We’re moving! Datasets in the NIAGADS database are being transitioned to the DSS database, click to learn more.

Biblio

Found 155 results
Author Keyword Title Type [ Year(Desc)]
Filters: First Letter Of Keyword is H  [Clear All Filters]
2004
V. Busby, Goossens, S., Nowotny, P., Hamilton, G., Smemo, S., Harold, D., Turic, D., Jehu, L., Myers, A., Womick, M., Woo, D., Compton, D., Doil, L. M., Tacey, K. M., Lau, K. F., Al-Saraj, S., Killick, R., Pickering-Brown, S., Moore, P., Hollingworth, P., Archer, N., Foy, C., Walter, S., Lendon, C., Iwatsubo, T., Morris, J. C., Norton, J., Mann, D., Janssens, B., Hardy, J., O'Donovan, M., Jones, L., Williams, J., Holmans, P., Owen, M. J., Grupe, A., Powell, J., van Hengel, J., Goate, A., Van Roy, F., and Lovestone, S., Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease., Neuromolecular Med, vol. 5, no. 2, pp. 133-46, 2004.
J. M. van der Walt, Dementieva, Y. A., Martin, E. R., Scott, W. K., Nicodemus, K. K., Kroner, C. C., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Small, G. W., Schmechel, D. E., P Doraiswamy, M., Gilbert, J. R., Haines, J. L., Vance, J. M., and Pericak-Vance, M. A., Analysis of European mitochondrial haplogroups with Alzheimer disease risk., Neurosci Lett, vol. 365, no. 1, pp. 28-32, 2004.
J. M. van der Walt, Dementieva, Y. A., Martin, E. R., Scott, W. K., Nicodemus, K. K., Kroner, C. C., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Small, G. W., Schmechel, D. E., P Doraiswamy, M., Gilbert, J. R., Haines, J. L., Vance, J. M., and Pericak-Vance, M. A., Analysis of European mitochondrial haplogroups with Alzheimer disease risk., Neurosci Lett, vol. 365, no. 1, pp. 28-32, 2004.
K. K. Nicodemus, Stenger, J. E., Schmechel, D. E., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Gilbert, J. R., Vance, J. M., Haines, J. L., Pericak-Vance, M. A., and Martin, E. R., Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease., Neurogenetics, vol. 5, no. 4, pp. 201-8, 2004.
K. K. Nicodemus, Stenger, J. E., Schmechel, D. E., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Gilbert, J. R., Vance, J. M., Haines, J. L., Pericak-Vance, M. A., and Martin, E. R., Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease., Neurogenetics, vol. 5, no. 4, pp. 201-8, 2004.
M. Saleh, Vaillancourt, J. P., Graham, R. K., Huyck, M., Srinivasula, S. M., Alnemri, E. S., Steinberg, M. H., Nolan, V., Baldwin, C. T., Hotchkiss, R. S., Buchman, T. G., Zehnbauer, B. A., Hayden, M. R., Farrer, L. A., Roy, S., and Nicholson, D. W., Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms., Nature, vol. 429, no. 6987, pp. 75-9, 2004.
J. H. Lee, Mayeux, R., Mayo, D., Mo, J., Santana, V., Williamson, J., Flaquer, A., Ciappa, A., Rondon, H., Estevez, P., Lantigua, R., Kawarai, T., Toulina, A., Medrano, M., Torres, M., Stern, Y., Tycko, B., Rogaeva, E., St George-Hyslop, P., and Knowles, J. A., Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics., Mol Psychiatry, vol. 9, no. 11, pp. 1042-51, 2004.
J. H. Lee, Mayeux, R., Mayo, D., Mo, J., Santana, V., Williamson, J., Flaquer, A., Ciappa, A., Rondon, H., Estevez, P., Lantigua, R., Kawarai, T., Toulina, A., Medrano, M., Torres, M., Stern, Y., Tycko, B., Rogaeva, E., St George-Hyslop, P., and Knowles, J. A., Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics., Mol Psychiatry, vol. 9, no. 11, pp. 1042-51, 2004.
A. J. Myers, Marshall, H., Holmans, P., Compton, D., Crook, R. J. P., Mander, A. P., Nowotny, P., Smemo, S., Dunstan, M., Jehu, L., Wang, J. C., Hamshere, M., Morris, J. C., Norton, J., Chakraventy, S., Tunstall, N., Lovestone, S., Petersen, R., O'Donovan, M., Jones, L., Williams, J., Owen, M. J., Hardy, J., and Goate, A., Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD., Am J Med Genet B Neuropsychiatr Genet, vol. 124B, no. 1, pp. 29-37, 2004.
A. J. Myers, Marshall, H., Holmans, P., Compton, D., Crook, R. J. P., Mander, A. P., Nowotny, P., Smemo, S., Dunstan, M., Jehu, L., Wang, J. C., Hamshere, M., Morris, J. C., Norton, J., Chakraventy, S., Tunstall, N., Lovestone, S., Petersen, R., O'Donovan, M., Jones, L., Williams, J., Owen, M. J., Hardy, J., and Goate, A., Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD., Am J Med Genet B Neuropsychiatr Genet, vol. 124B, no. 1, pp. 29-37, 2004.
2005
P. Nowotny, Hinrichs, A. L., Smemo, S., Kauwe, J. S. K., Maxwell, T., Holmans, P., Hamshere, M., Turic, D., Jehu, L., Hollingworth, P., Moore, P., Bryden, L., Myers, A., Doil, L. M., Tacey, K. M., Gibson, A. M., McKeith, I. G., Perry, R. H., Morris, C. M., Thal, L., Morris, J. C., O'Donovan, M. C., Lovestone, S., Grupe, A., Hardy, J., Owen, M. J., Williams, J., and Goate, A., Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme., Am J Med Genet B Neuropsychiatr Genet, vol. 136B, no. 1, pp. 62-8, 2005.
P. Nowotny, Hinrichs, A. L., Smemo, S., Kauwe, J. S. K., Maxwell, T., Holmans, P., Hamshere, M., Turic, D., Jehu, L., Hollingworth, P., Moore, P., Bryden, L., Myers, A., Doil, L. M., Tacey, K. M., Gibson, A. M., McKeith, I. G., Perry, R. H., Morris, C. M., Thal, L., Morris, J. C., O'Donovan, M. C., Lovestone, S., Grupe, A., Hardy, J., Owen, M. J., Williams, J., and Goate, A., Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme., Am J Med Genet B Neuropsychiatr Genet, vol. 136B, no. 1, pp. 62-8, 2005.
F. W. Lohoff, Sander, T., Ferraro, T. N., Dahl, J. P., Gallinat, J., and Berrettini, W. H., Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder., Am J Med Genet B Neuropsychiatr Genet, vol. 139B, no. 1, pp. 51-3, 2005.
N. Ertekin-Taner, Ronald, J., Feuk, L., Prince, J., Tucker, M., Younkin, L., Hella, M., Jain, S., Hackett, A., Scanlin, L., Kelly, J., Kihiko-Ehman, M., Neltner, M., Hersh, L., Kindy, M., Markesbery, W., Hutton, M., de Andrade, M., Petersen, R. C., Graff-Radford, N., Estus, S., Brookes, A. J., and Younkin, S. G., Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene., Hum Mol Genet, vol. 14, no. 3, pp. 447-60, 2005.
R. K. Gopalraj, Zhu, H., Kelly, J. F., Mendiondo, M., Pulliam, J. F., Bennett, D. A., and Estus, S., Genetic association of low density lipoprotein receptor and Alzheimer's disease., Neurobiol Aging, vol. 26, no. 1, pp. 1-7, 2005.