999, Gut.

Endoscopic ligation of gastric varices

J. Fujimoto, A. Whitehead, E. Okamoto, 1996, The Lancet.