PubMed for id: 457

Year	Number of Results
1980	1
1989	1
1991	6
1992	5
1993	3
1994	2
1995	4
1996	3
1997	6
1998	5
1999	3
2000	7
2001	8
2002	7
2003	10
2004	13
2005	14
2006	10
2007	16
2008	18
2009	19
2010	16
2011	12
2012	21
2013	14
2014	1
2023	1
2024	0

1

Acid sphingomyelinase regulates platelet cell membrane scrambling, secretion, and thrombus formation.

Münzer P, Borst O, Walker B, Schmid E, Feijge MA, Cosemans JM, Chatterjee M, Schmidt EM, Schmidt S, Towhid ST, Leibrock C, Elvers M, Schaller M, Seizer P, Ferlinz K, May AE, Gulbins E, Heemskerk JW, Gawaz M, Lang F. Münzer P, et al. Arterioscler Thromb Vasc Biol. 2014 Jan;34(1):61-71. doi: 10.1161/ATVBAHA.112.300210. Epub 2013 Nov 14. Arterioscler Thromb Vasc Biol. 2014. PMID: 24233488

2

Acid sphingomyelinase plays a key role in palmitic acid-amplified inflammatory signaling triggered by lipopolysaccharide at low concentrations in macrophages.

Jin J, Zhang X, Lu Z, Perry DM, Li Y, Russo SB, Cowart LA, Hannun YA, Huang Y. Jin J, et al. Am J Physiol Endocrinol Metab. 2013 Oct 1;305(7):E853-67. doi: 10.1152/ajpendo.00251.2013. Epub 2013 Aug 6. Am J Physiol Endocrinol Metab. 2013. PMID: 23921144 Free PMC article.

3

Rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease.

Foo JN, Liany H, Bei JX, Yu XQ, Liu J, Au WL, Prakash KM, Tan LC, Tan EK. Foo JN, et al. Neurobiol Aging. 2013 Dec;34(12):2890.e13-5. doi: 10.1016/j.neurobiolaging.2013.06.010. Epub 2013 Jul 18. Neurobiol Aging. 2013. PMID: 23871123

4

Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann-Pick disease patients: mutation profile and description of a novel mutation.

Aykut A, Karaca E, Onay H, Ucar SK, Coker M, Cogulu O, Ozkinay F. Aykut A, et al. Gene. 2013 Sep 10;526(2):484-6. doi: 10.1016/j.gene.2013.03.116. Epub 2013 Apr 22. Gene. 2013. PMID: 23618813

5

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.

Gan-Or Z, Ozelius LJ, Bar-Shira A, Saunders-Pullman R, Mirelman A, Kornreich R, Gana-Weisz M, Raymond D, Rozenkrantz L, Deik A, Gurevich T, Gross SJ, Schreiber-Agus N, Giladi N, Bressman SB, Orr-Urtreger A. Gan-Or Z, et al. Neurology. 2013 Apr 23;80(17):1606-10. doi: 10.1212/WNL.0b013e31828f180e. Epub 2013 Mar 27. Neurology. 2013. PMID: 23535491 Free PMC article.

6

Identification of a distinct mutation spectrum in the SMPD1 gene of Chinese patients with acid sphingomyelinase-deficient Niemann-Pick disease.

Zhang H, Wang Y, Gong Z, Li X, Qiu W, Han L, Ye J, Gu X. Zhang H, et al. Orphanet J Rare Dis. 2013 Jan 28;8:15. doi: 10.1186/1750-1172-8-15. Orphanet J Rare Dis. 2013. PMID: 23356216 Free PMC article.

7

Hyperresponsiveness of mice deficient in plasma-secreted sphingomyelinase reveals its pivotal role in early phase of host response.

Jbeily N, Suckert I, Gonnert FA, Acht B, Bockmeyer CL, Grossmann SD, Blaess MF, Lueth A, Deigner HP, Bauer M, Claus RA. Jbeily N, et al. J Lipid Res. 2013 Feb;54(2):410-24. doi: 10.1194/jlr.M031625. Epub 2012 Dec 10. J Lipid Res. 2013. PMID: 23230083 Free PMC article.

8

Oxidative stress triggers Ca-dependent lysosome trafficking and activation of acid sphingomyelinase.

Li X, Gulbins E, Zhang Y. Li X, et al. Cell Physiol Biochem. 2012;30(4):815-26. doi: 10.1159/000341460. Epub 2012 Aug 10. Cell Physiol Biochem. 2012. PMID: 22890197 Free PMC article.

9

Accumulated bending energy elicits neutral sphingomyelinase activity in human red blood cells.

López DJ, Egido-Gabas M, López-Montero I, Busto JV, Casas J, Garnier M, Monroy F, Larijani B, Goñi FM, Alonso A. López DJ, et al. Biophys J. 2012 May 2;102(9):2077-85. doi: 10.1016/j.bpj.2012.03.020. Biophys J. 2012. PMID: 22824271 Free PMC article.

10

A novel SMPD1 mutation in two Chinese sibling patients with type B Niemann-Pick disease.

Hua R, Wu H, Cui Z, Chen JX, Wang Z. Hua R, et al. Chin Med J (Engl). 2012 Apr;125(8):1511-2. Chin Med J (Engl). 2012. PMID: 22613662

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