About: David T. Curiel

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

American cancer biologist

Attributes	Values
rdf:type	Item
description	American cancer biologist (en)
rdfs:label	David Curiel (cs) David T. Curiel (en) David T. Curiel (es) David T. Curiel (nl) David T. Curiel (ast)
skos:prefLabel	David Curiel (cs) David T. Curiel (en) David T. Curiel (es) David T. Curiel (nl) David T. Curiel (ast)
name	David Curiel (cs) David T. Curiel (en) David T. Curiel (es) David T. Curiel (nl) David T. Curiel (ast)
given name	wds:Q64384545-B0EAF1AD-F5C5-4E3A-9F43-DAAA26A09570
given name	David
instance of	wds:Q64384545-470B091C-23C8-4F9F-B54D-D615F24B7E4E
NL CR AUT ID	wds:Q64384545-E34545C5-6E07-4119-911E-EEB1E0CB4684
instance of	Homo sapiens
NL CR AUT ID	jn20031111029
skos:altLabel	Curiel (en) David Curiel (en) David T Curiel (en) Curiel D (en) Curiel D. (en) Curiel D. T. (en) Curiel DT (en) D Curiel (en) D T Curiel (en) D. Curiel (en) D. T. Curiel (en) David Terry Curiel (en)
occupation	wds:Q64384545-d127faa1-c1bc-4078-84b7-e65db6a5c6c2
NUKAT ID	wds:Q64384545-43476D6F-86F4-475A-913E-C9ED4D6B47D9
sex or gender	wds:Q64384545-87E561BB-BD54-4B63-AD23-42F73866A8ED
ISNI	wds:Q64384545-DDDB1CEC-2FC2-4701-836B-10F8EE71C569
VIAF ID	wds:Q64384545-323264CE-CE92-4EDE-9BAB-D175584067BE
IdRef ID	wds:Q64384545-9CBCF8C2-3CD1-496A-895D-4D870AFF1F32
date of birth	wds:Q64384545-5AC38090-8D4B-43C6-A382-66DBE4E7854C
family name	wds:q64384545-9e8722c5-491f-430d-d1aa-63991022c912
WorldCat Identities ID (superseded)	wds:Q64384545-3423996D-19FB-4747-9F0F-AB575B9753C9
National Library of Israel J9U ID	wds:Q64384545-F510192A-44EA-43F4-8511-9D6429C4434C
VIAF ID	http://viaf.org/viaf/21434052
IdRef ID	http://www.idref.fr/069231133/id
occupation	biologist
NUKAT ID	n2012144925
sex or gender	male
ISNI	0000000035186758
VIAF ID	21434052
IdRef ID	069231133
date of birth	1956-01-01 00:00:00Z (xsd:dateTime)
family name	Curiel
WorldCat Identities ID (superseded)	lccn-n97802979
National Library of Israel J9U ID	987007323431005171
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q64384545 David T. Curiel
is author of	Three-dimensional structure of canine adenovirus serotype 2 capsid Selected strategies to augment polynucleotide immunization Vorinostat and sorafenib synergistically kill tumor cells via FLIP suppression and CD95 activation Current issues and future directions of oncolytic adenoviruses Members of adenovirus species B utilize CD80 and CD86 as cellular attachment receptors Modulation of renal glomerular disease using remote delivery of adenoviral‐encoded solubletype II TGF‐β receptor fusion molecule Gene therapy for the treatment of cancer High-efficiency gene transfer employing adenovirus-polylysine-DNA complexes Targeting strategies for cancer radiotherapy In vivo localization of [(111)In]-DTPA-D-Phe1-octreotide to human ovarian tumor xenografts induced to express the somatostatin receptor subtype 2 using an adenoviral vector Enhancement of radiolabeled antibody binding and tumor localization through adenoviral transduction of the human carcinoembryonic antigen gene Approaches to enhance cancer radiotherapy employing gene transfer methods In vivo molecular chemotherapy and noninvasive imaging with an infectivity-enhanced adenovirus Specific membrane receptor gene expression targeted with radiolabeled peptide employing the erbB-2 and DF3 promoter elements in adenoviral vectors Localization of iodine-125-mIP-Des-Met14-bombesin (7-13)NH2 in ovarian carcinoma induced to express the gastrin releasing peptide receptor by adenoviral vector-mediated gene transfer Blockade of B7-H1 improves myeloid dendritic cell–mediated antitumor immunity Incorporating the survivin promoter in an infectivity enhanced CRAd-analysis of oncolysis and anti-tumor effects in vitro and in vivo. Cell cycle arrest and apoptosis induced by SART-1 gene transduction Antineoplastic effect of anti-erbB-2 intrabody is not correlated with scFv affinity for its target Improved gene transfer efficiency to primary and established human pancreatic carcinoma target cells via epidermal growth factor receptor and integrin-targeted adenoviral vectors Adenovirus-mediated ribozyme targeting of HER-2/neu inhibits in vivo growth of breast cancer cells Reciprocal regulation of plasmacytoid dendritic cells and monocytes during viral infection Inhibition of tumor necrosis factor alpha decreases inflammation and prolongs adenovirus gene expression in lung and liver Interleukin-6 induces both cell growth and VEGF production in malignant mesotheliomas The level of erbB2 expression predicts sensitivity to the cytotoxic effects of an intracellular anti-erbB2 sFv. An intracellular anti-erbB-2 single-chain antibody is specifically cytotoxic to human breast carcinoma cells overexpressing erbB-2. Engineering of adenovirus vectors containing heterologous peptide sequences in the C terminus of capsid protein IX. Genetic incorporation of a herpes simplex virus type 1 thymidine kinase and firefly luciferase fusion into the adenovirus protein IX for functional display on the virion Genetic incorporation of HSV-1 thymidine kinase into the adenovirus protein IX for functional display on the virion Fluorescently labeled adenovirus with pIX-EGFP for vector detection Derivation of a triple mosaic adenovirus based on modification of the minor capsid protein IX. Use of a novel cross-linking method to modify adenovirus tropism Paracrine expression of a native soluble vascular endothelial growth factor receptor inhibits tumor growth, metastasis, and mortality rate Adenovirus enhancement of transferrin-polylysine-mediated gene delivery Conditionally replicative adenoviral vectors for cancer gene therapy Maturation of dendritic cells accompanies high-efficiency gene transfer by a CD40-targeted adenoviral vector Treatment of ovarian cancer with a tropism modified oncolytic adenovirus. The flt-1 promoter for transcriptional targeting of teratocarcinoma. Self-assembling nanoclusters in living systems: application for integrated photothermal nanodiagnostics and nanotherapy A targetable, injectable adenoviral vector for selective gene delivery to pulmonary endothelium in vivo Re-expression of p16INK4a in mesothelioma cells results in cell cycle arrest, cell death, tumor suppression and tumor regression.

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