Sarkissian CN - Search Results

1

Structure-based chemical modification strategy for enzyme replacement treatment of phenylketonuria.

Wang L, Gamez A, Sarkissian CN, Straub M, Patch MG, Han GW, Striepeke S, Fitzpatrick P, Scriver CR, Stevens RC. Wang L, et al. Among authors: sarkissian cn. Mol Genet Metab. 2005 Sep-Oct;86(1-2):134-40. doi: 10.1016/j.ymgme.2005.05.012. Epub 2005 Jul 11. Mol Genet Metab. 2005. PMID: 16006165

2

A different approach to treatment of phenylketonuria: phenylalanine degradation with recombinant phenylalanine ammonia lyase.

Sarkissian CN, Shao Z, Blain F, Peevers R, Su H, Heft R, Chang TM, Scriver CR. Sarkissian CN, et al. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2339-44. doi: 10.1073/pnas.96.5.2339. Proc Natl Acad Sci U S A. 1999. PMID: 10051643 Free PMC article.

3

PAHdb: a locus-specific knowledgebase.

Scriver CR, Waters PJ, Sarkissian C, Ryan S, Prevost L, Côté D, Novak J, Teebi S, Nowacki PM. Scriver CR, et al. Hum Mutat. 2000;15(1):99-104. doi: 10.1002/(SICI)1098-1004(200001)15:1<99::AID-HUMU18>3.0.CO;2-P. Hum Mutat. 2000. PMID: 10612829

4

A heteroallelic mutant mouse model: A new orthologue for human hyperphenylalaninemia.

Sarkissian CN, Boulais DM, McDonald JD, Scriver CR. Sarkissian CN, et al. Mol Genet Metab. 2000 Mar;69(3):188-94. doi: 10.1006/mgme.2000.2974. Mol Genet Metab. 2000. PMID: 10767173

5

Measurement of phenyllactate, phenylacetate, and phenylpyruvate by negative ion chemical ionization-gas chromatography/mass spectrometry in brain of mouse genetic models of phenylketonuria and non-phenylketonuria hyperphenylalaninemia.

Sarkissian CN, Scriver CR, Mamer OA. Sarkissian CN, et al. Anal Biochem. 2000 May 1;280(2):242-9. doi: 10.1006/abio.2000.4542. Anal Biochem. 2000. PMID: 10790306

6

The phenylketonuria mouse model: a meeting review.

McDonald JD, Andriolo M, Calì F, Mirisola M, Puglisi-Allegra S, Romano V, Sarkissian CN, Smith CB. McDonald JD, et al. Among authors: sarkissian cn. Mol Genet Metab. 2002 Aug;76(4):256-61. doi: 10.1016/s1096-7192(02)00115-4. Mol Genet Metab. 2002. PMID: 12208130 No abstract available.

7

PAHdb 2003: what a locus-specific knowledgebase can do.

Scriver CR, Hurtubise M, Konecki D, Phommarinh M, Prevost L, Erlandsen H, Stevens R, Waters PJ, Ryan S, McDonald D, Sarkissian C. Scriver CR, et al. Hum Mutat. 2003 Apr;21(4):333-44. doi: 10.1002/humu.10200. Hum Mutat. 2003. PMID: 12655543 Review.

8

Development of pegylated forms of recombinant Rhodosporidium toruloides phenylalanine ammonia-lyase for the treatment of classical phenylketonuria.

Gámez A, Sarkissian CN, Wang L, Kim W, Straub M, Patch MG, Chen L, Striepeke S, Fitzpatrick P, Lemontt JF, O'Neill C, Scriver CR, Stevens RC. Gámez A, et al. Among authors: sarkissian cn. Mol Ther. 2005 Jun;11(6):986-9. doi: 10.1016/j.ymthe.2005.02.013. Mol Ther. 2005. PMID: 15922970 Free article.

9

Phenylalanine ammonia lyase, enzyme substitution therapy for phenylketonuria, where are we now?

Sarkissian CN, Gámez A. Sarkissian CN, et al. Mol Genet Metab. 2005 Dec;86 Suppl 1:S22-6. doi: 10.1016/j.ymgme.2005.06.016. Epub 2005 Sep 13. Mol Genet Metab. 2005. PMID: 16165390 Review.

10

Quantitation of phenylalanine and its trans-cinnamic, benzoic and hippuric acid metabolites in biological fluids in a single GC-MS analysis.

Sarkissian CN, Scriver CR, Mamer OA. Sarkissian CN, et al. J Mass Spectrom. 2007 Jun;42(6):811-7. doi: 10.1002/jms.1218. J Mass Spectrom. 2007. PMID: 17511014

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