scholarly article | Q13442814 |
P50 | author | Daniel G. Miller | Q42094335 |
P2093 | author name string | George Stamatoyannopoulos | |
David W Emery | |||
Julie Tubb | |||
Mari Aker | |||
P2860 | cites work | 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 | ||
Matrix attachment regions as targets for retroviral integration | Q24811093 | ||
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1 | Q28210584 | ||
High-resolution genome-wide mapping of transposon integration in mammals | Q28769896 | ||
Transcription start regions in the human genome are favored targets for MLV integration | Q29618456 | ||
HIV-1 integration in the human genome favors active genes and local hotspots | Q29618457 | ||
Weak palindromic consensus sequences are a common feature found at the integration target sites of many retroviruses | Q33724262 | ||
Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver | Q33737640 | ||
Symmetrical base preferences surrounding HIV-1, avian sarcoma/leukosis virus, and murine leukemia virus integration sites | Q33771092 | ||
The ups and downs of gene expression and retroviral DNA integration | Q33820016 | ||
Combination of interleukins 3 and 6 preserves stem cell function in culture and enhances retrovirus-mediated gene transfer into hematopoietic stem cells | Q34319610 | ||
Foamy virus vector integration sites in normal human cells | Q34334976 | ||
Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibers | Q34344656 | ||
Transcriptional Interference by Independently Regulated Genes Occurs in Any Relative Arrangement of the Genes and Is Influenced by Chromosomal Integration Position | Q34440230 | ||
RTCGD: retroviral tagged cancer gene database | Q34923778 | ||
American Society of Gene Therapy (ASGT) ad hoc subcommittee on retroviral-mediated gene transfer to hematopoietic stem cells | Q35195407 | ||
A chromatin insulator protects retrovirus vectors from chromosomal position effects | Q35198059 | ||
Targeting survival: integration site selection by retroviruses and LTR-retrotransposons | Q35563809 | ||
Chance or necessity? Insertional mutagenesis in gene therapy and its consequences | Q35637501 | ||
Protection and selection for gene therapy in the hematopoietic system | Q35673396 | ||
Recurrent retroviral vector integration at the Mds1/Evi1 locus in nonhuman primate hematopoietic cells | Q35848227 | ||
Stem cell clonality and genotoxicity in hematopoietic cells: gene activation side effects should be avoidable. | Q35929299 | ||
Goodness-of-fit tests for discrete data: a review and an application to a health impairment scale | Q36776980 | ||
A safe packaging line for gene transfer: separating viral genes on two different plasmids | Q36865708 | ||
Genome-wide analyses of avian sarcoma virus integration sites | Q37583468 | ||
Performance- and safety-enhanced lentiviral vectors containing the human interferon-beta scaffold attachment region and the chicken beta-globin insulator | Q40670749 | ||
A GFP reporter system to assess gene transfer and expression in human hematopoietic progenitor cells | Q41066600 | ||
Genome-wide analysis of chromosomal features repressing human immunodeficiency virus transcription. | Q42755157 | ||
Topological constraints governing the use of the chicken HS4 chromatin insulator in oncoretrovirus vectors | Q43980881 | ||
Preferential selection of human T-cell leukemia virus type I provirus integration sites in leukemic versus carrier states | Q45478033 | ||
Retroviral vector integration occurs in preferred genomic targets of human bone marrow-repopulating cells | Q45856240 | ||
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 | ||
Clonal dominance of hematopoietic stem cells triggered by retroviral gene marking. | Q54662841 | ||
Evidence for nucleosome depletion at active regulatory regions genome-wide | Q54998820 | ||
New genes involved in cancer identified by retroviral tagging | Q74624557 | ||
Murine leukemia induced by retroviral gene marking | Q77975543 | ||
P433 | issue | 2 | |
P921 | main subject | bias | Q742736 |
P304 | page(s) | 226-235 | |
P577 | publication date | 2006-05-02 | |
P1433 | published in | Molecular Therapy | Q15762400 |
P1476 | title | Integration bias of gammaretrovirus vectors following transduction and growth of primary mouse hematopoietic progenitor cells with and without selection | |
P478 | volume | 14 |
Q38707236 | Bidirectional Retroviral Integration Site PCR Methodology and Quantitative Data Analysis Workflow |
Q35751562 | Gammaretroviral vector integration occurs overwhelmingly within and near DNase hypersensitive sites |
Q37795125 | Gene therapy for β-thalassaemia: the continuing challenge |
Q33713390 | Genomic and functional assays demonstrate reduced gammaretroviral vector genotoxicity associated with use of the cHS4 chromatin insulator |
Q33325922 | HTLV-1 integration into transcriptionally active genomic regions is associated with proviral expression and with HAM/TSP |
Q35260206 | Retroviral integration site selection. |
Q38913136 | Significant differences in integration sites of Moloney murine leukemia virus/Moloney murine sarcoma virus retroviral vector carrying recombinant coagulation factor IX in two human cell lines |
Q37830029 | The Use of Chromatin Insulators to Improve the Expression and Safety of Integrating Gene Transfer Vectors |
Q39509837 | The sea urchin sns5 insulator protects retroviral vectors from chromosomal position effects by maintaining active chromatin structure. |
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