242 related articles for article (PubMed ID: 15459963)
1. Widespread gene transduction to the central nervous system by adenovirus in utero: implication for prenatal gene therapy to brain involvement of lysosomal storage disease.
Shen JS; Meng XL; Maeda H; Ohashi T; Eto Y
J Gene Med; 2004 Nov; 6(11):1206-15. PubMed ID: 15459963
[TBL] [Abstract][Full Text] [Related]
2. Widespread and highly persistent gene transfer to the CNS by retrovirus vector in utero: implication for gene therapy to Krabbe disease.
Shen JS; Meng XL; Yokoo T; Sakurai K; Watabe K; Ohashi T; Eto Y
J Gene Med; 2005 May; 7(5):540-51. PubMed ID: 15685691
[TBL] [Abstract][Full Text] [Related]
3. Adenovirus-mediated prenatal gene transfer to murine central nervous system.
Shen JS; Meng XL; Ohashi T; Eto Y
Gene Ther; 2002 Jun; 9(12):819-23. PubMed ID: 12040464
[TBL] [Abstract][Full Text] [Related]
4. Systemic hyperosmolality improves beta-glucuronidase distribution and pathology in murine MPS VII brain following intraventricular gene transfer.
Ghodsi A; Stein C; Derksen T; Martins I; Anderson RD; Davidson BL
Exp Neurol; 1999 Nov; 160(1):109-16. PubMed ID: 10630195
[TBL] [Abstract][Full Text] [Related]
5. Genetic correction of the fetal brain increases the lifespan of mice with the severe multisystemic disease mucopolysaccharidosis type VII.
Karolewski BA; Wolfe JH
Mol Ther; 2006 Jul; 14(1):14-24. PubMed ID: 16624622
[TBL] [Abstract][Full Text] [Related]
6. Engraftment of genetically engineered amniotic epithelial cells corrects lysosomal storage in multiple areas of the brain in mucopolysaccharidosis type VII mice.
Kosuga M; Sasaki K; Tanabe A; Li XK; Okawa H; Ogino I; Okuda O; Arai H; Sakuragawa N; Kamata Y; Azuma N; Suzuki S; Yamada M; Okuyama T
Mol Ther; 2001 Feb; 3(2):139-48. PubMed ID: 11237670
[TBL] [Abstract][Full Text] [Related]
7. Long-term normalization in the central nervous system, ocular manifestations, and skeletal deformities by a single systemic adenovirus injection into neonatal mice with mucopolysaccharidosis VII.
Kamata Y; Tanabe A; Kanaji A; Kosuga M; Fukuhara Y; Li XK; Suzuki S; Yamada M; Azuma N; Okuyama T
Gene Ther; 2003 Mar; 10(5):406-14. PubMed ID: 12601395
[TBL] [Abstract][Full Text] [Related]
8. Sustained production of beta-glucuronidase from localized sites after AAV vector gene transfer results in widespread distribution of enzyme and reversal of lysosomal storage lesions in a large volume of brain in mucopolysaccharidosis VII mice.
Skorupa AF; Fisher KJ; Wilson JM; Parente MK; Wolfe JH
Exp Neurol; 1999 Nov; 160(1):17-27. PubMed ID: 10630187
[TBL] [Abstract][Full Text] [Related]
9. Widespread distribution of adenovirus-transduced monkey amniotic epithelial cells after local intracerebral injection: implication for cell-mediated therapy for lysosome storage disorders.
Kosuga M; Takahashi S; Tanabe A; Fujino M; Li XK; Suzuki S; Yamada M; Kakishita K; Ono F; Sakuragawa N; Okuyama T
Cell Transplant; 2001; 10(4-5):435-9. PubMed ID: 11549068
[TBL] [Abstract][Full Text] [Related]
10. In utero fetal liver cell transplantation without toxic irradiation alleviates lysosomal storage in mice with mucopolysaccharidosis type VII.
Barker JE; Deveau S; Lessard M; Hamblen N; Vogler C; Levy B
Blood Cells Mol Dis; 2001; 27(5):861-73. PubMed ID: 11783949
[TBL] [Abstract][Full Text] [Related]
11. Brain transplantation of genetically modified bone marrow stromal cells corrects CNS pathology and cognitive function in MPS VII mice.
Sakurai K; Iizuka S; Shen JS; Meng XL; Mori T; Umezawa A; Ohashi T; Eto Y
Gene Ther; 2004 Oct; 11(19):1475-81. PubMed ID: 15295619
[TBL] [Abstract][Full Text] [Related]
12. Brain transplantation of genetically engineered human neural stem cells globally corrects brain lesions in the mucopolysaccharidosis type VII mouse.
Meng XL; Shen JS; Ohashi T; Maeda H; Kim SU; Eto Y
J Neurosci Res; 2003 Oct; 74(2):266-77. PubMed ID: 14515356
[TBL] [Abstract][Full Text] [Related]
13. Viral-mediated delivery of the late-infantile neuronal ceroid lipofuscinosis gene, TPP-I to the mouse central nervous system.
Haskell RE; Hughes SM; Chiorini JA; Alisky JM; Davidson BL
Gene Ther; 2003 Jan; 10(1):34-42. PubMed ID: 12525835
[TBL] [Abstract][Full Text] [Related]
14. Feline immunodeficiency virus vectors. Gene transfer to mouse retina following intravitreal injection.
Derksen TA; Sauter SL; Davidson BL
J Gene Med; 2002; 4(5):463-9. PubMed ID: 12221638
[TBL] [Abstract][Full Text] [Related]
15. Adenovirus-mediated gene therapy for corneal clouding in mice with mucopolysaccharidosis type VII.
Kamata Y; Okuyama T; Kosuga M; O'hira A; Kanaji A; Sasaki K; Yamada M; Azuma N
Mol Ther; 2001 Oct; 4(4):307-12. PubMed ID: 11592832
[TBL] [Abstract][Full Text] [Related]
16. Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors.
Mitchell M; Jerebtsova M; Batshaw ML; Newman K; Ye X
Gene Ther; 2000 Dec; 7(23):1986-92. PubMed ID: 11175309
[TBL] [Abstract][Full Text] [Related]
17. Somatic gene therapy for a neurodegenerative disease using microencapsulated recombinant cells.
Ross CJ; Ralph M; Chang PL
Exp Neurol; 2000 Dec; 166(2):276-86. PubMed ID: 11085893
[TBL] [Abstract][Full Text] [Related]
18. In vivo treatment of hemophilia A and mucopolysaccharidosis type VII using nonprimate lentiviral vectors.
Stein CS; Kang Y; Sauter SL; Townsend K; Staber P; Derksen TA; Martins I; Qian J; Davidson BL; McCray PB
Mol Ther; 2001 Jun; 3(6):850-6. PubMed ID: 11407898
[TBL] [Abstract][Full Text] [Related]
19. Long-term and significant correction of brain lesions in adult mucopolysaccharidosis type VII mice using recombinant AAV vectors.
Bosch A; Perret E; Desmaris N; Heard JM
Mol Ther; 2000 Jan; 1(1):63-70. PubMed ID: 10933913
[TBL] [Abstract][Full Text] [Related]
20. Use of nonviral promoters in adenovirus-mediated gene therapy: reduction of lysosomal storage in the aspartylglucosaminuria mouse.
Virta S; Rapola J; Jalanko A; Laine M
J Gene Med; 2006 Jun; 8(6):699-706. PubMed ID: 16518877
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
