Items where Division is "Faculty of Medicine > Infection, Inflammation and Immunity" and Year is 1999

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Number of items: 14.

Arthur, M.J.P., Iredale, J.P. and Mann, D.A. (1999) Tissue Inhibitors of Metalloproteinases: Role in Liver Fibrosis and Alcoholic Liver Disease. Alcoholism Clinical and Experimental Research, 23, (5), 940-943. (doi:10.1111/j.1530-0277.1999.tb04208.x).

Dalrymple-Hay, M. J, Lucas, J.S., Connett, G. and Lea, R. E. (1999) Lung resection for the treatment of severe localised bronchiectasis in cystic fibrosis patients. Acta Chirurgica Hungarica, 38, (1), 23-25. (PMID:10439089).

Feelisch, Martin, Kotsonis, Peter, Siebe, Jan, Clement, Bernd and Schmidt, Harald H.HW (1999) The soluble guanylyl cyclase inhibitor 1H-[1,2,4]oxadiazolo[4,3,-a] quinoxalin-1-one is a nonselective heme protein inhibitor of nitric oxide synthase and other cytochrome P-450 enzymes involved in nitric oxide donor bioactivation. Molecular Pharmacology, 56, (2), 243-253. (PMID:10419542).

Healy, Eugene, Todd, Carole, Jackson , Ian J., Birch-Machin, Mark and Rees, Jonathan L. (1999) Skin type, melanoma and melanocortin 1 receptor variants. Journal of Investigative Dermatology, 112, (4), 512-513. (doi:10.1046/j.1523-1747.1999.00554.x ). (PMID:10201538).

Holloway, J. W., Beghé, B. and Holgate, S. T. (1999) The genetic basis of atopic asthma. Clinical & Experimental Allergy, 29, (8), 1023-1032. (doi:10.1046/j.1365-2222.1999.00599.x). (PMID:10457104).

Ji, G.J., Fleischmann, B.K., Bloch, W., Feelisch, M., Andressen, C., Addicks, K. and Hescheler, J. (1999) Regulation of the L-type Ca2+ channel during cardiomyogenesis: switch from NO to adenylyl cyclase-mediated inhibition. The FASEB Journal : the Journal of the Federation of American Societies for Experimental Biology, 13, (2), 313-324. (PMID:9973319).

Korge, B. P., Healy, Eugene, Traupe, H., Pünter, C., Mauch, C., Hamm, H., Birch-Machin, M. A., Belgaid, C. E., Stephenson, A. M., Holmes, S. C., Darlington, S., Messenger, A. G., Rees, J. L. and Munro, C. S. (1999) Point mutations in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five families. Experimental Dermatology, 8, (4), 310-312. (doi:10.1111/j.1600-0625.1999.tb00384.x). (PMID:10439241).

Korge, Bernhard P., Hamm, Henning, Jury, Catherine S., Traupe , Heiko, Irvine, Alan D., Healy, Eugene, Birch-Machin, Mark, Rees, Jonthan L., Messenger, Andrew G., Holmes, Susan C., Parry, David A. D. and Munro, Colin S. (1999) Identification of noval mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype. Journal of Investigative Dermatology, 113, (4), 607-612. (doi:10.1046/j.1523-1747.1999.00722.x). (PMID:10504448).

Kotsonis, Peter, Frey, Armin, Fröhlich, Lothar G., Hofmann, Heinrich, Reif, Andreas, Wink, David A., Feelisch, Martin and Schmidt, Harald H.H.W. (1999) Autoinhibition of neuronal nitric oxide synthase: distinct effects of reactive nitrogen and oxygen species on enzyme activity. Biochemical Journal, 340, 745-752. (PMID:10359660).

Ma, Xin L., Gao, Feng, Liu, Gao-Lin, Lopez, Bernard L., Christopher, Theodore A., Fukuto, Jon M. , Wink, David A. and Feelisch, Martin (1999) Opposite effects of nitric oxide and nitroxyl on postischemic myocardial injury. Proceedings of the National Academy of Sciences of the United States of America, 96, (25), 14617-14622. (doi:10.1073/pnas.96.25.14617). (PMID:10588754).

Rowan, Andrew, Bataille, Veronique, MacKie, Rona, Healy, Eugene, Bicknell , David, Bodmer, Walter and Tomlinson, Ian (1999) Somatic mutations in the Peutz-Jeghers (LKB1/STK11) gene in sporadic malignant melanomas. Journal of Investigative Dermatology, 112, (4), 509-511. (doi:10.1046/j.1523-1747.1999.00551.x). (PMID:10201537).

Ruiz-Perez, Victor L., Carter, Simon A., Healy, Eugene, Todd, Carole, Rees, Jonathan L., Steijlen, Peter M., Carmichael, Andrew J., Lewis, Helen M., Hohl, D., Itin, Peter, Valquist, Anders, Gobello, T., Mazzanti, C., Reggazini, R., Nagy, Gyula, Munro, Colin S. and Strachan, Tom (1999) ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class. Human Molecular Genetics, 8, (9), 1621-1630. (doi:10.1093/hmg/8.9.1621). (PMID:10441324).

Stone, Edwin M., Lotery, Andrew J., Munier, Francis L., Héon, Elise, Piguet, Bertrand, Guymer, Robyn H., Vandenburgh, Kimberlie, Cousin, Pascal, Nishimura, Darryl, Swiderski, Ruth E., Silvestri, Giuliana, Mackey, David A., Hageman, Gregory S., Bird, Alan C., Sheffield, Val C. and Schorderet, Daniel F. (1999) A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. Nature Genetics, 22, (2), 199-202. (doi:10.1038/9722 ). (PMID:10369267).

Wolzt, Michael, MacAllister, Raymond J., Davis, Dana, Feelisch, Martin, Moncada, Salvador, Vallance, Patrick and Hobbs, Adrian J. (1999) Biochemical characterization of S-nitrosohemoglobin. Mechanisms underlying synthesis, no release, and biological activity. The Journal of Biological Chemistry, 274, (41), 28983-28990. (doi:10.1074/jbc.274.41.28983). (PMID:10506146).

This list was generated on Tue Nov 25 01:33:26 2014 GMT.