Similar articles for PMID: 10840053

Year	Number of Results
1976	1
1985	1
1987	1
1992	1
1993	1
1994	2
1995	2
1996	2
1997	6
1998	3
1999	7
2000	8
2001	7
2002	8
2003	8
2004	9
2005	4
2006	10
2007	14
2008	8
2009	8
2010	11
2011	7
2012	9
2013	13
2014	9
2015	6
2016	10
2017	4
2018	11
2019	7
2020	6
2021	9
2022	6
2023	3
2024	0

1

Long-term enzyme correction and lipid reduction in multiple organs of primary and secondary transplanted Fabry mice receiving transduced bone marrow cells.

Takenaka T, Murray GJ, Qin G, Quirk JM, Ohshima T, Qasba P, Clark K, Kulkarni AB, Brady RO, Medin JA. Takenaka T, et al. Proc Natl Acad Sci U S A. 2000 Jun 20;97(13):7515-20. doi: 10.1073/pnas.120177997. Proc Natl Acad Sci U S A. 2000. PMID: 10840053 Free PMC article.

2

Adeno-associated viral vector-mediated gene transfer results in long-term enzymatic and functional correction in multiple organs of Fabry mice.

Jung SC, Han IP, Limaye A, Xu R, Gelderman MP, Zerfas P, Tirumalai K, Murray GJ, During MJ, Brady RO, Qasba P. Jung SC, et al. Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2676-81. doi: 10.1073/pnas.051634498. Proc Natl Acad Sci U S A. 2001. PMID: 11226298 Free PMC article.

3

Preselective gene therapy for Fabry disease.

Qin G, Takenaka T, Telsch K, Kelley L, Howard T, Levade T, Deans R, Howard BH, Malech HL, Brady RO, Medin JA. Qin G, et al. Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3428-33. doi: 10.1073/pnas.061020598. Epub 2001 Mar 6. Proc Natl Acad Sci U S A. 2001. PMID: 11248095 Free PMC article.

4

Long-term correction of globotriaosylceramide storage in Fabry mice by recombinant adeno-associated virus-mediated gene transfer.

Park J, Murray GJ, Limaye A, Quirk JM, Gelderman MP, Brady RO, Qasba P. Park J, et al. Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3450-4. doi: 10.1073/pnas.0537900100. Epub 2003 Mar 6. Proc Natl Acad Sci U S A. 2003. PMID: 12624185 Free PMC article.

5

Efficient correction of Fabry mice and patient cells mediated by lentiviral transduction of hematopoietic stem/progenitor cells.

Yoshimitsu M, Higuchi K, Ramsubir S, Nonaka T, Rasaiah VI, Siatskas C, Liang SB, Murray GJ, Brady RO, Medin JA. Yoshimitsu M, et al. Gene Ther. 2007 Feb;14(3):256-65. doi: 10.1038/sj.gt.3302839. Epub 2006 Aug 24. Gene Ther. 2007. PMID: 16929352

6

Partial correction of the alpha-galactosidase A deficiency and reduction of glycolipid storage in Fabry mice using synthetic vectors.

Przybylska M, Wu IH, Zhao H, Ziegler RJ, Tousignant JD, Desnick RJ, Scheule RK, Cheng SH, Yew NS. Przybylska M, et al. J Gene Med. 2004 Jan;6(1):85-92. doi: 10.1002/jgm.468. J Gene Med. 2004. PMID: 14716680

7

Long-term systemic therapy of Fabry disease in a knockout mouse by adeno-associated virus-mediated muscle-directed gene transfer.

Takahashi H, Hirai Y, Migita M, Seino Y, Fukuda Y, Sakuraba H, Kase R, Kobayashi T, Hashimoto Y, Shimada T. Takahashi H, et al. Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13777-82. doi: 10.1073/pnas.222221899. Epub 2002 Oct 7. Proc Natl Acad Sci U S A. 2002. PMID: 12370426 Free PMC article.

8

Circulating alpha-galactosidase A derived from transduced bone marrow cells: relevance for corrective gene transfer for Fabry disease.

Takenaka T, Qin G, Brady RO, Medin JA. Takenaka T, et al. Hum Gene Ther. 1999 Aug 10;10(12):1931-9. doi: 10.1089/10430349950017293. Hum Gene Ther. 1999. PMID: 10466627

9

An in vitro model of Fabry disease.

Shu L, Murphy HS, Cooling L, Shayman JA. Shu L, et al. J Am Soc Nephrol. 2005 Sep;16(9):2636-45. doi: 10.1681/ASN.2005040383. Epub 2005 Jul 20. J Am Soc Nephrol. 2005. PMID: 16033856

10

Correction of enzymatic and lysosomal storage defects in Fabry mice by adenovirus-mediated gene transfer.

Ziegler RJ, Yew NS, Li C, Cherry M, Berthelette P, Romanczuk H, Ioannou YA, Zeidner KM, Desnick RJ, Cheng SH. Ziegler RJ, et al. Hum Gene Ther. 1999 Jul 1;10(10):1667-82. doi: 10.1089/10430349950017671. Hum Gene Ther. 1999. PMID: 10428212

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