| Year |
Citation |
Score |
| 2016 |
Bagley SJ, Vitale S, Zhang S, Aggarwal C, Evans TL, Alley EW, Cohen RB, Langer CJ, Blair IA, Vachani A, Whitehead AS. Pretreatment Red Blood Cell Total Folate Concentration Is Associated With Response to Pemetrexed in Stage IV Nonsquamous Non-Small-cell Lung Cancer. Clinical Lung Cancer. PMID 27863923 DOI: 10.1016/J.Cllc.2016.10.010 |
0.301 |
|
| 2014 |
Summers CM, Hammons AL, Arora J, Zhang S, Jochems J, Blair IA, Whitehead AS. Methotrexate modulates folate phenotype and inflammatory profile in EA.hy 926 cells. European Journal of Pharmacology. 732: 60-7. PMID 24657277 DOI: 10.1016/J.Ejphar.2014.03.004 |
0.612 |
|
| 2013 |
Baldwin DA, Sarnowski CP, Reddy SA, Blair IA, Clapper M, Lazarus P, Li M, Muscat JE, Penning TM, Vachani A, Whitehead AS. Development of a genotyping microarray for studying the role of gene-environment interactions in risk for lung cancer. Journal of Biomolecular Techniques : Jbt. 24: 198-217. PMID 24294113 DOI: 10.7171/Jbt.13-2404-004 |
0.319 |
|
| 2012 |
Hammons AL, Summers CM, Jochems J, Arora JS, Zhang S, Blair IA, Whitehead AS. Pemetrexed alters folate phenotype and inflammatory profile in EA.hy 926 cells grown under low-folate conditions. European Journal of Pharmacology. 696: 12-7. PMID 22975265 DOI: 10.1016/J.Ejphar.2012.08.008 |
0.629 |
|
| 2011 |
Suh E, Paramasivam S, Zhang S, Arora JS, Cooper HS, Whitehead AS, Blair IA, Clapper ML. Abstract 856: Association of high levels of folate with increased risk for colitis-associated colorectal neoplasia Cancer Research. 71: 856-856. DOI: 10.1158/1538-7445.Am2011-856 |
0.309 |
|
| 2010 |
Stanisławska-Sachadyn A, Woodside JV, Sayers CM, Yarnell JW, Young IS, Evans AE, Mitchell LE, Whitehead AS. The transcobalamin (TCN2) 776C>G polymorphism affects homocysteine concentrations among subjects with low vitamin B(12) status. European Journal of Clinical Nutrition. 64: 1338-43. PMID 20808328 DOI: 10.1038/Ejcn.2010.157 |
0.302 |
|
| 2010 |
Summers CM, Mitchell LE, Stanislawska-Sachadyn A, Baido SF, Blair IA, Von Feldt JM, Whitehead AS. Genetic and lifestyle variables associated with homocysteine concentrations and the distribution of folate derivatives in healthy premenopausal women. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 679-88. PMID 20544798 DOI: 10.1002/Bdra.20683 |
0.61 |
|
| 2009 |
Stanisławska-Sachadyn A, Mitchell LE, Woodside JV, Buckley PT, Kealey C, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women. Annals of Human Genetics. 73: 484-91. PMID 19650776 DOI: 10.1111/J.1469-1809.2009.00529.X |
0.376 |
|
| 2009 |
Hammons AL, Summers CM, Woodside JV, McNulty H, Strain JJ, Young IS, Murray L, Boreham CA, Scott JM, Mitchell LE, Whitehead AS. Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1. Clinical Immunology (Orlando, Fla.). 133: 132-7. PMID 19625220 DOI: 10.1016/J.Clim.2009.06.008 |
0.628 |
|
| 2009 |
Mitchell LE, Morales M, Khartulyari S, Huang Y, Murphy K, Mei M, Von Feldt JM, Blair IA, Whitehead AS. Folate and homocysteine phenotypes: Comparative findings using research and clinical laboratory data. Clinical Biochemistry. 42: 1275-81. PMID 19427846 DOI: 10.1016/J.Clinbiochem.2009.04.014 |
0.304 |
|
| 2009 |
Lu ZY, Jensen LE, Huang Y, Kealey C, Blair IA, Whitehead AS. The up-regulation of monocyte chemoattractant protein-1 (MCP-1) in Ea.hy 926 endothelial cells under long-term low folate stress is mediated by the p38 MAPK pathway. Atherosclerosis. 205: 48-54. PMID 19152916 DOI: 10.1016/J.Atherosclerosis.2008.12.008 |
0.303 |
|
| 2008 |
Edgar KS, Woodside JV, Skidmore P, Cardwell C, Farelll K, McKinley MC, Young IS, Whitehead AS, Gey KF, Yarnell JW, Evans A. Thiol and cardiovascular risk factor status in a male northern Irish population. International Journal For Vitamin and Nutrition Research. Internationale Zeitschrift FüR Vitamin- Und ErnäHrungsforschung. Journal International De Vitaminologie Et De Nutrition. 78: 208-16. PMID 19326344 DOI: 10.1024/0300-9831.78.45.208 |
0.346 |
|
| 2008 |
Lu ZY, Morales M, Khartulyari S, Mei M, Murphy KM, Stanislawska-Sachadyn A, Summers CM, Huang Y, Von Feldt JM, Blair IA, Mitchell LE, Whitehead AS. Genetic and biochemical determinants of serum concentrations of monocyte chemoattractant protein-1, a potential neural tube defect risk factor. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 736-41. PMID 18937353 DOI: 10.1002/Bdra.20507 |
0.629 |
|
| 2008 |
Summers CM, Cucchiara AJ, Nackos E, Hammons AL, Mohr E, Whitehead AS, Von Feldt JM. Functional polymorphisms of folate-metabolizing enzymes in relation to homocysteine concentrations in systemic lupus erythematosus. The Journal of Rheumatology. 35: 2179-86. PMID 18785313 DOI: 10.3899/Jrheum.080071 |
0.595 |
|
| 2008 |
Huang Y, Khartulyari S, Morales ME, Stanislawska-Sachadyn A, Von Feldt JM, Whitehead AS, Blair IA. Quantification of key red blood cell folates from subjects with denned MTHFR 677C>T genotypes using stable isotope dilution liquid chromatography/mass spectrometry Rapid Communications in Mass Spectrometry. 22: 2403-2412. PMID 18634122 DOI: 10.1002/Rcm.3624 |
0.301 |
|
| 2008 |
Summers CM, Hammons AL, Mitchell LE, Woodside JV, Yarnell JW, Young IS, Evans A, Whitehead AS. Influence of the cystathionine beta-synthase 844ins68 and methylenetetrahydrofolate reductase 677C>T polymorphisms on folate and homocysteine concentrations. European Journal of Human Genetics : Ejhg. 16: 1010-3. PMID 18398434 DOI: 10.1038/Ejhg.2008.69 |
0.63 |
|
| 2008 |
Stanisławska-Sachadyn A, Brown KS, Mitchell LE, Woodside JV, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women. Human Genetics. 123: 289-95. PMID 18247058 DOI: 10.1007/S00439-008-0475-Y |
0.412 |
|
| 2008 |
Stanisławska-Sachadyn A, Woodside JV, Brown KS, Young IS, Murray L, McNulty H, Strain JJ, Boreham CA, Scott JM, Whitehead AS, Mitchell LE. Evidence for sex differences in the determinants of homocysteine concentrations. Molecular Genetics and Metabolism. 93: 355-62. PMID 18180190 DOI: 10.1016/J.Ymgme.2007.11.004 |
0.345 |
|
| 2007 |
Casley WL, Ogrodowczyk C, Larocque L, Jaentschke B, LeBlanc-Westwood C, Menzies JA, Whitehouse L, Hefford MA, Aubin RA, Thorn CF, Whitehead AS, Li X. Cytotoxic doses of ketoconazole affect expression of a subset of hepatic genes Journal of Toxicology and Environmental Health - Part a: Current Issues. 70: 1946-1955. PMID 17966066 DOI: 10.1080/15287390701551407 |
0.31 |
|
| 2007 |
Laing ME, Dicker P, Moloney FJ, Ho WL, Murphy GM, Conlon P, Whitehead AS, Shields DC. Association of methylenetetrahydrofolate reductase polymorphism and the risk of squamous cell carcinoma in renal transplant patients. Transplantation. 84: 113-6. PMID 17627246 DOI: 10.1097/01.Tp.0000266069.41882.28 |
0.309 |
|
| 2007 |
Schelleman H, Chen Z, Kealey C, Whitehead AS, Christie J, Price M, Brensinger CM, Newcomb CW, Thorn CF, Samaha FF, Kimmel SE. Warfarin response and vitamin K epoxide reductase complex 1 in African Americans and Caucasians. Clinical Pharmacology and Therapeutics. 81: 742-7. PMID 17329985 DOI: 10.1038/Sj.Clpt.6100144 |
0.321 |
|
| 2007 |
Kealey C, Chen Z, Christie J, Thorn CF, Whitehead AS, Price M, Samaha FF, Kimmel SE. Warfarin and cytochrome P450 2C9 genotype: possible ethnic variation in warfarin sensitivity. Pharmacogenomics. 8: 217-25. PMID 17324110 DOI: 10.2217/14622416.8.3.217 |
0.327 |
|
| 2006 |
Stanisławska-Sachadyn A, Jensen LE, Kealey C, Woodside JV, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. Association between the NAT1 1095C > A polymorphism and homocysteine concentration. American Journal of Medical Genetics. Part A. 140: 2374-7. PMID 17036310 DOI: 10.1002/Ajmg.A.31475 |
0.338 |
|
| 2006 |
Jensen LE, Hoess K, Mitchell LE, Whitehead AS. Loss of function polymorphisms in NAT1 protect against spina bifida. Human Genetics. 120: 52-7. PMID 16680433 DOI: 10.1007/S00439-006-0181-6 |
0.362 |
|
| 2006 |
Jensen LE, Etheredge AJ, Brown KS, Mitchell LE, Whitehead AS. Maternal genotype for the monocyte chemoattractant protein 1 A(-2518)G promoter polymorphism is associated with the risk of spina bifida in offspring. American Journal of Medical Genetics. Part A. 140: 1114-8. PMID 16596675 DOI: 10.1002/Ajmg.A.31212 |
0.34 |
|
| 2005 |
Jensen LE, Hoess K, Whitehead AS, Mitchell LE. The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 512-6. PMID 15959877 DOI: 10.1002/Bdra.20143 |
0.324 |
|
| 2005 |
Kealey C, Brown KS, Woodside JV, Young I, Murray L, Boreham CA, McNulty H, Strain JJ, McPartlin J, Scott JM, Whitehead AS. A common insertion/deletion polymorphism of the thymidylate synthase (TYMS) gene is a determinant of red blood cell folate and homocysteine concentrations. Human Genetics. 116: 347-53. PMID 15682292 DOI: 10.1007/S00439-004-1243-2 |
0.384 |
|
| 2004 |
Kelly CB, McDonnell AP, Johnston TG, Mulholland C, Cooper SJ, McMaster D, Evans A, Whitehead AS. The MTHFR C677T polymorphism is associated with depressive episodes in patients from Northern Ireland. Journal of Psychopharmacology (Oxford, England). 18: 567-71. PMID 15582924 DOI: 10.1177/0269881104047285 |
0.306 |
|
| 2004 |
Jensen LE, Barbaux S, Hoess K, Fraterman S, Whitehead AS, Mitchell LE. The human T locus and spina bifida risk. Human Genetics. 115: 475-82. PMID 15449172 DOI: 10.1007/S00439-004-1185-8 |
0.371 |
|
| 2004 |
Jensen LE, Wall AM, Cook M, Hoess K, Thorn CF, Whitehead AS, Mitchell LE. A common ABCC2 promoter polymorphism is not a determinant of the risk of spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 396-9. PMID 15211708 DOI: 10.1002/Bdra.20023 |
0.332 |
|
| 2004 |
Brown KS, Kluijtmans LA, Young IS, Murray L, McMaster D, Woodside JV, Yarnell JW, Boreham CA, McNulty H, Strain JJ, McPartlin J, Scott JM, Mitchell LE, Whitehead AS. The 5,10-methylenetetrahydrofolate reductase C677T polymorphism interacts with smoking to increase homocysteine. Atherosclerosis. 174: 315-22. PMID 15136061 DOI: 10.1016/J.Atherosclerosis.2004.01.023 |
0.332 |
|
| 2004 |
Brown KS, Cook M, Hoess K, Whitehead AS, Mitchell LE. Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 101-6. PMID 15039923 DOI: 10.1002/Bdra.20002 |
0.359 |
|
| 2004 |
Thorn CF, Lu ZY, Whitehead AS. Regulation of the human acute phase serum amyloid A genes by tumour necrosis factor-alpha, interleukin-6 and glucocorticoids in hepatic and epithelial cell lines. Scandinavian Journal of Immunology. 59: 152-8. PMID 14871291 DOI: 10.1111/J.0300-9475.2004.01369.X |
0.325 |
|
| 2004 |
Brown KS, Kluijtmans LA, Young IS, McNulty H, Mitchell LE, Yarnell JW, Woodside JV, Boreham CA, McMaster D, Murray L, Strain JJ, Whitehead AS. The thymidylate synthase tandem repeat polymorphism is not associated with homocysteine concentrations in healthy young subjects. Human Genetics. 114: 182-5. PMID 14586640 DOI: 10.1007/S00439-003-1039-9 |
0.381 |
|
| 2003 |
Jensen LE, Whitehead AS. Ubiquitin activated tumor necrosis factor receptor associated factor-6 (TRAF6) is recycled via deubiquitination Febs Letters. 553: 190-194. PMID 14550571 DOI: 10.1016/S0014-5793(03)00998-0 |
0.318 |
|
| 2003 |
Thorn CF, Lu ZY, Whitehead AS. Tissue-specific regulation of the human acute-phase serum amyloid A genes, SAA1 and SAA2, by glucocorticoids in hepatic and epithelial cells. European Journal of Immunology. 33: 2630-9. PMID 12938239 DOI: 10.1002/Eji.200323985 |
0.326 |
|
| 2003 |
Jensen LE, Whitehead AS. Expression of alternatively spliced interleukin-1 receptor accessory protein mRNAs is differentially regulated during inflammation and apoptosis Cellular Signalling. 15: 793-802. PMID 12781872 DOI: 10.1016/S0898-6568(03)00039-1 |
0.314 |
|
| 2003 |
Brown KS, Kluijtmans LA, Young IS, Woodside J, Yarnell JW, McMaster D, Murray L, Evans AE, Boreham CA, McNulty H, Strain JJ, Mitchell LE, Whitehead AS. Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 1014-20. PMID 12689917 DOI: 10.1161/01.Atv.0000071348.70527.F4 |
0.338 |
|
| 2003 |
Kluijtmans LA, Young IS, Boreham CA, Murray L, McMaster D, McNulty H, Strain JJ, McPartlin J, Scott JM, Whitehead AS. Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults. Blood. 101: 2483-8. PMID 12642343 DOI: 10.1182/Blood.V101.7.2483 |
0.363 |
|
| 2003 |
Meleady R, Ueland PM, Blom H, Whitehead AS, Refsum H, Daly LE, Vollset SE, Donohue C, Giesendorf B, Graham IM, Ulvik A, Zhang Y, Bjorke Monsen AL. Thermolabile methylenetetrahydrofolate reductase, homocysteine, and cardiovascular disease risk: the European Concerted Action Project. The American Journal of Clinical Nutrition. 77: 63-70. PMID 12499324 DOI: 10.1093/Ajcn/77.1.63 |
0.319 |
|
| 2002 |
Thorn CF, Whitehead AS. Differential transcription of the mouse acute phase serum amyloid A genes in response to pro-inflammatory cytokines. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 9: 229-36. PMID 12557750 DOI: 10.3109/13506120209114098 |
0.327 |
|
| 2002 |
Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida. American Journal of Human Genetics. 71: 1222-6. PMID 12375236 DOI: 10.1086/344209 |
0.334 |
|
| 2002 |
Thorn CF, Whitehead AS. Differential glucocorticoid enhancement of the cytokine-driven transcriptional activation of the human acute phase serum amyloid A genes, SAA1 and SAA2. Journal of Immunology (Baltimore, Md. : 1950). 169: 399-406. PMID 12077270 DOI: 10.4049/Jimmunol.169.1.399 |
0.323 |
|
| 2002 |
Steiner M, Schuff-Werner P, Freund M, Köhne C, Stevenson JP, Whitehead AS, O’Dwyer PJ. Combined Chemotherapy Trials Require Combined Pharmacogenetic Approaches Journal of Clinical Oncology. 20: 1425-1426. PMID 11870191 DOI: 10.1200/Jco.2002.20.5.1425 |
0.305 |
|
| 2001 |
Gaughan DJ, Kluijtmans LA, Barbaux S, McMaster D, Young IS, Yarnell JW, Evans A, Whitehead AS. The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations. Atherosclerosis. 157: 451-6. PMID 11472746 DOI: 10.1016/S0021-9150(00)00739-5 |
0.395 |
|
| 2001 |
Rygg M, Uhlar CM, Thorn C, Jensen LE, Gaughan DJ, Varley AW, Munford RS, Göke R, Chen Y, Whitehead AS. In vitro evaluation of an enhanced human serum amyloid A (SAA2) promoter-regulated soluble TNF receptor fusion protein for anti-inflammatory gene therapy. Scandinavian Journal of Immunology. 53: 588-95. PMID 11422907 DOI: 10.1046/J.1365-3083.2001.00919.X |
0.312 |
|
| 2001 |
Jensen LE, Whitehead AS. IRAK1b, a Novel Alternative Splice Variant of Interleukin-1 Receptor-associated Kinase (IRAK), Mediates Interleukin-1 Signaling and Has Prolonged Stability Journal of Biological Chemistry. 276: 29037-29044. PMID 11397809 DOI: 10.1074/Jbc.M103815200 |
0.305 |
|
| 2001 |
Whitehead AS, FitzGerald GA. Twenty-first century phox: not yet ready for widespread screening. Circulation. 103: 7-9. PMID 11136676 DOI: 10.1161/01.Cir.103.1.7 |
0.306 |
|
| 2001 |
Cahill M, Karabatzaki M, Donoghue C, Meleady R, Mynett-Johnson LA, Mooney D, Graham IM, Whitehead AS, Shields DC. Thermolabile MTHFR genotype and retinal vascular occlusive disease. The British Journal of Ophthalmology. 85: 88-90. PMID 11133719 DOI: 10.1136/Bjo.85.1.88 |
0.315 |
|
| 2000 |
Shields DC, Ramsbottom D, Donoghue C, Pinjon E, Kirke PN, Molloy AM, Edwards YH, Mills JL, Mynett-Johnson L, Weir DG, Scott JM, Whitehead AS. Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury). American Journal of Medical Genetics. 92: 206-11. PMID 10817656 DOI: 10.1002/(Sici)1096-8628(20000529)92:3<206::Aid-Ajmg9>3.0.Co;2-W |
0.336 |
|
| 2000 |
Barbaux S, Plomin R, Whitehead AS. Polymorphisms of genes controlling homocysteine/folate metabolism and cognitive function. Neuroreport. 11: 1133-6. PMID 10790895 DOI: 10.1097/00001756-200004070-00044 |
0.331 |
|
| 2000 |
Murphy RP, Donoghue C, Nallen RJ, D'Mello M, Regan C, Whitehead AS, Fitzgerald DJ. Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy. Arteriosclerosis, Thrombosis, and Vascular Biology. 20: 266-70. PMID 10634828 DOI: 10.1161/01.Atv.20.1.266 |
0.305 |
|
| 2000 |
Barbaux S, Kluijtmans LAJ, Whitehead AS. Accurate and Rapid “Multiplex Heteroduplexing” Method for Genotyping Key Enzymes Involved in Folate/Homocysteine Metabolism Clinical Chemistry. 46: 907-912. DOI: 10.1093/Clinchem/46.7.907 |
0.358 |
|
| 1999 |
Harmon DL, Shields DC, Woodside JV, McMaster D, Yarnell JWG, Young IS, Peng K, Shane B, Evans AE, Whitehead AS. Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations Genetic Epidemiology. 17: 298-309. PMID 10520212 DOI: 10.1002/(Sici)1098-2272(199911)17:4<298::Aid-Gepi5>3.0.Co;2-V |
0.402 |
|
| 1999 |
Uhlar CM, Whitehead AS. Serum amyloid A, the major vertebrate acute-phase reactant. European Journal of Biochemistry. 265: 501-23. PMID 10504381 DOI: 10.1046/J.1432-1327.1999.00657.X |
0.348 |
|
| 1999 |
Mahmud N, Molloy A, McPartlin J, Corbally R, Whitehead AS, Scott JM, Weir DG. Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications. Gut. 45: 389-94. PMID 10446107 DOI: 10.1136/Gut.45.3.389 |
0.326 |
|
| 1999 |
Shields DC, Kirke PN, Mills JL, Ramsbottom D, Molloy AM, Burke H, Weir DG, Scott JM, Whitehead AS. 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. American Journal of Human Genetics. 64: 1045-55. PMID 10090889 DOI: 10.1086/302310 |
0.335 |
|
| 1998 |
Jensen LE, Whitehead AS. Regulation of serum amyloid A protein expression during the acute-phase response Biochemical Journal. 334: 489-503. PMID 9729453 DOI: 10.1042/Bj3340489 |
0.343 |
|
| 1998 |
Molloy AM, Mills JL, Kirke PN, Ramsbottom D, McPartlin JM, Burke H, Conley M, Whitehead AS, Weir DG, Scott JM. Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor. American Journal of Medical Genetics. 78: 155-9. PMID 9674907 DOI: 10.1002/(Sici)1096-8628(19980630)78:2<155::Aid-Ajmg11>3.0.Co;2-M |
0.361 |
|
| 1998 |
Molloy AM, Mills JL, Kirke PN, Whitehead AS, Weir DG, Scott JM. Whole-Blood Folate Values in Subjects with Different Methylenetetrahydrofolate Reductase Genotypes: Differences Between the Radioassay and Microbiological Assays Clinical Chemistry. 44: 186-188. DOI: 10.1093/Clinchem/44.1.186A |
0.314 |
|
| 1997 |
Grehan S, Herbert J, Whitehead AS. Down-regulation of the major circulating precursors of proteins deposited in secondary amyloidosis by a recombinant mouse interleukin-1 receptor antagonist. European Journal of Immunology. 27: 2593-9. PMID 9368615 DOI: 10.1002/Eji.1830271019 |
0.333 |
|
| 1997 |
Harmon DL, McMaster D, Shields DC, Whitehead AS, Rea IM. MTHFR thermolabile genotype frequencies and longevity in Northern Ireland Atherosclerosis. 131: 137-138. PMID 9180255 DOI: 10.1016/S0021-9150(97)06096-6 |
0.331 |
|
| 1997 |
Molloy AM, Daly S, Mills JL, Kirke PN, Whitehead AS, Ramsbottom D, Conley MR, Weir DG, Scott JM. Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: implications for folate intake recommendations. Lancet. 349: 1591-3. PMID 9174561 DOI: 10.1016/S0140-6736(96)12049-3 |
0.332 |
|
| 1997 |
Butler A, Whitehead AS. Structure of the mouse serum amyloid A 5 (Saa5) gene: relationship to other members of the serum amyloid A family. Scandinavian Journal of Immunology. 45: 160-5. PMID 9042428 DOI: 10.1046/J.1365-3083.1997.D01-385.X |
0.309 |
|
| 1996 |
Gallagher PM, Meleady R, Shields DC, Tan KS, McMaster D, Rozen R, Evans A, Graham IM, Whitehead AS. Homocysteine and risk of premature coronary heart disease: Evidence for a common gene mutation Circulation. 94: 2154-2158. PMID 8901666 DOI: 10.1161/01.Cir.94.9.2154 |
0.337 |
|
| 1995 |
Gaughan DJ, Steel DM, Whitehead AS. Ribozyme mediated cleavage of acute phase serum amyloid A (A-SAA) mRNA in vitro. Febs Letters. 374: 241-5. PMID 7589544 DOI: 10.1016/0014-5793(95)01118-X |
0.31 |
|
| 1995 |
Whitehead AS, Gallagher P, Mills JL, Kirke PN, Burke H, Molloy AM, Weir DG, Shields DC, Scott JM. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects Qjm: An International Journal of Medicine. 88: 763-766. DOI: 10.1093/Oxfordjournals.Qjmed.A069003 |
0.335 |
|
| 1994 |
Uhlar CM, Burgess CJ, Sharp PM, Whitehead AS. Evolution of the serum amyloid A (SAA) protein superfamily. Genomics. 19: 228-35. PMID 8188253 DOI: 10.1006/Geno.1994.1052 |
0.331 |
|
| 1994 |
Sellar GC, Jordan SA, Bickmore WA, Fantes JA, Van Heyningen V, Whitehead AS. The human serum amyloid A protein (SAA) superfamily gene cluster: Mapping to chromosome 11p15.1 by physical and genetic linkage analysis Genomics. 19: 221-227. PMID 8188252 DOI: 10.1006/Geno.1994.1051 |
0.311 |
|
| 1994 |
Sellar GC, Whitehead AS. The putative fifth human serum amyloid A protein (SAA)-related gene "SAA5" is defined by SAA3. Biochemical and Biophysical Research Communications. 200: 202-5. PMID 8166688 DOI: 10.1006/Bbrc.1994.1434 |
0.333 |
|
| 1994 |
Zahedi KA, Uhlar CM, Rits M, Prada AE, Whitehead AS. The mouse interleukin 1 receptor antagonist protein: gene structure and regulation in vitro. Cytokine. 6: 1-9. PMID 8003626 DOI: 10.1016/1043-4666(94)90001-9 |
0.314 |
|
| 1993 |
Zahedi K, Whitehead AS. Regulation of mouse serum amyloid P gene expression by cytokines in vitro. Biochimica Et Biophysica Acta. 1176: 162-8. PMID 8452873 DOI: 10.1016/0167-4889(93)90192-R |
0.351 |
|
| 1993 |
Steel DM, Rogers JT, DeBeer MC, DeBeer FC, Whitehead AS. 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. The Biochemical Journal. 291: 701-7. PMID 8387777 DOI: 10.1042/Bj2910701 |
0.324 |
|
| 1993 |
Sellar GC, Whitehead AS. Localization of four human serum amyloid A (SAA) protein superfamily genes to chromosome 11p: characterization of a fifth SAA-related gene sequence. Genomics. 16: 774-6. PMID 8325654 DOI: 10.1006/Geno.1993.1265 |
0.332 |
|
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