نتایج جستجو برای: lentiviral vector containing bvdv

تعداد نتایج: 539407  

2018
Felix Urusov Dina Glazkova Denis Omelchenko Elena Bogoslovskaya Galina Tsyganova Katerina Kersting German Shipulin Vadim Pokrovsky

C-C chemokine receptor type 5 (CCR5) is utilized by human immunodeficiency virus (HIV) as a co-receptor for cell entry. Suppression of the CCR5 gene by artificial microRNAs (amiRNAs) could confer cell resistance. In previous work, we created a lentivector that encoded the polycistron of two identical amiRNAs that could effectively suppress CCR5. However, tandem repeats in lentiviral vectors led...

Abbas Sahebghadam Lotfi, Behzad Adibi Mahboobe Ghaedi Masoud Soleimani, Mehdi Shamsara Sare Arjmand

In this study, in order to facilitate and accelerate the production of eukaryotic protein alpha 1-antitrypsin (AAT) with correct post-translational modifications, a protein production system based on the transduction of CHO and COS-7 cells using lentiviral vectors was developed. Human AAT cDNA was cloned into a replication-defective lentiviral vector. The transgene AAT-Jred chimer was transferr...

Journal: :Journal of the American Veterinary Medical Association 2004
Kris K Fairbanks Carol L Rinehart Wm Charles Ohnesorge Marie M Loughin Christopher C L Chase

OBJECTIVE To evaluate the efficacy of a modified-live virus (MLV) combination vaccine containing type 1 and type 2 bovine viral diarrhea virus (BVDV) in providing fetal protection against challenge with heterologous type 1 and type 2 BVDV. DESIGN Prospective study. ANIMALS 55 heifers. PROCEDURE Heifers were vaccinated with a commercial MLV combination vaccine or given a sham vaccine (ster...

Journal: :iranian journal of biotechnology 2009
mahboobe ghaedi abbas sahebghadam lotfi masoud soleimani mehdi shamsara sare arjmand

in this study, in order to facilitate and accelerate the production of eukaryotic protein alpha 1-antitrypsin (aat) with correct post-translational modifications, a protein production system based on the transduction of cho and cos-7 cells using lentiviral vectors was developed. human aat cdna was cloned into a replication-defective lentiviral vector. the transgene aat-jred chimer was transferr...

خداشناس لیمونی, شعبانعلی, سلیمی, فاطمه, فروزنده مقدم, مهدی,

Background and purpose: Exosome as drug delivery system is a novel and smart methodology enabling delivery of exosome cargo into specific tissue. This aim could be accessed by manipulation of exosome producer cells for expression of specific transmembrane-anchored ligand on exosomes surface. Accordingly, Lysosomal Associated Membrane Protein (LAMP) is one of the best choices for anchoring and c...

Journal: :Gene Reports 2022

Beta thalassemia is a common monogenic disorder caused by partial or complete reduction of beta globin chains synthesis. In recent years allogeneic bone marrow transplantation (BMT) has been considered to be the successful cure for patients with major, however this restricted due limited number HLA-matched donors. Therefore, molecular approaches including gene therapy direct normal transmission...

Journal: :Stem cells 2007
Betty Ying Zhou Zhaohui Ye Guibin Chen Zhigang Peter Gao Yu A Zhang Linzhao Cheng

We report here a lentiviral vector system for regulated transgene expression. We used the tetracycline repressor fused with a transcriptional suppression domain (tTS) to specifically suppress transgene expression. Human cells were first transduced with a tTS-expressing vector and subsequently transduced with a second lentiviral vector-containing transgene controlled by a regular promoter adjace...

Journal: :research in pharmaceutical sciences 0

lentiviral vectors are among the promising viral based-vectors in gene therapy applications, but the efficiency of their targeting needs to be improved. (strept)avidin-biotin adaptor system is a novel approach to modify the lentiviral envelope for better targeting properties. herein, we describe utilization of this adaptor system by designing a candidate envelope protein-bearing biotin acceptor...

Journal: :PLoS Pathogens 2007
Sabine Brandt Maik Blißenbach Bastian Grewe Rebecca Konietzny Thomas Grunwald Klaus Überla

The main function attributed to the Rev proteins of immunodeficiency viruses is the shuttling of viral RNAs containing the Rev responsive element (RRE) via the CRM-1 export pathway from the nucleus to the cytoplasm. This restricts expression of structural proteins to the late phase of the lentiviral replication cycle. Using Rev-independent gag-pol expression plasmids of HIV-1 and simian immunod...

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