scholarly article | Q13442814 |
P50 | author | Steven Rosenberg | Q2347448 |
P2093 | author name string | David J Munroe | |
Thomas Ried | |||
Paul F Robbins | |||
Cynthia E Dunbar | |||
Kenneth Cornetta | |||
Claudia Stewart | |||
Richard A Morgan | |||
Zhili Zheng | |||
Peter D Peng | |||
Juhua Zhou | |||
Cyrille J Cohen | |||
Danny Wangsa | |||
Cary Hsu | |||
Xinglei Shen | |||
Stephanie A Jones | |||
Keith Kerstann | |||
Theotonius J Gomes | |||
P2860 | cites work | Multicolor Spectral Karyotyping of Human Chromosomes | Q22065566 |
Adoptive cell transfer therapy following non-myeloablative but lymphodepleting chemotherapy for the treatment of patients with refractory metastatic melanoma | Q24548019 | ||
Distinct genomic integration of MLV and SIV vectors in primate hematopoietic stem and progenitor cells | Q24796392 | ||
Retroviral DNA integration: ASLV, HIV, and MLV show distinct target site preferences | Q24798872 | ||
COOH-terminal-modified interleukin-3 is retained intracellularly and stimulates autocrine growth. | Q38343544 | ||
Capture of antigen-specific T lymphocytes from human blood by selective immortalization to establish long-term T-cell lines maintaining primary cell characteristics | Q40323954 | ||
Divergent telomerase and CD28 expression patterns in human CD4 and CD8 T cells following repeated encounters with the same antigenic stimulus | Q40683550 | ||
Ectopic human telomerase catalytic subunit expression maintains telomere length but is not sufficient for CD8+ T lymphocyte immortalization | Q40846658 | ||
Efficient gene transfer into rhesus repopulating hematopoietic stem cells using a simian immunodeficiency virus-based lentiviral vector system | Q45674295 | ||
Virus-induced CD8+ T cell clonal expansion is associated with telomerase up-regulation and telomere length preservation: a mechanism for rescue from replicative senescence | Q45750058 | ||
Polyclonal long-term repopulating stem cell clones in a primate model | Q45855127 | ||
Gene therapy insertional mutagenesis insights | Q45871758 | ||
Insertion of retroviral vectors in NOD/SCID repopulating human peripheral blood progenitor cells occurs preferentially in the vicinity of transcription start regions and in introns | Q45879077 | ||
Retroviral transduction of human peripheral blood lymphocytes with Bcl-X(L) promotes in vitro lymphocyte survival in pro-apoptotic conditions | Q45885040 | ||
In vitro cellular aging in T-lymphocyte cultures: analysis of DNA content and cell size | Q47391554 | ||
Transfer of the human telomerase reverse transcriptase (TERT) gene into T lymphocytes results in extension of replicative potential. | Q52018513 | ||
Clonal dominance of hematopoietic stem cells triggered by retroviral gene marking. | Q54662841 | ||
Telomere length dynamics in human lymphocyte subpopulations measured by flow cytometry. | Q55067752 | ||
Murine leukemia induced by retroviral gene marking | Q77975543 | ||
IL-15 activates telomerase and minimizes telomere loss and may preserve the replicative life span of memory CD8+ T cells in vitro | Q81546505 | ||
Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells | Q27860926 | ||
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1 | Q28210584 | ||
Gene therapy: therapeutic gene causing lymphoma | Q28236795 | ||
Transcription start regions in the human genome are favored targets for MLV integration | Q29618456 | ||
Specific inhibition of gene expression by small double-stranded RNAs in invertebrate and vertebrate systems | Q33933613 | ||
Interleukin 15: biology and relevance to human disease | Q34116304 | ||
Rules for making human tumor cells | Q34159004 | ||
Telomere length of transferred lymphocytes correlates with in vivo persistence and tumor regression in melanoma patients receiving cell transfer therapy. | Q34314036 | ||
Retroviral vector integration deregulates gene expression but has no consequence on the biology and function of transplanted T cells. | Q34334845 | ||
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1. | Q34508425 | ||
High-efficiency transfection of primary human and mouse T lymphocytes using RNA electroporation | Q34657652 | ||
Recognition of fresh human tumor by human peripheral blood lymphocytes transduced with a bicistronic retroviral vector encoding a murine anti-p53 TCR. | Q34657661 | ||
Primary human T lymphocytes engineered with a codon-optimized IL-15 gene resist cytokine withdrawal-induced apoptosis and persist long-term in the absence of exogenous cytokine | Q34657676 | ||
Transfer of a TCR gene derived from a patient with a marked antitumor response conveys highly active T-cell effector functions | Q34669675 | ||
Focus on acute leukemias | Q34747215 | ||
Occurrence of leukaemia following gene therapy of X-linked SCID. | Q35166805 | ||
Gene Therapy Targeting Hematopoietic Cells: Better Not Leave It to Chance | Q35570283 | ||
Chance or necessity? Insertional mutagenesis in gene therapy and its consequences | Q35637501 | ||
Acute myeloid leukemia is associated with retroviral gene transfer to hematopoietic progenitor cells in a rhesus macaque | Q35848273 | ||
Forkhead transcription factors in immunology. | Q36047235 | ||
Cytogenetic findings in pediatric T-lymphoblastic lymphomas: one institution's experience and a review of the literature | Q36279935 | ||
Hematopoietic stem cell gene therapy: dead or alive? | Q36282424 | ||
Enhanced antitumor activity of murine-human hybrid T-cell receptor (TCR) in human lymphocytes is associated with improved pairing and TCR/CD3 stability | Q36286127 | ||
Survival of the fittest: in vivo selection and stem cell gene therapy | Q36306141 | ||
Bcl-2 overexpression enhances tumor-specific T-cell survival | Q36327125 | ||
Regulated expression of telomerase activity in human T lymphocyte development and activation | Q36366852 | ||
Fatal leukemia in interleukin 15 transgenic mice follows early expansions in natural killer and memory phenotype CD8+ T cells. | Q36369031 | ||
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors. | Q36424249 | ||
Diverse functions of IL-2, IL-15, and IL-7 in lymphoid homeostasis | Q36427380 | ||
Chromatin structural elements and chromosomal translocations in leukemia | Q36558869 | ||
Chromosome abnormalities in advanced stage lymphoblastic lymphoma of children and adolescents: a report from CCG-E08. | Q36686740 | ||
Transduction of an IL-2 gene into human melanoma-reactive lymphocytes results in their continued growth in the absence of exogenous IL-2 and maintenance of specific antitumor activity | Q36726945 | ||
Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements | Q36893995 | ||
Safety Issues Related to Retroviral-Mediated Gene Transfer in Humans | Q37219609 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 5168-5177 | |
P577 | publication date | 2007-03-12 | |
P1433 | published in | Blood | Q885070 |
P1476 | title | Cytokine-independent growth and clonal expansion of a primary human CD8+ T-cell clone following retroviral transduction with the IL-15 gene | |
P478 | volume | 109 |
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Q37110303 | Advances in clinical research in sickle cell disease |
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Q37909894 | Cell transfer immunotherapy for metastatic solid cancer--what clinicians need to know. |
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Q37129671 | Enhancing the in vivo expansion of adoptively transferred EBV-specific CTL with lymphodepleting CD45 monoclonal antibodies in NPC patients |
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Q42696988 | Experimental priapism is associated with increased oxidative stress and activation of protein degradation pathways in corporal tissue. |
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Q37965815 | Genetic engineering of T cells for the immunotherapy of haematological malignancies. |
Q36909362 | Genetic modification of T cells for immunotherapy |
Q30839014 | Hepatocyte-secreted extracellular vesicles modify blood metabolome and endothelial function by an arginase-dependent mechanism. |
Q37110809 | Hypoxia-mediated impaired erythrocyte Lands' Cycle is pathogenic for sickle cell disease |
Q37536195 | IL-12-secreting CD19-targeted cord blood-derived T cells for the immunotherapy of B-cell acute lymphoblastic leukemia |
Q36005345 | IL-15 protects NKT cells from inhibition by tumor-associated macrophages and enhances antimetastatic activity. |
Q35328354 | Identification of chimeric antigen receptors that mediate constitutive or inducible proliferation of T cells |
Q35580645 | Immortalization of human and rhesus macaque primary antigen-specific T cells by retrovirally transduced telomerase reverse transcriptase |
Q33731552 | Immunotherapy in acute leukemia |
Q28068378 | Improving Adoptive T Cell Therapy: The Particular Role of T Cell Costimulation, Cytokines, and Post-Transfer Vaccination |
Q33716478 | In vivo targeting of adoptively transferred T-cells with antibody- and cytokine-conjugated liposomes |
Q34745695 | Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease |
Q61813271 | Lymphocytes in Cellular Therapy: Functional Regulation of CAR T Cells |
Q36928580 | Molecular Pathways: Breaking the Epithelial Cancer Barrier for Chimeric Antigen Receptor and T-cell Receptor Gene Therapy |
Q36945148 | Network model of survival signaling in large granular lymphocyte leukemia |
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Q49401353 | Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors |
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Q37867674 | Pulmonary hypertension in children with sickle cell disease. |
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Q39493084 | Retroviral insertional mutagenesis can contribute to immortalization of mature T lymphocytes |
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Q39839500 | Transfer of Her-2/neu specificity into cytokine-induced killer (CIK) cells with RNA encoding chimeric immune receptor (CIR). |
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