Priestman DA - Search Results

1

A Mouse Systems Genetics Approach Reveals Common and Uncommon Genetic Modifiers of Hepatic Lysosomal Enzyme Activities and Glycosphingolipids.

Durán A, Priestman DA, Las Heras M, Rebolledo-Jaramillo B, Olguín V, Calderón JF, Zanlungo S, Gutiérrez J, Platt FM, Klein AD. Durán A, et al. Among authors: priestman da. Int J Mol Sci. 2023 Mar 3;24(5):4915. doi: 10.3390/ijms24054915. Int J Mol Sci. 2023. PMID: 36902345 Free PMC article.

2

Identification of genetic modifiers of murine hepatic β-glucocerebrosidase activity.

Durán A, Rebolledo-Jaramillo B, Olguin V, Rojas-Herrera M, Las Heras M, Calderón JF, Zanlungo S, Priestman DA, Platt FM, Klein AD. Durán A, et al. Among authors: priestman da. Biochem Biophys Rep. 2021 Aug 18;28:101105. doi: 10.1016/j.bbrep.2021.101105. eCollection 2021 Dec. Biochem Biophys Rep. 2021. PMID: 34458595 Free PMC article.

3

Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapy.

Platt FM, Jeyakumar M, Andersson U, Priestman DA, Dwek RA, Butters TD, Cox TM, Lachmann RH, Hollak C, Aerts JM, Van Weely S, Hrebícek M, Moyses C, Gow I, Elstein D, Zimran A. Platt FM, et al. Among authors: priestman da. J Inherit Metab Dis. 2001 Apr;24(2):275-90. doi: 10.1023/a:1010335505357. J Inherit Metab Dis. 2001. PMID: 11405346 Review.

4

Altered Expression of Ganglioside Metabolizing Enzymes Results in GM3 Ganglioside Accumulation in Cerebellar Cells of a Mouse Model of Juvenile Neuronal Ceroid Lipofuscinosis.

Somogyi A, Petcherski A, Beckert B, Huebecker M, Priestman DA, Banning A, Cotman SL, Platt FM, Ruonala MO, Tikkanen R. Somogyi A, et al. Among authors: priestman da. Int J Mol Sci. 2018 Feb 22;19(2):625. doi: 10.3390/ijms19020625. Int J Mol Sci. 2018. PMID: 29470438 Free PMC article.

5

Glycosphingolipid levels and glucocerebrosidase activity are altered in normal aging of the mouse brain.

Hallett PJ, Huebecker M, Brekk OR, Moloney EB, Rocha EM, Priestman DA, Platt FM, Isacson O. Hallett PJ, et al. Among authors: priestman da. Neurobiol Aging. 2018 Jul;67:189-200. doi: 10.1016/j.neurobiolaging.2018.02.028. Epub 2018 Mar 29. Neurobiol Aging. 2018. PMID: 29735433 Free PMC article.

6

Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson's disease.

Huebecker M, Moloney EB, van der Spoel AC, Priestman DA, Isacson O, Hallett PJ, Platt FM. Huebecker M, et al. Among authors: priestman da. Mol Neurodegener. 2019 Nov 8;14(1):40. doi: 10.1186/s13024-019-0339-z. Mol Neurodegener. 2019. PMID: 31703585 Free PMC article.

7

Glycosphingolipid metabolism and its role in ageing and Parkinson's disease.

Wallom KL, Fernández-Suárez ME, Priestman DA, Te Vruchte D, Huebecker M, Hallett PJ, Isacson O, Platt FM. Wallom KL, et al. Among authors: priestman da. Glycoconj J. 2022 Feb;39(1):39-53. doi: 10.1007/s10719-021-10023-x. Epub 2021 Nov 10. Glycoconj J. 2022. PMID: 34757540 Free PMC article. Review.

8

Increased glycosphingolipid levels in serum and aortae of apolipoprotein E gene knockout mice.

Garner B, Priestman DA, Stocker R, Harvey DJ, Butters TD, Platt FM. Garner B, et al. Among authors: priestman da. J Lipid Res. 2002 Feb;43(2):205-14. J Lipid Res. 2002. PMID: 11861662 Free article.

9

Analysis of fluorescently labeled glycosphingolipid-derived oligosaccharides following ceramide glycanase digestion and anthranilic acid labeling.

Neville DC, Coquard V, Priestman DA, te Vruchte DJ, Sillence DJ, Dwek RA, Platt FM, Butters TD. Neville DC, et al. Among authors: priestman da. Anal Biochem. 2004 Aug 15;331(2):275-82. doi: 10.1016/j.ab.2004.03.051. Anal Biochem. 2004. PMID: 15265733

10

Correction to: Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson's disease.

Huebecker M, Moloney EB, van der Spoel AC, Priestman DA, Isacson O, Hallett PJ, Platt FM. Huebecker M, et al. Among authors: priestman da. Mol Neurodegener. 2020 Jan 15;15(1):6. doi: 10.1186/s13024-019-0355-z. Mol Neurodegener. 2020. PMID: 31937358 Free PMC article.

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