Iwahashi C - Search Results

1

Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome.

Napoli E, Ross-Inta C, Wong S, Omanska-Klusek A, Barrow C, Iwahashi C, Garcia-Arocena D, Sakaguchi D, Berry-Kravis E, Hagerman R, Hagerman PJ, Giulivi C. Napoli E, et al. Among authors: iwahashi c. Hum Mol Genet. 2011 Aug 1;20(15):3079-92. doi: 10.1093/hmg/ddr211. Epub 2011 May 10. Hum Mol Genet. 2011. PMID: 21558427 Free PMC article.

2

FMR1 RNA within the intranuclear inclusions of fragile X-associated tremor/ataxia syndrome (FXTAS).

Tassone F, Iwahashi C, Hagerman PJ. Tassone F, et al. Among authors: iwahashi c. RNA Biol. 2004 Jul;1(2):103-5. doi: 10.4161/rna.1.2.1035. Epub 2004 Jul 17. RNA Biol. 2004. PMID: 17179750

3

A quantitative ELISA assay for the fragile x mental retardation 1 protein.

Iwahashi C, Tassone F, Hagerman RJ, Yasui D, Parrott G, Nguyen D, Mayeur G, Hagerman PJ. Iwahashi C, et al. J Mol Diagn. 2009 Jul;11(4):281-9. doi: 10.2353/jmoldx.2009.080118. Epub 2009 May 21. J Mol Diagn. 2009. PMID: 19460937 Free PMC article.

4

Fibroblast phenotype in male carriers of FMR1 premutation alleles.

Garcia-Arocena D, Yang JE, Brouwer JR, Tassone F, Iwahashi C, Berry-Kravis EM, Goetz CG, Sumis AM, Zhou L, Nguyen DV, Campos L, Howell E, Ludwig A, Greco C, Willemsen R, Hagerman RJ, Hagerman PJ. Garcia-Arocena D, et al. Among authors: iwahashi c. Hum Mol Genet. 2010 Jan 15;19(2):299-312. doi: 10.1093/hmg/ddp497. Epub 2009 Oct 28. Hum Mol Genet. 2010. PMID: 19864489 Free PMC article.

5

Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome.

Ross-Inta C, Omanska-Klusek A, Wong S, Barrow C, Garcia-Arocena D, Iwahashi C, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Giulivi C. Ross-Inta C, et al. Among authors: iwahashi c. Biochem J. 2010 Aug 1;429(3):545-52. doi: 10.1042/BJ20091960. Biochem J. 2010. PMID: 20513237 Free PMC article.

6

Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.

Arocena DG, Iwahashi CK, Won N, Beilina A, Ludwig AL, Tassone F, Schwartz PH, Hagerman PJ. Arocena DG, et al. Hum Mol Genet. 2005 Dec 1;14(23):3661-71. doi: 10.1093/hmg/ddi394. Epub 2005 Oct 20. Hum Mol Genet. 2005. PMID: 16239243

7

CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS.

Hoem G, Raske CR, Garcia-Arocena D, Tassone F, Sanchez E, Ludwig AL, Iwahashi CK, Kumar M, Yang JE, Hagerman PJ. Hoem G, et al. Hum Mol Genet. 2011 Jun 1;20(11):2161-70. doi: 10.1093/hmg/ddr101. Epub 2011 Mar 9. Hum Mol Genet. 2011. PMID: 21389081 Free PMC article.

8

Clinical and molecular implications of mosaicism in FMR1 full mutations.

Pretto D, Yrigollen CM, Tang HT, Williamson J, Espinal G, Iwahashi CK, Durbin-Johnson B, Hagerman RJ, Hagerman PJ, Tassone F. Pretto D, et al. Front Genet. 2014 Sep 17;5:318. doi: 10.3389/fgene.2014.00318. eCollection 2014. Front Genet. 2014. PMID: 25278957 Free PMC article.

9

Isolation of pathology-associated intranuclear inclusions.

Iwahashi C, Hagerman PJ. Iwahashi C, et al. Methods Mol Biol. 2008;463:181-90. doi: 10.1007/978-1-59745-406-3_13. Methods Mol Biol. 2008. PMID: 18951169

10

Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation.

Hessl D, Wang JM, Schneider A, Koldewyn K, Le L, Iwahashi C, Cheung K, Tassone F, Hagerman PJ, Rivera SM. Hessl D, et al. Among authors: iwahashi c. Biol Psychiatry. 2011 Nov 1;70(9):859-65. doi: 10.1016/j.biopsych.2011.05.033. Epub 2011 Jul 23. Biol Psychiatry. 2011. PMID: 21783174 Free PMC article.

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