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1
Factor VIII inhibitors: von Willebrand factor makes a difference in vitro and in vivo.
J Thromb Haemost. 2012 Nov;10(11):2328-37. doi: 10.1111/j.1538-7836.2012.04902.x.
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Characterization of the von Willebrand factor/factor VIII complex produced by a novel purification process.
Arch Pharm Res. 2020 Jul;43(7):714-723. doi: 10.1007/s12272-020-01245-y. Epub 2020 Jul 14.
5
The impact of GPIbα on platelet-targeted FVIII gene therapy in hemophilia A mice with pre-existing anti-FVIII immunity.
J Thromb Haemost. 2019 Mar;17(3):449-459. doi: 10.1111/jth.14379. Epub 2019 Feb 3.
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Recombinant VWF fragments improve bioavailability of subcutaneous factor VIII in hemophilia A mice.
Blood. 2021 Feb 25;137(8):1072-1081. doi: 10.1182/blood.2020006468.
10
Influence of von Willebrand factor on the reactivity of human factor VIII inhibitors with factor VIII.
Haemophilia. 2001 Jul;7(4):369-74. doi: 10.1046/j.1365-2516.2001.00526.x.

引用本文的文献

1
Factor VIII antibody immune complexes modulate the humoral response to factor VIII in an epitope-dependent manner.
Front Immunol. 2023 Aug 31;14:1233356. doi: 10.3389/fimmu.2023.1233356. eCollection 2023.
4
Platelet-Targeted FVIII Gene Therapy Restores Hemostasis and Induces Immune Tolerance for Hemophilia A.
Front Immunol. 2020 Jun 12;11:964. doi: 10.3389/fimmu.2020.00964. eCollection 2020.
5
Platelet-inspired therapeutics: current status, limitations, clinical implications, and future potential.
Drug Deliv Transl Res. 2021 Feb;11(1):24-48. doi: 10.1007/s13346-020-00751-2.
6
Platelet-Targeted Gene Therapy for Hemophilia.
Mol Ther Methods Clin Dev. 2018 Feb 7;9:100-108. doi: 10.1016/j.omtm.2018.01.011. eCollection 2018 Jun 15.
7
The impact of von Willebrand factor on factor VIII memory immune responses.
Blood Adv. 2017 Aug 22;1(19):1565-1574. doi: 10.1182/bloodadvances.2017009209. Epub 2017 Aug 18.
10
and Model Systems for Hemophilia A Gene Therapy.
J Genet Syndr Gene Ther. 2013 Jan 17;Suppl 1. doi: 10.4172/2157-7412.S1-014.

本文引用的文献

2
How we choose factor VIII to treat hemophilia.
Blood. 2012 May 3;119(18):4108-14. doi: 10.1182/blood-2012-01-394411. Epub 2012 Mar 12.
3
Current controversies in the formation and treatment of alloantibodies to factor VIII in congenital hemophilia A.
Hematology Am Soc Hematol Educ Program. 2011;2011:407-12. doi: 10.1182/asheducation-2011.1.407.
4
Immune tolerance induction in haemophilia: evidence and the way forward.
J Thromb Haemost. 2011 Jul;9 Suppl 1:216-25. doi: 10.1111/j.1538-7836.2011.04349.x.
5
Current options and new developments in the treatment of haemophilia.
Drugs. 2011 Feb 12;71(3):305-20. doi: 10.2165/11585340-000000000-00000.
6
Von Willebrand factor-containing factor VIII concentrates and inhibitors in haemophilia A. A critical literature review.
Thromb Haemost. 2010 Nov;104(5):931-40. doi: 10.1160/TH10-03-0151. Epub 2010 Sep 13.
8
Management of difficult-to-treat inhibitor patients.
Haemophilia. 2010 May;16 Suppl 3:52-7. doi: 10.1111/j.1365-2516.2010.02261.x.
9
The "normal" factor VIII concentration in plasma.
Thromb Res. 2010 Aug;126(2):119-23. doi: 10.1016/j.thromres.2010.04.004. Epub 2010 May 7.

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