Horowitz M - Search Results

1

UPR activation and CHOP mediated induction of GBA1 transcription in Gaucher disease.

Braunstein H, Maor G, Chicco G, Filocamo M, Zimran A, Horowitz M. Braunstein H, et al. Among authors: horowitz m. Blood Cells Mol Dis. 2018 Feb;68:21-29. doi: 10.1016/j.bcmd.2016.10.025. Epub 2016 Nov 3. Blood Cells Mol Dis. 2018. PMID: 27856178

2

Characterization of the ERAD process of the L444P mutant glucocerebrosidase variant.

Bendikov-Bar I, Ron I, Filocamo M, Horowitz M. Bendikov-Bar I, et al. Among authors: horowitz m. Blood Cells Mol Dis. 2011 Jan 15;46(1):4-10. doi: 10.1016/j.bcmd.2010.10.012. Epub 2010 Nov 23. Blood Cells Mol Dis. 2011. PMID: 21106416

3

Ambroxol as a pharmacological chaperone for mutant glucocerebrosidase.

Bendikov-Bar I, Maor G, Filocamo M, Horowitz M. Bendikov-Bar I, et al. Among authors: horowitz m. Blood Cells Mol Dis. 2013 Feb;50(2):141-5. doi: 10.1016/j.bcmd.2012.10.007. Epub 2012 Nov 14. Blood Cells Mol Dis. 2013. PMID: 23158495 Free PMC article.

4

ITCH regulates degradation of mutant glucocerebrosidase: implications to Gaucher disease.

Maor G, Filocamo M, Horowitz M. Maor G, et al. Among authors: horowitz m. Hum Mol Genet. 2013 Apr 1;22(7):1316-27. doi: 10.1093/hmg/dds535. Epub 2012 Dec 18. Hum Mol Genet. 2013. PMID: 23255161

5

Unfolded protein response in Gaucher disease: from human to Drosophila.

Maor G, Rencus-Lazar S, Filocamo M, Steller H, Segal D, Horowitz M. Maor G, et al. Among authors: horowitz m. Orphanet J Rare Dis. 2013 Sep 11;8:140. doi: 10.1186/1750-1172-8-140. Orphanet J Rare Dis. 2013. PMID: 24020503 Free PMC article.

6

New Directions in Gaucher Disease.

Horowitz M, Elstein D, Zimran A, Goker-Alpan O. Horowitz M, et al. Hum Mutat. 2016 Nov;37(11):1121-1136. doi: 10.1002/humu.23056. Epub 2016 Aug 21. Hum Mutat. 2016. PMID: 27449603 Review.

7

The effect of mutant GBA1 on accumulation and aggregation of α-synuclein.

Maor G, Rapaport D, Horowitz M. Maor G, et al. Among authors: horowitz m. Hum Mol Genet. 2019 Jun 1;28(11):1768-1781. doi: 10.1093/hmg/ddz005. Hum Mol Genet. 2019. PMID: 30615125

8

Lysosomal functions and dysfunctions: Molecular and cellular mechanisms underlying Gaucher disease and its association with Parkinson disease.

Horowitz M, Braunstein H, Zimran A, Revel-Vilk S, Goker-Alpan O. Horowitz M, et al. Adv Drug Deliv Rev. 2022 Aug;187:114402. doi: 10.1016/j.addr.2022.114402. Epub 2022 Jun 25. Adv Drug Deliv Rev. 2022. PMID: 35764179 Review.

9

Mutations causing Gaucher disease.

Horowitz M, Zimran A. Horowitz M, et al. Hum Mutat. 1994;3(1):1-11. doi: 10.1002/humu.1380030102. Hum Mutat. 1994. PMID: 8118460 Review.

10

Cytokine mRNA in Gaucher disease.

Lichtenstein M, Zimran A, Horowitz M. Lichtenstein M, et al. Among authors: horowitz m. Blood Cells Mol Dis. 1997 Dec;23(3):395-401. doi: 10.1006/bcmd.1997.0156. Blood Cells Mol Dis. 1997. PMID: 9446753

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