Browse by Divisions pre August 2011

Baralle, M., Baralle, D., De Conti, L., Mattocks, C., Whittaker, J., Knezevich, A., Ffrench-Constant, C. and Baralle, F.E. (2003) Identification of a mutation that perturbs NF1 agene splicing using genomic DNA samples and a minigene assay. Journal of Medical Genetics, 40, (3), 220-222. (doi:10.1136/jmg.40.3.220).

Baxter, E. J., Kulkarni, S., Vizmanos, J. L., Jaju, R., Martinelli, G., Testoni, N., Hughes, G., Salamanchuk, Z., Calasanz, M. J., Lahortiga, I., Pocock, C. F., Dang, R., Fidler, C., Wainscoat, J. S., Boultwood, J. and Cross, N. C. (2003) Novel translocations that disrupt the platelet-derived growth factor receptor beta (PDGFRB) gene in BCR-ABL-negative chronic myeloproliferative disorders. British journal of haematology, 120, (2), 251 - 256. (doi:10.1046/j.1365-2141.2003.04051.x).

Beghé, B., Barton, S., Rorke, S., Peng, Q., Sayers, I., Gaunt, T., Keith, T.P., Clough, J.B., Holgate, S.T. and Holloway, J.W. (2003) Polymorphisms in the interleukin-4 and interleukin-4 receptor α chain genes confer susceptibility to asthma and atopy in a Caucasian population. Clinical and Experimental Allergy, 33, (8), 1111-1117. (doi:10.1046/j.1365-2222.2003.01731.x).

Beyzade, Seyyare, Zhang, Shaoli, Wong, Yuk-ki, Day, Ian N.M., Eriksson, Per and Ye, Shu (2003) Influences of matrix metalloproteinase-3 gene variation on extent of coronary atherosclerosis and risk of myocardial infarction. Journal of the American College of Cardiology, 41, (12), 2130-2137. (doi:10.1016/S0735-1097(03)00482-0).

Bower, K. L., Dennis, N. R., Wellesley, D., Williams, C. P., Hodgkins, P., Tyreman, C., Browne, C. E. and Barber, J. C. (2003) New case of "apple-peel" intestinal atresia and ocular anomalies with mosaic variegated aneuploidy. American Journal of Medical Genetics, 117A, (2), 200 - 201. (doi: 10.1002/ajmg.a.10035).

Brickwood, S., Bonthron, D. T., Al-Gazali, L. I., Piper, K., Hearn, T., Wilson, D. I. and Hanley, N. A. (2003) Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3. Journal of Medical Genetics, 40, (9), 685 - 689.

Brümmendorf, Tim H., Ersöz, InciI, Hartmann, Ulrike, Bartolovic, Kerol, Balabanov, Stefan, Wahl, Alexandra, Paschka, Peter, Kreil, Sebastian, Lahaye, Tanja, Berger, Ute, Gschaidmeier, Harald, Bokemeyer, Carsten, Hehlmann, Rüdiger, Dietz, Klaus, Lansdorp, Peter M., Kanz, Lothar and Hochhaus, Andreas (2003) Telomere length in peripheral blood granulocytes reflects response to treatment with imatinib in patients with chronic myeloid leukemia. Blood, 101, (1), 375.

Bunyan, D., Thomas, N.S., Cross, N.C.P. and Harvey, J.F. (2003) Importance of mutation screening in 'false-positive' MLPA cases. Journal of Medical Genetics, 40, pp.S80.

Carroll, Michael, Levasseur, Mark, Wood, Chris, Whitaker, Michael, Jones, Keith T. and McDougall, Alex (2003) Exploring the mechanism of action of the sperm-triggered calcium-wave pacemaker in ascidian zygotes. Journal of Cell Science, 116, (24), 4997-5004. (doi:10.1242/10.1242/jcs.00846).

Chase, A., Higley, K., Baxter, J.F.E. and Cross, N.C.P. (2003) Testing in-vitro for imatinib sensitivity in BCR-ABL negative myeloproliferative disorders. Blood, 102, (11), pp.658A.

Chase, Alex J. and Newby, Andrew C. (2003) Regulation of matrix metalloproteinase (matrixin) genes in blood vessels: a multi-step recruitment model for pathological remodelling. Journal of Vascular Research, 40, (4), 329-343. (doi:10.1159/000072697).

Child, N.J.A., Yang, I.A., Pulletz, M.C.K., de Courcy-Golder, K., Andrews, A.-L., Pappachan, V.J. and Holloway, J.W. (2003) Polymorphisms in Toll-like receptor 4 and the systemic inflammatory response syndrome. Biochemical Society Transactions, 31, (3), 652-653.

Cockwell, Annette E., Jacobs, Patricia A., Beal, Sarah J. and Crolla, John A. (2003) A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities. Human Genetics, 112, (3), 298-302. (doi:10.1007/s00439-002-0887-z).

Day, Ian N.M. (2003) Genetics of Monogenic Hypercholesterolemia. In, Cooper, David (ed.) Nature Encyclopedia of the Human Genome. London, Nature Publishing Group, 69-74.

Deguchi, Kenji, Ayton, Paul M., Carapeti, Melina, Kutok, Jeffery L., Snyder, Cynthia S., Williams, Ifor R., Cross, Nicholas C.P., Glass, Christopher K., Cleary, Michael L. and Gilliland, D. Gary (2003) MOZ-TIF2-induced acute myeloid leukemia requires the MOZ nucleosome binding motif and TIF2-mediated recruitment of CBP. Cancer Cell, 3, (3), 259-271. (doi:10.1016/S1535-6108(03)00051-5).

Douglas, Jenny, Hanks, Sandra, Temple, I. Karen, Davies, Sally, Murray, Alexandra, Upadhyaya, Meena, Tomkins, Susan, Hughes, Helen E., Cole, Trevor R.P. and Rahman, Nazneen (2003) NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes. American Journal of Human Genetics, 72, (1), 132-143. (doi:10.1086/345647).

Fiegler, H., Gribble, S.M., Burford, D.C., Carr, P., Prigmore, E., Porter, K.M., Clegg, S., Crolla, J.A., Dennis, N.R., Jacobs, P. and Carter, N.P. (2003) Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays. Journal of Medical Genetics, 40, (9), 664-670. (doi:10.1136/jmg.40.9.664).

Foulds, Nicola, Fairhurst, Jo, Temple, I. Karen, Cade, Steven, Groves, Charlotte and Lancaster, Tessa (2003) A female case of Sedaghatian type spondylometaphyseal dysplasia. American Journal of Medical Genetics Part A, 118A, (4), 377-381. (doi:10.1002/ajmg.a.10199).

Gaunt, Tom R., Hinks, Lesley J., Rassoulian, Hamid and Day, Ian N.M. (2003) Manual 768 or 384 well microplate gel 'dry' electrophoresis for PCR checking and SNP genotyping. Nucleic Acids Research, 31, (9) (doi:10.1093/nar/gng048).

Good, Catriona D., Lawrence, Kate, Thomas, N. Simon, Price, Cathy J., Ashburner, John, Friston, Karl J., Frackowiak, Richard S.J., Oreland, Lars and Skuse, David H. (2003) Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans. Brain, 126, (11), 2431-2446. (doi:10.1093/brain/awg242).

Guy, Jane, Hearn, Tom, Crosier, Moira, Mudge, Jonathan, Viggiano, Luigi, Koczan, Dirk, Thiesen, Hans-Jurgen, Bailey, Jeffrey A., Horvath, Julie E., Eichler, Evan E., Earthrowl, Mark E., Deloukas, Panos, French, Lisa, Rogers, Jane, Bentley, David and Jackson, Michael S. (2003) Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p. Genome Research, 13, (2), 159-172. (doi:10.1101/gr.644503). (PMID:12566394).

Hodgkinson, Conrad P. and Ye, Shu (2003) Microarray analysis of peroxisome proliferator-activated receptor-γ induced changes in gene expression in macrophages. Biochemical and Biophysical Research Communications, 308, (3), 505-510. (doi:10.1016/S0006-291X(03)01416-5).

Holgate, S.T., Davies, D.E., Murphy, G., Powell, R.M. and Holloway, J.W. (2003) Editorial. ADAM 33: just another asthma gene or a breakthrough in understanding the origins of bronchial hyperresponsiveness? Thorax, 58, (6), 466-469. (doi:10.1136/thorax.58.6.466).

Hollox, E.J., Armour, A.L. and Barber, J.C.K. (2003) Extensive normal copy number variation of a β-defensin antimicrobial-gene cluster. American Journal of Human Genetics, 73, (3), 591-600. (doi:10.1086/378157).

Houghton, Franchesca D., Humpherson, Peter G., Hawkhead, Judith A., Hall, Christine J. and Leese, Henry J. (2003) Na+, K+, ATPase activity in the human and bovine preimplantation embryo. Developmental Biology, 263, (2), 360-366. (doi:10.1016/j.ydbio.2003.07.014).

Kajantie, Eero, Dunkel, Leo, Turpeinen, Ursula, Stenman, Ulf-Hakan, Wood, Peter J., Nuutila, Mika and Andersson, Sture (2003) Placental 11β-Hydroxysteroid Dehydrogenase-2 and fetal cortisol/cortisone shuttle in small preterm infants. The Journal of Clinical Endocrinology and Metabolism, 88, (1), 493-500.

Ke, X. and Collins, A. (2003) CpG islands in human X-inactivation. Annals of Human Genetics, 67, (3), 242-249. (doi:10.1046/j.1469-1809.2003.00038.x).

Kevern, Liam, Warwick, David, Wellesley, Diana, Senbaga, Raj and Clarke, N.M. (2003) Prenatal ultrasound: detection and diagnosis of limb abnormalities. Journal of Pediatric Orthopedics, 23, (2), 251-253.

Kimber, J., McLean, B.N., Prevett, M. and Hammans, S.R. (2003) Allgrove or 4 "A" syndrome: An autosomal recessive syndrome causing multisystem neurological disease. Journal of Neurology, Neurosurgery and Psychiatry, 74, (5), 654-657. (doi:10.1136/jnnp.74.5.654).

Lawrence, K.M., Scarabelli, T.M., Turtle, L., Chanalaris, A., Townsend, P.A., Carroll, C.J., Hubank, M., Stephanou, A., Knight, R.A. and Latchman, D.S. (2003) Urocortin protects cardiac myocytes from ischemia/reperfusion injury by attenuating calcium-insensitive phospholipase A2 gene expression. The Federation of American Societies for Experimental Biology (FASEB) Journal, 17, (15), 2313-2315. (doi:10.1096/fj.02-0832fje).

Lei, H. and Vorechovsky, I. (2003) BACH1 517C--> T transition impairs protein translocation to nucleus: a role in breast cancer susceptibility? International journal of cancer, 104, (3), 389 - 391. (doi:10.1002/ijc.10947).

Lonjou, Christine, Zhang, Weihua, Collins, Andrew, Tapper, William J., Elahi, Eiram, Maniatis, Nikolas and Morton, Newton E. (2003) Linkage disequilibrium in human populations. Proceedings of the National Academy of Sciences of the United States of America, 100, (10), 6069-6074. (doi:10.1073/pnas.1031521100).

Lotery, Andrew J., Yang, Grace S., Mullins, Robert F., Russell, Stephen R., Schmidt, Michael, Stone, Edwin M., Lindbloom, Jonathan D., Chiorini, John A., Kotin, Robert M. and Davidson, Beverly L. (2003) Adeno-associated virus type 5: transduction efficiency and cell-type specificity in the primate retina. Human Gene Therapy, 14, (17), 1663-1671. (doi:10.1089/104303403322542301).

Macdonald, D., Reiter, A. and Cross, N.C.P. (2003) The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1. In, Bain, B.J. (ed.) Chronic Myeloproliferative Disorders: Cytogenetic and Molecular Genetic Abnormalities. Basel, Switzerland, Karger, 62-68. (doi:10.1159/000068098).

Macpherson, J., Waghorn, A., Hammans, S. and Jacobs, P. (2003) Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia. Human Genetics, 112, (5-6), 619 - 620. (doi:10.1007/s00439-003-0939-z).

Maggouta, F., Roberts, S.E., Dennis, N.R., Veltman, M.W. and Crolla, J.A. (2003) A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype. Journal of Medical Genetics, 40, (7), e84.

Marchbanks, R.M., Ryan, Margaret, Day, I.N.M., Owen, M., McGuffin, P. and Whatley, S.A. (2003) A mitochondrial DNA sequence variant associated with schizophrenia and oxidative stress. Schizophrenia Research, 65, (1), 33 - 38. (doi:10.1016/S0920-9964(03)00011-2).

Masud, S. and Ye, S. (2003) Effect of the peroxisome proliferator activated receptor-gamma gene Pro12Ala variant on body mass index: a meta-analysis. Journal of Medical Genetics, 40, (10), 773 - 780.

Mattocks, C., Harvey, J.F. and Cross, N.C.P. (2003) An evaluation of the AutoGen NA-3000EU automatic nucleic acid isolation system. Journal of Medical Genetics, 40, pp.S78.

Mattocks, C., Tarpey, P.S., Whittaker, J.L., Harvey, J.F. and Cross, N.C.P. (2003) A large scale validation of prototype software for high throughput Comparative Sequence Analysis. Journal of Medical Genetics, 40, pp.S79.

Morgan, A., Zhang, B., Tapper, W., Collins, A. and Ye, S. (2003) Haplotypic analysis of the matrix metalloproteinase-9 gene in relation to coronary artery disease. Atherosclerosis Supplements, 4, (2), p.321. (doi:10.1016/S1567-5688(03)91377-8).

Morgan, Angharad R., Zhang, Baiping, Tapper, William, Collins, Andrew and Ye, Shu (2003) Haplotypic analysis of the MMP-9 gene in relation to coronary artery disease. Journal of Molecular Medicine, 81, (5), 321-326. (doi:10.1007/s00109-003-0441-z).

Morton, Newton E. (2003) Recollections of James Neel. Mutation Research, 543, (2), 97-104. (doi:10.1016/S1383-5742(03)00006-1).

Morton, Newton. E. (2003) Genetic epidemiology, genetic maps and positional cloning. Philosophical Transactions of the Royal Society B: Biological Sciences, 358, (1438), 1701-1708. (doi:10.1098/rstb.2003.1357).

Pardanani, A., Elliott, M., Reeder, T., Li, C.Y., Baxter, E.J., Cross, N.C.P. and Tefferi, A. (2003) Imatinib for systemic mast-cell disease. Lancet, 362, (9383), 535-536. (doi:10.1016/S0140-6736(03)14115-3).

Pardanani, Animesh, Ketterling, Rhett P., Brockman, Stephanie R., Flynn, Heather C., Paternoster, Sarah F., Shearer, Brandon M., Reeder, Terra L., Li, Chin-Yang, Cross, Nicholas C.P., Cools, Jan, Gilliland, Gary, Dewald, Gordon W. and Tefferi, Ayalew (2003) CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy. Blood, 102, (9), 3093-3096. (doi:10.1182/blood-2003-05-1627).

Pardanani, Animesh, Reeder, Terra, Porrata, Luis F., Li, Chin-Yang, Tazelaar, Henry D., Baxter, E. Joanna, Witzig, Thomas E., Cross, Nicholas C.P. and Tefferi, Ayalew (2003) Imatinib therapy for hypereosinophilic syndrome and other eosinophilic disorders. Blood, 101, (9), 3391-3397. (doi:10.1182/blood-2002-10-3103).

Powell, Robert M., Hamilton, Lynnsey M., Holgate, Stephen T., Davies, Donna E. and Holloway, John W. (2003) ADAM33: a novel therapeutic target for asthma. Expert Opinion on Therapeutic Targets, 7, (4), 485-494. (doi:10.1517/14728222.7.4.485).

Rauz, S., Cheung, C.M., Wood, P.J., Coca-Prados, M., Walker, E.A., Murray, P.I. and Stewart, P.M. (2003) Inhibition of 11ß-hydroxysteroid dehydrogenase type 1 lowers intraocular pressure in patients with ocular hypertension. QJM, 96, (7), 481-490.

Reiter, A.E.K., Walz, C.F.H., Schoch, C., Chase, A.J., Fuchs, R., Weisser, A., Hochhaus, A., Hehlmann, R. and Cross, N.C.P. (2003) Characterization of two new fusion genes in the 8p11 myeloproliferative syndrome (EMS) generated by disruption of FGFR. Blood, 102, (11), pp.108A.

Renforth, G. L. and Wilson, D. I. (2003) Adults with congenital heart disease: a genetic perspective. In, Gatzoulis, Michael A., Webb, Gary D. and Daubeney, Piers E.R. (eds.) Diagnosis and Management of Adult Congenital Heart Disease. London, UK, Churchill Livingstone, 19-25.

Reynolds, Rebecca M., Syddall, Holly E., Walker, Brian R., Wood, Peter J. and Phillips, David I. (2003) Predicting cardiovascular risk factors from plasma cortisol measured during oral glucose tolerance tests. Metabolism, 52, (5), 524-527. (doi:10.1053/meta.2003.50090).

Roberts, S. E., Maggouta, F., Thomas, N. S., Jacobs, P. A. and Crolla, J. A. (2003) Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity. American Journal of Human Genetics, 73, (5), 1061 - 1072.

Roberts, S.E. and Thomas, N.S. (2003) A quantitative polymerase chain reaction method for determining copy number within the Prader-Willi/Angelman syndrome critical region. Clinical Genetics, 64, (1), 76-78. (doi:10.1034/j.1399-0004.2003.00094.x).

Sayers, I., Barton, S., Rorke, S., Beghe, B., Hayward, B., Van Eerdewegh, P., Keith, T., Clough, J.B., Ye, S., Holloway, J.W., Sampson, A.P. and Holgate, S.T. (2003) Allelic association and functional studies of promoter polymorphism in the leukotriene C4 synthase gene (LTC4S) in asthma. Thorax, 58, (5), 417-424. (doi:10.1136/thorax.58.5.417).

Sayers, I., Barton, S., Rorke, S., Sawyer, J., Peng, Q., Beghe, B., Ye, S., Keith, T., Clough, J.B., Holloway, J.W., Sampson, A.P. and Holgate, S.T. (2003) Promoter polymorphism in the 5-lipoxygenase (ALOX5) and 5-lipoxygenase-activating protein (ALOX5AP) genes and asthma susceptibility in a Caucasian population. Clinical and Experimental Allergy, 33, (8), 1103-1110. (doi:10.1046/j.1365-2222.2003.01733.x).

Sayers, I., Sampson, A.P., Ye, S. and Holgate, S.T. (2003) Promoter polymorphism influences the effect of dexamethasone on transcriptional activation of the LTC4 synthase gene. European Journal of Human Genetics, 11, (8), 619-622. (doi:10.1038/sj.ejhg.5201015).

Shepard, A.R., Jacobson, N., Sui, R., Steely, H.T., Lotery, A.J., Stone, E.M. and Clark, A.F. (2003) Characterization of rabbit myocilin: Implications for human myocilin glycosylation and signal peptide usage. BMC genetics, 4, 5-5. (doi:10.1186/1471-2156-4-5).

Steer, E.J. and Cross, N.C.P. (2003) Myeloproliferative disorders with translocations of chromosome 5q31-35: role of the platelet-derived growth factor receptor beta. In, Bain, B.J. (ed.) Chronic Myeloproliferative Disorders: Cytogenetic and Molecular Genetic Abnormalities. Basel, Switzerland, Karger, 69-79. (doi:10.1159/000068099).

Tabiner, M., Youings, S., Dennis, N., Baldwin, D., Buis, C., Mayers, A.G., Jacobs, P.A. and Crolla, J.A. (2003) Poster session P.3. Anxiety disorder and anxiolytic, P.3.033. Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines. European Neuropsychopharmacology, 13, (Supplement 4), p.S367. (doi:10.1016/S0924-977X(03)92153-5).

Tabiner, M., Youings, S., Dennis, N., Buis, C., Mayers, A.G., Jacobs, P.A., Crolla, J.A. and Baldwin, D.S. (2003) Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines. Journal of Psychopharmacology, 17, (3), p.A25.

Tabiner, Melody, Youings, Sheila, Dennis, Nicholas, Baldwin, David, Buis, Christel, Mayers, Andrew, Jacobs, Patricia A. and Crolla, John A. (2003) Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines. American Journal of Human Genetics, 72, (3), 535-538. (doi:10.1086/367777).

Tapper, W.J., Maniatis, N., Morton, N.E. and Collins, A. (2003) A metric linkage disequilibrium map of a human chromosome. Annals of Human Genetics, 67, (6), 487 -494. (doi:10.1046/j.1469-1809.2003.00050.x).

Thomas, N.S. and Hassold, T.J. (2003) Aberrant recombination and the origin of Klinefelter syndrome. Human Reproduction Update, 9, (4), 309-317. (doi:10.1093/humupd/dmg028).

Thomas, N.S., Roberts, S.E. and Browne, C.E. (2003) Estimate of the prevalence of chromosome 15q11-q13 duplications. American Journal of Medical Genetics - A, 120, (4), 596 - 598. (doi:10.1002/ajmg.a.20140).

Thomas, S., Maloney, V., Bunyan, D.J., Cross, N.C.P. and Harvey, J.F. (2003) Investigation of the SHOX gene and Pseudoautosomal Region 1 in cases of Leri-Weill dyschondrosteosis. Journal of Medical Genetics, 40, pp.S84.

Thurston, L.M., Norgate, D.P., Jonas, K.C., Gregory, L., Wood, P.J., Cooke, B.A. and Michael, A.E. (2003) Ovarian modulators of type 1 11beta-hydroxysteroid dehydrogenase (11betaHSD) activity and intra-follicular cortisol:cortisone ratios correlate with the clinical outcome of IVF. Human Reproduction, 18, (8), 1603-1612. (doi:10.1093/humrep/deg322).

Thurston, L.M., Norgate, D.P., Jonas, K.C., Gregory, L., Wood, P.J., Cooke, B.A. and Michael, A.E. (2003) Ovarian modulators of type 1 11β-hydroxysteroid dehydrogenase (11βHSD) activity and intra-follicular cortisol:cortisone ratios correlate with the clinical outcome of IVF. Human Reproduction, 18, (8), 1603-1612.

Walz, C., Grimwade, D., Saussele, S., Weisser, A., Lafage-Pochitaloff, M., Hochhaus, A., Schoch, C., Schnittger, S., Lengfelder, E., Cross, N.C.P., Hehlmann, R. and Reiter, A. (2003) Mechanisms underlying loss of reciprocal fusion gene expression in acute promyelocytic leukaemia: evidence for deletions on der(17) and complex rearrangements yielding novel fusion gene transcripts. Blood, 102, (11), pp.846A.

Winfield, M., Ibrahim, A.H., Jones, A., Protheroe, R.K.M., Gunaserkera, J.B.L., Wragg, C.S., Vilain-Holmes, A. and Ross, F.M. (2003) Interphase FISH analysis in multiple myeloma. Journal of Medical Genetics, 40, pp.S23.

Yang, Ian A., Holloway, John W. and Ye, Shu (2003) TLR4 Asp299Gly polymorphism is not associated with coronary artery stenosis. Atherosclerosis, 170, (1), 187-190. (doi:10.1016/S0021-9150(03)00286-7).

Ye, S., Dhillon, S., Seear, R., Dunleavey, L., Day, L.B., Bannister, W., Day, I.N. and Simpson, I. (2003) Epistatic interaction between variations in the angiotensin I converting enzyme and angiotensin II type 1 receptor genes in relation to extent of coronary atherosclerosis. Heart, 89, (10), 1195-1199. (doi:10.1136/heart.89.10.1195).

Ye, Shu, Dunleavey, Louise, Bannister, Wendy, Day, Lorna B., Tapper, William, Collins, Andrew R., Day, Ian N.M. and Simpson, Iain (2003) Independent effects of the -219 G>T and ε2/ ε3/ ε4 polymorphisms in the apolipoprotein E gene on coronary artery disease: the Southampton Atherosclerosis Study. European Journal of Human Genetics, 11, (6), 437-443. (doi:10.1038/sj.ejhg.5200983).

Zhang, B., Ye, S., Sayer, A.A., Hammans, S.R., Adio, S., Hinks, L.J., Smythe, P.J., Groot, D., Cooper, C. and Day, I.N.M. (2003) A study of mitochondrial DNA mutations in peripheral lymphocytes in an aging cohort. Biochemical Society Transactions, 31, (2), 444-446.

Zhang, Baiping, Fugleholm, Kaare, Day, Lorna B., Ye, Shu, Weller, Roy O. and Day, Ian N.M. (2003) Molecular pathogenesis of subarachnoid haemorrhage. The International Journal of Biochemistry & Cell Biology, 35, (9), 1341-1360. (doi:10.1016/S1357-2725(03)00043-8).

Zhang, L.Y., Ibbotson, R.E., Orchard, J.A., Gardiner, A.C., Seear, R.V., Chase, A.J., Oscier, D.G. and Cross, N.C.P. (2003) P2X7 polymorphism and chronic lymphocytic leukaemia: lack of correlation with incidence, survival and abnormalities of chromosome 12. Leukemia, 17, (11), 2097-2100. (doi:10.1038/sj.leu.2403125).