Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tania Radziewic"'
Autor:
David A.F. Loebel, Kristen Barratt, Vanessa Jones, Doreen Liebhold, Nicolas Fossat, Tania Radziewic, Melinda Power, Patrick P.L. Tam, Karin Tourle, Joshua B. Studdert
Publikováno v:
EMBO reports. 15:903-910
Cytidine (C) to Uridine (U) RNA editing is a post-transcriptional modification that is accomplished by the deaminase APOBEC1 and its partnership with the RNA-binding protein A1CF. We identify and characterise here a novel RNA-binding protein, RBM47,
Autor:
Melinda Power, Alister P. W. Funnell, Ka Sin Mak, Andrew C. Perkins, Natalie A. Twine, Laura J. Norton, Patrick P.L. Tam, Stuart T. Fraser, Tania Radziewic, Richard C. M. Pearson, Marc R. Wilkins, Gregory J. Pelka, Kim S. Bell-Anderson, Merlin Crossley
Publikováno v:
Molecular and Cellular Biology. 33:2976-2987
Krüppel-like factors 3 and 8 (KLF3 and KLF8) are highly related transcriptional regulators that bind to similar sequences of DNA. We have previously shown that in erythroid cells there is a regulatory hierarchy within the KLF family, whereby KLF1 dr
Publikováno v:
Genesis (New York, N.Y. : 2000). 54(3)
Rbm47 encodes a RNA binding protein that is necessary for Cytidine to Uridine RNA editing. Rbm47(gt/gt) mutant mice that harbor inactivated Rbm47 display poor viability. Here it was determined that the loss of Rbm47(gt/gt) offspring is due to embryon
Autor:
David A.F. Loebel, Vanessa Jones, Melinda Power, Kirsten A. Steiner, Lorraine Robb, Leigh Coultas, Renuka S. Rao, Nicolas Fossat, Patrick P.L. Tam, Yvette Jackson, Joshua B. Studdert, Tania Radziewic
Publikováno v:
Small GTPases
Rhou encodes a Cdc42-related atypical Rho GTPase that influences actin organization in cultured cells. In mouse embryos at early-somite to early-organogenesis stages, Rhou is expressed in the columnar endoderm epithelium lining the lateral and ventra
Autor:
John Christodoulou, Melinda Hayward, Patrick P.L. Tam, Tania Radziewic, Catherine M. Watson, Hooshang Lahooti, Gregory J. Pelka
Publikováno v:
Brain. 129:887-898
Rett syndrome (RTT) is a debilitating neurological condition associated with mutations in the X-linked MECP2 gene, where apparently normal development is seen prior to the onset of cognitive and motor deterioration at 6-18 months of life. A targeted
Publikováno v:
Methods in Molecular Biology ISBN: 9781603272902
We are using knockdown of gene expression in mouse embryos by constitutive expression of small hairpin (sh)RNAs as a means of observing loss-of-function phenotypes more rapidly than gene targeting. Plasmid constructs that direct shRNA expression via
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03962fa1e3717e56a54b8fb1fbb2ab0e
https://doi.org/10.1007/978-1-60327-292-6_8
https://doi.org/10.1007/978-1-60327-292-6_8
Autor:
Gabriel A. Quinlan, Monica L. Gordon, Karin S. Sturm, Tania Radziewic, Paul A. Trainor, Maala Parameswaran, Patrick P.L. Tam, Catherine M. Watson, Gregory J. Pelka, Sheila X. Zhou
Publikováno v:
METHODS IN MOLECULAR BIOLOGY™ ISBN: 9781588294319
Cell lineage analyses trace the hierarchy of cell types derived from a progenitor population. Critical to these analyses is the ability to track reliably all or defined subsets of the clonal descendants of the progenitor population. This necessitates
Autor:
Gregory J. Pelka, Catherine M. Watson, Tania Radziewic, Melinda Hayward, Hooshang Lahooti, John Christodoulou, Patrick P. L. Tam
Publikováno v:
Brain: A Journal of Neurology; Apr2006, Vol. 129 Issue 4, p887-898, 12p