About: Xandra O. Breakefield

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

American neurologist

Attributes	Values
rdf:type	Item
description	investigador (es) wetenschapper (nl) дослідниця (uk) वैज्ञानिक (hi) American neurologist (en) طبيبة أعصاب أمريكية (ar)
rdfs:label	Xandra O. Breakefield (en) Xandra O. Breakefield (es) Xandra O. Breakefield (nl) Xandra O. Breakefield (ast)
skos:prefLabel	Xandra O. Breakefield (en) Xandra O. Breakefield (es) Xandra O. Breakefield (nl) Xandra O. Breakefield (ast)
name	Xandra O. Breakefield (en) Xandra O. Breakefield (es) Xandra O. Breakefield (nl) Xandra O. Breakefield (ast)
instance of	wds:Q63607934-28387602-49c8-1ff0-b868-12760c5d6b6d
instance of	Homo sapiens
award received	wds:Q63607934-0f5a79f2-47c4-6814-631f-8524a3a835ea
award received	Mika Salpeter Lifetime Achievement Award
Google Knowledge Graph ID	wds:Q63607934-26FE455E-2D5F-4142-B1CC-94CFBAB8C727
Google Knowledge Graph ID	http://g.co/kg/g/113qqgfjl
Google Knowledge Graph ID	/g/113qqgfjl
Google Scholar author ID	wds:Q63607934-504a86f0-4c64-a948-6c26-b08ccac85a45
Google Scholar author ID	X2FA3NoAAAAJ
skos:altLabel	X O Breakefield (en) X. O. Breakefield (en) X.O. Breakefield (en) Xandra Breakefield (en) Xandra O Breakefield (en) Xandra O Breakefield (nl) Xandra Owens Breakefield (en)
NORAF ID	wds:Q63607934-f6046ec3-4436-1de2-6a39-bb56bd694795
occupation	wds:Q63607934-1572d1a1-460f-deed-d64e-bb40bca5ac43
CiNii Research ID	wds:Q63607934-5AD36C52-263F-4DA1-80BE-B27DA045FCA0
sex or gender	wds:Q63607934-e72b94b2-4682-7a7c-bd34-d426ffa0894a
ISNI	wds:Q63607934-9fa2eb8e-475a-314c-33bb-170e57731216
VIAF ID	wds:Q63607934-16eb38d8-4b63-2cb1-0c73-645d3c177945
Library of Congress authority ID	wds:Q63607934-8cc7cde0-426e-ed32-e28e-fc11c5c6b41c
country of citizenship	wds:Q63607934-5ca0a4f3-4922-c62e-d502-b670b21a0ef4
NACSIS-CAT author ID	wds:Q63607934-d30f8bd3-43a6-1f31-f58c-08fbf7fe5745
National Library of Israel J9U ID	wds:Q63607934-d45ce64e-402b-53dd-52c5-ad181a63c089
NORAF ID	https://livedata.bibsys.no/authority/3054441
CiNii Research ID	https://cir.nii.ac.jp/crid/1140000791608426496.rdf
VIAF ID	http://viaf.org/viaf/8650249
Library of Congress authority ID	http://id.loc.gov/authorities/names/n78080984
NACSIS-CAT author ID	https://ci.nii.ac.jp/author/DA08176871#entity
NORAF ID	3054441
occupation	neurologist
CiNii Research ID	1140000791608426496
sex or gender	female organism
ISNI	0000000024109482
VIAF ID	8650249
Library of Congress authority ID	n78080984
country of citizenship	United States of America
NACSIS-CAT author ID	DA08176871
National Library of Israel J9U ID	987007332589605171
ORCID iD	wds:Q63607934-86BCC843-B373-433A-A8C8-68396E290245
ORCID iD	https://orcid.org/0000-0001-6036-0399
ORCID iD	0000-0001-6036-0399
is owl:sameAs of	Xandra O. Breakefield
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q63607934 Xandra Breakefield
is author of	miR-296 regulates growth factor receptor overexpression in angiogenic endothelial cells Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy Implanted fibroblasts genetically engineered to produce brain-derived neurotrophic factor prevent 1-methyl-4-phenylpyridinium toxicity to dopaminergic neurons in the rat. Degradation of fibrillar collagen in a human melanoma xenograft improves the efficacy of an oncolytic herpes simplex virus vector MiR-21 in the extracellular vesicles (EVs) of cerebrospinal fluid (CSF): a platform for glioblastoma biomarker development The TOR1A (DYT1) gene family and its role in early onset torsion dystonia TorsinA: movement at many levels Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cells Dopamine release is impaired in a mouse model of DYT1 dystonia Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier. FGF-2 regulation of neurogenesis in adult hippocampus after brain injury Genetically engineered microvesicles carrying suicide mRNA/protein inhibit schwannoma tumor growth Microvesicle-associated AAV vector as a novel gene delivery system Generation of stable retrovirus packaging cell lines after transduction with herpes simplex virus hybrid amplicon vectors Retrovirus-mediated gene therapy of experimental brain neoplasms using the herpes simplex virus-thymidine kinase/ganciclovir paradigm Transgene inheritance and retroviral infection contribute to the efficiency of gene expression in solid tumors inoculated with retroviral vector producer cells Selective killing of glioma cells in culture and in vivo by retrovirus transfer of the herpes simplex virus thymidine kinase gene Uptake and binding of dopamine and 6-hydroxydopamine in murine neuroblastoma and fibroblast cells Nerve growth factor released by transgenic astrocytes enhances the function of adrenal chromaffin cell grafts in a rat model of Parkinson's disease Introduction to Extracellular Vesicles: Biogenesis, RNA Cargo Selection, Content, Release, and Uptake Extracellular Vesicles: Unique Intercellular Delivery Vehicles Therapeutic applications of extracellular vesicles: clinical promise and open questions Tumour microvesicles contain retrotransposon elements and amplified oncogene sequences Gene delivery to glioma cells in rat brain by grafting of a retrovirus packaging cell line A defective HSV-1 vector expresses Escherichia coli beta-galactosidase in cultured peripheral neurons Therapeutic efficiency and safety of a second-generation replication-conditional HSV1 vector for brain tumor gene therapy. TorsinA and heat shock proteins act as molecular chaperones: suppression of alpha-synuclein aggregation Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene Dystonia-causing mutant torsinA inhibits cell adhesion and neurite extension through interference with cytoskeletal dynamics Untethering the nuclear envelope and cytoskeleton: biologically distinct dystonias arising from a common cellular dysfunction Protein typing of circulating microvesicles allows real-time monitoring of glioblastoma therapy TorsinA in the nuclear envelope Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain

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