| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/NG0393-224 |
| P698 | PubMed publication ID | 8485577 |
| P50 | author | Michel Jean Robert Perricaudet | Q64398414 |
| P2093 | author name string | Kahn A | |
| Caillaud C | |||
| Poenaru L | |||
| Perricaudet M | |||
| Vigne E | |||
| Akli S | |||
| Peschanski MR | |||
| Stratford-Perricaudet LD | |||
| P2860 | cites work | A short amino acid sequence able to specify nuclear location | Q29547781 |
| Use of a recombinant retrovirus to study post-implantation cell lineage in mouse embryos | Q33880924 | ||
| Widespread long-term gene transfer to mouse skeletal muscles and heart | Q35605664 | ||
| Adenovirus as an expression vector in muscle cells in vivo | Q36910386 | ||
| Cytotoxicity of a replication-defective mutant of herpes simplex virus type 1 | Q40065369 | ||
| Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice | Q41572953 | ||
| In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium | Q41644008 | ||
| Adenovirus-mediated transfer of a recombinant alpha 1-antitrypsin gene to the lung epithelium in vivo | Q41894646 | ||
| In Vivo Gene Transfer with Retroviral Vector-Producer Cells for Treatment of Experimental Brain Tumors | Q42818740 | ||
| Herpesvirus vector gene transfer and expression of beta-glucuronidase in the central nervous system of MPS VII mice | Q45175987 | ||
| Adenovirus-mediated in vivo gene transfer and expression in normal rat liver | Q45878870 | ||
| In Vivo Expression of β-Galactosidase in Hippocampal Neurons by HSV-Mediated Gene Transfer | Q48544329 | ||
| Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector | Q64378881 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Adenoviridae | Q193447 |
| P304 | page(s) | 224-228 | |
| P577 | publication date | 1993-03-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Transfer of a foreign gene into the brain using adenovirus vectors | |
| P478 | volume | 3 |
| Q90049700 | A Student's Guide to Neural Circuit Tracing |
| Q45861866 | A model for long-term transgene expression in spinal cord regeneration studies |
| Q40608616 | A multi-domain protein system based on the HC fragment of tetanus toxin for targeting DNA to neuronal cells |
| Q39733540 | A new hybrid system capable of efficient lentiviral vector production and stable gene transfer mediated by a single helper-dependent adenoviral vector |
| Q41130941 | A recombinant adenovirus that directs secretion of biologically active kappa-bungarotoxin from mammalian cells |
| Q28582416 | A role for the cadherin family of cell adhesion molecules in hippocampal long-term potentiation |
| Q30958033 | A simple and efficient method for constructing an adenoviral cDNA expression library |
| Q44420155 | Adeno-associated virus-mediated aspartoacylase gene transfer to the brain of knockout mouse for canavan disease |
| Q28141743 | Adenoviral and adeno-associated viral transfer of genes to the peripheral nervous system |
| Q45868483 | Adenoviral gene transfer of basic fibroblast growth factor promotes angiogenesis in rat brain |
| Q40890513 | Adenoviral gene transfer of ciliary neurotrophic factor and brain-derived neurotrophic factor leads to long-term survival of axotomized motor neurons |
| Q45887941 | Adenoviral gene transfer to spinal-cord neurons: intrathecal vs. intraparenchymal administration |
| Q48653102 | Adenoviral vector-directed expression of neurotrophin-3 in rat dorsal root ganglion explants results in a robust neurite outgrowth response |
| Q41068462 | Adenoviral vector-mediated GDNF gene therapy in a rodent lesion model of late stage Parkinson's disease |
| Q48633464 | Adenoviral vector-mediated expression of B-50/GAP-43 induces alterations in the membrane organization of olfactory axon terminals in vivo. |
| Q52197420 | Adenoviral vector-mediated gene transfer and neurotransplantation: possibilities and limitations in grafting of the fetal rat suprachiasmatic nucleus. |
| Q45861869 | Adenoviral vectors for in vivo gene delivery to oligodendrocytes: transgene expression and cytopathic consequences |
| Q45871546 | Adenoviral-mediated gene transfer to renal tubular cells in vivo |
| Q48431347 | Adenoviral-mediated transfection of the Lac-Z gene into rat dissociated embryonic central nervous system cells before and after seeding |
| Q42613158 | Adenovirus expression of IL-1 and NF-kappaB inhibitors does not inhibit acute adenoviral-induced brain inflammation, but delays immune system-mediated elimination of transgene expression. |
| Q43836200 | Adenovirus mediated expression of therapeutic plasma levels of human factor IX in mice |
| Q43717552 | Adenovirus vector-directed expression of the neurotrophin-3 receptor (TrkC) in mouse astrocytes |
| Q40489615 | Adenovirus vectors enter the brain |
| Q48581119 | Adenovirus-mediated expression of AMPA-type glutamate receptor channels in PC12 cells |
| Q37277727 | Adenovirus-mediated gene delivery into neuronal precursors of the adult mouse brain |
| Q40456070 | Adenovirus-mediated gene transfer into striated muscles. |
| Q44020421 | Adenovirus-mediated gene transfer of B7.1 induces immunological anti-tumor effects in a murine brain tumor |
| Q44409499 | Adenovirus-mediated gene transfer of interferon α improves dimethylnitrosamine-induced liver cirrhosis in rat model |
| Q48564941 | Adenovirus-mediated gene transfer to cultured nodose sensory neurons. |
| Q41450015 | Adenovirus-mediated gene transfer to the brain: methodological assessment |
| Q45856171 | Adenovirus-mediated suicide gene therapy in an in vitro model of reactive gliosis |
| Q40832016 | Adenovirus-mediated transfer of the neurotrophin-3 gene into skeletal muscle of pmn mice: therapeutic effects and mechanisms of action |
| Q73516016 | Adenovirus-mediated transfer of tissue-type plasminogen activator gene to human endothelial cells |
| Q44697885 | Adenovirus/herpes simplex-thymidine kinase/ganciclovir complex: preliminary results of a phase I trial in patients with recurrent malignant gliomas. |
| Q64380167 | Akt/protein kinase B prevents injury-induced motoneuron death and accelerates axonal regeneration |
| Q44858702 | An adenoviral vector expressing the glucose transporter protects cultured striatal neurons from 3-nitropropionic acid |
| Q42812872 | Analysis of adenovirus gene transfer into adult neural stem cells |
| Q73479964 | Apoptosis signaling pathway in T cells is composed of ICE/Ced-3 family proteases and MAP kinase kinase 6b |
| Q45856230 | Application of gene therapy to treat age-related loss of dopamine D2 receptor |
| Q48594392 | Application of recombinant adenovirus for in vivo gene delivery to spinal cord |
| Q43413361 | Attenuation of stroke size in rats using an adenoviral vector to induce overexpression of interleukin-1 receptor antagonist in brain |
| Q43662965 | Bcl-2 expression by retrograde transport of adenoviral vectors with Cre-loxP recombination system in motor neurons of mutant SOD1 transgenic mice. |
| Q27316954 | CAR-associated vesicular transport of an adenovirus in motor neuron axons |
| Q45867447 | Cationic liposome conjugation to recombinant adenoviral vector reduces viral antigenicity |
| Q48913603 | Co-administration of adenovirus vector expressing CTLA4-Ig prolongs transgene expression in the brain of mice sensitized with adenovirus |
| Q34898869 | Comparison of the efficacy of four viral vectors for transducing hypothalamic magnocellular neurosecretory neurons in the rat supraoptic nucleus |
| Q41258616 | Construction of recombinant adenovirus containing picorna-viral 2A-peptide sequence for the co-expression of neuro-protective growth factors in human umbilical cord blood cells |
| Q57254245 | Continuous renewal of the axonal pathway sensor apparatus by insertion of new sensor molecules into the growth cone membrane |
| Q28581577 | Corticostriatopallidal neuroprotection by adenovirus-mediated ciliary neurotrophic factor gene transfer in a rat model of progressive striatal degeneration |
| Q40646326 | Cre/loxP-mediated adenovirus type 5 packaging signal excision demonstrates that core element VI is sufficient for virus packaging |
| Q33641230 | Cyclophosphamide increases transgene expression mediated by an oncolytic adenovirus in glioma-bearing mice monitored by bioluminescence imaging |
| Q43641898 | DNA fragmentation and HSP72 gene expression by adenovirus-mediated gene transfer in postischemic gerbil hippocampus and ventricle |
| Q48493406 | Degeneration in vivo of rat hippocampal neurons by wild-type Alzheimer amyloid precursor protein overexpressed by adenovirus-mediated gene transfer. |
| Q34038253 | Development of an adenoviral vector for intracerebral delivery of the dopamine D(2) receptor |
| Q40905804 | Differential effects of glial cell line-derived neurotrophic factor (GDNF) in the striatum and substantia nigra of the aged Parkinsonian rat. |
| Q34904038 | Differentiated neuroprogenitor cells incubated with human or canine adenovirus, or lentiviral vectors have distinct transcriptome profiles |
| Q39465848 | Direct gene transfer into rat liver cells by in vivo electroporation |
| Q37459272 | Disruption of the coxsackievirus and adenovirus receptor-homodimeric interaction triggers lipid microdomain- and dynamin-dependent endocytosis and lysosomal targeting. |
| Q48726011 | Dissociative expression of adenoviral-mediated E. coli LacZ gene between ischemic and reperfused rat brains |
| Q64381079 | Dopa-producing astrocytes generated by adenoviral transduction of human tyrosine hydroxylase gene: in vitro study and transplantation to hemiparkinsonian model rats |
| Q64382528 | Efficient gene expression in mammalian clock pacemaker cell in vitro by an adenovirus vector |
| Q44014363 | Efficient gene transfer and long-term expression in neurons using a recombinant adenovirus with a neuron-specific promoter |
| Q24600841 | Efficient transfer of genetic material into mammalian cells using Starburst polyamidoamine dendrimers |
| Q53060851 | Electroporation markedly improves Sleeping Beauty transposon-induced tumorigenesis in mice. |
| Q62971299 | Engineering Herpes Simplex |
| Q41209927 | EphB signaling controls lineage plasticity of adult neural stem cell niche cells |
| Q26744103 | Evaluation of Gene Therapy as an Intervention Strategy to Treat Brain Injury from Stroke |
| Q45760694 | Evaluation of recombinant adeno-associated virus as a gene transfer vector for the retina |
| Q44184245 | Ex vivo adenoviral vector-mediated neurotrophin gene transfer to olfactory ensheathing glia: effects on rubrospinal tract regeneration, lesion size, and functional recovery after implantation in the injured rat spinal cord. |
| Q34949959 | Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke |
| Q36367568 | Gene Therapy for the Treatment of Neurological Disorders: Central Nervous System Neoplasms. |
| Q41091912 | Gene delivery into neuronal and glial cells by using a replication-deficient adenovirus vector: prospects for neurological gene therapy |
| Q45773320 | Gene delivery into the brain using virus vectors |
| Q64382253 | Gene therapy for Parkinson's disease |
| Q35152561 | Gene therapy for brain tumors: regression of experimental gliomas by adenovirus-mediated gene transfer in vivo |
| Q35045240 | Gene therapy for cerebral vascular disease: update 2003. |
| Q33582065 | Gene therapy for diseases of the nervous system. |
| Q34997896 | Gene therapy for the central nervous system in the lysosomal storage disorders |
| Q34987206 | Gene therapy for treatment of cerebral ischemia using defective recombinant adeno-associated virus vectors |
| Q34114285 | Gene therapy in lysosomal diseases |
| Q41625113 | Gene therapy of Duchenne muscular dystrophy. |
| Q45881242 | Gene therapy of murine motor neuron disease using adenoviral vectors for neurotrophic factors |
| Q45866023 | Gene transfer into hippocampal slice cultures with an adenovirus vector driven by cytomegalovirus promoter: stable co-expression of green fluorescent protein and lacZ genes |
| Q33904294 | Gene transfer into rat brain using adenoviral vectors. |
| Q45081316 | Gene transfer to the cerebellum |
| Q45867822 | Gene transfer to the rhesus monkey brain using SV40-derived vectors is durable and safe |
| Q37967602 | Genetic approaches to study glial cells in the rodent brain. |
| Q45869609 | Helper-dependent adenovirus vectors: their use as a gene delivery system to neurons |
| Q45884040 | High-capacity, helper-dependent, "gutless" adenoviral vectors for gene transfer into brain |
| Q35891440 | Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector. |
| Q41526863 | Human Adenovirus Vectors for Gene Transfer into Mammalian Cells |
| Q64380983 | Humoral immune responses to adenovirus vectors in the brain |
| Q30495926 | Imaging and recording subventricular zone progenitor cells in live tissue of postnatal mice |
| Q54563329 | Immune Responses to Reporter Proteins and High Viral Dose Limit Duration of Expression with Adenoviral Vectors: Comparison of E2a Wild Type and E2a Deleted Vectors |
| Q40922367 | Immune responses to adenovirus vectors in the nervous system |
| Q44907561 | Immunological instability of persistent adenovirus vectors in the brain: peripheral exposure to vector leads to renewed inflammation, reduced gene expression, and demyelination |
| Q41321011 | In VivoAdenovirus-Mediated Gene Transfer of theEscherichia coliCytosine Deaminase Gene to Human Colon Carcinoma-Derived Tumors Induces Chemosensitivity to 5-Fluorocytosine |
| Q40798274 | In vivo adenovirus-mediated gene transfer and expression in ischemic rabbit spinal cord |
| Q40886793 | In vivo adenovirus-mediated gene transfer and the expression in ischemic and reperfused rat brain |
| Q64382369 | In vivo adenovirus-mediated gene transfer to newborn rat retinal pigment epithelial cells |
| Q43856184 | In vivo assessment of adenoviral vector-mediated gene expression of dopamine D(2) receptors in the rat striatum by positron emission tomography |
| Q48529105 | In vivo gene transfer into the adult mammalian central nervous system by continuous injection of plasmid DNA-cationic liposome complex |
| Q33216908 | In vivo transgene expression from an adenoviral vector is altered following a 6-OHDA lesion of the dopamine system. |
| Q47953700 | Infection Efficiency of Human and Mouse Embryonic Stem Cells Using Adenoviral and Adeno-Associated Viral Vectors |
| Q45861874 | Inflammatory responses and their impact on beta-galactosidase transgene expression following adenovirus vector delivery to the primate caudate nucleus |
| Q45862705 | Inhibiting AIDS in the central nervous system: gene delivery to protect neurons from HIV. |
| Q40097069 | Inhibition of hepatitis C virus infection and expression in vitro and in vivo by recombinant adenovirus expressing short hairpin RNA. |
| Q45870327 | Intracisternal rSV40 administration provides effective pan-CNS transgene expression |
| Q48443362 | Lateral connectivity and contextual interactions in macaque primary visual cortex |
| Q48165069 | Lipid mediated gene delivery in the adult rat brain: quantitative analysis of expression |
| Q45880758 | Lipofectin-facilitated transfer of cholecystokinin gene corrects behavioral abnormalities of rats with audiogenic seizures |
| Q40565599 | Liver-directed adenoviral gene transfer in murine succinate semialdehyde dehydrogenase deficiency. |
| Q44903416 | Local adenovirus-mediated CTLA4-immunoglobulin expression suppresses the immune responses to adenovirus vectors in the brain |
| Q48692017 | Long-Term Transgene Expression in Fetal Rat Suprachiasmatic Nucleus Neurografts Followingex VivoAdenoviral Vector-Mediated Gene Transfer |
| Q64377654 | Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene |
| Q42280576 | Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain |
| Q45742031 | Long-term gene expression in the anterior horn motor neurons after intramuscular inoculation of a live herpes simplex virus vector |
| Q34223710 | Low-efficiency of percutaneous adenovirus-mediated arterial gene transfer in the atherosclerotic rabbit |
| Q41051027 | Manganese superoxide dismutase protects nNOS neurons from NMDA and nitric oxide-mediated neurotoxicity. |
| Q74587447 | Manipulation of gene expression in the mammalian nervous system: application in the study of neurite outgrowth and neuroregeneration-related proteins |
| Q34135050 | Molecular therapy in a model neuroendocrine disease: developing clinical gene therapy for pituitary tumours. |
| Q40437473 | Myoblast transfer and gene therapy in muscular dystrophies |
| Q31424820 | NAC-1 is a brain POZ/BTB protein that can prevent cocaine-induced sensitization in the rat. |
| Q26802140 | Neuroanatomy goes viral! |
| Q41235622 | Neuronal progenitors as tools for cell replacement in the nervous system |
| Q34209742 | Noninvasive imaging of lipid nanoparticle-mediated systemic delivery of small-interfering RNA to the liver |
| Q33985663 | Nonneurotropic adenovirus: a vector for gene transfer to the brain and gene therapy of neurological disorders |
| Q64380685 | Novel method for the labeling of distant neuromuscular junctions |
| Q45881303 | Overexpression of interleukin-1 receptor antagonist in the mouse brain reduces ischemic brain injury |
| Q35161530 | Peripheral infection with adenovirus causes unexpected long-term brain inflammation in animals injected intracranially with first-generation, but not with high-capacity, adenovirus vectors: toward realistic long-term neurological gene therapy for ch |
| Q44686121 | Persistent phenotypic correction of central diabetes insipidus using adeno-associated virus vector expressing arginine-vasopressin in Brattleboro rats |
| Q34000123 | Phenotype correction in retinal pigment epithelium in murine mucopolysaccharidosis VII by adenovirus-mediated gene transfer |
| Q48628421 | Phenotypic alteration of astrocytes induced by ciliary neurotrophic factor in the intact adult brain, As revealed by adenovirus-mediated gene transfer. |
| Q45297193 | Prospectives for cell and gene therapy in Huntington's disease |
| Q64382515 | Rapid gene transfer into cultured hippocampal neurons and acute hippocampal slices using adenoviral vectors |
| Q34361466 | Regulatable and cell-type specific transgene expression in glial cells: prospects for gene therapy for neurological disorders |
| Q47832394 | Reproducible and efficient murine CNS gene delivery using a microprocessor-controlled injector |
| Q21142695 | Restoration of full-length SMN promoted by adenoviral vectors expressing RNA antisense oligonucleotides embedded in U7 snRNAs |
| Q33545312 | Restorative gene therapy approaches to Parkinson's disease |
| Q37273145 | Retargeted adenoviruses for radiation-guided gene delivery |
| Q42553132 | Retrograde adenoviral vector targeting of nociresponsive pontospinal noradrenergic neurons in the rat in vivo |
| Q44823262 | Retrograde labeling of mouse spinal descending tracts by a recombinant adenovirus |
| Q42117065 | Retrograde viral vector-mediated inhibition of pontospinal noradrenergic neurons causes hyperalgesia in rats. |
| Q33778711 | Retroviral transfection of the lacZ gene from Liz-9 packaging cells to glioma spheroids |
| Q34644825 | Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblasts |
| Q43655399 | Sequential histopathological changes in vivo after suicide gene therapy of gastric cancer induced by N-methyl-N'-nitro-N-nitrosoguanidine in rats |
| Q47227825 | Single intracerebroventricular bolus injection of a recombinant adenovirus expressing leptin results in reduction of food intake and body weight in both lean and obese Zucker fa/fa rats |
| Q41450039 | Somatic gene transfer approaches to manipulate neural networks |
| Q48291049 | Spinal cord injury: bridging the lesion and the role of neurotrophic factors in repair. |
| Q45867412 | Strategies for CNS-directed gene delivery: in vivo gene transfer to the brain using SV40-derived vectors |
| Q48348307 | Suppression of inflammation by dexamethasone prolongs adenoviral vector-mediated transgene expression in the facial nucleus of the rat. |
| Q48633480 | Targeted transduction of CNS neurons with adenoviral vectors carrying neurotrophic factor genes confers neuroprotection that exceeds the transduced population |
| Q34942440 | Techniques for gene transfer into neurons. |
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| Q48521197 | Transgene expression in rat fetal brain grafts is maintained for 7 months after ex vivo adenoviral vector-mediated gene transfer |
| Q41139955 | Transient gene transfer to neurons and glia: analysis of adenoviral vector performance in the CNS and PNS. |
| Q44515156 | Transplantation to the rat brain of human neural progenitors that were genetically modified using adenoviruses |
| Q45864999 | Tumour regression in a ligand inducible manner mediated by a chimeric tumour suppressor derived from p53. |
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