Ian Holt

Author PubWeight™ 10.93^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.	PLoS Genet	2009	1.22
2	Emerin interacts in vitro with the splicing-associated factor, YT521-B.	Eur J Biochem	2003	1.12
3	Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features.	PLoS One	2008	1.01
4	Expanded CUG repeats Dysregulate RNA splicing by altering the stoichiometry of the muscleblind 1 complex.	J Biol Chem	2011	0.97
5	Analysis of exonic regions involved in nuclear localization, splicing activity, and dimerization of Muscleblind-like-1 isoforms.	J Biol Chem	2011	0.94
6	Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues.	DNA Repair (Amst)	2012	0.86
7	Characterization of MSH2 variants by endogenous gene modification in mouse embryonic stem cells.	Hum Mutat	2011	0.86
8	High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell lines.	Hum Mol Genet	2013	0.86
9	Characterisation of the transcription factor, SIX5, using a new panel of monoclonal antibodies.	J Cell Biochem	2005	0.81
10	Nesprin-1 and nesprin-2 regulate endothelial cell shape and migration.	Cytoskeleton (Hoboken)	2014	0.80
11	Endosomal location of dopamine receptors in neuronal cell cytoplasm.	J Mol Histol	2007	0.76
12	A rapid immunohistochemical test to distinguish congenital myotonic dystrophy from X-linked myotubular myopathy.	Neuromuscul Disord	2011	0.76