Mice with Ppt1Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons

Infantile Neuronal Ceroid Lipofuscinosis (INCL) results from mutations in the palmitoyl protein thioesterase (PPT1, CLN1) gene and is characterized by dramatic death of cortical neurons. We generated Ppt1Δex4 mice by a targeted deletion of exon 4 of the mouse Ppt1 gene. Similar to the clinical pheno...

Cijeli opis

Bibliografski detalji

Glavni autori:	Anu Jalanko, Jouni Vesa, Tuula Manninen, Carina von Schantz, Helena Minye, Anna-Liisa Fabritius, Tarja Salonen, Juhani Rapola, Massimiliano Gentile, Outi Kopra, Leena Peltonen
Format:	Artigo
Jezik:	Inglês
Izdano:	Elsevier 2005-02-01
Serija:	Neurobiology of Disease
Teme:	INCL Inflammation Mouse model Neurodegeneration Palmitoyl protein thioesterase
Online pristup:	http://www.sciencedirect.com/science/article/pii/S0969996104001858
Oznake:	Dodaj oznaku Bez oznaka, Budi prvi tko označuje ovaj zapis!