High-efficiency gene transfer into mammalian cells: generation of helper-free recombinant retrovirus with broad mammalian host range.
about
P1343
Molecular cloning of a cDNA encoding interleukin 11, a stromal cell-derived lymphopoietic and hematopoietic cytokineIdentification and molecular cloning of a soluble human granulocyte-macrophage colony-stimulating factor receptorAmino-terminal basic residues of Src mediate membrane binding through electrostatic interaction with acidic phospholipidsIdentification of a membrane-binding domain within the amino-terminal region of human immunodeficiency virus type 1 Gag protein which interacts with acidic phospholipidsConstruction of recombinant murine retroviruses that express the human T-cell leukemia virus type II and human T-cell lymphotropic virus type III trans activator genesA versatile viral system for expression and depletion of proteins in mammalian cellsThe rat leukocyte antigen MRC OX-44 is a member of a new family of cell surface proteins which appear to be involved in growth regulationMolecular engineering of viral gene delivery vehiclesPhorbol ester-induced terminal differentiation is inhibited in human U-937 monoblastic cells expressing a v-myc oncogene.Retrovirus-mediated transduction of adult hepatocytes.Oncogene v-src transforms and establishes embryonic rodent fibroblasts but not diploid human fibroblasts.Activated type I phosphatidylinositol kinase is associated with the epidermal growth factor (EGF) receptor following EGF stimulationSafe and efficient generation of recombinant retroviruses with amphotropic and ecotropic host rangesRequirements for efficient production and transduction of human immunodeficiency virus type 1-based vectors.Development of improved adenosine deaminase retroviral vectors.DNA as therapeutics; an update.Sequences in the cytoplasmic tail of the gibbon ape leukemia virus envelope protein that prevent its incorporation into lentivirus vectorsHoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b.Progress with retroviral gene vectors.Replication of enhancer-deficient amphotropic murine leukemia virus in human cellsRas-mediated cell cycle arrest is altered by nuclear oncogenes to induce Schwann cell transformation.Impairment of natural killer functions by interleukin 6 increases lymphoblastoid cell tumorigenicity in athymic mice.Rapidly and slowly replicating human immunodeficiency virus type 1 isolates can be distinguished according to target-cell tropism in T-cell and monocyte cell lines.Retrovirus-mediated gene transfer to purified hemopoietic stem cells with long-term lympho-myelopoietic repopulating ability.A versatile and potentially general approach to the targeting of specific cell types by retroviruses: application to the infection of human cells by means of major histocompatibility complex class I and class II antigens by mouse ecotropic murine leAntisense RNA complementary to 3' coding and noncoding sequences of creatine kinase is a potent inhibitor of translation in vivoOncoretrovirus and lentivirus vectors pseudotyped with lymphocytic choriomeningitis virus glycoprotein: generation, concentration, and broad host rangeDefective HLA class II expression in a regulatory mutant is partially complemented by activated ras oncogenes.Enhancer sequences of a retroviral vector determine expression of a gene in multipotent hematopoietic progenitors and committed erythroid cells.Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer.Expression of human class II major histocompatibility complex antigens using retrovirus vectors.Palmitoylation of p59fyn is reversible and sufficient for plasma membrane associationRetroviruses as genetic tools to isolate transcriptionally active chromosomal regions.Gene therapy for the inner ear: challenges and promises.Blocking of retroviral infection at a step prior to reverse transcription in cells transformed to constitutively express interferon beta.Gene therapy of monogenic and cardiovascular disorders.Enhanced transfection efficiency and improved cell survival after electroporation of G2/M-synchronized cells and treatment with sodium butyrate.A new approach to the molecular basis of neoplastic transformation in the brain.Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cellsRetrovirus-mediated transfer of human adenosine deaminase gene sequences into cells in culture and into murine hematopoietic cells in vivo.
P2860
Q24298662-2FB4E525-B0E2-4D78-AE89-CEE0E44A8549Q24562055-D4E08A5D-5FB2-440C-A1C7-5A4A0764BA37Q24564497-D82E3976-2C8A-44A4-AF18-9624CDEC29D4Q24646680-6E3412F6-FE66-4875-AF16-836169204288Q24655892-6EDA1ACC-A65C-46D5-A462-582D3B1F2F75Q28475909-EAA680B9-6BC7-41AA-B3A8-9863C8AF381DQ28771383-406209D8-9B53-4506-BF11-EE1AF5B15305Q33353795-CD863EA8-5E5F-4B39-B834-C3594172C2CDQ33567289-3B1E5C80-8DB1-41DB-A55E-69AD64CFCFF1Q33570031-22A4CAB8-C4C6-4A1A-9AD7-DA61A2ECDFE8Q33581671-2F9CE75E-FD89-4F7B-8096-CB18B9156069Q33587507-4F3A3CD9-FF19-4AE8-9D00-8C5DF5FB2D7EQ33644899-5AB75911-248F-47ED-BDEE-846B85728E30Q33652758-941766E6-2B6B-413D-A5F9-13777C849BB8Q33782258-13F8BD2B-0329-4D83-B368-46B874E02EBAQ33836499-E3E19C85-C308-46A3-9276-AEDE6B6016C6Q33839293-365B60BA-AD08-4970-860C-DBB54BC0ACEAQ33889059-5126321E-73DF-47E6-9CA7-6783BB4BB0A4Q33920752-892CDFC4-B8B9-436C-8B83-546D290E1078Q33943938-F79C5636-FD8D-46F5-95B3-2F147E2B54FCQ34164036-7E90B7DB-FDF0-44E3-A651-7B4CE160E408Q34225642-9128F7EB-3BFD-416C-BD87-69604CD98F0EQ34304672-6BD09038-3A23-4051-8111-846DE02E4AB7Q34319023-F2C2469A-7350-4A1A-8960-730C5BD023C7Q34321338-B0828662-BFCD-4B76-B3EB-68B9AC35AA65Q34326292-15F489C8-55FA-4579-8A6B-5FB771C95EF0Q34329994-D09B6A39-B7EB-4F49-98F2-EABC205EAF4EQ34373203-67D35982-9DFC-4131-B8CC-1F01D88C81F6Q34373796-768412A5-95BF-41EF-8994-AA30E78FE050Q34585324-BD08CB06-8865-4D37-815E-E01922DEF0C9Q34611661-D3F60A7E-F1BE-4998-AC56-6EB43E779989Q34671604-EEE25D6C-54D3-4FBF-B452-5A32EDEBB39FQ35034076-B0C47854-D230-4AC8-9C43-FE839668546AQ35095260-154A4C63-576E-4335-9A7A-433B01536829Q35129626-A25BC3E9-AD55-458A-A1BD-D495803E7A9EQ35207521-295E1576-89ED-48D6-BA6A-C29E7F3ACEC3Q35228280-5F32C966-4FED-47ED-B286-6C0DCA2CA6A9Q35236403-91EBC5D4-6574-428A-A28D-AD09C6CAF453Q35586549-6FB8D083-4E9A-4D9C-88AD-71F9EA58AEBBQ35600024-7B704127-6EF7-48E6-8A92-4A1A2CC2AF87
P2860
High-efficiency gene transfer into mammalian cells: generation of helper-free recombinant retrovirus with broad mammalian host range.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 1984
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
High-efficiency gene transfer ...... th broad mammalian host range.
@en
High-efficiency gene transfer ...... th broad mammalian host range.
@nl
type
label
High-efficiency gene transfer ...... th broad mammalian host range.
@en
High-efficiency gene transfer ...... th broad mammalian host range.
@nl
prefLabel
High-efficiency gene transfer ...... th broad mammalian host range.
@en
High-efficiency gene transfer ...... th broad mammalian host range.
@nl
P2860
P356
P1476
High-efficiency gene transfer ...... th broad mammalian host range.
@en
P2093
R C Mulligan
P2860
P304
P356
10.1073/PNAS.81.20.6349
P407
P4510
P577
1984-10-01T00:00:00Z