The Mottled Mouse as a Model for Human Menkes Disease: Identification of Mutations in the Atp7a Gene

By Cecchi Chiara   Biasotto Michel   Tosi Mario   Avner Philip  

Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 425-433

Oxford University Press

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Novel membrane traffic steps regulate the exocytosis of the Menkes disease ATPase

By Cobbold Christian  

Human Molecular Genetics, Vol. 11, Iss. 23, 2002-11 ,pp. : 2855-2866

Oxford University Press

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The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal

By Petris Michael J.  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2107-2115

Oxford University Press

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Immunocytochemical Localization of the Menkes Copper Transport Protein (ATP7A) to the Trans -Golgi Network

By Dierick Herman A.   Adam Ayla N.   Escara-Wilke June F.   Glover Thomas W.  

Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 409-416

Oxford University Press

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Constitutive skipping of alternatively spliced exon 10 in the ATP7A gene abolishes Golgi localization of the Menkes protein and produces the occipital horn syndrome

By Qi M.   Byers P.H.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 465-469

Oxford University Press

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