Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres

By Trollet Capucine   Anvar Seyed Yahya   Venema Andrea   Hargreaves Iain P.   Foster Keith   Vignaud Alban   Ferry Arnaud   Negroni Elisa   Hourde Christophe   Baraibar Martin A.   't Hoen Peter A.C.   Davies Janet E.   Rubinsztein David C.   Heales Simon J.   Mouly Vincent   van der Maarel Silvre M.   Butler-Browne Gillian   Raz Vered   Dickson George  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2191-2207

Oxford University Press

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Cardiovascular defects in a mouse model of HOXA1 syndrome

By Makki Nadja   Capecchi Mario R.  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 26-31

Oxford University Press

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Lethal, neonatal ichthyosis with increased proteolytic processing of filaggrin in a mouse model of Netherton syndrome

By Hewett Duncan R.  

Human Molecular Genetics, Vol. 14, Iss. 2, 2005-01 ,pp. : 335-346

Oxford University Press

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Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger–Huët anomaly

By Shultz Leonard D.  

Human Molecular Genetics, Vol. 12, Iss. 1, 2003-01 ,pp. : 61-69

Oxford University Press

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Disruption of scribble ( Scrb1 ) causes severe neural tube defects in the circletail mouse

By Murdoch Jennifer N.  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-01 ,pp. : 87-98

Oxford University Press

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