25 results for author:"Dickson G." in Literature citations
Results Customize
› Repeat search in UniProtKB (10)
| Combinatorial use of bone morphogenetic protein 6, noggin and SOST significantly predicts cancer progression. Yuen H.F., McCrudden C.M., Grills C., Zhang S.D., Huang Y.H., Chan K.K., Chan Y.P., Wong M.L., Law S., Srivastava G. et al. Cancer Sci. 103:1145-1154(2012) · Mapped (12) |
| Evidence for alteration of EZH2, BMI1, and KDM6A and epigenetic reprogramming in human papillomavirus type 16 E6/E7-expressing keratinocytes. Hyland P.L., McDade S.S., McCloskey R., Dickson G.J., Arthur K., McCance D.J., Patel D. J. Virol. 85:10999-11006(2011) · Mapped (29) |
| Differential Hox expression in murine embryonic stem cell models of normal and malignant hematopoiesis. Wheadon H., Ramsey J.M., Dobbin E., Dickson G.J., Corrigan P.M., Freeburn R.W., Thompson A. Stem Cells Dev. 20:1465-1476(2011) · Mapped (8) |
| Transcriptomic analysis of dystrophin RNAi knockdown reveals a central role for dystrophin in muscle differentiation and contractile apparatus organization. Ghahramani Seno M.M., Trollet C., Athanasopoulos T., Graham I.R., Hu P., Dickson G. BMC Genomics 11:345-345(2010) · Mapped (11) |
| Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres. Trollet C., Anvar S.Y., Venema A., Hargreaves I.P., Foster K., Vignaud A., Ferry A., Negroni E., Hourde C., Baraibar M.A. et al. Hum. Mol. Genet. 19:2191-2207(2010) · Mapped (7) |
| Hoxa6 potentiates short-term hemopoietic cell proliferation and extended self-renewal. Dickson G.J., Kwasniewska A., Mills K.I., Lappin T.R., Thompson A. Exp. Hematol. 37:322-33.e3(2009) · Mapped (6) |
| Preliminary evaluation of a self-complementary AAV2/8 vector for hepatic gene transfer of human apoE3 to inhibit atherosclerotic lesion development in apoE-deficient mice. Osman E., Evans V., Graham I.R., Athanasopoulos T., McIntosh J., Nathwani A.C., Simons J.P., Dickson G., Owen J.S. Atherosclerosis 204:121-126(2009) · Mapped (14) |
| RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology. Ghahramani Seno M.M., Graham I.R., Athanasopoulos T., Trollet C., Pohlschmidt M., Crompton M.R., Dickson G. Hum. Mol. Genet. 17:2622-2632(2008) · Mapped (8) |
| Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscle. Arechavala-Gomeza V., Graham I.R., Popplewell L.J., Adams A.M., Aartsma-Rus A., Kinali M., Morgan J.E., van Deutekom J.C., Wilton S.D., Dickson G. et al. Hum. Gene Ther. 18:798-810(2007) · Mapped (69) |
| Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice. Ito K., Kimura S., Ozasa S., Matsukura M., Ikezawa M., Yoshioka K., Ueno H., Suzuki M., Araki K., Yamamura K. et al. Hum. Mol. Genet. 15:2266-2275(2006) · Mapped (10) |
| Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene. Sakamoto M., Yuasa K., Yoshimura M., Yokota T., Ikemoto T., Suzuki M., Dickson G., Miyagoe-Suzuki Y., Takeda S. Biochem. Biophys. Res. Commun. 293:1265-1272(2002) · Mapped (11) |
| Acute regression of advanced and retardation of early aortic atheroma in immunocompetent apolipoprotein-E (apoE) deficient mice by administration of a second generation [E1(-), E3(-), polymerase(-)] adenovirus vector expressing human apoE. Harris J.D., Graham I.R., Schepelmann S., Stannard A.K., Roberts M.L., Hodges B.L., Hill V., Amalfitano A., Hassall D.G., Owen J.S. et al. Hum. Mol. Genet. 11:43-58(2002) · Mapped (13) |
| Independent localization of dystrophin N- and C-terminal regions to the sarcolemma of mdx mouse myofibres in vivo. Dunckley M.G., Wells K.E., Piper T.A., Wells D.J., Dickson G. J. Cell. Sci. 107:1469-1475(1994) · Mapped (8) |
| Liposome-mediated gene transfer into normal and dystrophin-deficient mouse myoblasts. Trivedi R.A., Dickson G. J. Neurochem. 64:2230-2238(1995) · Mapped (8) |
| Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Wells D.J., Wells K.E., Asante E.A., Turner G., Sunada Y., Campbell K.P., Walsh F.S., Dickson G. Hum. Mol. Genet. 4:1245-1250(1995) · Mapped (8) |
| Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32. Zeviani M., Darras B.T., Rizzuto R., Salviati G., Betto R., Bonilla E., Miranda A.F., Du J., Samitt C., Dickson G. et al. Genomics 2:249-256(1988) · UniProtKB (3) |
| Complete sequence and in vitro expression of a tissue-specific phosphatidylinositol-linked N-CAM isoform from skeletal muscle. Barton C.H., Dickson G., Gower H.J., Rowett L.H., Putt W., Elsom V., Moore S.E., Goridis C., Walsh F.S. Development 104:165-173(1988) · UniProtKB (1) |
| Alternative splicing generates a secreted form of N-CAM in muscle and brain. Gower H.J., Barton C.H., Elsom V.L., Thompson J., Moore S.E., Dickson G., Walsh F.S. Cell 55:955-964(1988) · UniProtKB (1) |
| Human muscle neural cell adhesion molecule (N-CAM): identification of a muscle-specific sequence in the extracellular domain. Dickson G., Gower H.J., Barton C.H., Prentice H.M., Elsom V.L., Moore S.E., Cox R.D., Quinn C., Putt W., Walsh F.S. Cell 50:1119-1130(1987) · UniProtKB (1) |
| An autosomal transcript in skeletal muscle with homology to dystrophin. Love D.R., Hill D.F., Dickson G., Spurr N.K., Byth B.C., Marsden R.F., Walsh F.S., Edwards Y.H., Davies K.E. |
| Cloning and characterization of a myoblast cell surface antigen defined by 24.1D5 monoclonal antibody. Gower H.J., Moore S.E., Dickson G., Elsom V.L., Nayak R., Walsh F.S. Development 105:723-731(1989) · UniProtKB (1) |
| The muscle specific domain of mouse N-CAM: structure and alternative splicing patterns. Hamshere M., Dickson G., Eperon I. Nucleic Acids Res. 19:4709-4716(1991) · UniProtKB (1) · Mapped (7) |
| Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells. Blake D.J., Love D.R., Tinsley J., Morris G.E., Turley H., Gatter K., Dickson G., Edwards Y.H., Davies K.E. Hum. Mol. Genet. 1:103-109(1992) · UniProtKB (1) · Mapped (2) |
| Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice. Wells D.J., Wells K.E., Walsh F.S., Davies K.E., Goldspink G., Love D.R., Chan-Thomas P., Dunckley M.G., Piper T., Dickson G. Hum. Mol. Genet. 1:35-40(1992) · Mapped (8) |
| Co-localization and molecular association of dystrophin with laminin at the surface of mouse and human myotubes. Dickson G., Azad A., Morris G.E., Simon H., Noursadeghi M., Walsh F.S. J. Cell. Sci. 103:1223-1233(1992) · Mapped (8) |