The Menkes disease ATPase (ATP7A) is internalized via a Rac1-regulated, clathrin- and caveolae-independent pathway

By Cobbold C.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1523-1533

Oxford University Press

Access to resources Recommend Favorite

A comparison of the mutation spectra of Menkes disease and Wilson disease

By Hsi Gloria   Cox Diane  

Human Genetics, Vol. 114, Iss. 2, 2004-01 ,pp. : 165-172

Springer Publishing Company

Access to resources Recommend Favorite

Menkes disease with discordant phenotype in female monozygotic twins

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2826-2829

John Wiley & Sons Inc

Access to resources Recommend Favorite

Defective copper-induced trafficking and localization of the Menkes protein in patients with mild and copper-treated classical Menkes disease

By Ambrosini Loreta   Mercer Julian F. B.   Danks D.M.   Procopis P.   Vulpe C.   Mercer J.F.B.   Chelly J.   Pederson P.L.   Odermatt A.   Camakaris J.   Petris M.J.   La Fontaine S.   Ackland M.L.   Goka T.J.   Camakaris J.   Dierick H.   Tümer Z.   Danks D.M.   Danks D.M.   Christodoulou J.   Shapiro M.B.   Yamaguchi Y.   Lutsenko S.   Ladinsky M.S.   Molloy S.S.   Kaler S.G.   Strausak D.   Payne A.S.   Qi M.   Petris M.J.   Kaler S.G.   Das S.   Tümer Z.   Paynter J.A.   Sambrook J.   Miller S.A.   Mercer J.F.B.   Bull P.C.   Theophilos M.B.   Wu J.   Sambongi Y.   Fu D.  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1547-1555

Oxford University Press

Access to resources Recommend Favorite

Molecular Basis of the Brindled Mouse Mutant ( Mobr ): A Murine Model of Menkes Disease

By Grimes Andrew   Hearn Catherine J.   Lockhart Paul   Newgreen Don F.   Mercer Julian F. B.  

Human Molecular Genetics, Vol. 6, Iss. 7, 1997-01 ,pp. : 1037-1042

Oxford University Press

Access to resources Recommend Favorite