Matalon R - Search Results

1

Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiency.

Surendran S, Ezell EL, Quast MJ, Wei J, Tyring SK, Michals-Matalon K, Matalon R. Surendran S, et al. Among authors: matalon r. Neurosci Lett. 2004 Mar 18;358(1):29-32. doi: 10.1016/j.neulet.2003.12.105. Neurosci Lett. 2004. PMID: 15016427

2

Adeno-associated virus-mediated aspartoacylase gene transfer to the brain of knockout mouse for canavan disease.

Matalon R, Surendran S, Rady PL, Quast MJ, Campbell GA, Matalon KM, Tyring SK, Wei J, Peden CS, Ezell EL, Muzyczka N, Mandel RJ. Matalon R, et al. Among authors: matalon km. Mol Ther. 2003 May;7(5 Pt 1):580-7. doi: 10.1016/s1525-0016(03)00066-2. Mol Ther. 2003. PMID: 12718900 Free article.

3

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 disease.

Surendran S, Rady PL, Michals-Matalon K, Quast MJ, Rassin DK, Campbell GA, Ezell EL, Wei J, Tyring SK, Szucs S, Matalon R. Surendran S, et al. Among authors: matalon r. Brain Res Bull. 2003 Aug 30;61(4):427-35. doi: 10.1016/s0361-9230(03)00158-8. Brain Res Bull. 2003. PMID: 12909286

4

Canavan disease: a monogenic trait with complex genomic interaction.

Surendran S, Michals-Matalon K, Quast MJ, Tyring SK, Wei J, Ezell EL, Matalon R. Surendran S, et al. Among authors: matalon r. Mol Genet Metab. 2003 Sep-Oct;80(1-2):74-80. doi: 10.1016/j.ymgme.2003.08.015. Mol Genet Metab. 2003. PMID: 14567959 Review.

5

Molecular basis of Canavan's disease: from human to mouse.

Surendran S, Matalon KM, Tyring SK, Matalon R. Surendran S, et al. Among authors: matalon r, matalon km. J Child Neurol. 2003 Sep;18(9):604-10. doi: 10.1177/08830738030180090601. J Child Neurol. 2003. PMID: 14572138 Review.

6

Metabolic changes in the knockout mouse for Canavan's disease: implications for patients with Canavan's disease.

Surendran S, Matalon KM, Szucs S, Tyring SK, Matalon R. Surendran S, et al. Among authors: matalon r, matalon km. J Child Neurol. 2003 Sep;18(9):611-5. doi: 10.1177/08830738030180090701. J Child Neurol. 2003. PMID: 14572139

7

Aspartoacylase deficiency does not affect N-acetylaspartylglutamate level or glutamate carboxypeptidase II activity in the knockout mouse brain.

Surendran S, Ezell EL, Quast MJ, Wei J, Tyring SK, Michals-Matalon K, Matalon R. Surendran S, et al. Among authors: matalon r. Brain Res. 2004 Aug 6;1016(2):268-71. doi: 10.1016/j.brainres.2004.05.035. Brain Res. 2004. PMID: 15246864

8

Mouse neural progenitor cells differentiate into oligodendrocytes in the brain of a knockout mouse model of Canavan disease.

Surendran S, Shihabuddin LS, Clarke J, Taksir TV, Stewart GR, Parsons G, Yang W, Tyring SK, Michals-Matalon K, Matalon R. Surendran S, et al. Among authors: matalon r. Brain Res Dev Brain Res. 2004 Oct 15;153(1):19-27. doi: 10.1016/j.devbrainres.2004.07.003. Brain Res Dev Brain Res. 2004. PMID: 15464214

9

Aspartoacylase gene knockout results in severe vacuolation in the white matter and gray matter of the spinal cord in the mouse.

Surendran S, Campbell GA, Tyring SK, Matalon R. Surendran S, et al. Among authors: matalon r. Neurobiol Dis. 2005 Mar;18(2):385-9. doi: 10.1016/j.nbd.2004.10.014. Neurobiol Dis. 2005. PMID: 15686967

10

Aspartoacylase gene knockout in the mouse: impact on reproduction.

Surendran S, Szucs S, Tyring SK, Matalon R. Surendran S, et al. Among authors: matalon r. Reprod Toxicol. 2005 Jul-Aug;20(2):281-3. doi: 10.1016/j.reprotox.2005.02.001. Reprod Toxicol. 2005. PMID: 15907664

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