Carina von Schantz

Brain gene expression profiles of Cln1and Cln5deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases (2008)

Von Schantz, Carina, Saharinen, Juha, Kopra, Outi, Cooper, Jonathan D, Gentile, Massimiliano, Hovatta, Iiris, ...

Abstract Background The neuronal ceroid lipofuscinoses (NCL) are a group of children's inherited neurodegenerative disorders, characterized by blindness, early dementia and pronounced cortical...

Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1) – distinct characteristics in neurons (2007)

Lyly, Annina, Von Schantz, Carina, Salonen, Tarja, Kopra, Outi, Saarela, Jani, Jauhiainen, Matti, ...

Abstract Background Neuronal ceroid lipofuscinoses (NCLs) are collectively the most common type of recessively inherited childhood encephalopathies. The most severe form of NCL, infantile neuronal...

A Mouse Model for Finnish Variant Late Infantile Neuronal Ceroid Lipofuscinosis, CLN5, reveals neuropathology associated with early aging (2004)

Kopra, Outi, Vesa, Jouni, Von Schantz, Carina, Manninen, Tuula, Minye, Helena, Fabritius, Anna-Liisa, ...

Neuronal ceroid lipofuscinoses (NCL) comprise the most common group of childhood encephalopathies caused by mutations in eight genetic loci, CLN1-CLN8. Here we have developed a novel mouse model for...

A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging (2004)

Kopra, Outi, Vesa, Jouni, Von Schantz, Carina, Manninen, Tuula, Minye, Helena, Fabritius, Anna-Liisa, ...

Neuronal ceroid lipofuscinoses (NCL) comprise the most common group of childhood encephalopathies caused by mutations in eight genetic loci, CLN1–CLN8. Here, we have developed a novel mouse model...

A Mouse Model for Finnish Variant Late Infantile Neuronal Ceroid Lipofuscinosis, CLN5, reveals neuropathology associated with early aging (2004)

Kopra, Outi, Vesa, Jouni, Von Schantz, Carina, Manninen, Tuula, Minye, Helena, Fabritius, Anna-Liisa, ...

Neuronal ceroid lipofuscinoses (NCL) comprise the most common group of childhood encephalopathies caused by mutations in eight genetic loci, CLN1-CLN8. Here we have developed a novel mouse model for...

Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1) – distinct characteristics in neurons

Lyly, Annina, Von Schantz, Carina, Salonen, Tarja, Kopra, Outi, Saarela, Jani, Jauhiainen, Matti, ...

Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases

Von Schantz, Carina, Saharinen, Juha, Kopra, Outi, Cooper, Jonathan D, Gentile, Massimiliano, Hovatta, Iiris, ...