Sialin, an anion transporter defective in sialic acid storage diseases, shows highly variable expression in adult mouse brain, and is developmentally regulated
Natalia Yarovaya(Murdoch Children's Research Institute), Deon J. Venter(The University of Melbourne), Rachel Schot(Erasmus MC), Colin L. Masters(Mental Health Research Institute), Alexis Mahoney(Murdoch Children's Research Institute), Elly Verbeek(Erasmus MC), Grazia M.S. Mancini(Erasmus MC), Peter J. van der Spek(Erasmus MC), Rachel Williams, An De Bondt, Andrew Stubbs, Michelle A. McMahon(Murdoch Children's Research Institute), Frans W. Verheijen(Erasmus MC), Mark Hampson, Lisa R. Fodero(The University of Melbourne)
Cited by 36
Related Papers
Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease
|New England Journal of Medicine|2012|3.8k
Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease
|Nature Medicine|2019|948
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
|Nature Genetics|2012|752
Metalloenzyme-like Activity of Alzheimer's Disease β-Amyloid
|Journal of Biological Chemistry|2002|575