Spectroscopy of 16O using α + 12C resonant scattering in inverse kinematics von Ashwood, N I, Freer, M, Achouri, N L, Bloxham, T R, Catford, W N, Curtis, N, Haigh, P J, Harlin, C W, Patterson, N P, Price, D L, Soić, N, Thomas, J S

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Search for the 2+ excitation of the Hoyle state in 12C using the 12C(12C,3α)12C reaction von Muñoz-Britton, T, Freer, M, Ashwood, N I, Brown, T A D, Catford, W N, Curtis, N, Fox, S P, Fulton, B R, Harlin, C W, Laird, A M, Mumby-Croft, P, Murphy, A St J, Papka, P, Price, D L, Vaughan, K, Watson, D L, Weisser, D C

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Spectroscopy of 16 O using α + 12 C resonant scattering in inverse kinematics von Ashwood, N I, Freer, M, Achouri, N L, Bloxham, T R, Catford, W N, Curtis, N, Haigh, P J, Harlin, C W, Patterson, N P, Price, D L, Soić, N, Thomas, J S

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Spectroscopy of {sup 16}O Using {alpha}+{sup 12}C Resonant Scattering in Inverse Kinematics von Ashwood, N. I., Freer, M., Bloxham, T. R., Curtis, N., Haigh, P. J., Price, D. L., Achouri, N. L., Catford, W. N., Harlin, C. W., Patterson, N. P., Thomas, J. S., Soic, N.

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A full Genome Scan for Late Onset Alzheimer's Disease von Kehoe, Patrick, Vrieze, Fabienne Wavrant-De, Crook, Richard, Wu, William S., Holmans, Peter, Fenton, Iain, Spurlock, Gillian, Norton, Nadine, Williams, Hywel, Williams, Nigel, Lovestone, Simon, Perez-Tur, Jordi, Hutton, Mike, Chartier-Harlin, Marie-Christine, Shears, Shantia, Roehl, Kimberly, Booth, Jeremy, Van Voorst, Wendy, Ramic, Dzanan, Williams, Julie, Goate, Alison, Hardy, John, Owen, Michael J.

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Spectroscopy of 16O using alpha + 12C resonant scattering in inverse kinematics von Ashwood, N I, Freer, M, Achouri, N L, Bloxham, T R, Catford, W N, Curtis, N, Haigh, P J, Harlin, C W, Patterson, N P, Price, D L, Soic, N, Thomas, J S

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Spectroscopy of 16O Using alpha+12C Resonant Scattering in Inverse Kinematics von Ashwood, N I, Freer, M, Achouri, N L, Bloxham, T R, Catford, W N, Curtis, N, Haigh, P J, Harlin, C W, Patterson, N P, Price, D L, Soic, N, Thomas, J S

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Search for the 2 + excitation of the Hoyle state in 12 C using the 12 C( 12 C,3α) 12 C reaction von Muñoz-Britton, T, Freer, M, Ashwood, N I, Brown, T A D, Catford, W N, Curtis, N, Fox, S P, Fulton, B R, Harlin, C W, Laird, A M, Mumby-Croft, P, Murphy, A St J, Papka, P, Price, D L, Vaughan, K, Watson, D L, Weisser, D C

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α-decaying states in Be 10 , 12 populated in the Be 10 ( C 14 , Be 10 , 12 ) reaction von Curtis, N., Ashwood, N. I., Baby, L. T., Baldwin, T. D., Bloxham, T. R., Catford, W. N., Caussyn, D. D., Freer, M., Harlin, C. W., McEwan, P., Price, D. L., Spingler, D., Wiedenhover, I.

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The Possible Role of Volatile Secretions as Intra- and Interspecific Alarm Signals in Gyrinus Species von Karlsson, Anna-Karin Borg, Henrikson, Britt-Inger, Härlin, Carina, Ivarsson, Per, Jan A. E. Stenson, Svensson, Bo W.

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Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease von Wu, William S, Holmans, Peter, Wavrant-DeVrièze, Fabienne, Shears, Shantia, Kehoe, Patrick, Crook, Richard, Booth, Jeremy, Williams, Nigel, Pérez-Tur, Jordi, Roehl, Kimberly, Fenton, Iain, Chartier-Harlin, Marie-Christine, Lovestone, Simon, Williams, Julie, Hutton, Mike, Hardy, John, Owen, Michael J, Goate, Alison

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Nitrogen Isotopes as Indicators of NO x Source Contributions to Atmospheric Nitrate Deposition Across the Midwestern and Northeastern United States von Elliott, E. M, Kendall, C, Wankel, S. D, Burns, D. A, Boyer, E. W, Harlin, K, Bain, D. J, Butler, T. J

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Presenilin-1 polymorphism and Alzheimer's disease von Scott, WilliamK, Roses, AllenD, Haines, JonathanL, Pericak-Vance, MargaretA, Pérez-Tur, J., Wavrant-De Vrieze, F., Lambert, J.C., Chartier-Harlin, M-C., the Alzheimer's Study Group

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Nitrogen Isotopes as Indicators of NOx Source Contributions to Atmospheric Nitrate Deposition Across the Midwestern and Northeastern United States von ELLIOTT, E. M., KENDALL, C., WANKEL, S. D., BURNS, D. A., BOYER, E. W., HARLIN, K., BAIN, D. J., BUTLER, T. J.

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Dual nitrate isotopes in dry deposition: Utility for partitioning NOx source contributions to landscape nitrogen deposition von Elliott, E. M., Kendall, C., Boyer, E. W., Burns, D. A., Lear, G. G., Golden, H. E., Harlin, K., Bytnerowicz, A., Butler, T. J., Glatz, R.

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Characterization of DCTN1 genetic variability in neurodegeneration von VILARINO-GÜELL, C, WIDER, C, UITTI, R. J, GRAFF-RADFORD, N. R, BOEVE, B. F, JOSEPHS, K. A, MILLER, B, BOYLAN, K. B, GWINN, K, ADLER, C. H, AASLY, J. O, HENTATI, F, SOTO-ORTOLAZA, A. I, DESTEE, A, KRYGOWSKA-WAJS, A, CHARTIER-HARLIN, M.-C, ROSS, O. A, RADEMAKERS, R, FARRER, M. J, COBB, S. A, KACHERGUS, J. M, KEELING, B. H, DACHSEL, J. C, HULIHAN, M. M, DICKSON, D. W, WSZOLEK, Z. K

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Evolutionary analysis of KED-rich proteins in plants von Zhang, Xing-Hai, Swait, David, Jin, Xiao-Lu, Vichyavichien, Paveena, Nifakos, Nicholas, Kaplan, Noah, Raymond, Lucwilerna, Harlin, John M

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UCHL1 is a Parkinson's disease susceptibility gene von Maraganore, Demetrius M., Lesnick, Timothy G., Elbaz, Alexis, Chartier-Harlin, Marie-Christine, Gasser, Thomas, Krüger, Rejko, Hattori, Nobutaka, Mellick, George D., Quattrone, Aldo, Satoh, Jun-Ichi, Toda, Taksushi, Wang, Jian, Ioannidis, John P.A., de Andrade, Mariza, Rocca, Walter A.

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The magic nature of 132 Sn explored through the single-particle states of 133 Sn von Jones, K. L, Adekola, A. S, Bardayan, D. W, Blackmon, J. C, Chae, K. Y, Chipps, K. A, Cizewski, J. A, Erikson, L, Harlin, C, Hatarik, R, Kapler, R, Kozub, R. L, Liang, J. F, Livesay, R, Ma, Z, Moazen, B. H, Nesaraja, C. D, Nunes, F. M, Pain, S. D, Patterson, N. P, Shapira, D, Shriner, J. F, Smith, M. S, Swan, T. P, Thomas, J. S

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NADPH oxidases in Parkinson's disease: a systematic review von Belarbi, Karim, Cuvelier, Elodie, Destée, Alain, Gressier, Bernard, Chartier-Harlin, Marie-Christine

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