Laipis P - Search Results

1

Maternal phenylketonuria syndrome: studies in mice suggest a potential approach to a continuing problem.

Zeile WL, McCune HC, Musson DG, O'Donnell B, O'Neill CA, Tsuruda LS, Zori RT, Laipis PJ. Zeile WL, et al. Among authors: laipis pj. Pediatr Res. 2018 Apr;83(4):889-896. doi: 10.1038/pr.2017.323. Epub 2018 Jan 31. Pediatr Res. 2018. PMID: 29278642 Free PMC article.

2

Partial rescue of neuropathology in the murine model of PKU following administration of recombinant phenylalanine ammonia lyase (pegvaliase).

Goldfinger M, Zeile WL, Corado CR, O'Neill CA, Tsuruda LS, Laipis PJ, Cooper JD. Goldfinger M, et al. Among authors: laipis pj. Mol Genet Metab. 2017 Sep;122(1-2):33-35. doi: 10.1016/j.ymgme.2017.04.013. Epub 2017 Apr 29. Mol Genet Metab. 2017. PMID: 28506393 Free article.

3

Formulation and PEGylation optimization of the therapeutic PEGylated phenylalanine ammonia lyase for the treatment of phenylketonuria.

Bell SM, Wendt DJ, Zhang Y, Taylor TW, Long S, Tsuruda L, Zhao B, Laipis P, Fitzpatrick PA. Bell SM, et al. Among authors: laipis p. PLoS One. 2017 Mar 10;12(3):e0173269. doi: 10.1371/journal.pone.0173269. eCollection 2017. PLoS One. 2017. PMID: 28282402 Free PMC article.

4

Epilepsy in phenylketonuria: a complex dependence on serum phenylalanine levels.

Martynyuk AE, Ucar DA, Yang DD, Norman WM, Carney PR, Dennis DM, Laipis PJ. Martynyuk AE, et al. Among authors: laipis pj. Epilepsia. 2007 Jun;48(6):1143-50. doi: 10.1111/j.1528-1167.2007.01115.x. Epub 2007 May 1. Epilepsia. 2007. PMID: 17484755 Free article.

5

Structural and kinetic analysis of proton shuttle residues in the active site of human carbonic anhydrase III.

Elder I, Fisher Z, Laipis PJ, Tu C, McKenna R, Silverman DN. Elder I, et al. Among authors: laipis pj. Proteins. 2007 Jul 1;68(1):337-43. doi: 10.1002/prot.21403. Proteins. 2007. PMID: 17427958

6

PKU is a reversible neurodegenerative process within the nigrostriatum that begins as early as 4 weeks of age in Pah(enu2) mice.

Embury JE, Charron CE, Martynyuk A, Zori AG, Liu B, Ali SF, Rowland NE, Laipis PJ. Embury JE, et al. Among authors: laipis pj. Brain Res. 2007 Jan 5;1127(1):136-50. doi: 10.1016/j.brainres.2006.09.101. Epub 2006 Nov 15. Brain Res. 2007. PMID: 17112485 Free PMC article.

7

A murine model for human sepiapterin-reductase deficiency.

Yang S, Lee YJ, Kim JM, Park S, Peris J, Laipis P, Park YS, Chung JH, Oh SP. Yang S, et al. Among authors: laipis p. Am J Hum Genet. 2006 Apr;78(4):575-87. doi: 10.1086/501372. Epub 2006 Jan 31. Am J Hum Genet. 2006. PMID: 16532389 Free PMC article.

8

Impaired glutamatergic synaptic transmission in the PKU brain.

Martynyuk AE, Glushakov AV, Sumners C, Laipis PJ, Dennis DM, Seubert CN. Martynyuk AE, et al. Among authors: laipis pj. Mol Genet Metab. 2005 Dec;86 Suppl 1:S34-42. doi: 10.1016/j.ymgme.2005.06.014. Epub 2005 Sep 8. Mol Genet Metab. 2005. PMID: 16153867 Review.

9

Pathologic and immunohistochemical findings in hypothalamic and mesencephalic regions in the pah(enu2) mouse model for phenylketonuria.

Embury JE, Reep RR, Laipis PJ. Embury JE, et al. Among authors: laipis pj. Pediatr Res. 2005 Aug;58(2):283-7. doi: 10.1203/01.PDR.0000170000.78670.44. Epub 2005 Jul 31. Pediatr Res. 2005. PMID: 16055931 Free PMC article.

10

Human carbonic anhydrase III: structural and kinetic study of catalysis and proton transfer.

Duda DM, Tu C, Fisher SZ, An H, Yoshioka C, Govindasamy L, Laipis PJ, Agbandje-McKenna M, Silverman DN, McKenna R. Duda DM, et al. Among authors: laipis pj. Biochemistry. 2005 Aug 2;44(30):10046-53. doi: 10.1021/bi050610h. Biochemistry. 2005. PMID: 16042381

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