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Items where Division is "Faculty of Medicine > Clinical and Experimental Sciences" and Year is 2000

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Number of items: 27.

Blake, A.S., Petley, G.W. and Deakin, C.D. (2000) Effects of changes in packed cell volume on the specific heat capacity of blood: implications for studies measuring heat exchange in extracorporeal circuits British Journal of Anaesthesia, 84, (1), pp. 28-32. (PMID:10740543).

Chadwick, P. R., Beards, G., Brown, D., Caul, E. O., Cheesbrough, J., Clarke, I. N., Curry, A., O'Brien, S., Quigley, K., Sellwood, J. and Westmoreland, D. (2000) Management of hospital outbreaks of gastro-enteritis due to small round structured viruses Journal of Hospital Infection, 45, (1), pp. 1-10. (PMID:10833336).

Clarke, I.N. and Lambden, P.R. (2000) Viral gastroenteritis: the human caliciviruses CPD Infection, 2, (1), pp. 14-17.

Dellamary, Luis A., Tarara, Thomas E., Smith, Dan J., Woelk, Christopher H., Adractas, Anastasios, Costello, Michael L., Gill, Howard and Weers, Jeffry G. (2000) Hollow porous particles in metered dose inhalers Pharmaceutical Research, 17, (2), pp. 168-174. (PMID:10751031).

Espey, Michael Graham, Miranda, Katrina M., Feelisch, Martin, Fukuto, Jon, Grisham, Mathew B., Vitek, Michael P. and Wink, David A. (2000) Mechanisms of cell death governed by the balance between nitrosative and oxidative stress Annals of the New York Academy of Sciences, 899, pp. 209-221. (doi:10.1111/j.1749-6632.2000.tb06188.x). (PMID:10863541).

Flanagan, Niamh, Healy, Eugene, Ray, Amanda, Philips, Sion, Todd, Carole, Jackson, Ian J., Birch-Machin, Mark A. and Rees, Jonathan L. (2000) Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation Human Molecular Genetics, 9, (17), pp. 2531-2537. (doi:10.1093/hmg/9.17.2531). (PMID:11030758).

Harding, Rosalind M., Healy, Eugene, Ray, Amanda J., Ellis, Nichola S., Flanagan, Niamh, Todd, Carol, Dixon, Craig, Sajantila, Antti, Jackson, Ian J., Birch-Machin, Mark A. and Rees, Jonathan L. (2000) Evidence for variable selective pressures at MC1R The American Journal of Human Genetics, 66, (4), pp. 1351-1361.

Healy, Eugene, Flanagan, Niamh, Ray, Amanda, Todd, Carole, Jackson, Ian J., Matthews, John N. S., Birch-Machin, Mark A. and Rees, Jonathan L. (2000) Melanocortin 1 receptor gene and sun sensitivity in individuals without red hair Lancet, 355, (9209), pp. 1072-1073. (PMID:10744096).

Jenkins, Gareth M., Woelk, Christopher H., Rambaut, Andrew and Holmes, Edward C. (2000) Testing the extent of sequence similarity among viroids, satellite RNAs and hepatitis delta virus Journal of Molecular Evolution, 50, (1), pp. 98-102. (doi:10.1007/s002399910011). (PMID:10654264).

Jordens, J.Z., Lanham, S.A., Pickett, M.A., Amarasekara, S., Abeywickrema, I. and Watt, Peter J. (2000) Amplification with molecular beacon primers and reverse line blotting for the detection and typing of human papillomaviruses Journal of Virological Methods, 89, pp. 29-37. (doi:10.1016/S0166-0934(00)00195-6). (PMID:10996637).

Jourd'heuil, David, Hallén, Katarina, Feelisch, Martin and Grisham, Matthew B. (2000) Dynamic state of S-nitrosothiols in human plasma and whole blood Free Radical Biology and Medicine, 28, (3), pp. 409-417. (doi:10.1016/S0891-5849(99)00257-9). (PMID:10699753).

Kennedy, C.R., Kimm, L., Thornton, A.R.D. and Davis, A. (2000) False positives in universal neonatal screening for permanent childhood hearing impairment Lancet, 356, (9245), pp. 1903-1904. (doi:10.1016/S0140-6736(00)03267-0).

Khakoo, S.I., Ling, R., Scott, I., Dodi, A.I., Harrison, T.J., Dusheiko, G.M. and Madrigal, J.A. (2000) Cytotoxic T lymphocyte responses and CTL epitope escape mutation in HBsAg, anti-HBe positive individuals Gut, 47, (1), pp. 137-143. (doi:10.1136/gut.47.1.137). (PMID:10861276).

Khakoo, Salim I., Rajalingam, Raja, Shum, Benny P., Weidenbach, Kristin, Flodin, Laura, Muir, David G., Canavez, Flavio, Cooper, Stewart L., Valiante, Nicholas M., Lanier, Lewis L. and Parnham, Peter (2000) Rapid evolution of NK cell receptor systems demonstrated by comparison of chimpanzees and humans Immunity, 12, (6), pp. 687-698. (doi:10.1016/S1074-7613(00)80219-8). (PMID:10894168).

Komarov, Andrei M., Wink, David A., Feelisch, Martin and Schmidt, Harald H.H.W. (2000) Electron-paramagnetic resonance spectroscopy using N-methyl-D-glucamine dithiocarbamate iron cannot discriminate between nitric oxide and nitroxyl: implications for the detection of reaction products for nitric oxide synthase Free Radical Biology and Medicine, 28, (5), pp. 739-742. (doi:10.1016/S0891-5849(00)00156-8). (PMID:10754269).

Lotery, Andrew J., Munier, Francis L., Fishman, Gerald A., Weleber, Richard G., Jacobson, Samuel G., Affatigato, Louisa M., Nichols, Brian E., Schorderet, Daniel F., Sheffield, Val C. and Stone, Edwin M. (2000) Allelic variation in the VMD2 gene in best disease and age-related macular degeneration Investigative Ophthalmology & Visual Science, 41, (6), pp. 1291-1296. (PMID:10798642).

Lotery, Andrew J., Namperumalsamy, P., Jacobson, Samuel G., Weleber, Richard G., Fishman, Gerald A., Musarella, Maria A., Hoyt, Creig S., Héon, Elise, Levin, Alex, Jan, James, Lam, Byron, Carr, Ronald E., Franklin, Alan, Radha, S., Andorf, Jeaneen L., Sheffield, Val C. and Stone, Edwin M. (2000) Mutation analysis of 3 genes in patients with Leber congenital amaurosis Archives of Ophthalmology, 118, (4), pp. 538-543. (doi:10.1001/archopht.118.4.538). (PMID:10766140).

Lotery, Andrew J., Wiggam, M. Ivan, Jackson, A. Jonathan, Silvestri, Guiliana, Refson, Kathlene, Fullerton, Kenneth J., Gilmore, David H. and Beringer, Timothy R.O. (2000) Correctable visual impairment in stroke rehabilitation patients Age and Ageing, 29, (3), pp. 221-222. (doi:10.1093/ageing/29.3.221). (PMID:10855903).

Lucas, Jane S., Foreman, Claire T. and Clough, Joanne B. (2000) Measuring pulmonary function in infancy The Indian Journal of Pediatrics, 67, (2), pp. 123-127. (doi:10.1007/BF02726186). (PMID:10832239).

Marley, Richard, Feelisch, Martin, Holt, Stephen and Moore, Kevin (2000) A chemiluminescense-based assay for S-nitrosoalbumin and other plasma S-nitrosothiols Free Radical Research, 32, (1), pp. 1-9. (doi:10.1080/10715760000300011). (PMID:10625212).

Oh, Kean T., Weleber, Richard G., Lotery, Andrew J., Oh, Dawn M., Billingslea, Andrea M. and Stone, Edwin M. (2000) Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutation Archives of Ophthalmology, 118, (9), pp. 1269-1276. (doi:10.1001/archopht.118.9.1269). (PMID:10980774).

Orsi, Antonia, Beltrán, Belén, Clementi, Emilio, Hallén, Katarina, Feelisch, Martin and Moncada, Salvador (2000) Continuous exposure to high concentrations of nitric oxide leads to persistent inhibition of oxygen consumption by J774 cells as well as extraction of oxygen by the extracellular medium Biochemical Journal, 346, pp. 407-412. (PMID:10677360).

Papadopoulos, N.G., Bates, P.J., Bardin, P.G., Papi, A., Leir, S.H., Fraenkel, D.J., Meyer, J., Lackie, P.M., Sanderson, G., Holgate, S.T. and Johnston, S.L. (2000) Rhinoviruses infect the lower airways The Journal of Infectious Diseases, 181, (6), pp. 1875-1884. (doi:10.1086/315513). (PMID:10837165).

Petley, G.W., Taylor, P.A., Murrills, A.J., Dennison, E., Pearson, G. and Cooper, C. (2000) An investigation of the diagnostic value of bilateral femoral neck bone mineral density measurements Osteoporosis International, 11, (8), pp. 675-679. (PMID:11095170).

Smith, F. J. D., Fisher, M. P., Healy, E., Rees, J. L., Bonifas, J. M., Epstein, E. H., Tan, E. M. L., Uitto, J. and McLean, W. H. I. (2000) Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma Experimental Dermatology, 9, (3), pp. 170-177. (doi:10.1034/j.1600-0625.2000.009003170.x). (PMID:10839714).

Sudbrack, Ralf, Brown, Joanna, Dobson-Stone, Carol, Carter, Simon, Ramser, Juliane, White, Jacqueline, Healy, Eugene, Dissanayake, Manuel, Larrègue, Marc, Perrussel, Marc, Lehrach, Hans, Munro, Colin S., Strachan, Tom, Burge, Susan, Hovnanian, Alain and Monaco, Anthony P. (2000) Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump Human Molecular Genetics, 9, (7), pp. 1131-1140. (doi:10.1093/hmg/9.7.1131).

Zampolli, Antonella, Basta, Giuseppina, Lazzerini, Guido, Feelisch, Martin and De Caterina, Raffaele (2000) Inhibition of endothelial cell activation by nitric oxide donors The Journal of Pharmacology and Experimental Therapeutics, 295, (2), pp. 818-823. (PMID:11046123).

This list was generated on Wed Apr 12 15:48:57 2017 BST.
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