Browse by Divisions pre August 2011

Alvarez, Yolanda, Alonso, Maria Teresa, Vendrell, Victor, Zelarayan, Laura Cecilia, Chamero, Pablo, Theil, Thomas, Bösl, Michael R., Kato, Shigeaki, Maconochie, Mark, Riethmacher, Dieter and Schimmang, Thomas (2003) Requirements for FGF3 and FGF10 during inner ear formation. Development, 130, (25), 6329-6338. (doi:10.1242/10.1242/dev.00881).

Arshad, S.H., Bateman, B. and Matthews, S.M. (2003) Primary prevention of asthma and atopy during childhood by allergen avoidance in infancy: a randomised controlled study. Thorax, 58, (6), 489-493. (doi:10.1136/thorax.58.6.489).

Baralle, Diana, Mattocks, Chris, Kalidas, Kamini, Elmslie, Frances, Whittaker, Joanne, Lees, Melissa, Ragge, Nicola, Patton, Michael A., Winter, Robin M. and ffrench-Constant, Charles (2003) Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS). American Journal of Medical Genetics Part A, 119A, (1), 1-8. (doi:10.1002/ajmg.a.20023).

Baralle, M., Baralle, D., De Conti, L., Mattocks, C., Whittaker, J., Knezevich, A., ffrench-Constant, C. and Baralle, F.E. (2003) Letter to JMG. 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).

Brummendorf, T.H., Ersoz, I., Hartmann, U., Balabanov, S., Wolke, H., Paschka, P., Lahaye, T., Berner, B., Bartolovic, K., Kreil, S., Berger, U., Gschaidmeier, H., Bokemeyer, C., Hehlmann, R., Dietz, K., Lansdorp, P.M., Kanz, L. and Hochhaus, A. (2003) Normalization of previously shortened telomere length under treatment with imatinib argues against a preexisting telomere length deficit in normal hematopoietic stem cells from patients with chronic myeloid leukemia. Annals of the New York Academy of Sciences, 996, (Hematopoietic S), 26-38. (doi:10.1111/j.1749-6632.2003.tb03229.x).

Cabanas, E.D., Boyle, T., Browne, C. and Barber, J. (2003) Two new transmitted imbalances without apparent phenotypic effect. Journal of Medical Genetics, 40, pp.S56.

Campbell, C., Barber, J.C.K., Latif, G., Sullivan, C.M. and Waters, C.S. (2003) The phenotypic effect of the abnormal cell line in six patients showing mosaicism for a structural chromosome abnormality. Journal of Medical Genetics, 40, pp.S52.

Clegg, A., Colquitt, J., Sidhu, M., Royle, P. and Walker, A. (2003) Clinical and cost effectiveness of surgery for morbid obesity: a systematic review and economic evaluation. International Journal of Obesity, 27, (10), 1167-1177. (doi:10.1038/sj.ijo.0802394).

Collins, A. (2003) Genetics maps: integration. In, Cooper, David (ed.) Nature Encyclopedia of the Human Genome. London, UK, Nature Publishing Group, 888-891.

Cools, Jan, DeAngelo, Daniel J., Gotlib, Jason, Stover, Elizabeth H., Legare, Robert D., Cortes, Jorges, Kutok, Jeffrey, Clark, Jennifer, Galinsky, Ilene, Griffin, James D., Cross, Nicholas C. P., Tefferi, Ayalew, Malone, James, Alam, Rafeul, Schrier, Stanley L., Schmid, Janet, Rose, Michal, Vandenberghe, Peter, Verhoef, Gregor, Boogaerts, Marc, Wlodarska, Iwona, Kantarjian, Hagop, Marynen, Peter, Coutre, Steven E., Stone, Richard and Gilliland, D. Gary (2003) A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. The New England Journal of Medicine, 348, (13), 1201-1214.

Cross, Nicholas C.P. and Hochhaus, Andreas (2003) Minimal residual disease in chronic myelogenous leukemia: results of RT-PCR detection of BCR-ABL transcripts. In, Schreiber, Martin H., Zipf, Theodore F. and Johnston, Dennis A. (eds.) Leukemia and Lymphoma: Detection of Minimal Residual Disease. , Humana Press, 179-199.

Cumberland, P., Sethi, D., Roderick, P.J., Wheeler, J.G., Cowden, J.M., Roberts, J.A., Rodrigues, L.C., Hudson, M.J. and Tompkins, D.S. (2003) The infectious intestinal disease study of England: a prospective evaluation of symptoms and health care use after an acute episode. Epidemiology and Infection, 130, (3), 453-460. (doi:10.1017/S0950268803008410). (PMID:12825729).

Curley, Anna E., Sweet, David G., Thornton, Claire M., O'Hara, M. Denis, Chesshyre, Emily, Pizzotti, Jessica, Wilbourn, Mark S., Halliday, Henry L. and Warner, Jane A. (2003) Chorioamnionitis and increased neonatal lung lavage fluid matrix metalloproteinase-9 levels: implications for antenatal origins of chronic lung disease. American Journal of Obstetrics and Gynecology, 188, (4), 871-875. (doi:10.1067/mob.2003.215).

Curtis, Neil, New, Andrew, Taylor, Mark and Browne, Martin (2003) Effect of component alignment and ligament balancing on the passive stability of the replaced knee. In, Proceedings of the 2003 Summer Bioengineering Conference. 2003 Summer Bioengineering Conference New York, USA, American Society Of Mechanical Engineers (ASME), 1177-1178.

Davies, J.H., Evans, B.A.J., Jenney, M.E.M. and Gregory, J.W. (2003) Effects of chemotherapeutic agents on the function of primary human osteoblast-like cells derived from children. Journal of Clinical Endocrinology & Metabolism, 88, (12), 6088-6097. (doi:10.1210/jc.2003-030712).

Davies, J.H. and Gregory, J.W. (2003) Radiographic long bone appearance in a child administered cyclical pamidronate. Archives of Disease in Childhood, 88, (10), p.854. (doi:10.1136/adc.88.10.854).

Day, Ian N.M. (2003) Genetics of monogenic hypercholesterolemia. Volume 4. In, Cooper, David (ed.) Nature Encyclopedia of the Human Genome. London, UK, Nature Publishing Group, 69-74.

De Falco, Francesca, Cainarca, Silvia, Andolfi, Grazia, Ferrentino, Rosa, Berti, Caterina, Criado, German Rodríguez, Rittinger, Olaf, Dennis, Nick, Odent, Sylvie, Rastogi, Amit, Liebelt, Jan, Chitayat, David, Winter, Robin, Jawanda, Harinder, Ballabio, Andrea, Franco, Brunella and Meroni, Germana (2003) X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum. American Journal of Medical Genetics Part A, 120A, (2), 222-228. (doi:10.1002/ajmg.a.10265).

Dopson, Sue, Locock, Louise, Gabbay, John, Ferlie, Ewan and Fitzgerald, Louise (2003) Evidence-based medicine and the implementation gap. Health, 7, (3), 311-330. (doi:10.1177/1363459303007003004).

Ennis, S., Collins, A. and Morton, N.E. (2003) SNP-based haplotypes and LD blocks in the fragile X region. Journal of Medical Genetics, 40, p.S15.

Ennis, S., Collins, A. and Morton, N.E. (2003) The use of SNP-based haplotypes and LD blocks to positionally clone modifying determinants of expansion of the Fragile X triplet repeat. American Journal of Human Genetics, 73, (5), 377.

Fisher, A., Tyreman, C., Cullis, J. and Ross, F.M. (2003) Five cases of myeloid neoplasia with idic(21)(q22): a possible novel mechanism of chromosome 21 amplification. Journal of Medical Genetics, 40, pp.S50.

Gutman, George A., Chandy, K. George, Adelman, John P., Aiyar, Jayashree, Bayliss, Douglas A., Clapham, David E., Covarriubias, Manuel, Desir, Gary V., Furuichi, Kiyoshi, Ganetzky, Barry, Garcia, Maria L., Grissmer, Stephan, Jan, Lily Y., Karschin, Andreas, Kim, Donghee, Kuperschmidt, Sabina, Kurachi, Yoshihisa, Lazdunski, Michel, Lesage, Florian, Lester, Henry A., McKinnon, David, Nichols, Colin G., O'Kelly, Ita, Robbins, Jonathan, Robertson, Gail A., Rudy, Bernardo, Sanguinetti, Michael, Seino, Susumu, Stuehmer, Walter, Tamkun, Michael M., Vandenberg, Carol A., Wei, Aguan, Wulff, Heike and Wymore, Randy S. (2003) International Union of Pharmacology. XLI. Compendium of voltage-gated ion channels: potassium channels. Pharmacological Reviews, 55, (4), 583-586. (doi:10.1124/pr.55.4.9).

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

Holme, S.A., Davies, J.H. and Mills, C.M. (2003) Iatrogenic injury in childhood staphylococcal scalded skin syndrome. Journal of Paediatrics and Child Health, 39, (1), 73-74. (doi:10.1046/j.1440-1754.2003.00092.x).

Holmes, C., El-Okl, M., Williams, A.L., Cunningham, C., Wilcockson, D. and Perry, V.H. (2003) Systemic infection, interleukin 1 beta, and cognitive decline in Alzheimer's disease. Journal of Neurology, Neurosurgery and Psychiatry, 74, 788-789. (doi:10.1136/jnnp.74.6.788).

Howell, W. Martin, Smith, Katherine C., Fussell, Helen M. and Bateman, Adrian C. (2003) Influence of cytokine gene polymorphisms on susceptibility to and prognosis in breast cancer. Genes and immunity, 4, (Supplement S1), p.S35. (doi:10.1038/sj.gene.6363994).

Hughes, Elinor R., Leighton, Timothy G., Petley, Graham W., White, Paul R. and Chivers, Robert C. (2003) Estimation of critical and viscous frequencies for Biot theory in cancellous bone. Ultrasonics, 41, (5), 365-368. (doi:10.1016/S0041-624X(03)00107-0).

Jacobs, P. (2003) Recurrent reciprocal translocations and inversions detectable by light microscopy. Journal of Medical Genetics, 40, pp.S26.

Joyce, Rachel and Peacock, Janet (2003) A comparison of methods of adjusting stillbirth and neonatal mortality rates for birthweight in hospital and geographical populations. Paediatric and Perinatal Epidemiology, 17, (2), 119-124. (doi:10.1046/j.1365-3016.2003.00486.x).

Killick, S.B., Mufti, G., Cavenagh, J.D., Mijovic, A., Peacock, J.L., Gordon-Smith, E.C., Bowen, D.T. and Marsh, J.C. (2003) A pilot study of antithymocyte globulin (ATG) in the treatment of patients with 'low-risk' myelodysplasia. British journal of haematology, 120, (4), 679-684.

Kirkbride, H.A., Jessop, E.G. and Peacock, J.L. (2003) Hostile Hartlepool and genteel Guildford: hostility and health in 10 English towns. Public Health, 117, (5), 312-316. (doi:10.1016/S0033-3506(03)00101-X).

Lachlan, K., Temple, I.K. and Wellesley, D. (2003) Intracerebral calcification in a child with 22q11 deletion syndrome. Journal of Medical Genetics, 40, pp.S35.

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, Haixin and Vorechovsky, Igor (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).

Lewith, George T. (2003) Evaluating traditionally based systems of medicine with particular reference to acupuncture. Clinical Acupuncture and Oriental Medicine, 4, (2-3), 78-83.

Loveman, E, Cave, C, Green, C, Royle, P, Dunn, N and Waugh, N (2003) The clinical and cost-effectiveness of patient education models for diabetes: a systematic review and economic evaluation. Health Technology Assessment, 7, (22), 1-190.

Maloney, V., Barber, J. and Crolla, A. (2003) Expansion in the use and availability of FISH probes via the National Genetics Reference Laboratory (NGRL) Wessex and international human genomic resources. Journal of Medical Genetics, 40, pp.S58.

Maniatis, Nikolas, Collins, Andrew, Gibson, Jane, Zhang, Weihua, Tapper, William and Morton, Newton E. (2003) Positional cloning by linkage disequilibrium. American Journal of Human Genetics, 73, (5), 846-855. (doi:10.1086/383589).

Martinelli, G., Cilloni, D., Ottaviani, E., Malagola, M., Cross, N., Rosti, G., Gaitani, S., Pane, F., Giannini, B., Testoni, N., Mecucci, C., Soverini, S., Piccaluga, P., Rondoni, M., Amabile, M., Tirabelli, M., Bosi, C., Poerio, A., Zuffa, E., Zaccaria, A., Grafone, T., De Vivo, A., Ascani, S., Pileri, S., Visani, G., Fattori, P., Bocchia, M., Serra, A., Gottardi, E., Maurillo, L., Merante, S., Cazzola, M., Fanin, R., Saglio, G., Bertieri, R. and Baccarani, M. (2003) Italian cooperative study on idiopathic hypereosinophilic syndrome (HES): FIP1-L1/PDGFRA rearrangement can be effectively treated with imatinib. Blood, 102, (11), pp.386A.

Melton, Lisa M., Keith, Alexander B., Davis, Sue, Oakley, Arthur E., Edwardson, James A. and Morris, Christopher M. (2003) Chronic glial activation, neurodegeneration, and APP immunoreactive deposits following acute administration of double-stranded RNA. Glia, 44, (1), 1-12. (doi:10.1002/glia.10276).

Mistry, A.R., Felix, C.A., Whitmarsh, R., Mason, A., Reiter, A., Cassinat, B., Parry, A., Walz, C., Ades, L., Blair, I.A., Osheroff, N., Littlewood, T.J., Lafage-Pochitaloff, M., Cross, N.C.P., Chomienne, C., Solomon, E., Fenaux, P. and Grimwade, D. (2003) Mitoxantrone induces DNA topoisomerase II cleavage at translocation breakpoint hotspot in PML gene in acute promyelocytic leukemia. Blood, 102, (11), pp.215A.

Montgomery, Alan A, Peters, Tim J and Little, Paul (2003) Design, analysis and presentation of factorial randomised controlled trials. BMC Medical Research Methodology, 26, (3) (doi:10.1186/1471-2288-3-26).

Morof, Diane, Barrett, Geraldine, Peacock, Janet, Victor, Christina R. and Manyonda, Isaac (2003) Postnatal depression and sexual health after childbirth. Obstetrics and Gynecology, 102, (6), 1318-1325. (doi:10.1016/j.obstetgynecol.2003.08.020).

Morton, N. E. (2003) Blocks of limited haplotype diversity. In, Cooper, D. (ed.) Nature Encyclopedia of the Human Genome. London, UK, Nature Publishing Group, 331-332.

Morton, N.E. (2003) Wright, Sewall. In, Cooper, D. (ed.) Encyclopedia of the Human Genome. London, UK, Prectice Hall, 775-775.

Muller, M.C., Gattermann, N., Lahaye, T., Deininger, M.W., Berndt, A., Fruehauf, S., Neubauer, A., Fischer, T., Hossfeld, D.K., Schneller, F., Krause, S.W., Nerl, C., Sayer, H.G., Ottmann, O.G., Waller, C., Aulitzky, W., Le Coutre, P., Freund, M., Merx, K., Paschka, P., Konig, H., Kreil, S., Berger, U., Gschaidmeier, H., Hehlmann, R. and Hochhaus, A. (2003) Dynamics of BCR-ABL mRNA expression in first-line therapy of chronic myelogenous leukemia patients with imatinib or interferon alpha/ara-C. Leukemia, 17, (12), 2392-2400. (doi:10.1038/sj.leu.2403157).

O'Kelly, Ita, Butler, Margaret, Zilberberg, Noam and Goldstein, Steve A.N. (2003) A general mechanism for forward transport of proteins subject to retention in endoplasmic reticulum via dibasic signals. Biophysical Journal, 84, (2, Abstract Sup), p.62A.

Palaniyar, Nades, Clark, Howard, Nadesalingam, Jeya, Hawgood, Samuel and Reid, Kenneth B.M. (2003) Surfactant protein D binds genomic DNA and apoptotic cells, and enhances their clearance, in vivo. Annals of the New York Academy of Sciences, 1010, 471-475.

Palmer, K.T. and Coggon, D. (2003) Investigating the workplace. In, Snashall, David and Patel , Dipti (eds.) ABC of Occupational and Environmental Medicine. 2nd edition. London, GB, BMJ Publishing Group.

Paschka, P., Muller, M.C., Merx, K., Kreil, S., Schoch, C., Lahaye, T., Weisser, A., Petzold, A., Konig, H., Berger, U., Gschaidmeier, H., Hehlmann, R. and Hochhaus, A. (2003) Molecular monitoring of response to imatinib (Glivec) in CML patients pretreated with interferon alpha. Low levels of residual disease are associated with continuous remission. Leukemia, 17, (9), 1687-1694. (doi:10.1038/sj.leu.2403033).

Pathan, N., Faust, S.N. and Levin, M. (2003) Pathophysiology of meningococcal meningitis and septicaemia. Archives of Disease in Childhood, 88, (7), 601-607. (doi:10.1136/adc.88.7.601).

Peacock, J.L., Symonds, P., Jackson, P., Bremner, S.A., Scarlett, J.F., Strachan, D.P. and Anderson, H.R. (2003) Acute effects of winter air pollution on respiratory function in schoolchildren in southern England. Occupational and Environmental Medicine, 60, (2), 82-89. (doi:10.1136/oem.60.2.82).

Rauz, S., Cheung, C.M.G., Wood, P.J., Coca-Prados, M., Walker, E.A., Murray, P.I. and Stewart, P.M. (2003) Inhibition of 11beta-hydroxysteroid dehydrogenase type 1 lowers intraocular pressure in patients with ocular hypertension. Q J Med, 96, (7), 481-490. (doi:10.1093/qjmed/hcg085).

Reiter, Andreas, Saussele, Susanne, Grimwade, David, Wiemels, Joseph L., Segal, Mark R., Lafage-Pochitaloff, Marina, Walz, Christoph, Weisser, Andreas, Hochhaus, Andreas, Willer, Andreas, Reichert, Anja, Buchner, Thomas, Lengfelder, Eva, Hehlmann, Rüdiger and Cross, Nicholas C.P. (2003) Genomic anatomy of the specific reciprocal translocation t(15;17) in acute promyelocytic leukemia. Genes, Chromosomes and Cancer, 36, (2), 175-188. (doi:10.1002/gcc.10154).

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).

Schmucker, Johannes, Ader, Marius, Brockschnieder, Damian, Brodarac, Andreja, Bartsch, Udo and Riethmacher, Dieter (2003) erbB3 is dispensable for oligodendrocyte development in vitro and in vivo. Glia, 44, (1), 67-75. (doi:10.1002/glia.10275).

Simonis, R.B., Parnell, E.J., Ray, P.S. and Peacock, J.L. (2003) Electrical treatment of tibial non-union: a prospective, randomised, double-blind trial. Injury, 34, (5), 357-362.

Steer, E.J. and Cross, N.C.P. (2003) Myeloproliferative disorders with 5q31-35 rearrangements. In, Bain, B.J. (ed.) Chronic Myeloproliferative Disorders: Cytogenetic and Molecular Genetic Abnormalities. , S Karger AG, 69-79.

Strong, P., Townsend, P., Mackay, Rosemarie, Reid, K.B.M. and Clark, H.W. (2003) A recombinant fragment of human SP-D reduces allergic responses in mice sensitized to house dust mite allergens. Clinical and Experimental Immunology, 134, (2), 181-7. (doi:10.1046/j.1365-2249.2003.02281.x).

Swords, F.M., Carroll, P.V., Kisalu, J., Wood, P.J., Taylor, N.F. and Monson, J.P. (2003) The effects of growth hormone deficiency and replacement on glucocorticoid exposure in hypopituitary patients on cortisone acetate and hydrocortisone replacement. Clinical Endocrinology (Oxf), 59, (5), 613-620. (doi:10.1046/j.1365-2265.2003.01894.x).

Thomas, Alan J., Davis, Sue, Ferrier, I. Nichol, Kalaria, Rajesh N. and O'Brien, John T. (2003) Elevation of cell adhesion molecule immunoreactivity in the anterior cingulated bipolar disorder. Biological Psychiatry, 55, (6), 652-655. (doi:10.1016/j.biopsych.2003.10.015). (PMID:15013836).

Thomas, M., Greenough, A., Johnson, A., Limb, E., Marlow, N., Peacock, J.L. and Calvert, S. (2003) Frequent wheeze at follow up of very preterm infants: which factors are predictive? [In: Fetal and Neonatal Edition]. Archives of Disease in Childhood, 88, (4), F329-F332. (doi:10.1136/fn.88.4.F329).

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).

Velissaris, Theodore, Stuklis, Robert G., Hett, David A. and Ohri, Sunil K. (2003) Right pleuropericardial release: a useful technique in off-pump coronary surgery. Asian Cardiovascular & Thoracic Annals, 11, (2), 174-176.

Wilkinson, Tom M.A., Patel, Irem S., Wilks, Mark, Donaldson, Gavin C. and Wedzicha, Jadwiga A. (2003) Airway bacterial load and FEV1 decline in patients with chronic obstructive pulmonary disease. American Journal of Respiratory and Critical Care Medicine, 167, (8), 1090-1095. (doi:10.1164/rccm.200210-1179OC).

Wilson, D., Cox, H., Fiegler, H., Wilkinson, K., Fowler, D., Moore, K., Carter, N.P., Wellesley, D. and Barber, J. (2003) Congenital heart disease, deafness and duplications of 3q: refining a new critical region. Journal of Medical Genetics, 40, pp.S60.

Wilson, D.I. and Hanley, N.A. (2003) Human developmental molecular genetics. In, Cooper, D. (ed.) Nature Encyclopedia of the Human Genome. London, UK, Nature Publishing Group, 312-316.

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).

Zweier, C., Temple, I.K., Beemer, F., Zackai, E., Lerman-Sagie, T., Weschke, B., Anderson, C.E. and Rauch, A. (2003) Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome. Journal of Medical Genetics, 40, (8), 601-605. (doi:10.1136/jmg.40.8.601).