Identification of the gene responsible for Best macular dystrophy von Petrukhin, Konstantin, Wadelius, Claes, Koisti, Markus J, Bakall, Benjamin, Li, Wen, Xie, Guochun, Marknell, Towa, Sandgren, Ola, Forsman, Kristina, Holmgren, Gösta, Andreasson, Sten, Vujic, Mihailo, Bergen, Arthur A. B, McGarty-Dugan, Valarie, Figueroa, David, Austin, Christopher P, Metzker, Michael L, Caskey, C.Thomas

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Evaluation of 13 short tandem repeat loci for use in personal identification applications von HAMMOND, H. A, LI JIN, ZHONG, Y, CASKEY, C. T, RANAJIT CHAKRABORTY

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A New Adenoviral Vector: Replacement of All Viral Coding Sequences with 28 kb of DNA Independently Expressing Both Full-Length Dystrophin and β -Galactosidase von Kochanek, Stefan, Clemens, Paula R., Mitani, Kohnosuke, Chen, Hsiao-Huei, Chan, Suzanne, Caskey, C. Thomas

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Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses von Monckton, Darren G., Wong, Lee-Jun C., Ashizawa, Tetsuo, Caskey, C. Thomas

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Hyperuricemia and urate nephropathy in urate oxidase-deficient mice von Wu, X, Wakamiya, M, Vaishnav, S, Geske, R, Montgomery, C. Jr, Jones, P, Bradley, A, Caskey, C.T

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Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats von REINER, O, CARROZZO, R, YING SHEN, WEHNERT, M, FAUSTINELLA, F, DOBYNS, W. B, CASKEY, C. T, LEDBETTER, D. H

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DNA typing and genetic mapping with trimeric and tetrameric tandem repeats von EDWARDS, A. I, CIVITELLO, A, HAMMOND, H. A, CASKEY, C. T

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Novel Proteins with Binding Specificity for DNA CTG Repeats And RNA Cug Repeats: Implications for Myotonic Dystrophy von Timchenko, L. T., Timchenko, N. A., Caskey, C. T., Roberts, R.

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Monitoring expression of genes involved in drug metabolism and toxicology using DNA microarrays von GERHOLD, DAVID, LU, MEIQING, XU, JIAN, AUSTIN, CHRISTOPHER, CASKEY, C. THOMAS, RUSHMORE, THOMAS

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Alu Polymerase Chain Reaction: A Method for Rapid Isolation of Human-Specific Sequences from Complex DNA Sources von Nelson, David L., Ledbetter, Susan A., Corbo, Laura, Victoria, Maureen F., Ramírez-Solis, Ramiro, Webster, Thomas D., Ledbetter, David H., Caskey, C. Thomas

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Identification of Urotensin II as the Endogenous Ligand for the Orphan G-Protein-Coupled Receptor GPR14 von Liu, Qingyun, Pong, Sheng-Shung, Zeng, Zhizhen, Zhang, Qing, Howard, Andrew D., Williams, David L., Davidoff, Michael, Wang, Ruiping, Austin, Christopher P., McDonald, Terrence P., Bai, Chang, George, Susan R., Evans, Jilly F., Caskey, C.Thomas

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Absence of expression of the FMR-1 gene in fragile X syndrome von Pieretti, Maura, Zhang, Fuping, Fu, Ying-Hui, Warren, Stephen T., Oostra, Ben A., Caskey, C.Thomas, Nelson, David L.

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox von Fu, Ying-Hui, Kuhl, Derek P.A., Pizzuti, Antonio, Pieretti, Maura, Sutcliffe, James S., Richards, Stephen, Verkert, Annemieke J.M.H., Holden, Jeanette J.A., Fenwick, Raymond G., Warren, Stephen T., Oostra, Ben A., Nelson, David L., Caskey, C.Thomas

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Urate Oxidase: Primary Structure and Evolutionary Implications von Wu, Xiangwei, Lee, Cheng Chi, Muzny, Donna M., Caskey, C. Thomas

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Rescue, Propagation, and Partial Purification of a Helper Virus-Dependent Adenovirus Vector von Mitani, Kohnosuke, Graham, Frank L., Caskey, C. Thomas, Kochanek, Stefan

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An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy von Fu, Y. H., Pizzuti, A., Fenwick, R. G., King, J., Rajnarayan, S., Dunne, P. W., Dubel, J., Nasser, G. A., Ashizawa, T., De Jong, P., Wieringa, B., Korneluk, R., Perryman, M. B., Epstein, H. F., Caskey, C. Thomas

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Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies von ALLIKMETS, R, SEDDON, J. M, CASKEY, C. T, DEAN, M, PETRUKHIN, K, BERNSTEIN, P. S, HUTCHINSON, A, ATKINSON, A, SHARMA, S, GERRARD, B, WEN LI, METZKER, M. L, WADELIUS, C

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Characterization of the human cysteinyl leukotriene CysLT1 receptor von Lynch, Kevin R., O'Neill, Gary P., Liu, Qingyun, Im, Dong-Soon, Sawyer, Nicole, Metters, Kathleen M., Coulombe, Nathalie, Abramovitz, Mark, Figueroa, David J., Zeng, Zhizhen, Connolly, Brett M., Bai, Chang, Austin, Christopher P., Chateauneuf, Anne, Stocco, Rino, Greig, Gillian M., Kargman, Stacia, Hooks, Shelley B., Hosfield, Elizabeth, Williams, David L., Ford-Hutchinson, Anthony W., Caskey, C. Thomas, Evans, Jilly F.

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Triplet Repeat Mutations in Human Disease von Caskey, C. Thomas, Pizzuti, Antonio, Fu, Ying-Hui, Fenwick, Raymond G., Nelson, David L.

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Triplet repeat disorders: discussion of molecular mechanisms von Timchenko, L. T, Caskey, C. T

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