Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Brain Research. Developmental Brain Research|October 7, 2004
Mouse neural progenitor cells differentiate into oligodendrocytes in the brain of a knockout mouse model of Canavan diseaseSankar Surendran, Lamya S Shihabuddin, Jennifer Clarke, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's diseaseChikkathur N Madhavarao, Peethambaran Arun, John R Moffett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 17, 2004
Biopterin responsive phenylalanine hydroxylase deficiencyReuben Matalon, Richard Koch, Kimberlee Michals-Matalon, et al.
Pediatrics|December 5, 2003
Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcomeFlemming Güttler, Colleen Azen, Per Guldberg, et al.
Pediatrics|December 5, 2003
Pregnancy experiences in the woman with mild hyperphenylalaninemiaHarvey L Levy, Susan E Waisbren, Flemming Güttler, et al.
Iscience|May 31, 2022
Therapeutic development for Canavan disease using patient iPSCs introduced with the wild-type <i>ASPA</i> geneJianfei Chao, Lizhao Feng, Peng Ye, et al.
Pediatrics|March 30, 2016
Acute Otitis Media and Other Complications of Viral Respiratory InfectionTasnee Chonmaitree, Rocio Trujillo, Kristofer Jennings, et al.
Brain Research Bulletin|August 12, 2003
Expression of glutamate transporter, GABRA6, serine proteinase inhibitor 2 and low levels of glutamate and GABA in the brain of knock-out mouse for Canavan diseaseSankar Surendran, Peter L Rady, Kimberlee Michals-Matalon, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 5, 2016
rAAV Gene Therapy in a Canavan's Disease Mouse Model Reveals Immune Impairments and an Extended Pathology Beyond the Central Nervous SystemSeemin Seher Ahmed, Stefan A Schattgen, Ashley E Frakes, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 24, 2004
Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutationsHeidi Erlandsen, Angel L Pey, Alejandra Gámez, et al.
Pageof 6