review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | William M Pardridge | Q33489592 |
P2860 | cites work | The blood-brain barrier: bottleneck in brain drug development | Q22336985 |
Avidin | Q28292166 | ||
Brain-specific expression of an exogenous gene after i.v. administration | Q33948080 | ||
EGF mutant receptor vIII as a molecular target in cancer therapy | Q33950534 | ||
Human insulin receptor monoclonal antibody undergoes high affinity binding to human brain capillaries in vitro and rapid transcytosis through the blood-brain barrier in vivo in the primate | Q34058435 | ||
Vector-mediated delivery of a polyamide ("peptide") nucleic acid analogue through the blood-brain barrier in vivo | Q34239620 | ||
EGFR and cancer prognosis | Q34399312 | ||
The effects of polycations on vascular permeability in the rat. A proposed role for charge sites | Q34607667 | ||
Neuroprotection with noninvasive neurotrophin delivery to the brain | Q34802946 | ||
Gene silencing in mammals by small interfering RNAs | Q34931992 | ||
Noninvasive gene targeting to the brain | Q35163431 | ||
Pharmacokinetics and blood-brain barrier transport of [3H]-biotinylated phosphorothioate oligodeoxynucleotide conjugated to a vector-mediated drug delivery system | Q38287477 | ||
Non–Sequence-Specific Inhibition of Transferrin Receptor Expression in HL-60 Leukemia Cells by Phosphorothioate Oligodeoxynucleotides | Q38337527 | ||
Comparative inhibition of chloramphenicol acetyltransferase gene expression by antisense oligonucleotide analogues having alkyl phosphotriester, methylphosphonate and phosphorothioate linkages | Q40389198 | ||
Imaging endogenous gene expression in brain cancer in vivo with 111In-peptide nucleic acid antisense radiopharmaceuticals and brain drug-targeting technology. | Q40506666 | ||
Intravenous RNA interference gene therapy targeting the human epidermal growth factor receptor prolongs survival in intracranial brain cancer | Q40550050 | ||
Antisense oligonucleotides as therapeutic agents--is the bullet really magical? | Q40834751 | ||
Transport across the primate blood-brain barrier of a genetically engineered chimeric monoclonal antibody to the human insulin receptor | Q40881449 | ||
An antibody-avidin fusion protein specific for the transferrin receptor serves as a delivery vehicle for effective brain targeting: initial applications in anti-HIV antisense drug delivery to the brain. | Q41694333 | ||
Imaging brain tumors by targeting peptide radiopharmaceuticals through the blood-brain barrier. | Q41712976 | ||
Targeting rat anti-mouse transferrin receptor monoclonal antibodies through blood-brain barrier in mouse. | Q41721402 | ||
Partial protection of oncogene, anti-sense oligodeoxynucleotides against serum nuclease degradation using terminal methylphosphonate groups | Q41760845 | ||
Neuroprotection in transient focal brain ischemia after delayed intravenous administration of brain-derived neurotrophic factor conjugated to a blood-brain barrier drug targeting system | Q43626844 | ||
Contribution of plasmid DNA to hepatotoxicity after systemic administration of lipoplexes | Q43653658 | ||
In vitro stability of alpha-helical peptide nucleic acids (alphaPNAs). | Q43723268 | ||
Receptor-mediated delivery of an antisense gene to human brain cancer cells | Q43947685 | ||
Rapid transferrin efflux from brain to blood across the blood-brain barrier | Q44085165 | ||
Widespread expression of an exogenous gene in the eye after intravenous administration. | Q44119141 | ||
RNAi in human cells: basic structural and functional features of small interfering RNA. | Q44199577 | ||
Intravenous nonviral gene therapy causes normalization of striatal tyrosine hydroxylase and reversal of motor impairment in experimental parkinsonism. | Q44305889 | ||
Organ-specific gene expression in the rhesus monkey eye following intravenous non-viral gene transfer | Q44613306 | ||
Enhanced neuroprotective effects of basic fibroblast growth factor in regional brain ischemia after conjugation to a blood-brain barrier delivery vector | Q44661842 | ||
Normalization of striatal tyrosine hydroxylase and reversal of motor impairment in experimental parkinsonism with intravenous nonviral gene therapy and a brain-specific promoter | Q44821882 | ||
Antisense gene therapy of brain cancer with an artificial virus gene delivery system | Q45731908 | ||
Stabilization of poly-L-lysine/DNA polyplexes for in vivo gene delivery to the liver | Q45856362 | ||
Liposome-mediated, nonviral gene transfer induces a systemic inflammatory response which can exacerbate pre-existing inflammation | Q45870694 | ||
Receptor-mediated gene targeting to tissues in vivo following intravenous administration of pegylated immunoliposomes | Q45880218 | ||
Disposition of the 14C-labeled phosphorothioate oligonucleotide ISIS 2105 after intravenous administration to rats. | Q46032203 | ||
Gene targeting in vivo with pegylated immunoliposomes | Q46173833 | ||
Delivery of beta-galactosidase to mouse brain via the blood-brain barrier transferrin receptor | Q46454399 | ||
In vivo knockdown of gene expression in brain cancer with intravenous RNAi in adult rats | Q48122926 | ||
PTEN decreases in vivo vascularization of experimental gliomas in spite of proangiogenic stimuli | Q48319236 | ||
Global non-viral gene transfer to the primate brain following intravenous administration | Q48393623 | ||
Decline in exogenous gene expression in primate brain following intravenous administration is due to plasmid degradation | Q48494993 | ||
Selective transport of an anti-transferrin receptor antibody through the blood-brain barrier in vivo | Q48643049 | ||
Central nervous system pharmacologic effect in conscious rats after intravenous injection of a biotinylated vasoactive intestinal peptide analog coupled to a blood-brain barrier drug delivery system. | Q48909700 | ||
Conjugation of brain-derived neurotrophic factor to a blood-brain barrier drug targeting system enables neuroprotection in regional brain ischemia following intravenous injection of the neurotrophin | Q49047711 | ||
Organ-specific expression of the lacZ gene controlled by the opsin promoter after intravenous gene administration in adult mice | Q57677348 | ||
Targeting genes: delivery and persistent expression of a foreign gene driven by mammalian regulatory elements in vivo | Q69752125 | ||
Electron microscopic visualization of insulin translocation into the cytoplasm and nuclei of intact H35 hepatoma cells using covalently linked Nanogold-insulin | Q72332030 | ||
Insulin receptors in human ocular tissues. Immunohistochemical demonstration in normal and diabetic eyes | Q73619625 | ||
Free cationic liposomes inhibit the inflammatory response to cationic lipid-DNA complex injected intravenously and enhance its transfection efficiency | Q78944400 | ||
P433 | issue | 2-3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 141-152 | |
P577 | publication date | 2007-03-16 | |
P1433 | published in | Advanced Drug Delivery Reviews | Q2825362 |
P1476 | title | shRNA and siRNA delivery to the brain | |
P478 | volume | 59 |
Q90230646 | Activation of cyclin D1 affects mitochondrial mass following traumatic brain injury |
Q30488727 | An engineered substance P variant for receptor-mediated delivery of synthetic antibodies into tumor cells |
Q37851969 | Antibody-targeted nanoparticles for cancer therapy |
Q46710298 | Cellular uptake of fluorescent labelled biotin-streptavidin microspheres |
Q60467863 | Chitosan and its derivatives as nanocarriers for siRNA delivery |
Q36345289 | Click synthesis of a polyamidoamine dendrimer-based camptothecin prodrug. |
Q37217876 | Concepts in in vivo siRNA delivery for cancer therapy |
Q38160246 | Delivery of RNAi therapeutics: work in progress |
Q34293708 | Delivery of siRNA therapeutics: barriers and carriers |
Q37481282 | Delivery of small-interfering RNA (siRNA) to the brain |
Q40286912 | Development of antibody-modified chitosan nanoparticles for the targeted delivery of siRNA across the blood-brain barrier as a strategy for inhibiting HIV replication in astrocytes. |
Q42646979 | Diagnosing and Treating Nervous System Disorders by Targeting Novel Classes of Non-coding RNAs |
Q37425213 | Differential receptor-mediated drug targeting to the diseased brain |
Q37590479 | Electro-Magnetic Nano-Particle Bound Beclin1 siRNA Crosses the Blood-Brain Barrier to Attenuate the Inflammatory Effects of HIV-1 Infection in Vitro |
Q48164145 | Elevated plasma CaM expression in patients with acute cerebral infarction predicts poor outcomes and is inversely associated with miR-26b expression |
Q35090897 | Functional motor recovery from brain ischemic insult by carbon nanotube-mediated siRNA silencing |
Q33732849 | Genetic approach for intracerebroventricular delivery |
Q39437235 | Glioma growth inhibition in vitro and in vivo by single chain variable fragments of the transferrin receptor conjugated to survivin small interfering RNA. |
Q35093276 | Gold nanorod--siRNA induces efficient in vivo gene silencing in the rat hippocampus |
Q38042256 | Immunoconjugates and long circulating systems: origins, current state of the art and future directions |
Q54957884 | Improved method for synthesis of low molecular weight protamine-siRNA conjugate. |
Q35846848 | Increased brain radioactivity by intranasal P-labeled siRNA dendriplexes within in situ-forming mucoadhesive gels |
Q33687594 | Intranasal drug delivery of small interfering RNA targeting Beclin1 encapsulated with polyethylenimine (PEI) in mouse brain to achieve HIV attenuation |
Q40070009 | Intravenous siRNA of brain cancer with receptor targeting and avidin-biotin technology |
Q89482934 | Intravenously Administered Novel Liposomes, DCL64, Deliver Oligonucleotides to Cerebellar Purkinje Cells |
Q37342330 | Knockdown of tyrosine hydroxylase in the nucleus of the solitary tract reduces elevated blood pressure during chronic intermittent hypoxia |
Q38756973 | Lentivirus mediated RNA interference of EMMPRIN (CD147) gene inhibits the proliferation, matrigel invasion and tumor formation of breast cancer cells |
Q39964739 | Manipulation of PKC isozymes by RNA interference and inducible expression of PKC constructs |
Q27002604 | MicroRNA Regulation of Brain Tumour Initiating Cells in Central Nervous System Tumours |
Q33346479 | MicroRNAs: regulators of oncogenesis and stemness |
Q43038942 | Molecular medicine: entry granted |
Q21223671 | Multifunctional Nanocarriers for diagnostics, drug delivery and targeted treatment across blood-brain barrier: perspectives on tracking and neuroimaging |
Q37948968 | Nanocarrier possibilities for functional targeting of bioactive peptides and proteins: state-of-the-art |
Q37800505 | Nanoparticulate Systems for Drug Delivery and Targeting to the Central Nervous System |
Q33420721 | Nanotechnology approach for drug addiction therapy: gene silencing using delivery of gold nanorod-siRNA nanoplex in dopaminergic neurons |
Q44066855 | Neuroprotective effects of microRNA-210 on hypoxic-ischemic encephalopathy |
Q37024768 | Nonviral delivery of synthetic siRNAs in vivo |
Q37360226 | Nonviral methods for siRNA delivery |
Q38091009 | Novel siRNA delivery strategy: a new "strand" in CNS translational medicine? |
Q37981217 | Nucleic-acid based gene therapeutics: delivery challenges and modular design of nonviral gene carriers and expression cassettes to overcome intracellular barriers for sustained targeted expression |
Q42225268 | Optimization and apoptosis induction by RNAi with UTMD technology in vitro |
Q46021217 | Physicochemical properties of a zinc phthalocyanine - pyrene conjugate adsorbed onto single walled carbon nanotubes. |
Q37780603 | Potential use of RNA interference in cancer therapy |
Q33574535 | REV3L confers chemoresistance to cisplatin in human gliomas: the potential of its RNAi for synergistic therapy |
Q47338076 | RNAi mechanisms in Huntington's disease therapy: siRNA versus shRNA. |
Q89638520 | SREBP1 siRNA enhance the docetaxel effect based on a bone-cancer dual-targeting biomimetic nanosystem against bone metastatic castration-resistant prostate cancer |
Q35848195 | Single reporter for targeted multimodal in vivo imaging |
Q37593705 | Site-specific antibody drug conjugates for cancer therapy |
Q37598928 | Strategies for short hairpin RNA delivery in cancer gene therapy |
Q37619111 | Strategies for targeted nonviral delivery of siRNAs in vivo |
Q38090672 | Strategies to assess blood-brain barrier penetration |
Q39427146 | Substance P derivatives as versatile tools for specific delivery of various types of biomolecular cargo |
Q92354290 | Synthesis and characterization of nanometer-sized liposomes for encapsulation and microRNA transfer to breast cancer cells |
Q47152520 | Targeted Delivery of siRNA Therapeutics to Malignant Tumors. |
Q41312221 | Targeted delivery of siRNA to macrophages for anti-inflammatory treatment |
Q41790608 | Targeting individual calpain isoforms for neuroprotection |
Q48238485 | Targeting the insulin receptor: nanoparticles for drug delivery across the blood-brain barrier (BBB). |
Q26858788 | The involvement of microRNAs in neurodegenerative diseases |
Q24657247 | The promises and pitfalls of RNA-interference-based therapeutics |
Q38268541 | Therapeutic face of RNAi: in vivo challenges |
Q44696669 | Transport of nanoparticles through the blood-brain barrier for imaging and therapeutic applications |
Q37270325 | Vessel microport technique for applications in cerebrovascular research |
Q36905867 | microRNAs: innovative targets for cerebral ischemia and stroke. |
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