14578207,20962279,17954912,17079175,24388731,34106956,9482915,36736320,35711931,1594045,16954197,7753840[uid] - Search Results

Year	Number of Results
1992	1
1995	1
1998	1
2003	1
2006	2
2007	2
2010	1
2013	1
2014	1
2021	1
2022	1
2023	1
2024	0

1

Viable mouse models of acid beta-glucosidase deficiency: the defect in Gaucher disease.

Xu YH, Quinn B, Witte D, Grabowski GA. Xu YH, et al. Am J Pathol. 2003 Nov;163(5):2093-101. doi: 10.1016/s0002-9440(10)63566-3. Am J Pathol. 2003. PMID: 14578207 Free PMC article.

2

Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage.

Mistry PK, Liu J, Yang M, Nottoli T, McGrath J, Jain D, Zhang K, Keutzer J, Chuang WL, Mehal WZ, Zhao H, Lin A, Mane S, Liu X, Peng YZ, Li JH, Agrawal M, Zhu LL, Blair HC, Robinson LJ, Iqbal J, Sun L, Zaidi M. Mistry PK, et al. Proc Natl Acad Sci U S A. 2010 Nov 9;107(45):19473-8. doi: 10.1073/pnas.1003308107. Epub 2010 Oct 20. Proc Natl Acad Sci U S A. 2010. PMID: 20962279 Free PMC article.

3

Murine models of acute neuronopathic Gaucher disease.

Enquist IB, Lo Bianco C, Ooka A, Nilsson E, Månsson JE, Ehinger M, Richter J, Brady RO, Kirik D, Karlsson S. Enquist IB, et al. Proc Natl Acad Sci U S A. 2007 Oct 30;104(44):17483-8. doi: 10.1073/pnas.0708086104. Epub 2007 Oct 22. Proc Natl Acad Sci U S A. 2007. PMID: 17954912 Free PMC article.

4

Generation of a conditional knockout of murine glucocerebrosidase: utility for the study of Gaucher disease.

Sinclair GB, Jevon G, Colobong KE, Randall DR, Choy FY, Clarke LA. Sinclair GB, et al. Mol Genet Metab. 2007 Feb;90(2):148-56. doi: 10.1016/j.ymgme.2006.09.008. Epub 2006 Oct 31. Mol Genet Metab. 2007. PMID: 17079175

5

Neuroinflammation and α-synuclein accumulation in response to glucocerebrosidase deficiency are accompanied by synaptic dysfunction.

Ginns EI, Mak SK, Ko N, Karlgren J, Akbarian S, Chou VP, Guo Y, Lim A, Samuelsson S, LaMarca ML, Vazquez-DeRose J, Manning-Boğ AB. Ginns EI, et al. Mol Genet Metab. 2014 Feb;111(2):152-62. doi: 10.1016/j.ymgme.2013.12.003. Epub 2013 Dec 11. Mol Genet Metab. 2014. PMID: 24388731

6

Decreased glucocerebrosidase activity and substrate accumulation of glycosphingolipids in a novel GBA1 D409V knock-in mouse model.

Polinski NK, Martinez TN, Gorodinsky A, Gareus R, Sasner M, Herberth M, Switzer R, Ahmad SO, Cosden M, Kandebo M, Drolet RE, Buckett PD, Shan W, Chen Y, Pellegrino LJ, Ellsworth GD, Dungan LB, Hirst WD, Clark SW, Dave KD. Polinski NK, et al. PLoS One. 2021 Jun 9;16(6):e0252325. doi: 10.1371/journal.pone.0252325. eCollection 2021. PLoS One. 2021. PMID: 34106956 Free PMC article.

7

Mice with type 2 and 3 Gaucher disease point mutations generated by a single insertion mutagenesis procedure.

Liu Y, Suzuki K, Reed JD, Grinberg A, Westphal H, Hoffmann A, Döring T, Sandhoff K, Proia RL. Liu Y, et al. Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2503-8. doi: 10.1073/pnas.95.5.2503. Proc Natl Acad Sci U S A. 1998. PMID: 9482915 Free PMC article.

8

Direct activation of microglia by β-glucosylceramide causes phagocytosis of neurons that exacerbates Gaucher disease.

Shimizu T, Schutt CR, Izumi Y, Tomiyasu N, Omahdi Z, Kano K, Takamatsu H, Aoki J, Bamba T, Kumanogoh A, Takao M, Yamasaki S. Shimizu T, et al. Immunity. 2023 Feb 14;56(2):307-319.e8. doi: 10.1016/j.immuni.2023.01.008. Epub 2023 Feb 2. Immunity. 2023. PMID: 36736320

9

Establishment and Phenotypic Analysis of the Novel Gaucher Disease Mouse Model With the Partially Humanized Gba1 Gene and F213I Mutation.

Guo JN, Guan M, Jiang N, Li N, Li YJ, Zhang J, Ma D. Guo JN, et al. Front Genet. 2022 May 27;13:892457. doi: 10.3389/fgene.2022.892457. eCollection 2022. Front Genet. 2022. PMID: 35711931 Free PMC article.

10

Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene.

Tybulewicz VL, Tremblay ML, LaMarca ME, Willemsen R, Stubblefield BK, Winfield S, Zablocka B, Sidransky E, Martin BM, Huang SP, et al. Tybulewicz VL, et al. Nature. 1992 Jun 4;357(6377):407-10. doi: 10.1038/357407a0. Nature. 1992. PMID: 1594045

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