Michals-Matalon K - Search Results

1

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

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

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

5

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.

6

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.

7

Prenatal diagnosis of Canavan disease.

Matalon R, Michals-Matalon K. Matalon R, et al. Prenat Diagn. 1999 Jul;19(7):669-70. doi: 10.1002/(sici)1097-0223(199907)19:7<669::aid-pd630>3.0.co;2-n. Prenat Diagn. 1999. PMID: 10419617 Review. No abstract available.

8

Recent advances in Canavan disease.

Matalon R, Michals-Matalon K. Matalon R, et al. Adv Pediatr. 1999;46:493-506. Adv Pediatr. 1999. PMID: 10645473 Review.

9

Spongy degeneration of the brain, Canavan disease: biochemical and molecular findings.

Matalon RM, Michals-Matalon K. Matalon RM, et al. Front Biosci. 2000 Mar 1;5:D307-11. doi: 10.2741/matalon. Front Biosci. 2000. PMID: 10704428 Review.

10

Molecular basis of Canavan disease.

Matalon R, Michals-Matalon K. Matalon R, et al. Eur J Paediatr Neurol. 1998;2(2):69-76. doi: 10.1016/s1090-3798(98)80044-5. Eur J Paediatr Neurol. 1998. PMID: 10724099 Review. No abstract available.

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