標(biāo)題: Titlebook: Gene Therapy for HIV Infection; Clay Smith Book 1998 Springer-Verlag Berlin Heidelberg 1998 AIDS.HIV.Immunsystem.diseases.gene therapy.gen [打印本頁] 作者: memoir 時間: 2025-3-21 17:37
書目名稱Gene Therapy for HIV Infection影響因子(影響力)
書目名稱Gene Therapy for HIV Infection影響因子(影響力)學(xué)科排名
書目名稱Gene Therapy for HIV Infection網(wǎng)絡(luò)公開度
書目名稱Gene Therapy for HIV Infection網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Gene Therapy for HIV Infection被引頻次
書目名稱Gene Therapy for HIV Infection被引頻次學(xué)科排名
書目名稱Gene Therapy for HIV Infection年度引用
書目名稱Gene Therapy for HIV Infection年度引用學(xué)科排名
書目名稱Gene Therapy for HIV Infection讀者反饋
書目名稱Gene Therapy for HIV Infection讀者反饋學(xué)科排名
作者: Badger 時間: 2025-3-21 23:43
C. M. Finlayson,A. G. van der Valke system durably protected from rampant viral multiplication. This chapter reviews different gene therapy approaches that have been taken to inhibit HIV replication, using either viral components or cellular proteins as targets.作者: Tinea-Capitis 時間: 2025-3-22 00:40
https://doi.org/10.1007/978-3-642-31635-7y of HIV-1 pathogenesis. Several model systems use immunodeficient mice engrafted with human immune cells while other models use one of several species of macaque infected with SIV, a virus which is highly related to HIV-2 and more distantly related to HIV-1.. Some of these animal models of HIV and 作者: 大猩猩 時間: 2025-3-22 07:15
Book 1998apy by some, genetic material encoding HIV proteins is introduced into patient‘s cells in order to stimulate a cellular immune response above and beyond 3 5 that stimulated by the viral infection itself. - Two general genetic im- munotherapy strategies have been developed. Genes encoding HIV pro- te作者: GROVE 時間: 2025-3-22 11:39
Gene Therapy Strategies for Inhibition of HIV,e system durably protected from rampant viral multiplication. This chapter reviews different gene therapy approaches that have been taken to inhibit HIV replication, using either viral components or cellular proteins as targets.作者: notification 時間: 2025-3-22 13:32
Animal Models of Gene Therapy for AIDS,y of HIV-1 pathogenesis. Several model systems use immunodeficient mice engrafted with human immune cells while other models use one of several species of macaque infected with SIV, a virus which is highly related to HIV-2 and more distantly related to HIV-1.. Some of these animal models of HIV and 作者: notification 時間: 2025-3-22 19:59
https://doi.org/10.1007/978-3-662-11821-4AIDS; HIV; Immunsystem; diseases; gene therapy; gene transfer; hematopoietic stem cell; hematopoietic stem 作者: 勤勉 時間: 2025-3-23 00:03 作者: BARB 時間: 2025-3-23 01:38
An Algorithm for Predictive Ordination,The goal of gene therapy for the treatment of acquired immuno deficiency syndrome (AIDS) is suppression of human immunodeficiency virus (HIV) replication at any stage of the viral life cycle in order to promote host survival. As described in chapter 2, most current gene therapy efforts focus on:作者: 招惹 時間: 2025-3-23 07:28 作者: 頭盔 時間: 2025-3-23 13:03 作者: Evacuate 時間: 2025-3-23 15:43 作者: 未成熟 時間: 2025-3-23 21:37
https://doi.org/10.1007/978-94-011-0115-8 put into research on this disorder and its prevention and treatment. In 1986 the first study was published demonstrating beneficial effects of drug treatment. However, until recently the benefits of drug treatment have been modest and short lived. Therefore, alternative therapeutic approaches have 作者: 摻和 時間: 2025-3-23 22:25
C. M. Finlayson,A. G. van der Valk have been successfully inhibited in vitro and in T cell lines. However, challenging transduced primary T cells and macrophages with diverse strains of HIV is a more realistic system to test and compare the effectiveness of different gene therapy approaches. With several clinical trials planned or u作者: GNAT 時間: 2025-3-24 05:51 作者: dilute 時間: 2025-3-24 08:50
Age of Onset, Sex Incidence, Course,nase deficiency (ADA), purine nucleoside phosphorylase deficiency (PNP),leukocyte adhesion deficiency (LAD), and chronic granulomatus disease (CGD).. Other disease states have also become candidates for gene therapy approaches such as treatment of tumors through modification of tumor infiltrating ly作者: offense 時間: 2025-3-24 12:56
Victor Westhoff,Eddy Van Der Maareldominantly hematopoietic cells that express the CD. surface antigen, become infected with the type 1 human immunodeficiency virus (HIV). HIV is a small, enveloped RNA virus that belongs to the lentivirinae subfamily of retroviruses. The lentiviruses, in general, give rise to progressive disease stat作者: inhumane 時間: 2025-3-24 15:33
https://doi.org/10.1007/978-3-642-31635-7sted and must reproduce, at least in part, the pathogenesis of HIV-1 in infected people. The value of animal models for testing anti-HIV-1 gene therapy is clear from the inadequacy of tissue culture systems in reproducing the pathogenesis of patient derived strains of HIV-1. T lymphoblastoid cell li作者: 灰心喪氣 時間: 2025-3-24 19:46
Classifications and Scores of the Shoulderms with gene modified cells resistant to HIV infection. Enormous strides have been made in understanding the biology of hematopoietic stem cell transplantation over the last twenty years, in identifying a variety of hematopoietic stem cells and in minimizing the toxicity and expense of hematopoietic作者: Regurgitation 時間: 2025-3-25 01:23
Clay SmithHow to develop effective gene therapy to fight HIV infection.作者: stressors 時間: 2025-3-25 06:42
Age of Onset, Sex Incidence, Course,mphocytes.. The treatment of viral diseases including HIV, EBV and CMV infection with gene modified T lymphocytes is another area of intense research 4. T cells are attractive target cells for gene therapy strategies because they are easy to obtain from the peripheral blood and are relatively easy to expand, select and characterize..作者: judiciousness 時間: 2025-3-25 10:48
Classifications and Scores of the Shoulder stem cell transplantation. In this review, we will summarize the biology of hematopoietic stem cell transplantation as well as highlight some of the clinical considerations that are relevant to stem cell based approaches to HIV gene therapy.作者: 休閑 時間: 2025-3-25 15:43 作者: 裂隙 時間: 2025-3-25 16:39 作者: 群居動物 時間: 2025-3-25 21:27 作者: Ambiguous 時間: 2025-3-26 04:12
Victor Westhoff,Eddy Van Der Maarelrapeutic standpoint it may therefore be helpful to consider that individuals infected with HIV are essentially genetic mosaics, where some of their somatic cells carry a pathogenic genetic element. At this level, AIDS may be viewed as a genetic disease and may therefore be treatable through the emerging technologies of gene therapy.作者: lacrimal-gland 時間: 2025-3-26 07:17
Stem Cell-Based Gene Therapies in the Treatment of AIDS,rapeutic standpoint it may therefore be helpful to consider that individuals infected with HIV are essentially genetic mosaics, where some of their somatic cells carry a pathogenic genetic element. At this level, AIDS may be viewed as a genetic disease and may therefore be treatable through the emerging technologies of gene therapy.作者: slipped-disk 時間: 2025-3-26 10:28 作者: Amenable 時間: 2025-3-26 15:44 作者: CANON 時間: 2025-3-26 17:28 作者: 痛打 時間: 2025-3-27 00:30 作者: rods366 時間: 2025-3-27 02:10 作者: facilitate 時間: 2025-3-27 08:44
Trans-Splicing Ribozymes as Potential HIV Gene Inhibitors,atalysts as anti-HIV agents. Here we will provide an example of how this trans-splicing reaction can be employed to revise HIV transcripts to give them antiviral activity. Then we will quickly review the splicing reaction mediated by the group I ribozyme from . and highlight some of the facets of th作者: 奇怪 時間: 2025-3-27 10:37
T Lymphocyte Based HIV Gene Therapy Strategies,nase deficiency (ADA), purine nucleoside phosphorylase deficiency (PNP),leukocyte adhesion deficiency (LAD), and chronic granulomatus disease (CGD).. Other disease states have also become candidates for gene therapy approaches such as treatment of tumors through modification of tumor infiltrating ly作者: 記憶法 時間: 2025-3-27 13:49 作者: LURE 時間: 2025-3-27 21:03 作者: nurture 時間: 2025-3-27 23:39 作者: In-Situ 時間: 2025-3-28 02:23
