Sarkissian CN - Search Results

1

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.

2

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

3

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

4

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.

5

Structure-based epitope and PEGylation sites mapping of phenylalanine ammonia-lyase for enzyme substitution treatment of phenylketonuria.

Gámez A, Wang L, Sarkissian CN, Wendt D, Fitzpatrick P, Lemontt JF, Scriver CR, Stevens RC. Gámez A, et al. Among authors: sarkissian cn. Mol Genet Metab. 2007 Aug;91(4):325-34. doi: 10.1016/j.ymgme.2007.04.015. Epub 2007 Jun 8. Mol Genet Metab. 2007. PMID: 17560821

6

Evaluation of orally administered PEGylated phenylalanine ammonia lyase in mice for the treatment of Phenylketonuria.

Sarkissian CN, Kang TS, Gámez A, Scriver CR, Stevens RC. Sarkissian CN, et al. Mol Genet Metab. 2011 Nov;104(3):249-54. doi: 10.1016/j.ymgme.2011.06.016. Epub 2011 Jun 29. Mol Genet Metab. 2011. PMID: 21803624 Free PMC article.

7

Phenylalanine ammonia lyase (PAL): From discovery to enzyme substitution therapy for phenylketonuria.

Levy HL, Sarkissian CN, Scriver CR. Levy HL, et al. Among authors: sarkissian cn. Mol Genet Metab. 2018 Aug;124(4):223-229. doi: 10.1016/j.ymgme.2018.06.002. Epub 2018 Jun 9. Mol Genet Metab. 2018. PMID: 29941359 Review.

8

Converting an injectable protein therapeutic into an oral form: phenylalanine ammonia lyase for phenylketonuria.

Kang TS, Wang L, Sarkissian CN, Gámez A, Scriver CR, Stevens RC. Kang TS, et al. Among authors: sarkissian cn. Mol Genet Metab. 2010 Jan;99(1):4-9. doi: 10.1016/j.ymgme.2009.09.002. Mol Genet Metab. 2010. PMID: 19793667 Free PMC article.

9

Charles Scriver: Epitome of the physician scientist.

Sarkissian CN, Scriver PP, Prevost L, Levy HL. Sarkissian CN, et al. Mol Genet Metab. 2022 Dec;137(4):388-398. doi: 10.1016/j.ymgme.2022.11.001. Epub 2022 Nov 4. Mol Genet Metab. 2022. PMID: 36503822

10

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.

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