7 results for author:"D'Souza I." in Literature citations
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| Tau isoform regulation is region- and cell-specific in mouse brain. McMillan P., Korvatska E., Poorkaj P., Evstafjeva Z., Robinson L., Greenup L., Leverenz J., Schellenberg G.D., D'Souza I. J. Comp. Neurol. 511:788-803(2008) · Mapped (6) |
| A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia. Malkani R., D'Souza I., Gwinn-Hardy K., Schellenberg G.D., Hardy J., Momeni P. Neurobiol. Dis. 22:401-403(2006) · Mapped (6) |
| tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites. D'Souza I., Schellenberg G.D. J. Biol. Chem. 277:26587-26599(2002) · Mapped (6) |
| A genomic sequence analysis of the mouse and human microtubule-associated protein tau. Poorkaj P., Kas A., D'Souza I., Zhou Y., Pham Q., Stone M., Olson M.V., Schellenberg G.D. |
| Determinants of 4-repeat tau expression. Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion. D'Souza I., Schellenberg G.D. J. Biol. Chem. 275:17700-17709(2000) · Mapped (9) |
| A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration. Yasuda M., Kawamata T., Komure O., Kuno S., D'Souza I., Poorkaj P., Kawai J., Tanimukai S., Yamamoto Y., Hasegawa H. et al. Neurology 53:864-868(1999) · UniProtKB (1) |
| Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Clark L.N., Poorkaj P., Wszolek Z., Geschwind D.H., Nasreddine Z.S., Miller B., Li D., Payami H., Awert F., Markopoulou K. et al. Proc. Natl. Acad. Sci. U.S.A. 95:13103-13107(1998) · UniProtKB (1) |