| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0165-0270(96)00129-X |
| P8608 | Fatcat ID | release_ltkuwa6dsvgv5cnmlyfbkxfm4a |
| P698 | PubMed publication ID | 9125378 |
| P2093 | author name string | Houweling DA | |
| Verhaagen J | |||
| Hermens WT | |||
| Giger RJ | |||
| Holtmaat AJ | |||
| Dijkhuizen PA | |||
| P2860 | cites work | A new technique for the assay of infectivity of human adenovirus 5 DNA | Q27860797 |
| Characteristics of a human cell line transformed by DNA from human adenovirus type 5 | Q29547863 | ||
| Gene therapy for cystic fibrosis: challenges and future directions | Q35767578 | ||
| Molecular analysis of neuronal physiology by gene transfer into neurons with herpes simplex virus vectors | Q36708223 | ||
| Grafting genetically modified cells to the brain: possibilities for the future | Q39694407 | ||
| Nervous system modification by transplants and gene transfer | Q40582056 | ||
| In vivo and ex vivo gene transfer to the brain | Q40588469 | ||
| An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerve | Q40974241 | ||
| The principles of gene therapy for the nervous system | Q41120773 | ||
| Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis | Q41226051 | ||
| Characterization of 911: a new helper cell line for the titration and propagation of early region 1-deleted adenoviral vectors. | Q41237683 | ||
| FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirus-mediated gene transfer | Q41275978 | ||
| Characterization of an adenovirus gene transfer vector containing an E4 deletion | Q41286200 | ||
| Emergence of early region 1-containing replication-competent adenovirus in stocks of replication-defective adenovirus recombinants (delta E1 + delta E3) during multiple passages in 293 cells | Q41423332 | ||
| Somatic gene transfer approaches to manipulate neural networks | Q41450039 | ||
| Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice | Q41572953 | ||
| Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis | Q41607205 | ||
| In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium | Q41644008 | ||
| MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses. | Q41664847 | ||
| Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain | Q42280576 | ||
| Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis. | Q42483788 | ||
| Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis. | Q43535009 | ||
| The use of adenovirus vectors for intracerebral grafting of transfected nervous cells. | Q44038508 | ||
| Transplantation to the rat brain of human neural progenitors that were genetically modified using adenoviruses | Q44515156 | ||
| Anti-T cell receptor monoclonal antibody prolongs transgene expression following adenovirus-mediated in vivo gene transfer to mouse synovium. | Q44809129 | ||
| Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector | Q45769447 | ||
| Long-term hepatic adenovirus-mediated gene expression in mice following CTLA4Ig administration | Q45866667 | ||
| Recombinant IL-12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung. | Q45867442 | ||
| An adenovirus vector for gene transfer into neurons and glia in the brain | Q45874317 | ||
| Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors | Q45875094 | ||
| Transient expression of genes transferred in vivo into heart using first-generation adenoviral vectors: role of the immune response | Q45876235 | ||
| Adenovirus-mediated in vivo gene transfer and expression in normal rat liver | Q45878870 | ||
| A model system for in vivo gene transfer into the central nervous system using an adenoviral vector | Q48325479 | ||
| The facial "motor" nerve of the rat: control of vibrissal movement and examination of motor and sensory components | Q48344171 | ||
| Expression of a functional foreign gene in adult mammalian brain following in Vivo transfer via a herpes simplex virus type 1 defective viral vector | Q48675433 | ||
| Efficient adenoviral vector-directed expression of a foreign gene to neurons and sustentacular cells in the mouse olfactory neuroepithelium | Q48919784 | ||
| Organization of the facial nucleus in the rat. | Q49048171 | ||
| A neural cell-type-specific expression system using recombinant adenovirus vectors | Q49161577 | ||
| Adenoviral vector-mediated gene transfer and neurotransplantation: possibilities and limitations in grafting of the fetal rat suprachiasmatic nucleus. | Q52197420 | ||
| Adenoviral vector as a gene delivery system into cultured rat neuronal and glial cells. | Q54650303 | ||
| Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene | Q64377654 | ||
| Transfer of a foreign gene into the brain using adenovirus vectors | Q64377820 | ||
| Use of transient CD4 lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors | Q64382915 | ||
| Retrograde transfer of replication deficient recombinant adenovirus vector in the central nervous system for tracing studies | Q64383045 | ||
| Adenovirus gene transfer causes inflammation in the brain | Q64383186 | ||
| Oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells derived from adult rat spinal cord: in vitro characteristics and response to PDGF, bFGF and NT-3 | Q71488133 | ||
| Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis | Q71660966 | ||
| P433 | issue | 1 | |
| P921 | main subject | neuroglia | Q177105 |
| Adenoviridae | Q193447 | ||
| P304 | page(s) | 85-98 | |
| P577 | publication date | 1997-01-01 | |
| P1433 | published in | Journal of Neuroscience Methods | Q15764020 |
| P1476 | title | Transient gene transfer to neurons and glia: analysis of adenoviral vector performance in the CNS and PNS. | |
| P478 | volume | 71 |
| Q34987171 | Adeno-associated viral vectors as agents for gene delivery: application in disorders and trauma of the central nervous system. |
| Q28141743 | Adenoviral and adeno-associated viral transfer of genes to the peripheral nervous system |
| Q48653102 | Adenoviral vector-directed expression of neurotrophin-3 in rat dorsal root ganglion explants results in a robust neurite outgrowth response |
| 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 |
| Q43717552 | Adenovirus vector-directed expression of the neurotrophin-3 receptor (TrkC) in mouse astrocytes |
| Q41450015 | Adenovirus-mediated gene transfer to the brain: methodological assessment |
| Q45754375 | Analysis of a multi-mutant herpes simplex virus type 1 for gene transfer into sympathetic preganglionic neurons and a comparison to adenovirus vectors |
| Q41449995 | Antisense oligonucleotides induce functional deletion of ligand gated ion channels in cultured neurons and brain explants |
| Q41922961 | Comparative analysis of lentiviral vectors and modular protein nanovectors for traumatic brain injury gene therapy |
| Q44870612 | Evidence for the direct role of acetylcholinesterase in neurite outgrowth in primary dorsal root ganglion neurons. |
| 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. |
| Q42800909 | Extensive sprouting of sensory afferents and hyperalgesia induced by conditional expression of nerve growth factor in the adult spinal cord. |
| Q59361017 | Hypothalamic arcuate nucleus glucokinase regulates insulin secretion and glucose homeostasis |
| Q50745460 | Improved Golgi-like visualization in retrogradely projecting neurons after EGFP-adenovirus infection in adult rat and monkey. |
| Q48692017 | Long-Term Transgene Expression in Fetal Rat Suprachiasmatic Nucleus Neurografts Followingex VivoAdenoviral Vector-Mediated Gene Transfer |
| Q74587447 | Manipulation of gene expression in the mammalian nervous system: application in the study of neurite outgrowth and neuroregeneration-related proteins |
| Q28766660 | Methods, potentials, and limitations of gene delivery to regenerate central nervous system cells |
| Q37092541 | Modification of Schwann cell gene expression by electroporation in vivo |
| Q36387408 | Projections of preBötzinger complex neurons in adult rats. |
| Q64381948 | Promoter-independent regulation of cell-specific dopamine receptor expression |
| Q50754589 | Recombinant human nerve growth factor (rhNGF-β) gene transfer promotes regeneration of crush-injured mental nerve in rats. |
| Q48291049 | Spinal cord injury: bridging the lesion and the role of neurotrophic factors in repair. |
| Q48348307 | Suppression of inflammation by dexamethasone prolongs adenoviral vector-mediated transgene expression in the facial nucleus of the rat. |
| Q74248973 | The suprachiasmatic nucleus and the circadian time-keeping system revisited |
| Q48521197 | Transgene expression in rat fetal brain grafts is maintained for 7 months after ex vivo adenoviral vector-mediated gene transfer |
| Q45883608 | Viral vector-mediated gene expression in olfactory ensheathing glia implants in the lesioned rat spinal cord. |
Search more.