Howe Steven J相关文献与解析，生知库 | 链接生命科学的每一步

Rittié, Laure; Athanasopoulos, Takis; Calero-Garcia, Miguel; Davies, Marie L; Dow, David J; Howe, Steven J; Morrison, Alastair; Ricciardelli, Ida; Saudemont, Aurore; Jespers, Laurent; Clay, Timothy M

肿瘤

肿瘤免疫

发表日期：2019

文献求助收藏

Inhibition of Mitochondrial Complex I Impairs Release of Î±-Galactosidase by Jurkat Cells.

抑制线粒体复合物 I 会损害 Jurkat 细胞释放 α-半乳糖苷酶

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms20184349

Lambert Jonathan R A, Howe Steven J, Rahim Ahad A, Burke Derek G, Heales Simon J R

BMI-1 extends proliferative potential of human bronchial epithelial cells while retaining their mucociliary differentiation capacity

BMI-1可延长人支气管上皮细胞的增殖潜能，同时保留其黏液纤毛分化能力。

期刊:American Journal of Physiology-Lung Cellular and Molecular Physiology

影响因子:3.5

doi:10.1152/ajplung.00471.2016

Munye, Mustafa M; Shoemark, Amelia; Hirst, Robert A; Delhove, Juliette M; Sharp, Tyson V; McKay, Tristan R; O'Callaghan, Christopher; Baines, Deborah L; Howe, Steven J; Hart, Stephen L

Evidence for contribution of CD4+ CD25+ regulatory T cells in maintaining immune tolerance to human factor IX following perinatal adenovirus vector delivery

证据表明，CD4+CD25+调节性T细胞在围产期腺病毒载体递送后维持对人凝血因子IX的免疫耐受中发挥作用

期刊:Journal of Immunology Research

影响因子:3.6

doi:10.1155/2015/397879

Nivsarkar, Megha S; Buckley, Suzanne M K; Parker, Alan L; Perocheau, Dany; McKay, Tristan R; Rahim, Ahad A; Howe, Steven J; Waddington, Simon N

Hematopoietic stem cell and gene therapy corrects primary neuropathology and behavior in mucopolysaccharidosis IIIA mice

造血干细胞和基因疗法可纠正粘多糖贮积症 IIIA 小鼠的原发性神经病理学和行为异常

期刊:Molecular Therapy

影响因子:12

doi:10.1038/mt.2012.82

Langford-Smith, Alexander; Wilkinson, Fiona L; Langford-Smith, Kia J; Holley, Rebecca J; Sergijenko, Ana; Howe, Steven J; Bennett, William R; Jones, Simon A; Wraith, Je; Merry, Catherine Lr; Wynn, Robert F; Bigger, Brian W

Insertion sites in engrafted cells cluster within a limited repertoire of genomic areas after gammaretroviral vector gene therapy

γ逆转录病毒载体基因治疗后，移植细胞中的插入位点集中在有限的基因组区域内。

期刊:Molecular Therapy

影响因子:12

doi:10.1038/mt.2011.178

Deichmann, Annette; Brugman, Martijn H; Bartholomae, Cynthia C; Schwarzwaelder, Kerstin; Verstegen, Monique M A; Howe, Steven J; Arens, Anne; Ott, Marion G; Hoelzer, Dieter; Seger, Reinhard; Grez, Manuel; Hacein-Bey-Abina, Salima; Cavazzana-Calvo, Marina; Fischer, Alain; Paruzynski, Anna; Gabriel, Richard; Glimm, Hanno; Abel, Ulrich; Cattoglio, Claudia; Mavilio, Fulvio; Cassani, Barbara; Aiuti, Alessandro; Dunbar, Cynthia E; Baum, Christopher; Gaspar, H Bobby; Thrasher, Adrian J; von Kalle, Christof; Schmidt, Manfred; Wagemaker, Gerard

Perinatal gene transfer to the liver

围产期基因转移至肝脏

期刊:Current Pharmaceutical Design

影响因子:2.8

doi:10.2174/138161211797247541

McKay, Tristan R; Rahim, Ahad A; Buckley, Suzanne M K; Ward, Natalie J; Chan, Jerry K Y; Howe, Steven J; Waddington, Simon N

发表日期：2011

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Tolerance induction using lentiviral gene delivery delays onset and severity of collagen II arthritis.

利用慢病毒基因递送诱导耐受性可延缓 II 型胶原关节炎的发病和严重程度

期刊:Molecular Therapy

影响因子:12

doi:10.1038/mt.2009.299

Gjertsson Inger, Laurie Karen L, Devitt James, Howe Steven J, Thrasher Adrian J, Holmdahl Rikard, Gustafsson Kenth

Vector integration is nonrandom and clustered and influences the fate of lymphopoiesis in SCID-X1 gene therapy

载体整合是非随机的、聚集性的，并影响SCID-X1基因治疗中淋巴细胞生成的命运。

期刊:Journal of Clinical Investigation

影响因子:13.6

doi:10.1172/JCI31659

Deichmann, Annette; Hacein-Bey-Abina, Salima; Schmidt, Manfred; Garrigue, Alexandrine; Brugman, Martijn H; Hu, Jingqiong; Glimm, Hanno; Gyapay, Gabor; Prum, Bernard; Fraser, Christopher C; Fischer, Nicolas; Schwarzwaelder, Kerstin; Siegler, Maria-Luise; de Ridder, Dick; Pike-Overzet, Karin; Howe, Steven J; Thrasher, Adrian J; Wagemaker, Gerard; Abel, Ulrich; Staal, Frank J T; Delabesse, Eric; Villeval, Jean-Luc; Aronow, Bruce; Hue, Christophe; Prinz, Claudia; Wissler, Manuela; Klanke, Chuck; Weissenbach, Jean; Alexander, Ian; Fischer, Alain; von Kalle, Christof; Cavazzana-Calvo, Marina

The Landscape of Early Clinical Gene Therapies outside of Oncology

肿瘤学以外早期临床基因疗法的概况

Inhibition of Mitochondrial Complex I Impairs Release of Î±-Galactosidase by Jurkat Cells.

抑制线粒体复合物 I 会损害 Jurkat 细胞释放 α-半乳糖苷酶

BMI-1 extends proliferative potential of human bronchial epithelial cells while retaining their mucociliary differentiation capacity

BMI-1可延长人支气管上皮细胞的增殖潜能，同时保留其黏液纤毛分化能力。

Evidence for contribution of CD4+ CD25+ regulatory T cells in maintaining immune tolerance to human factor IX following perinatal adenovirus vector delivery

证据表明，CD4+CD25+调节性T细胞在围产期腺病毒载体递送后维持对人凝血因子IX的免疫耐受中发挥作用

Hematopoietic stem cell and gene therapy corrects primary neuropathology and behavior in mucopolysaccharidosis IIIA mice

造血干细胞和基因疗法可纠正粘多糖贮积症 IIIA 小鼠的原发性神经病理学和行为异常

Insertion sites in engrafted cells cluster within a limited repertoire of genomic areas after gammaretroviral vector gene therapy

γ逆转录病毒载体基因治疗后，移植细胞中的插入位点集中在有限的基因组区域内。

Perinatal gene transfer to the liver

围产期基因转移至肝脏

Tolerance induction using lentiviral gene delivery delays onset and severity of collagen II arthritis.

利用慢病毒基因递送诱导耐受性可延缓 II 型胶原关节炎的发病和严重程度

Vector integration is nonrandom and clustered and influences the fate of lymphopoiesis in SCID-X1 gene therapy

载体整合是非随机的、聚集性的，并影响SCID-X1基因治疗中淋巴细胞生成的命运。