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E A Chiocca

Researcher at Harvard University

Publications -  22
Citations -  2333

E A Chiocca is an academic researcher from Harvard University. The author has contributed to research in topics: Herpes simplex virus & Genetic enhancement. The author has an hindex of 20, co-authored 22 publications receiving 2276 citations. Previous affiliations of E A Chiocca include Ohio State University.

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Diagnostic criteria for schwannomatosis

TL;DR: Diagnostic criteria for schwannomatosis are needed for both clinicians and researchers, but final diagnostic certainly will await the identification of the schWannom atosis locus itself.
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Herpes simplex virus type 1 DNA amplified as bacterial artificial chromosome in Escherichia coli : rescue of replication-competent virus progeny and packaging of amplicon vectors

TL;DR: The capacity of generating infectious and replication-competent HSV-1 progeny following transfection into mammalian cells was restored after insertion of a pac signal into fHSV delta pac, and the resulting amplicon stocks are virtually free of contaminating helper virus.
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Pattern of self-organization in tumour systems: complex growth dynamics in a novel brain tumour spheroid model.

TL;DR: The concept of least resistance, most permission and highest attraction as an essential principle for tumour invasion is introduced and these results support the hypothesis of a self‐organizing adaptive biosystem.
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Transfer and expression of the lacZ gene in rat brain neurons mediated by herpes simplex virus mutants.

TL;DR: Three mutants of herpes simplex virus type 1 (HSV-1) were used to deliver and express the Escherichia coli lacZ gene in cells of the rat central nervous system, providing a means for the in situ delivery and expression of specific genes in neurons in thecentral nervous system with little adverse effect on animals.
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Gene Transfer into Experimental Brain Tumors Mediated by Adenovirus, Herpes Simplex Virus, and Retrovirus Vectors

TL;DR: Three vectors derived from retrovirus, herpes simplex virus type 1 (HSV), and adenovirus were compared in cultured rat 9L gliosarcoma cells for gene transfer efficiency and in a 9L rat brain tumor model for histologic pattern and distribution of foreign gene delivery, as well as for associated tumor necrosis and inflammation.