Michals-Matalon K - Search Results

1

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. Brain Res. 2004 Aug 6;1016(2):268-71. doi: 10.1016/j.brainres.2004.05.035. Brain Res. 2004. PMID: 15246864

2

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. Brain Res Bull. 2003 Aug 30;61(4):427-35. doi: 10.1016/s0361-9230(03)00158-8. Brain Res Bull. 2003. PMID: 12909286

3

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. 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.

4

High level of orexin A observed in the phenylketonuria mouse brain is due to the abnormal expression of prepro-orexin.

Surendran S, Rady PL, Szucs S, Michals-Matalon K, Tyring SK, Matalon R. Surendran S, et al. Biochem Biophys Res Commun. 2004 Apr 30;317(2):522-6. doi: 10.1016/j.bbrc.2004.03.079. Biochem Biophys Res Commun. 2004. PMID: 15063788

5

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. 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

6

Canavan disease: studies on the knockout mouse.

Matalon R, Michals-Matalon K, Surendran S, Tyring SK. Matalon R, et al. Among authors: michals matalon k. Adv Exp Med Biol. 2006;576:77-93; discussion 361-3. doi: 10.1007/0-387-30172-0_6. Adv Exp Med Biol. 2006. PMID: 16802706 Review.

7

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. Neurosci Lett. 2004 Mar 18;358(1):29-32. doi: 10.1016/j.neulet.2003.12.105. Neurosci Lett. 2004. PMID: 15016427

8

Biopterin responsive phenylalanine hydroxylase deficiency.

Matalon R, Koch R, Michals-Matalon K, Moseley K, Surendran S, Tyring S, Erlandsen H, Gamez A, Stevens RC, Romstad A, Møller LB, Guttler F. Matalon R, et al. Genet Med. 2004 Jan-Feb;6(1):27-32. doi: 10.1097/01.gim.0000108840.17922.a7. Genet Med. 2004. PMID: 14726806 Clinical Trial.

9

Hyaluronidase increases the biodistribution of acid alpha-1,4 glucosidase in the muscle of Pompe disease mice: an approach to enhance the efficacy of enzyme replacement therapy.

Matalon R, Surendran S, Campbell GA, Michals-Matalon K, Tyring SK, Grady J, Cheng S, Kaye E. Matalon R, et al. Among authors: michals matalon k. Biochem Biophys Res Commun. 2006 Nov 24;350(3):783-7. doi: 10.1016/j.bbrc.2006.09.133. Epub 2006 Oct 2. Biochem Biophys Res Commun. 2006. PMID: 17027913

10

Biochemistry and molecular biology of Canavan disease.

Matalon R, Michals-Matalon K. Matalon R, et al. Neurochem Res. 1999 Apr;24(4):507-13. doi: 10.1023/a:1022531829100. Neurochem Res. 1999. PMID: 10227683 Review.

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