Snowden A - Search Results

1

Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compounds.

Zhang R, Chen L, Jiralerspong S, Snowden A, Steinberg S, Braverman N. Zhang R, et al. Among authors: snowden a. Proc Natl Acad Sci U S A. 2010 Mar 23;107(12):5569-74. doi: 10.1073/pnas.0914960107. Epub 2010 Mar 8. Proc Natl Acad Sci U S A. 2010. PMID: 20212125 Free PMC article.

2

A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts.

Steinberg SJ, Snowden A, Braverman NE, Chen L, Watkins PA, Clayton PT, Setchell KD, Heubi JE, Raymond GV, Moser AB, Moser HW. Steinberg SJ, et al. Among authors: snowden a. J Inherit Metab Dis. 2009 Feb;32(1):109-19. doi: 10.1007/s10545-008-0969-8. Epub 2008 Dec 25. J Inherit Metab Dis. 2009. PMID: 19127411

3

The peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders.

Law KB, Bronte-Tinkew D, Di Pietro E, Snowden A, Jones RO, Moser A, Brumell JH, Braverman N, Kim PK. Law KB, et al. Among authors: snowden a. Autophagy. 2017 May 4;13(5):868-884. doi: 10.1080/15548627.2017.1291470. Autophagy. 2017. PMID: 28521612 Free PMC article.

4

Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutations.

Dranchak PK, Di Pietro E, Snowden A, Oesch N, Braverman NE, Steinberg SJ, Hacia JG. Dranchak PK, et al. Among authors: snowden a. J Cell Biochem. 2011 May;112(5):1250-8. doi: 10.1002/jcb.22979. J Cell Biochem. 2011. PMID: 21465523 Free PMC article.

5

X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism.

Wang Y, Busin R, Reeves C, Bezman L, Raymond G, Toomer CJ, Watkins PA, Snowden A, Moser A, Naidu S, Bibat G, Hewson S, Tam K, Clarke JT, Charnas L, Stetten G, Karczeski B, Cutting G, Steinberg S. Wang Y, et al. Among authors: snowden a. Mol Genet Metab. 2011 Sep-Oct;104(1-2):160-6. doi: 10.1016/j.ymgme.2011.05.016. Epub 2011 Jun 22. Mol Genet Metab. 2011. PMID: 21700483

6

Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3.

Itzkovitz B, Jiralerspong S, Nimmo G, Loscalzo M, Horovitz DD, Snowden A, Moser A, Steinberg S, Braverman N. Itzkovitz B, et al. Among authors: snowden a. Hum Mutat. 2012 Jan;33(1):189-97. doi: 10.1002/humu.21623. Epub 2011 Oct 31. Hum Mutat. 2012. PMID: 21990100

7

X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humans.

Curiel J, Steinberg SJ, Bright S, Snowden A, Moser AB, Eichler F, Dubbs HA, Hacia JG, Ely JJ, Bezner J, Gean A, Vanderver A. Curiel J, et al. Among authors: snowden a. Mol Genet Metab. 2017 Nov;122(3):130-133. doi: 10.1016/j.ymgme.2017.08.012. Epub 2017 Sep 1. Mol Genet Metab. 2017. PMID: 28919002

8

Animal lectins as self/non-self recognition molecules. Biochemical and genetic approaches to understanding their biological roles and evolution.

Vasta GR, Ahmed H, Fink NE, Elola MT, Marsh AG, Snowden A, Odom EW. Vasta GR, et al. Among authors: snowden a. Ann N Y Acad Sci. 1994 Apr 15;712:55-73. doi: 10.1111/j.1749-6632.1994.tb33562.x. Ann N Y Acad Sci. 1994. PMID: 8192353 Review.

9

Oxidized low density lipoproteins stimulate galactosyltransferase activity, ras activation, p44 mitogen activated protein kinase and c-fos expression in aortic smooth muscle cells.

Chatterjee S, Bhunia AK, Snowden A, Han H. Chatterjee S, et al. Among authors: snowden a. Glycobiology. 1997 Jul;7(5):703-10. doi: 10.1093/glycob/7.5.703. Glycobiology. 1997. PMID: 9254052

10

A dimeric lectin from coelomic fluid of the starfish Oreaster reticulatus cross-reacts with the sea urchin embryonic substrate adhesion protein, echinonectin.

Snowden AM, Vasta GR. Snowden AM, et al. Ann N Y Acad Sci. 1994 Apr 15;712:327-9. doi: 10.1111/j.1749-6632.1994.tb33585.x. Ann N Y Acad Sci. 1994. PMID: 8192340 No abstract available.

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