Cardiac malformations and midline skeletal defects in mice lacking filamin A

By Hart Alan W.   Morgan Joanne E.   Schneider Jürgen   West Katrine   McKie Lisa   Bhattacharya Shoumo   Jackson Ian J.   Cross Sally H.  

Human Molecular Genetics, Vol. 15, Iss. 16, 2006-08 ,pp. : 2457-2467

Oxford University Press

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A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification

By Zeeuwen P.L.J.M.  

Human Molecular Genetics, Vol. 11, Iss. 23, 2002-11 ,pp. : 2867-2875

Oxford University Press

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Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume

By Van Agtmael Tom   Bailey Matthew A.   Schltzer-Schrehardt Ursula   Craigie Eilidh   Jackson Ian J.   Brownstein David G.   Megson Ian L.   Mullins John J.  

Human Molecular Genetics, Vol. 19, Iss. 6, 2010-03 ,pp. : 1119-1128

Oxford University Press

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Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1

By Goold Robert   Hubank Michael   Hunt Abigail   Holton Janice   Menon Rajesh P.   Revesz Tamas   Pandolfo Massimo   Matilla-Dueas Antoni  

Human Molecular Genetics, Vol. 16, Iss. 17, 2007-09 ,pp. : 2122-2134

Oxford University Press

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Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice

By Tiranti V.  

Human Molecular Genetics, Vol. 12, Iss. 4, 2003-02 ,pp. : 399-413

Oxford University Press

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