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Phenylalanine hydroxylase deficient phenylketonuria comparative metabolomics identifies energy pathway disruption and oxidative stress.
Mol Genet Metab. 2021 Apr 7:S1096-7192(21)00686-7. doi: 10.1016/j.ymgme.2021.04.002. Online ahead of print.
Mol Genet Metab. 2021.
PMID: 33846068
Altered DNA methylation in PAH deficient phenylketonuria.
Dobrowolski SF, Lyons-Weiler J, Spridik K, Biery A, Breck J, Vockley J, Yatsenko S, Sultana T.
Dobrowolski SF, et al. Among authors: spridik k.
Mol Genet Metab. 2015 Jun-Jul;115(2-3):72-7. doi: 10.1016/j.ymgme.2015.04.002. Epub 2015 Apr 24.
Mol Genet Metab. 2015.
PMID: 25990862
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A bone mineralization defect in the Pahenu2 model of classical phenylketonuria involves compromised mesenchymal stem cell differentiation.
Dobrowolski SF, Tourkova IL, Robinson LJ, Secunda C, Spridik K, Blair HC.
Dobrowolski SF, et al. Among authors: spridik k.
Mol Genet Metab. 2018 Nov;125(3):193-199. doi: 10.1016/j.ymgme.2018.08.010. Epub 2018 Aug 27.
Mol Genet Metab. 2018.
PMID: 30201326
Free PMC article.
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Mesenchymal stem cell energy deficit and oxidative stress contribute to osteopenia in the Pahenu2 classical PKU mouse.
Dobrowolski SF, Sudano C, Phua YL, Tourkova IL, Spridik K, Goetzman ES, Vockley J, Blair HC.
Dobrowolski SF, et al. Among authors: spridik k.
Mol Genet Metab. 2021 Mar;132(3):173-179. doi: 10.1016/j.ymgme.2021.01.014. Epub 2021 Feb 11.
Mol Genet Metab. 2021.
PMID: 33602601
Free PMC article.
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Comparative metabolomics in the Pahenu2 classical PKU mouse identifies cerebral energy pathway disruption and oxidative stress.
Dobrowolski SF, Phua YL, Sudano C, Spridik K, Zinn PO, Wang Y, Bharathi S, Vockley J, Goetzman E.
Dobrowolski SF, et al. Among authors: spridik k.
Mol Genet Metab. 2022 May;136(1):38-45. doi: 10.1016/j.ymgme.2022.03.004. Epub 2022 Mar 18.
Mol Genet Metab. 2022.
PMID: 35367142
Free PMC article.
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DNA methylation in the pathophysiology of hyperphenylalaninemia in the PAH(enu2) mouse model of phenylketonuria.
Dobrowolski SF, Lyons-Weiler J, Spridik K, Vockley J, Skvorak K, Biery A.
Dobrowolski SF, et al. Among authors: spridik k.
Mol Genet Metab. 2016 Sep;119(1-2):1-7. doi: 10.1016/j.ymgme.2016.01.001. Epub 2016 Jan 14.
Mol Genet Metab. 2016.
PMID: 26822703
Free PMC article.
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Methylome repatterning in a mouse model of Maternal PKU Syndrome.
Dobrowolski SF, Lyons-Weiler J, Biery A, Spridik K, Vockley G, Kranik E, Skvorak K, Sultana T.
Dobrowolski SF, et al. Among authors: spridik k.
Mol Genet Metab. 2014 Nov;113(3):194-9. doi: 10.1016/j.ymgme.2014.08.006. Epub 2014 Aug 23.
Mol Genet Metab. 2014.
PMID: 25218179
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