Witte DP - Search Results

1

Temporal gene expression profiling reveals CEBPD as a candidate regulator of brain disease in prosaposin deficient mice.

Sun Y, Jia L, Williams MT, Zamzow M, Ran H, Quinn B, Aronow BJ, Vorhees CV, Witte DP, Grabowski GA. Sun Y, et al. Among authors: witte dp. BMC Neurosci. 2008 Aug 1;9:76. doi: 10.1186/1471-2202-9-76. BMC Neurosci. 2008. PMID: 18673548 Free PMC article.

2

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.

3

Specific saposin C deficiency: CNS impairment and acid beta-glucosidase effects in the mouse.

Sun Y, Ran H, Zamzow M, Kitatani K, Skelton MR, Williams MT, Vorhees CV, Witte DP, Hannun YA, Grabowski GA. Sun Y, et al. Among authors: witte dp. Hum Mol Genet. 2010 Feb 15;19(4):634-47. doi: 10.1093/hmg/ddp531. Epub 2009 Dec 16. Hum Mol Genet. 2010. PMID: 20015957 Free PMC article.

4

Tissue-specific effects of saposin A and saposin B on glycosphingolipid degradation in mutant mice.

Sun Y, Zamzow M, Ran H, Zhang W, Quinn B, Barnes S, Witte DP, Setchell KD, Williams MT, Vorhees CV, Grabowski GA. Sun Y, et al. Among authors: witte dp. Hum Mol Genet. 2013 Jun 15;22(12):2435-50. doi: 10.1093/hmg/ddt096. Epub 2013 Feb 27. Hum Mol Genet. 2013. PMID: 23446636 Free PMC article.

5

Prosaposin: threshold rescue and analysis of the "neuritogenic" region in transgenic mice.

Sun Y, Qi X, Witte DP, Ponce E, Kondoh K, Quinn B, Grabowski GA. Sun Y, et al. Among authors: witte dp. Mol Genet Metab. 2002 Aug;76(4):271-86. doi: 10.1016/s1096-7192(02)00114-2. Mol Genet Metab. 2002. PMID: 12208132

6

Analyses of temporal regulatory elements of the prosaposin gene in transgenic mice.

Sun Y, Witte DP, Jin P, Grabowski GA. Sun Y, et al. Among authors: witte dp. Biochem J. 2003 Mar 1;370(Pt 2):557-66. doi: 10.1042/BJ20021120. Biochem J. 2003. PMID: 12467496 Free PMC article.

7

Gaucher disease mouse models: point mutations at the acid beta-glucosidase locus combined with low-level prosaposin expression lead to disease variants.

Sun Y, Quinn B, Witte DP, Grabowski GA. Sun Y, et al. Among authors: witte dp. J Lipid Res. 2005 Oct;46(10):2102-13. doi: 10.1194/jlr.M500202-JLR200. Epub 2005 Aug 1. J Lipid Res. 2005. PMID: 16061944 Free article.

8

Conditional expression of human acid beta-glucosidase improves the visceral phenotype in a Gaucher disease mouse model.

Sun Y, Quinn B, Xu YH, Leonova T, Witte DP, Grabowski GA. Sun Y, et al. Among authors: witte dp. J Lipid Res. 2006 Oct;47(10):2161-70. doi: 10.1194/jlr.M600239-JLR200. Epub 2006 Jul 21. J Lipid Res. 2006. PMID: 16861620 Free article.

9

Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and alpha-hydroxy ceramide accumulation, and altered prosaposin trafficking.

Sun Y, Witte DP, Zamzow M, Ran H, Quinn B, Matsuda J, Grabowski GA. Sun Y, et al. Among authors: witte dp. Hum Mol Genet. 2007 Apr 15;16(8):957-71. doi: 10.1093/hmg/ddm040. Epub 2007 Mar 12. Hum Mol Genet. 2007. PMID: 17353235

10

Neurological deficits and glycosphingolipid accumulation in saposin B deficient mice.

Sun Y, Witte DP, Ran H, Zamzow M, Barnes S, Cheng H, Han X, Williams MT, Skelton MR, Vorhees CV, Grabowski GA. Sun Y, et al. Among authors: witte dp. Hum Mol Genet. 2008 Aug 1;17(15):2345-56. doi: 10.1093/hmg/ddn135. Epub 2008 May 14. Hum Mol Genet. 2008. PMID: 18480170 Free PMC article.

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