Szucs S - Search Results

1

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. Among authors: szucs s. 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

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. Among authors: szucs s. 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

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: szucs s. J Child Neurol. 2003 Sep;18(9):611-5. doi: 10.1177/08830738030180090701. J Child Neurol. 2003. PMID: 14572139

4

Future role of large neutral amino acids in transport of phenylalanine into the brain.

Matalon R, Surendran S, Matalon KM, Tyring S, Quast M, Jinga W, Ezell E, Szucs S. Matalon R, et al. Among authors: szucs s. Pediatrics. 2003 Dec;112(6 Pt 2):1570-4. Pediatrics. 2003. PMID: 14654667

5

Aspartoacylase gene knockout in the mouse: impact on reproduction.

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

6

Knock-out mouse for Canavan disease: a model for gene transfer to the central nervous system.

Matalon R, Rady PL, Platt KA, Skinner HB, Quast MJ, Campbell GA, Matalon K, Ceci JD, Tyring SK, Nehls M, Surendran S, Wei J, Ezell EL, Szucs S. Matalon R, et al. Among authors: szucs s. J Gene Med. 2000 May-Jun;2(3):165-75. doi: 10.1002/(SICI)1521-2254(200005/06)2:3<165::AID-JGM107>3.0.CO;2-R. J Gene Med. 2000. PMID: 10894262

7

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

Rady PL, Szucs S, Grady J, Hudnall SD, Kellner LH, Nitowsky H, Tyring SK, Matalon RK. Rady PL, et al. Among authors: szucs s. Am J Med Genet. 2002 Jan 15;107(2):162-8. doi: 10.1002/ajmg.10122. Am J Med Genet. 2002. PMID: 11807892

8

Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease.

Madhavarao CN, Arun P, Moffett JR, Szucs S, Surendran S, Matalon R, Garbern J, Hristova D, Johnson A, Jiang W, Namboodiri MA. Madhavarao CN, et al. Among authors: szucs s. Proc Natl Acad Sci U S A. 2005 Apr 5;102(14):5221-6. doi: 10.1073/pnas.0409184102. Epub 2005 Mar 22. Proc Natl Acad Sci U S A. 2005. PMID: 15784740 Free PMC article.

9

Genetic polymorphism (G80A) of reduced folate carrier gene in ethnic populations.

Rady PL, Szucs S, Matalon RK, Grady J, Hudnall SD, Kellner LH, Nitowsky H. Rady PL, et al. Among authors: szucs s. Mol Genet Metab. 2001 Jul;73(3):285-6. doi: 10.1006/mgme.2001.3197. Mol Genet Metab. 2001. PMID: 11461197 No abstract available.

10

Neuronal localization of the mitochondrial protein NIPSNAP1 in rat nervous system.

Nautiyal M, Sweatt AJ, MacKenzie JA, Mark Payne R, Szucs S, Matalon R, Wallin R, Hutson SM. Nautiyal M, et al. Among authors: szucs s. Eur J Neurosci. 2010 Aug;32(4):560-9. doi: 10.1111/j.1460-9568.2010.07326.x. Epub 2010 Jul 16. Eur J Neurosci. 2010. PMID: 20646061

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