Futerman AH - Search Results

1

The metabolism of glucocerebrosides - From 1965 to the present.

Futerman AH, Platt FM. Futerman AH, et al. Mol Genet Metab. 2017 Jan-Feb;120(1-2):22-26. doi: 10.1016/j.ymgme.2016.11.390. Epub 2016 Dec 2. Mol Genet Metab. 2017. PMID: 27955980 Review.

2

Inhibition of calcium uptake via the sarco/endoplasmic reticulum Ca2+-ATPase in a mouse model of Sandhoff disease and prevention by treatment with N-butyldeoxynojirimycin.

Pelled D, Lloyd-Evans E, Riebeling C, Jeyakumar M, Platt FM, Futerman AH. Pelled D, et al. Among authors: futerman ah. J Biol Chem. 2003 Aug 8;278(32):29496-501. doi: 10.1074/jbc.M302964200. Epub 2003 May 19. J Biol Chem. 2003. PMID: 12756243 Free article.

3

X-ray structure of human acid-beta-glucosidase, the defective enzyme in Gaucher disease.

Dvir H, Harel M, McCarthy AA, Toker L, Silman I, Futerman AH, Sussman JL. Dvir H, et al. Among authors: futerman ah. EMBO Rep. 2003 Jul;4(7):704-9. doi: 10.1038/sj.embor.embor873. EMBO Rep. 2003. PMID: 12792654 Free PMC article.

4

Phosphatidylcholine metabolism is altered in a monocyte-derived macrophage model of Gaucher disease but not in lymphocytes.

Trajkovic-Bodennec S, Bodennec J, Futerman AH. Trajkovic-Bodennec S, et al. Among authors: futerman ah. Blood Cells Mol Dis. 2004 Jul-Aug;33(1):77-82. doi: 10.1016/j.bcmd.2004.03.001. Blood Cells Mol Dis. 2004. PMID: 15223015

5

Gaucher disease: pathological mechanisms and modern management.

Jmoudiak M, Futerman AH. Jmoudiak M, et al. Among authors: futerman ah. Br J Haematol. 2005 Apr;129(2):178-88. doi: 10.1111/j.1365-2141.2004.05351.x. Br J Haematol. 2005. PMID: 15813845 Free article. Review.

6

Crystal structures of complexes of N-butyl- and N-nonyl-deoxynojirimycin bound to acid beta-glucosidase: insights into the mechanism of chemical chaperone action in Gaucher disease.

Brumshtein B, Greenblatt HM, Butters TD, Shaaltiel Y, Aviezer D, Silman I, Futerman AH, Sussman JL. Brumshtein B, et al. Among authors: futerman ah. J Biol Chem. 2007 Sep 28;282(39):29052-29058. doi: 10.1074/jbc.M705005200. Epub 2007 Jul 31. J Biol Chem. 2007. PMID: 17666401 Free article.

7

No evidence for activation of the unfolded protein response in neuronopathic models of Gaucher disease.

Farfel-Becker T, Vitner E, Dekel H, Leshem N, Enquist IB, Karlsson S, Futerman AH. Farfel-Becker T, et al. Among authors: futerman ah. Hum Mol Genet. 2009 Apr 15;18(8):1482-8. doi: 10.1093/hmg/ddp061. Epub 2009 Feb 3. Hum Mol Genet. 2009. PMID: 19193629

8

Common and uncommon pathogenic cascades in lysosomal storage diseases.

Vitner EB, Platt FM, Futerman AH. Vitner EB, et al. Among authors: futerman ah. J Biol Chem. 2010 Jul 2;285(27):20423-7. doi: 10.1074/jbc.R110.134452. Epub 2010 Apr 29. J Biol Chem. 2010. PMID: 20430897 Free PMC article. Review.

9

Altered expression and distribution of cathepsins in neuronopathic forms of Gaucher disease and in other sphingolipidoses.

Vitner EB, Dekel H, Zigdon H, Shachar T, Farfel-Becker T, Eilam R, Karlsson S, Futerman AH. Vitner EB, et al. Among authors: futerman ah. Hum Mol Genet. 2010 Sep 15;19(18):3583-90. doi: 10.1093/hmg/ddq273. Epub 2010 Jul 8. Hum Mol Genet. 2010. PMID: 20616152

10

Molecular basis of reduced glucosylceramidase activity in the most common Gaucher disease mutant, N370S.

Offman MN, Krol M, Silman I, Sussman JL, Futerman AH. Offman MN, et al. Among authors: futerman ah. J Biol Chem. 2010 Dec 31;285(53):42105-14. doi: 10.1074/jbc.M110.172098. Epub 2010 Oct 27. J Biol Chem. 2010. PMID: 20980259 Free PMC article.

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