Long-term expression of human adenosine deaminase in rhesus monkeys transplanted with retrovirus-infected bone-marrow cells.
about
Ganciclovir-mediated in vivo elimination of myeloid leukemic cells expressing the HSVtk gene induces HSVtk loss variants.Selection of transduced CD34+ progenitors and enzymatic correction of cells from Gaucher patients, with bicistronic vectorsHigh-efficiency gene transfer into normal and adenosine deaminase-deficient T lymphocytes is mediated by transduction on recombinant fibronectin fragments.Gene therapy for the hemoglobin disorders: past, present, and future.Evidence that retroviruses integrate into post-replication host DNAEntry of amphotropic and 10A1 pseudotyped murine retroviruses is restricted in hematopoietic stem cell lines.Effects of retroviral vector design on expression of human adenosine deaminase in murine bone marrow transplant recipients engrafted with genetically modified cells.Therapeutic potential of ribozymes in haematological disorders.Bone marrow extracellular matrix molecules improve gene transfer into human hematopoietic cells via retroviral vectors.Current status of retroviral vector mediated gene transfer into human hematopoietic stem cells.Gene therapy: here to stay.Long-term in vivo expression of the human glucocerebrosidase gene in nonhuman primates after CD34+ hematopoietic cell transduction with cell-free retroviral vector preparations.Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiencyRetroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblasts.Gene transfer into hematopoietic stem cells: long-term maintenance of in vitro activated progenitors without marrow ablation.Drug-selected coexpression of human glucocerebrosidase and P-glycoprotein using a bicistronic vector.Gaucher disease as a paradigm of current issues regarding single gene mutations of humansHuman cord blood cells as targets for gene transfer: potential use in genetic therapies of severe combined immunodeficiency disease.Peripheral blood progenitors as a target for genetic correction of p47phox-deficient chronic granulomatous diseaseExpression of the gibbon ape leukemia virus receptor-1 in rhesus macaque tissues.Development of gene therapy: potential in severe combined immunodeficiency due to adenosine deaminase deficiency.The level of mRNA encoding the amphotropic retrovirus receptor in mouse and human hematopoietic stem cells is low and correlates with the efficiency of retrovirus transduction.Transduction of pluripotent human hematopoietic stem cells demonstrated by clonal analysis after engraftment in immune-deficient mice.Changing faces in virology: the dutch shift from oncogenic to oncolytic viruses.Preclinical modeling of hematopoietic stem cell transplantation - advantages and limitations.Gene marking and autologous bone marrow transplantation.Current status of gene transfer into haemopoietic progenitor cells: application to Langerhans cell histiocytosisIn vivo methotrexate selection of murine hemopoietic cells transduced with a retroviral vector for Gaucher disease.In vitro T lymphopoiesis: a model system for stem cell gene therapy for AIDS.
P2860
Q33178788-16EA82E6-913B-4900-9F8E-B333B062A776Q33645840-8C152869-724F-405F-96F4-A5E33A9BD8ADQ33784122-FF4736A5-EF0B-49C2-8C6C-A5DFD6E1B971Q33915535-8E17F7AD-FE9E-4EAE-A4EB-2518A14698D6Q34064403-45EA5926-94FD-40E3-8AC1-0C38349EDF04Q34069853-E9E12AF6-2E0D-47D3-9B81-22E84BB2985DQ34073981-376D283B-BB7A-4F7D-9E8D-1710A32E3913Q34074840-6B892546-491B-48F4-9DEB-D52B9FDF1227Q34138051-F2D5DEBD-4D5F-43D0-9B14-FA42D2B65769Q34244510-23970D88-CE99-4974-923C-4484BEF181CFQ34279082-EE00A312-3120-45B4-9A3D-DB8E960CE10AQ34326769-1736DF3E-899A-44BD-B93E-72DAABBA6FAAQ34454454-45D70AA3-443C-4FF2-B0E1-3B287ED8DF27Q34644825-0FFB8A93-6EA1-49C8-8102-E998FE690066Q34958691-FF7BF4DC-D0DD-49AF-800A-BE73216F4969Q35159720-B4668016-7831-4F5A-902F-7432CA2265ACQ36353819-1E01643C-DBAE-4B4C-A463-AC97B3F57E18Q36362150-59674ECB-66F0-485A-B6EF-4A12C09745DAQ36470854-16BFEC5D-757E-477C-B98B-AF3A85DE7FB3Q36879120-A33419FA-710E-457F-B814-EF7F3278B55DQ37194056-5B53AD77-A71C-42A3-AF4B-B0096A499945Q37310938-5B352EE8-F042-4CC6-98D2-157B2B129D29Q37693995-58685CF0-4818-490F-B268-78E5902C215AQ38241666-AF6ADF9C-74E1-4F3C-B599-6C7542C95C80Q38660463-3206B53A-C338-4B2C-AEB8-40D02BD712FEQ40667892-EEB6F1DE-640C-4B3D-B36D-9DE51E1EB735Q40696526-FCA5EA00-3DFB-4807-83A2-100FC9B9E831Q45862789-B750A962-F1AE-4E30-B9BE-A51FC32F9850Q45879348-EAB043FD-2604-486C-96D5-0D54CE89D698
P2860
Long-term expression of human adenosine deaminase in rhesus monkeys transplanted with retrovirus-infected bone-marrow cells.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on August 1992
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Long-term expression of human ...... us-infected bone-marrow cells.
@en
Long-term expression of human ...... us-infected bone-marrow cells.
@nl
type
label
Long-term expression of human ...... us-infected bone-marrow cells.
@en
Long-term expression of human ...... us-infected bone-marrow cells.
@nl
prefLabel
Long-term expression of human ...... us-infected bone-marrow cells.
@en
Long-term expression of human ...... us-infected bone-marrow cells.
@nl
P2093
P2860
P356
P1476
Long-term expression of human ...... us-infected bone-marrow cells.
@en
P2093
van Beusechem VW
P2860
P304
P356
10.1073/PNAS.89.16.7640
P407
P577
1992-08-01T00:00:00Z