Melinda L Moseley-Alldredge

2022

A role for the Erk MAPK pathway in modulating SAX-7/L1CAM-dependent locomotion in Caenorhabditis elegans

Moseley-Alldredge, M., Sheoran, S., Yoo, H., O'Keefe, C., Richmond, J. E. & Chen, L., Feb 2022, In: Genetics. 220, 2, iyab215.

Research output: Contribution to journal › Article › peer-review

Open Access

4 Scopus citations

2016

EFN-4 functions in LAD-2-mediated axon guidance in Caenorhabditis elegans

Dong, B., Moseley-Alldredge, M., Schwieterman, A. A., Donelson, C. J., McMurry, J. L., Hudson, M. L. & Chen, L., Apr 1 2016, In: Development (Cambridge). 143, 7, p. 1182-1191 10 p.

Research output: Contribution to journal › Article › peer-review

Open Access

6 Scopus citations

2014

A novel nondevelopmental role of the sax-7/l1cam cell adhesion molecule in synaptic regulation in caenorhabditis elegans

Opperman, K., Moseley-Alldredge, M., Yochem, J., Bell, L., Kanayinkal, T. & Chen, L., Feb 1 2014, In: Genetics. 199, 2, p. 497-509 13 p.

Research output: Contribution to journal › Article › peer-review

Open Access

10 Scopus citations

2011

Non-ATG-initiated translation directed by microsatellite expansions

Zu, T., Gibbens, B., Doty, N. S., Gomes-Pereira, M., Huguet, A., Stone, M. D., Margolis, J., Peterson, M., Markowski, T. W., Ingram, M. A. C., Nan, Z., Forster, C., Low, W. C., Schoser, B., Somia, N. V., Clark, H. B., Schmechel, S., Bitterman, P. B., Gourdon, G. & Swanson, M. S. & 2 others, Moseley, M. & Ranum, L. P. W., Jan 4 2011, In: Proceedings of the National Academy of Sciences of the United States of America. 108, 1, p. 260-265 6 p.

Research output: Contribution to journal › Article › peer-review

722 Scopus citations

2010

Double the trouble: Bidirectional expression of the SCA8 CAG/CTG expansion mutation - Evidence for RNA and protein gain of function effects

Ranum, L. P. W., Daughters, R. S., Tuttle, D. L., Gao, W., Ikeda, Y., Moseley, M. L., Ebner, T. & Swanson, M. S., 2010, In: Clinical Neurology. 50, 11, p. 982-983 2 p.

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

2009

RNA gain-of-function in spinocerebellar ataxia type 8

Daughters, R. S., Tuttle, D. L., Gao, W., Ikeda, Y., Moseley, M. L., Ebner, T. J., Swanson, M. S. & Ranum, L. P. W., Aug 2009, In: PLoS genetics. 5, 8, e1000600.

Research output: Contribution to journal › Article › peer-review

237 Scopus citations

2006

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8

Moseley, M. L., Zu, T., Ikeda, Y., Gao, W., Mosemiller, A. K., Daughters, R. S., Chen, G., Weatherspoon, M. R., Clark, H. B., Ebner, T. J., Day, J. W. & Ranum, L. P. W., Jul 2006, In: Nature Genetics. 38, 7, p. 758-769 12 p.

Research output: Contribution to journal › Article › peer-review

369 Scopus citations

DM2 intronic expansions: Evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression

Margolis, J. M., Schoser, B. G., Moseley, M. L., Day, J. W. & Ranum, L. P. W., Jun 2006, In: Human molecular genetics. 15, 11, p. 1808-1815 8 p.

Research output: Contribution to journal › Article › peer-review

96 Scopus citations

2004

Insulin receptor splicing alteration in myotonic dystrophy type 2

Savkur, R. S., Philips, A. V., Cooper, T. A., Dalton, J. C., Moseley, M. L., Ranum, L. P. W. & Day, J. W., Jun 2004, In: American Journal of Human Genetics. 74, 6, p. 1309-1313 5 p.

Research output: Contribution to journal › Article › peer-review

139 Scopus citations

Spinocerebellar ataxia type 8: Molecular genetic comparisons and haplotype analysis of 37 families with ataxia

Ikeda, Y., Dalton, J. C., Moseley, M. L., Gardner, K. L., Bird, T. D., Ashizawa, T., Seltzer, W. K., Pandolfo, M., Milunsky, A., Potter, N. T., Shoji, M., Vincent, J. B., Day, J. W. & Ranum, L. P. W., Jul 2004, In: American Journal of Human Genetics. 75, 1, p. 3-16 14 p.

Research output: Contribution to journal › Article › peer-review

75 Scopus citations

2001

Myotonic dystrophy type 2 caused by a CCTG expansion in intron I of ZNF9

Liquori, C. L., Ricker, K., Moseley, M. L., Jacobsen, J. F., Kress, W., Naylor, S. L., Day, J. W. & Ranum, L. P. W., Aug 3 2001, In: Science. 293, 5531, p. 864-867 4 p.

Research output: Contribution to journal › Article › peer-review

1081 Scopus citations

2000

Erratum: The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1) (Human Molecular Genetics (2000) vol. 9 (1543-1551))

Nemes, J. P., Benzow, K. A., Moseley, M. L., Ranum, L. P. W. & Koob, M. D., Nov 1 2000, In: Human molecular genetics. 9, 18, 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

2 Scopus citations

Large, expanded repeats in sca8 are not confined to patients with cerebellar ataxia: Reply

Moseley, M. L., Schut, L. J., Bird, T. D., Day, J. W. & Ranum, L. P. W., Mar 2000, In: Nature Genetics. 24, 3, p. 215 1 p.

Research output: Contribution to journal › Article › peer-review

Open Access

10 Scopus citations

Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia

Worth, P. F., Houlden, H., Giunti, P., Davis, M. B., Wood, N. W., Moseley-Alldredge, M. L., Schut, L. J., Bird, T. D., Day, J. W. & Ranum, L. P. W., Mar 2000, In: Nature Genetics. 24, 3, p. 214-215 2 p.

Research output: Contribution to journal › Letter › peer-review

100 Scopus citations

SCA8 CTG repeat: En masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance

Moseley, M. L., Schut, L. J., Bird, T. D., Koob, M. D., Day, J. W. & Ranum, L. P. W., Sep 1 2000, In: Human molecular genetics. 9, 14, p. 2125-2130 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

104 Scopus citations

Spinocerebellar ataxia type 8: Clinical features in a large family

Day, J. W., Schut, L. J., Moseley, M. L., Durand, A. C. & Ranum, L. P. W., 2000, In: Neurology. 55, 5, p. 649-657 9 p.

Research output: Contribution to journal › Article › peer-review

128 Scopus citations

1999

A nonpathogenic GAAGGA repeat in the Friedreich gene: Implications for pathogenesis

Ohshima, K., Sakamoto, N., Labuda, M., Poirier, J., Moseley, M. L., Montermini, L., Ranum, L. P. W., Wells, R. D. & Pandolfo, M., Nov 10 1999, In: Neurology. 53, 8, p. 1854-1857 4 p.

Research output: Contribution to journal › Article › peer-review

46 Scopus citations

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

Koob, M. D., Moseley, M. L., Schut, L. J., Benzow, K. A., Bird, T. D., Day, J. W. & Ranum, L. P. W., Apr 1999, In: Nature Genetics. 21, 4, p. 379-384 6 p.

Research output: Contribution to journal › Article › peer-review

566 Scopus citations

1998

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

Moseley, M. L., Benzow, K. A., Schut, L. J., Bird, T. D., Gomez, C. M., Barkhaus, P. E., Blindauer, K. A., Labuda, M., Pandolfo, M., Koob, M. D. & Ranum, L. P. W., Dec 1998, In: Neurology. 51, 6, p. 1666-1671 6 p.

Research output: Contribution to journal › Article › peer-review

206 Scopus citations

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA

Koob, M. D., Benzow, K. A., Bird, T. D., Day, J. W., Moseley, M. L. & Ranum, L. P. W., 1998, In: Nature Genetics. 18, 1, p. 72-75 4 p.

Research output: Contribution to journal › Article › peer-review

93 Scopus citations

Melinda L Moseley-Alldredge

Research output

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