Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
about
Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosisConstruction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virusCas9 as a versatile tool for engineering biologyCorrection of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapyLentiviral vectors in gene therapy: their current status and future potentialCD226 (DNAM-1) is involved in lymphocyte function-associated antigen 1 costimulatory signal for naive T cell differentiation and proliferationPromising and delivering gene therapies for vision lossGene therapy of inherited retinal degenerations: prospects and challengesMüller glia activation in response to inherited retinal degeneration is highly varied and disease-specificCRISPR-Cas9 System as a Versatile Tool for Genome Engineering in Human CellsIdentification of key residues determining isomerohydrolase activity of human RPE65Review: the history and role of naturally occurring mouse models with Pde6b mutationsGene transfer mediated by recombinant baculovirus into mouse eyeAbnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B proteinRetinal degeneration progression changes lentiviral vector cell targeting in the retinaA third-generation lentivirus vector with a conditional packaging systemA lentivirus packaging system based on alternative RNA transport mechanisms to express helper and gene transfer vector RNAs and its use to study the requirement of accessory proteins for particle formation and gene delivery.A specific region of 37 amino acid residues in the SPRY (B30.2) domain of African green monkey TRIM5alpha determines species-specific restriction of simian immunodeficiency virus SIVmac infection.Novel bovine lentiviral vectors based on Jembrana disease virus.Gene therapy regenerates protein expression in cone photoreceptors in Rpe65(R91W/R91W) mice.Identification of synthetic endothelial cell-specific promoters by use of a high-throughput screen.Long-term safety of GDNF gene delivery in the retina.Inactivation of SMC2 shows a synergistic lethal response in MYCN-amplified neuroblastoma cells.A packaging cell line for lentivirus vectors.Development of a self-inactivating lentivirus vector.Development of multigene and regulated lentivirus vectors.Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitroMarking and gene expression by a lentivirus vector in transplanted human and nonhuman primate CD34(+) cellsA murine leukemia virus (MuLV) long terminal repeat derived from rhesus macaques in the context of a lentivirus vector and MuLV gag sequence results in high-level gene expression in human T lymphocytesMinimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors.Lentiviral vectors: turning a deadly foe into a therapeutic agent.A large-scale insertional mutagenesis screen in zebrafishGeneration of Rx+/Pax6+ neural retinal precursors from embryonic stem cellsRecent advances in the molecular basis of inherited photoreceptor degeneration.Lentiviral mediated transgenesis by in vivo manipulation of spermatogonial stem cells.Design of an HIV-1 lentiviral-based gene-trap vector to detect developmentally regulated genes in mammalian cells.Current status of viral gene therapy for brain tumours.Gene therapy and retinitis pigmentosa: advances and future challenges.P2Y(2) receptor agonist INS37217 enhances functional recovery after detachment caused by subretinal injection in normal and rds mice.Absence of functional and structural abnormalities associated with expression of EGFP in the retina.
P2860
Q21144697-FBB05A17-7609-4A52-9FBD-83D0BB107A49Q24529091-B2B926AA-170C-422D-AAD5-2A221E457654Q24564294-83C2B0D1-ED59-4CAC-99C3-6DE19817BFBCQ24621941-2E667315-9300-4A51-875F-9085E78231FCQ24629462-1B7041D5-4F56-46B5-98E8-B62783034B10Q24672761-45D32BC8-4723-423C-BED0-F8F3631430B6Q27007079-00E92F7A-3435-4BD7-A8CE-A0C971D85897Q27009261-9F68E9BC-E498-4038-ABAD-1D64AB82B589Q27311456-1E887337-D107-4C45-B2B9-D86E2D466858Q28076522-A1805CAE-16DC-4D47-B6A9-F309013CC0EEQ28245764-6FDCBFA8-2997-428B-B600-7AE0C3A132E0Q28304672-688CA832-BB70-4AC2-9546-93ADDD2AADE4Q28365551-56086384-02A5-4678-8843-2CE55084FF1CQ28505722-4415ED7C-7FFB-44A1-B941-9F078D2C35B3Q28741007-89CDF732-01E4-4E24-834B-D46392348418Q29616120-7D7B2E41-EECB-4E4B-99DD-B5AC273F6FBEQ30453492-8560891B-6AB8-41F7-B2B5-FDA86637F6F9Q30789664-3D62D2F1-08C4-41C7-A6F0-79D1B75C8BC0Q30885539-E23A58AD-418E-40A7-8E39-4D83AC934193Q30999247-7FDB0331-E9CE-4234-91E3-3E04070387B4Q31066742-60BFF194-8328-4D57-B117-66892ADC48B3Q33221962-2AD0088F-D733-4191-BF93-026FB16260E0Q33578581-A2110224-F467-4AE6-9CA3-8B1BFAE680F8Q33639623-947B56BE-F966-4DAE-90AA-25CF96BBAB76Q33784841-0A48F70C-D43A-485F-8007-364382552821Q33787285-06A1E967-4C8B-4477-97C5-64DAF157F3B9Q33787358-0CEE7101-0F32-4641-8DF2-242795B2A1CCQ33793274-7E1C41BE-7760-46BC-8FC6-A58377662C9EQ33802424-52919BBC-5C23-4DCE-80D0-875471E307ADQ33814215-4CD9EBB6-5B2A-4F0D-A42E-879674424A5FQ33840989-B51B753B-AFBA-4A42-B249-33C05F8FBFBDQ33878395-5776F850-2588-4C75-885E-56A1D8593588Q33913871-DB3572BA-05E8-4082-8CD8-C194F462704FQ33942183-EC200E48-205B-4EA2-B2A9-ED0AE8C81AB6Q33961652-BA45B81C-4536-4EA1-B2C2-F7FA928902CCQ34019566-A540875F-8A19-4A74-9A03-03912CA49A06Q34074791-7897DC7E-3BBC-4E66-AFB2-82AE7FCC540FQ34084443-A00292BE-20A6-482A-847A-2D1AF5CCFC1FQ34120951-9C6140E1-808A-4D90-AE69-9AD6C8E81F9CQ34120983-76895A4E-541E-48ED-ADB7-0749722BABC9
P2860
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
@ast
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
@en
type
label
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
@ast
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
@en
prefLabel
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
@ast
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
@en
P2093
P2860
P356
P1476
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.
@en
P2093
P2860
P304
10319-10323
P356
10.1073/PNAS.94.19.10319
P407
P577
1997-09-01T00:00:00Z