Samulski R J相关文献与解析，生知库 | 链接生命科学的每一步

Efficient transduction of vascular smooth muscle cells with a translational AAV2.5 vector: a new perspective for in-stent restenosis gene therapy

利用转化 AAV2.5 载体高效转导血管平滑肌细胞：支架内再狭窄基因治疗的新视角

doi:10.1038/gt.2013.13

A-M Lompré, L Hadri, E Merlet, Z Keuylian, N Mougenot, I Karakikes, J Chen, F Atassi, A Marchand, R Blaise, I Limon, S W J McPhee, R J Samulski, R J Hajjar, L Lipskaia

Translational Control

发表日期：2013

文献求助收藏

The influence of epileptic neuropathology and prior peripheral immunity on CNS transduction by rAAV2 and rAAV5

癫痫神经病理学和既往外周免疫对rAAV2和rAAV5介导的中枢神经系统转导的影响

期刊:Gene Therapy

影响因子:4.5

doi:10.1038/gt.2011.49

Weinberg, M S; Blake, B L; Samulski, R J; McCown, T J

Self-complementary AAV mediates gene targeting and enhances endonuclease delivery for double-strand break repair

自互补AAV介导基因靶向并增强核酸内切酶递送以修复双链断裂。

期刊:Gene Therapy

影响因子:4.5

doi:10.1038/gt.2010.65

Hirsch, M L; Green, L; Porteus, M H; Samulski, R J

发表日期：2010

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A small regulatory element from chromosome 19 enhances liver-specific gene expression

来自19号染色体的一个小调控元件增强肝脏特异性基因表达

期刊:Gene Therapy

影响因子:4.5

doi:10.1038/gt.2008.134

Li, C; Hirsch, M; Carter, P; Asokan, A; Zhou, X; Wu, Z; Samulski, R J

信号转导

发表日期：2009

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Ex vivo serotype-specific transduction of equine joint tissue by self-complementary adeno-associated viral vectors

利用自互补腺相关病毒载体对马关节组织进行体外血清型特异性转导

期刊:Human Gene Therapy

影响因子:4

doi:10.1089/hum.2009.030

Goodrich, L R; Choi, V W; Carbone, B A Duda; McIlwraith, C W; Samulski, R J

Embryonic substantia nigra grafts in the mesencephalon send neurites to the host striatum in non-human primate after overexpression of GDNF

在非人灵长类动物中，过表达GDNF后，中脑内移植的胚胎黑质组织会向宿主纹状体发出神经突。

期刊:Journal of Comparative Neurology

影响因子:2.1

doi:10.1002/cne.22028

Redmond, D E Jr; Elsworth, J D; Roth, R H; Leranth, C; Collier, T J; Blanchard, B; Bjugstad, K B; Samulski, R J; Aebischer, P; Sladek, J R Jr

Bioluminescent virion shells: new tools for quantitation of AAV vector dynamics in cells and live animals

生物发光病毒颗粒外壳：用于定量分析细胞和活体动物中AAV载体动力学的新工具

期刊:Gene Therapy

影响因子:4.5

doi:10.1038/gt.2008.127

Asokan, A; Johnson, J S; Li, C; Samulski, R J

Adeno-associated virus-mediated expression and constitutive secretion of NPY or NPY13-36 suppresses seizure activity in vivo

腺相关病毒介导的 NPY 或 NPY13-36 的表达和组成型分泌可抑制体内癫痫发作。

期刊:Gene Therapy

影响因子:4.5

doi:10.1038/sj.gt.3303013

Foti, S; Haberman, R P; Samulski, R J; McCown, T J

Characterization of a novel adeno-associated viral vector with preferential oligodendrocyte tropism

对一种具有优先嗜少突胶质细胞特性的新型腺相关病毒载体进行表征

Prediction of adeno-associated virus neutralizing antibody activity for clinical application

预测腺相关病毒中和抗体活性以用于临床应用

Efficient transduction of vascular smooth muscle cells with a translational AAV2.5 vector: a new perspective for in-stent restenosis gene therapy

利用转化 AAV2.5 载体高效转导血管平滑肌细胞：支架内再狭窄基因治疗的新视角

The influence of epileptic neuropathology and prior peripheral immunity on CNS transduction by rAAV2 and rAAV5

癫痫神经病理学和既往外周免疫对rAAV2和rAAV5介导的中枢神经系统转导的影响

Self-complementary AAV mediates gene targeting and enhances endonuclease delivery for double-strand break repair

自互补AAV介导基因靶向并增强核酸内切酶递送以修复双链断裂。

A small regulatory element from chromosome 19 enhances liver-specific gene expression

来自19号染色体的一个小调控元件增强肝脏特异性基因表达

Ex vivo serotype-specific transduction of equine joint tissue by self-complementary adeno-associated viral vectors

利用自互补腺相关病毒载体对马关节组织进行体外血清型特异性转导

Embryonic substantia nigra grafts in the mesencephalon send neurites to the host striatum in non-human primate after overexpression of GDNF

在非人灵长类动物中，过表达GDNF后，中脑内移植的胚胎黑质组织会向宿主纹状体发出神经突。

Bioluminescent virion shells: new tools for quantitation of AAV vector dynamics in cells and live animals

生物发光病毒颗粒外壳：用于定量分析细胞和活体动物中AAV载体动力学的新工具

Adeno-associated virus-mediated expression and constitutive secretion of NPY or NPY13-36 suppresses seizure activity in vivo

腺相关病毒介导的 NPY 或 NPY13-36 的表达和组成型分泌可抑制体内癫痫发作。