Year |
Citation |
Score |
2015 |
Castanotto D, Lin M, Kowolik C, Wang L, Ren XQ, Soifer HS, Koch T, Hansen BR, Oerum H, Armstrong B, Wang Z, Bauer P, Rossi J, Stein CA. A cytoplasmic pathway for gapmer antisense oligonucleotide-mediated gene silencing in mammalian cells. Nucleic Acids Research. PMID 26433227 DOI: 10.1093/Nar/Gkv964 |
0.36 |
|
2012 |
Soifer HS, Koch T, Lai J, Hansen B, Hoeg A, Oerum H, Stein CA. Silencing of gene expression by gymnotic delivery of antisense oligonucleotides. Methods in Molecular Biology (Clifton, N.J.). 815: 333-46. PMID 22131003 DOI: 10.1007/978-1-61779-424-7_25 |
0.353 |
|
2010 |
Stein CA, Hansen JB, Lai J, Wu S, Voskresenskiy A, Høg A, Worm J, Hedtjärn M, Souleimanian N, Miller P, Soifer HS, Castanotto D, Benimetskaya L, Ørum H, Koch T. Efficient gene silencing by delivery of locked nucleic acid antisense oligonucleotides, unassisted by transfection reagents. Nucleic Acids Research. 38: e3. PMID 19854938 DOI: 10.1093/Nar/Gkp841 |
0.45 |
|
2009 |
Kortylewski M, Swiderski P, Herrmann A, Wang L, Kowolik C, Kujawski M, Lee H, Scuto A, Liu Y, Yang C, Deng J, Soifer HS, Raubitschek A, Forman S, Rossi JJ, et al. In vivo delivery of siRNA to immune cells by conjugation to a TLR9 agonist enhances antitumor immune responses. Nature Biotechnology. 27: 925-32. PMID 19749770 DOI: 10.1038/Nbt.1564 |
0.357 |
|
2008 |
Soifer HS, Sano M, Sakurai K, Chomchan P, Saetrom P, Sherman MA, Collingwood MA, Behlke MA, Rossi JJ. A role for the Dicer helicase domain in the processing of thermodynamically unstable hairpin RNAs. Nucleic Acids Research. 36: 6511-22. PMID 18927112 DOI: 10.1093/Nar/Gkn687 |
0.315 |
|
2007 |
Castanotto D, Sakurai K, Lingeman R, Li H, Shively L, Aagaard L, Soifer H, Gatignol A, Riggs A, Rossi JJ. Combinatorial delivery of small interfering RNAs reduces RNAi efficacy by selective incorporation into RISC. Nucleic Acids Research. 35: 5154-64. PMID 17660190 DOI: 10.1093/Nar/Gkm543 |
0.35 |
|
2007 |
Höhn B, Soifer HS, Forman SJ, Rossi JJ. Bifunctional siRNA Design Targeting Non-Hodgkin’s Lymphoma. Blood. 110: 2357-2357. DOI: 10.1182/Blood.V110.11.2357.2357 |
0.438 |
|
2006 |
Soifer HS, Rossi JJ. Small interfering RNAs to the rescue: blocking L1 retrotransposition. Nature Structural & Molecular Biology. 13: 758-9. PMID 16955095 DOI: 10.1038/Nsmb0906-758 |
0.398 |
|
2006 |
Soifer HS. Do small RNAs interfere with LINE-1? Journal of Biomedicine & Biotechnology. 2006: 29049. PMID 16877812 DOI: 10.1155/Jbb/2006/29049 |
0.401 |
|
2006 |
Kubo S, Seleme MC, Soifer HS, Perez JL, Moran JV, Kazazian HH, Kasahara N. L1 retrotransposition in nondividing and primary human somatic cells. Proceedings of the National Academy of Sciences of the United States of America. 103: 8036-41. PMID 16698926 DOI: 10.1073/Pnas.0601954103 |
0.568 |
|
2005 |
Soifer HS, Zaragoza A, Peyvan M, Behlke MA, Rossi JJ. A potential role for RNA interference in controlling the activity of the human LINE-1 retrotransposon. Nucleic Acids Research. 33: 846-56. PMID 15701756 DOI: 10.1093/Nar/Gki223 |
0.449 |
|
2005 |
Kubo S, Soifer HS, Seleme MdC, Moran JV, Kazazian HH, Kasahara N. 1093. An Adenovirus-Retrotransposon Hybrid Vector Achieves Stable Transformation of Quiescent and Primary Human Somatic Cells Molecular Therapy. 11. DOI: 10.1016/J.Ymthe.2005.07.640 |
0.626 |
|
2004 |
Soifer HS, Kasahara N. Retrotransposon-adenovirus hybrid vectors: efficient delivery and stable integration of transgenes via a two-stage mechanism. Current Gene Therapy. 4: 373-84. PMID 15578988 DOI: 10.2174/1566523043346084 |
0.652 |
|
2004 |
Kubo S, Soifer H, Moran JV, Kazazian HH, Kasahara N. High-capacity adenovirus/ retrotransposon hybrid vectors for efficient and stable gene transfer Molecular Therapy. 9: 295. DOI: 10.1016/J.Ymthe.2004.06.869 |
0.589 |
|
2004 |
Soifer HS, Vishwanath R, Kim J, Heale B, Scherer LJ, Rossi JJ. 548. Cyclophilin A as a cellular target for gene therapy of HIV-1 Molecular Therapy. 9. DOI: 10.1016/J.Ymthe.2004.06.500 |
0.354 |
|
2002 |
Soifer H, Higo C, Logg CR, Jih LJ, Shichinohe T, Harboe-Schmidt E, Mitani K, Kasahara N. A novel, helper-dependent, adenovirus-retrovirus hybrid vector: stable transduction by a two-stage mechanism. Molecular Therapy : the Journal of the American Society of Gene Therapy. 5: 599-608. PMID 11991751 DOI: 10.1006/Mthe.2002.0586 |
0.598 |
|
2001 |
Soifer H, Higo C, Kazazian JH, Moran JV, Mitani K, Kasahara N. Stable integration of transgenes delivered by a retrotransposon-adenovirus hybrid vector Human Gene Therapy. 12: 1417-1428. PMID 11485633 DOI: 10.1089/104303401750298571 |
0.637 |
|
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