Sc Brown

发表

Strategies for disease identification

Emc Fisher, A Ballabio, Sc Brown, 1997 .

Cellular localisation of wild type and mutated FKRP

Martin Brockington, Francesco Muntoni, Sc Brown, 2004 .

Disorders of glycosylation: an emerging group of muscular dystrophies

Martin Brockington, Francesco Muntoni, Sc Brown, 2002 .

Dystroglycan expression during muscle development

Francesco Muntoni, Sc Brown, Lucy Feng, 2002 .

Clinical phenotype in patients with mutations in the fukutin-related protein (FKRP) gene

Martin Brockington, Francesco Muntoni, Sc Brown, 2002 .

Evaluation of the effect of a transient up-regulation of LARGE in the mouse m.tibialis anterior

Martin Brockington, Francesco Muntoni, Sc Brown, 2006 .

How much dystrophin to avoid muscular dystrophy

Francesco Muntoni, Luciano Merlini, Alessandra Ferlini, 2007 .

Primary or secondary laminin-alpha 2 deficiency?

Francesco Muntoni, Sc Brown, Caroline A. Sewry, 2004 .

Double lamin-emerin and lamin-desmin trouble

Francesco Muntoni, Sc Brown, Pascale Richard, 2005 .

A comprehensive ENU mutagenesis programme has produced novel neurological and behavioural phenotypes.

Josephine Peters, Emc Fisher, Je Martin, 1999 .

In situ hybridization of FKRP mRNA during mouse development

Martin Brockington, Francesco Muntoni, Sc Brown, 2004 .

The dystroglycan complex in patients with mutations in the gene encoding for fukutin-related protein (FKRP)

Martin Brockington, Francesco Muntoni, Sc Brown, 2002 .

A comprehensive ENU mutagenesis programme for the mouse genome.

Josephine Peters, Simon Greenaway, Sc Brown, 1997 .

Immunocytochemical analysis of muscle agrin in MDC1C and LGDM2I

Francesco Muntoni, Sc Brown, Lucy Feng, 2003 .

Characterization and genetics of a mouse model of hypophosphatasia

Emc Fisher, Sc Brown, Tertius Hough, 2004 .