Partial loss of presenilins causes seborrheic keratosis and autoimmune disease in mice

By Tournoy Jos   Bossuyt Xavier   Snellinx An   Regent Marleen   Garmyn Marian   Serneels Lutgarde   Saftig Paul   Craessaerts Katleen   De Strooper Bart   Hartmann Dieter  

Human Molecular Genetics, Vol. 13, Iss. 13, 2004-07 ,pp. : 1321-1331

Oxford University Press

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Mutant presenilins specifically elevate the levels of the 42 residue -amyloid peptide in vivo : evidence for augmentation of a 42-specific  secretase

By Jankowsky Joanna L.  

Human Molecular Genetics, Vol. 13, Iss. 2, 2004-01 ,pp. : 159-170

Oxford University Press

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Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization

By Rajpar M.H.  

Human Molecular Genetics, Vol. 11, Iss. 21, 2002-10 ,pp. : 2559-2565

Oxford University Press

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Impaired cotranslational processing of the calcium-sensing receptor due to signal peptide missense mutations in familial hypocalciuric hypercalcemia

By Pidasheva Svetlana  

Human Molecular Genetics, Vol. 14, Iss. 12, 2005-06 ,pp. : 1679-1690

Oxford University Press

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Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transport

By Dumanchin Cécile  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1263-1269

Oxford University Press

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