Increased SK3 expression in DM1 lens cells leads to impaired growth through a greater calcium-induced fragility

By Rhodes Jeremy D.   Monckton Darren G.   McAbney John P.   Prescott Alan R.   Duncan George  

Human Molecular Genetics, Vol. 15, Iss. 24, 2006-12 ,pp. : 3559-3568

Oxford University Press

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CLN3 protein is targeted to neuronal synapses but excluded from synaptic vesicles: new clues to Batten disease

By Lehtovirta M.   Luiro K.   Kopra O.   Jalanko A.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2123-2131

Oxford University Press

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A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis

By Kitzmller Claudia   Haines Rebecca L.   Codlin Sandra   Cutler Daniel F.   Mole Sara E.  

Human Molecular Genetics, Vol. 17, Iss. 2, 2008-01 ,pp. : 303-312

Oxford University Press

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Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models

By Chan Chun-Hung   Mitchison Hannah M.   Pearce David A.  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3332-3339

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Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

By Isosomppi J.  

Human Molecular Genetics, Vol. 11, Iss. 8, 2002-04 ,pp. : 885-891

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