Ran H - Search Results

1

In vivo and ex vivo evaluation of L-type calcium channel blockers on acid beta-glucosidase in Gaucher disease mouse models.

Sun Y, Liou B, Quinn B, Ran H, Xu YH, Grabowski GA. Sun Y, et al. Among authors: ran h. PLoS One. 2009 Oct 7;4(10):e7320. doi: 10.1371/journal.pone.0007320. PLoS One. 2009. PMID: 19809509 Free PMC article.

2

Accumulation and distribution of α-synuclein and ubiquitin in the CNS of Gaucher disease mouse models.

Xu YH, Sun Y, Ran H, Quinn B, Witte D, Grabowski GA. Xu YH, et al. Among authors: ran h. Mol Genet Metab. 2011 Apr;102(4):436-47. doi: 10.1016/j.ymgme.2010.12.014. Epub 2010 Dec 31. Mol Genet Metab. 2011. PMID: 21257328 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: ran h. 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

Neuronopathic Gaucher disease in the mouse: viable combined selective saposin C deficiency and mutant glucocerebrosidase (V394L) mice with glucosylsphingosine and glucosylceramide accumulation and progressive neurological deficits.

Sun Y, Liou B, Ran H, Skelton MR, Williams MT, Vorhees CV, Kitatani K, Hannun YA, Witte DP, Xu YH, Grabowski GA. Sun Y, et al. Among authors: ran h. Hum Mol Genet. 2010 Mar 15;19(6):1088-97. doi: 10.1093/hmg/ddp580. Epub 2010 Jan 4. Hum Mol Genet. 2010. PMID: 20047948 Free PMC article.

5

Isofagomine in vivo effects in a neuronopathic Gaucher disease mouse.

Sun Y, Ran H, Liou B, Quinn B, Zamzow M, Zhang W, Bielawski J, Kitatani K, Setchell KD, Hannun YA, Grabowski GA. Sun Y, et al. Among authors: ran h. PLoS One. 2011 Apr 20;6(4):e19037. doi: 10.1371/journal.pone.0019037. PLoS One. 2011. PMID: 21533102 Free PMC article.

6

Properties of neurons derived from induced pluripotent stem cells of Gaucher disease type 2 patient fibroblasts: potential role in neuropathology.

Sun Y, Florer J, Mayhew CN, Jia Z, Zhao Z, Xu K, Ran H, Liou B, Zhang W, Setchell KD, Gu J, Grabowski GA. Sun Y, et al. Among authors: ran h. PLoS One. 2015 Mar 30;10(3):e0118771. doi: 10.1371/journal.pone.0118771. eCollection 2015. PLoS One. 2015. PMID: 25822147 Free PMC article.

7

Combination of acid β-glucosidase mutation and Saposin C deficiency in mice reveals Gba1 mutation dependent and tissue-specific disease phenotype.

Liou B, Zhang W, Fannin V, Quinn B, Ran H, Xu K, Setchell KDR, Witte D, Grabowski GA, Sun Y. Liou B, et al. Among authors: ran h. Sci Rep. 2019 Apr 3;9(1):5571. doi: 10.1038/s41598-019-41914-7. Sci Rep. 2019. PMID: 30944381 Free PMC article.

8

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: ran h. 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

9

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: ran h. 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.

10

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: ran h. BMC Neurosci. 2008 Aug 1;9:76. doi: 10.1186/1471-2202-9-76. BMC Neurosci. 2008. PMID: 18673548 Free PMC article.

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