Showing results (21-30 of 58) with videos related to
Sort By:
Pageof 6
European Journal of Medical Genetics|April 7, 2011
A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasiaJill K Northup, Reuben Matalon, Lillian H Lockhart, et al.Neurochemical Research|December 3, 2003
High levels of orexin A in the brain of the mouse model for phenylketonuria: possible role of orexin A in hyperactivity seen in children with PKUSankar Surendran, Gerald A Campbell, Stephen K Tyring, et al.Experimental Animals|April 27, 2007
Absence-like and tonic seizures in aspartoacylase/attractin double-mutant miceHiroshi Gohma, Takashi Kuramoto, Reuben Matalon, et al.Neurobiology of Disease|July 20, 2010
Aspartoacylase deficiency affects early postnatal development of oligodendrocytes and myelinationNatalia S Mattan, Cristina A Ghiani, Marcia Lloyd, et al.Pediatrics|December 5, 2003
Future role of large neutral amino acids in transport of phenylalanine into the brainReuben Matalon, Sankar Surendran, Kimberlee Michals Matalon, et al.Pediatrics|December 5, 2006
Association of proinflammatory cytokine gene polymorphisms with susceptibility to otitis mediaJanak A Patel, Sangeeta Nair, Krystal Revai, et al.Brain Research|July 13, 2004
Aspartoacylase deficiency does not affect N-acetylaspartylglutamate level or glutamate carboxypeptidase II activity in the knockout mouse brainSankar Surendran, Edward L Ezell, Michael J Quast, et al.Journal of Neurochemistry|January 27, 2007
Bimodal occurrence of aspartoacylase in myelin and cytosol of brainJianfeng Wang, Reuben Matalon, Gita Bhatia, et al.Molecular Genetics and Metabolism|October 22, 2003
Canavan disease: a monogenic trait with complex genomic interactionSankar Surendran, Kimberlee Michals-Matalon, Michael J Quast, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 6, 2004
Trends in enzyme therapy for phenylketonuriaWoomi Kim, Heidi Erlandsen, Sankar Surendran, et al.Pageof 6