11 results for author:"Donnelly A." in Literature citations
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| Combined inhibition of Wee1 and Hsp90 activates intrinsic apoptosis in cancer cells. Iwai A., Bourboulia D., Mollapour M., Jensen-Taubman S., Lee S., Donnelly A.C., Yoshida S., Miyajima N., Tsutsumi S., Smith A.K. et al. Cell Cycle 11:3649-3655(2012) · Mapped (13) |
| Swe1Wee1-dependent tyrosine phosphorylation of Hsp90 regulates distinct facets of chaperone function. Mollapour M., Tsutsumi S., Donnelly A.C., Beebe K., Tokita M.J., Lee M.J., Lee S., Morra G., Bourboulia D., Scroggins B.T. et al. Mol. Cell 37:333-343(2010) · Mapped (9) |
| D2 receptor-mediated inhibition of dopamine release in the rat striatum in vitro is modulated by CB1 receptors: studies using fast cyclic voltammetry. O'Neill C., Evers-Donnelly A., Nicholson D., O'Boyle K.M., O'Connor J.J. J. Neurochem. 108:545-551(2009) · Mapped (2) |
| Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation. Tarpey P., Parnau J., Blow M., Woffendin H., Bignell G., Cox C., Cox J., Davies H., Edkins S., Holden S. et al. Am. J. Hum. Genet. 75:318-324(2004) · UniProtKB (1) · Mapped (3) |
| Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation. Kalscheuer V.M., Tao J., Donnelly A., Hollway G., Schwinger E., Kuebart S., Menzel C., Hoeltzenbein M., Tommerup N., Eyre H. et al. Am. J. Hum. Genet. 72:1401-1411(2003) · UniProtKB (1) · Mapped (1) |
| IKK-i and TBK-1 are enzymatically distinct from the homologous enzyme IKK-2: comparative analysis of recombinant human IKK-i, TBK-1, and IKK-2. Kishore N., Huynh Q.K., Mathialagan S., Hall T., Rouw S., Creely D., Lange G., Caroll J., Reitz B., Donnelly A. et al. J. Biol. Chem. 277:13840-13847(2002) · UniProtKB (1) · Mapped (2) |
| Kinetic mechanisms of IkappaB-related kinases (IKK) inducible IKK and TBK-1 differ from IKK-1/IKK-2 heterodimer. Huynh Q.K., Kishore N., Mathialagan S., Donnelly A.M., Tripp C.S. J. Biol. Chem. 277:12550-12558(2002) · Mapped (3) |
| Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation. Gecz J., Barnett S., Liu J., Hollway G., Donnelly A., Eyre H., Eshkevari H.S., Baltazar R., Grunn A., Nagaraja R. et al. Genomics 62:356-368(1999) · UniProtKB (2) |
| A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Donnelly A., Haan E., Manson J., Mulley J. Hum. Mutat. 11:334-334(1998) · Mapped (5) |
| Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Borjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient. Gecz J., Baker E., Donnelly A., Ming J.E., McDonnald-McGinn D.M., Spinner N.B., Zackai E.H., Sutherland G.R., Mulley J.C. Hum. Genet. 104:56-63(1999) · UniProtKB (1) |
| A novel mutation in exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia. Donnelly A., Colley A., Crimmins D., Mulley J. Hum. Mutat. 8:384-385(1996) · UniProtKB (1) |