Insulin Receptor Splicing Alteration in Myotonic Dystrophy Type 2 von Savkur, R.S., Philips, A.V., Cooper, T.A., Dalton, J.C., Moseley, M.L., Ranum, L.P.W., Day, J.W.

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Molecular genetics of spinocerebellar ataxia type 8 (SCA8) von Mosemiller, A.K., Dalton, J.C., Day, J.W., Ranum, L.P.W.

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140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management von Udd, B., Meola, G., Krahe, R., Thornton, C., Ranum, L.P.W., Bassez, G., Kress, W., Schoser, B., Moxley, R.

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Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families von MOSELEY, M. L, BENZOW, K. A, RANUM, L. P. W, SCHUT, L. J, BIRD, T. D, GOMEZ, C. M, BARKHAUS, P. E, BLINDAUER, K. A, LABUDA, M, PANDOLFO, M, KOOB, M. D

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Therapeutic strategies for C9orf72 amyotrophic lateral sclerosis and frontotemporal dementia von Hautbergue, G.M, Cleary, J.D, Guo, S, Ranum, L.P.W

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Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5 von LORENZO, D. N, FORREST, S. M, IKEDA, Y, DICK, K. A, RANUM, L. P. W, KNIGHT, M. A

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Molecular and clinical correlations in spinocerebellar ataxia type I : evidence for familial effects on the age at onset von RANUM, L. P. W, MING-YI CHUNG, GOMEZ, C, SANDKUIJL, L. A, ORR, H. T, ZOGHBI, H. Y, BANFI, S, BRYER, A, SCHUT, L. J, RAJ RAMESAR, DUVICK, L. A, MCCALL, A, SUBRAMONY, S. H, LEV GOLDFARB

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Isolation and characterization of the nitrate reductase structural gene of Chlamydomonas reinhardtii von Fernandez, E. (University of Minnesota, Saint Paul, MN), Schnell, R, Ranum, L.P.W, Hussey, S.C, Silflow, C.D, Lefebvre, P.A

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Dominant Non-Coding Repeat Expansions in Human Disease von Dick, K.A., Margolis, J.M., Day, J.W., Ranum, L.P.W.

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Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb von Banfi, S., Chung, M.-Y., Kwiatkowski, T.J., Ranum, L.P.W., McCall, A.E., Chinault, A.C., Orr, H.T., Zoghbi, H.Y.

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The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 l... von KWIATKOWSKI, T. J, ORR, H. T, SUBRAMONY, S. H, BEAUDET, A. L, TERRENATO, L, ZOGHBI, H. Y, RANUM, L. P. W, BANFI, S, MCCALL, A. E, JODICE, C, PERSICHETTI, F, NOVELLETTO, A, LE BORGNE-DE MARQUOY, F, DUVICK, L. A, FRONTALI, M

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Dinucleotide repeat polymorphism at the D6S109 locus von RANUM, L. P. W, CHUNG, M.-Y, DUVICK, L. A, ZOGHBI, H. Y, ORR, H. T

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Mapping and cloning of the critical region for the spineocerebellar ataxia Type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1. 2 Mb von Banfi, S., McCall, A.E., Zoghbi, H.Y., Kwiatkowski, T.J. Jr, Chinault, A.C., Ranum, L.P.W., Orr, H.T.

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Mutants resistant to anti-microtubule herbicides map to a locus on the uni linkage group in Chlamydomonas reinhardtii von James, S.W, Ranum, L.P.W, Silflow, C.D, Lefebvre, P.A

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Extragenic suppression and synthetic lethality among Chlamydomonas reinhardtii mutants resistant to anti-microtubule drugs von James, S.W. (University of Minnesota, St. Paul, MN), Silflow, C.D, Thompson, M.D, Ranum, L.P.W, Lefebvre, P.A

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Peripheral neuropathy in adult onset degenerative ataxia von Midani, H., Parry, G.J.G., Ranum, L.P.W., Gomez, C.

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