Severely altered guanidino compound levels, disturbed body weight homeostasis and impaired fertility in a mouse model of guanidinoacetate N-methyltransferase (GAMT) deficiency

By Schmidt Andreas   Marescau Bart   Boehm Ernest A.   Renema W. Klaas Jan   Peco Ruben   Das Anib   Steinfeld Robert   Chan Sharon   Wallis Julie   Davidoff Michail   Ullrich Kurt   Waldschütz Ralph   Heerschap Arend   De Deyn Peter P.   Neubauer Stefan   Isbrandt Dirk  

Human Molecular Genetics, Vol. 13, Iss. 9, 2004-05 ,pp. : 905-921

Oxford University Press

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Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome

By Balemans Monique C.M.   Nadif Kasri Nael   Kopanitsa Maksym V.   Afinowi Nurudeen O.   Ramakers Ger   Peters Theo A.   Beynon Andy J.   Janssen Sanne M.   van Summeren Rik C.J.   Eeftens Jorine M.   Eikelenboom Nathalie   Benevento Marco   Tachibana Makoto   Shinkai Yoichi   Kleefstra Tjitske   van Bokhoven Hans   Van der Zee Catharina E.E.M.  

Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 852-866

Oxford University Press

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Enzyme therapy for lysosomal acid lipase deficiency in the mouse

By Schiavi S.   Levine M.   Du H.   Mishra J.   Heur M.   Grabowski G.A.  

Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1639-1648

Oxford University Press

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Mouse model of N -acetylgalactosamine-6-sulfate sulfatase deficiency ( Galns −/− ) produced by targeted disruption of the gene defective in Morquio A disease

By Tomatsu Shunji  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3349-3358

Oxford University Press

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Knockout mouse model for Fxr2 : a model for mental retardation

By McAninch R.  

Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 487-498

Oxford University Press

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