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Adenovirus-associated virus vector-mediated gene transfer in hemophilia B.
N Engl J Med. 2011 Dec 22;365(25):2357-65. doi: 10.1056/NEJMoa1108046. Epub 2011 Dec 10.
2
Long-term safety and efficacy of factor IX gene therapy in hemophilia B.
N Engl J Med. 2014 Nov 20;371(21):1994-2004. doi: 10.1056/NEJMoa1407309.
4
Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant.
N Engl J Med. 2017 Dec 7;377(23):2215-2227. doi: 10.1056/NEJMoa1708538.
5
Optimized human factor IX expression cassettes for hepatic-directed gene therapy of hemophilia B.
Front Med. 2015 Mar;9(1):90-9. doi: 10.1007/s11684-015-0390-2. Epub 2015 Feb 7.
9
Gene therapy for hemophilia B mice with scAAV8-LP1-hFIX.
Front Med. 2016 Jun;10(2):212-8. doi: 10.1007/s11684-016-0438-y. Epub 2016 Apr 6.

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GD2T cells as a platform for single-dose and long-term delivery of biologics.
Nat Commun. 2025 Aug 29;16(1):8088. doi: 10.1038/s41467-025-63427-w.
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Epitope mapping using immunopeptidomics reveals novel immunodominant CD8 T cell epitopes of the AAV9 capsid.
Front Immunol. 2025 Aug 8;16:1641289. doi: 10.3389/fimmu.2025.1641289. eCollection 2025.
3
Are viral vector-mediated therapies compatible with aberrant glycosylation?
Mol Ther Methods Clin Dev. 2025 Jul 22;33(3):101540. doi: 10.1016/j.omtm.2025.101540. eCollection 2025 Sep 11.
4
Why is the uptake of gene therapy in hemophilia less than expected?
Res Pract Thromb Haemost. 2025 Jun 23;9(5):102948. doi: 10.1016/j.rpth.2025.102948. eCollection 2025 Jul.
5
Sustained high expression of human FVII following AAV8-mediated gene delivery in mice.
Mol Ther Methods Clin Dev. 2025 Jun 25;33(3):101523. doi: 10.1016/j.omtm.2025.101523. eCollection 2025 Sep 11.
8
Getting closer to hemophilia gene therapy for all?
Blood Adv. 2025 Jul 22;9(14):3629-3630. doi: 10.1182/bloodadvances.2025016642.
10
[Gene therapy marks the beginning of a potential "clinical cure" for hemophilia B patients].
Zhonghua Xue Ye Xue Za Zhi. 2025 May 14;46(5):385-388. doi: 10.3760/cma.j.cn121090-20250304-00111.

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4
Dystrophin immunity in Duchenne's muscular dystrophy.
N Engl J Med. 2010 Oct 7;363(15):1429-37. doi: 10.1056/NEJMoa1000228.
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Analysis of low frequency bleeding data: the association of joint bleeds according to baseline FVIII activity levels.
Haemophilia. 2011 Jan;17(1):41-4. doi: 10.1111/j.1365-2516.2010.02383.x. Epub 2010 Sep 2.
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Sustained transgene expression despite T lymphocyte responses in a clinical trial of rAAV1-AAT gene therapy.
Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16363-8. doi: 10.1073/pnas.0904514106. Epub 2009 Aug 12.
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Cellular immune response to cryptic epitopes during therapeutic gene transfer.
Proc Natl Acad Sci U S A. 2009 Jun 30;106(26):10770-4. doi: 10.1073/pnas.0902269106. Epub 2009 Jun 16.
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AAV-1-mediated gene transfer to skeletal muscle in humans results in dose-dependent activation of capsid-specific T cells.
Blood. 2009 Sep 3;114(10):2077-86. doi: 10.1182/blood-2008-07-167510. Epub 2009 Jun 8.
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Worldwide epidemiology of neutralizing antibodies to adeno-associated viruses.
J Infect Dis. 2009 Feb 1;199(3):381-90. doi: 10.1086/595830.
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Muscular exercise can cause highly pathological liver function tests in healthy men.
Br J Clin Pharmacol. 2008 Feb;65(2):253-9. doi: 10.1111/j.1365-2125.2007.03001.x. Epub 2007 Aug 31.

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