Literature DB >> 16802706

Canavan disease: studies on the knockout mouse.

Reuben Matalon1, Kimberlee Michals-Matalon, Sankar Surendran, Stephen K Tyring.   

Abstract

Canavan disease (CD) is an autosomal recessive disorder, characterized by spongy degeneration of the brain. Patients with CD have aspartoacylase (ASPA) deficiency, which results accumulation of N-acetylaspartic acid (NAA) in the brain and elevated excretion of urinary NAA. Clinically, patients with CD have macrocephaly, mental retardation and hypotonia. A knockout mouse for CD which was engineered, also has ASPA deficiency and elevated NAA. Molecular studies of the mouse brain showed abnormal expression of multiple genes in addition to ASPA deficiency. Adenoassociated virus mediated gene transfer and stem cell therapy in the knockout mouse are the latest attempts to alter pathophysiology in the CD mouse.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16802706     DOI: 10.1007/0-387-30172-0_6

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  1 in total

1.  rAAV Gene Therapy in a Canavan's Disease Mouse Model Reveals Immune Impairments and an Extended Pathology Beyond the Central Nervous System.

Authors:  Seemin Seher Ahmed; Stefan A Schattgen; Ashley E Frakes; Elif M Sikoglu; Qin Su; Jia Li; Thomas G Hampton; Andrew R Denninger; Daniel A Kirschner; Brian Kaspar; Reuben Matalon; Guangping Gao
Journal:  Mol Ther       Date:  2016-04-04       Impact factor: 11.454

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.