Biomedical subjects

J E Walsh

Publications and source records attributed to J E Walsh.

15 recordsLinked to original sources

PubMed1981

Molecular cloning of the complete Epstein-Barr virus genome as a set of overlapping restriction endonuclease fragments.

A complete collection of fragments of Epstein-Barr virus DNA, obtained by cleavage with restriction endonuclease Eco RI, has been cloned. Fourteen different internal fragments of the virus genome, derived from linear virion DNA of the B95-8 strain, and sequences corresponding to the terminal regions of virion DNA, derived from intracellular circular EBV DNA isolated from 895-8 cells, were cloned. Sizes of fragments were determined by agarose gel electrophoresis and their sum leads to an estimated molecular weight of 110 x 10(6) for virion DNA. Large Eco RI DNA fragments of special interest were also cloned in cosmids using another source of EBV DNA, that is, to circular viral DNA derived from Raji cells. In order to provide a set of overlapping sequences, all the 29 internal Bam HI fragments of B95-8 virion DNA were cloned in pBR322. The map location within the viral genome of each cloned DNA fragment was identified by hybridizing to blots of virion DNA cleaved with several different restriction endonucleases.

Cloning, Molecular↗

PubMed1980

Coding potential and regulatory signals of the polyoma virus genome.

The complete DNA sequence of the A2 strain of polyoma virus has been determined. It consists of 5,292 base pairs. The sequence is analysed in terms of its coding potential and sites of possible functional significance or structural interest. The polyoma virus genome is compared with those of related tumour viruses, simian virus 40 and BK virus.

Antigens, Viral↗

PubMed1980

Polyoma virus DNA: Sequence from the late region that specifies the leader sequence for late mRNA and codes for VP2, VP3, and the N-terminus of VP1.

The DNA sequence of part of the late region of the polyoma virus genome is presented. This sequence of 1,348 nucleotide pairs encompasses the leader region for late mRNA and the coding sequence for the two minor capsid proteins VP2 and VP3. The coding sequence for the N-terminus of the major capsid protein overlaps the C-terminus of VP2/VP3 by 32 nucleotide pairs. From the DNA sequence the sizes and sequences of VP2 and VP3 could be predicted. Potential splicing signals for the processing of late mRNA's could be identified. Comparisons are made between the sequence of polyoma virus DNA and corresponding regions of simian virus 40 DNA.

Amino Acid Sequence↗

PubMed1979

An invasive microwave antenna for locally-induced hyperthermia for cancer therapy.

A microwave system has been developed and characterized for delivering heat directly into tumors. This system employs a microwave power source (3-10W) operating in the 500 MHz to 1.3 GHz frequency range, coaxial transmission line, and a monopole antenna. Absorbed power was measured in saline, in tissue equivalent phantoms, and in tumors in live and dead mice. Antennas were designed to operate at 500 MHz and 1 GHz, and the critical design parameters have been identified for this system. Analytical and experimental results obtained in our laboratory suggest that this system is capable of providing controlled temperature distributions appropriate for hyperthermia in animal tumors. Theoretical results predict that 3 GHz may be an optimum choice for this system in animal tumors of approximately 1 cm diameter; the microwave antenna system provides a heat distribution superior to that obtained using a resistance heater of similar dimensions. We propose that further development of this approach may overcome some of the problems associated with other systems which use external radiation sources, and implications for clinical application of this system are discussed.

Animals↗

PubMed1979

Cancer therapy with localized hyperthermia using an invasive microwave system.

A system has been developed for producing local hyperthermia in small animal tumors by means of an invasive needle microwave antenna. Thermal distributions produced by this system using 1 GHz microwaves have been characterized in mammary adenocarcinomas (MTG-B) implanted in thighs of C3H mice. Therapeutic efficacy by hyperthermia was demonstrated by comparing MTG-B diameters in mice following control, sham or hyperthermia treatment. It is proposed that this system could be employed clinically to provide very local hyperthermia in deep-seated tumors.

Adenocarcinoma↗

PubMed1974