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Black Hole

Lensing of space time around a black hole. At Oxford we study black holes observationally and theoretically on all size and time scales - it is some of our core work.

Credit: ALAIN RIAZUELO, IAP/UPMC/CNRS. CLICK HERE TO VIEW MORE IMAGES.

Joseph Silk

Emeritus Savilian Professor

Sub department

  • Astrophysics

Research groups

  • Beecroft Institute for Particle Astrophysics and Cosmology
joseph.silk@physics.ox.ac.uk
Telephone: 01865 (2)73300
Denys Wilkinson Building, room 532G
  • About
  • Publications

Have Atmospheric Cerenkov Telescopes Observed Dark Matter?

ArXiv astro-ph/0404205 (2004)

Authors:

Dan Hooper, Ignacio de la Calle Perez, Joseph Silk, Francesc Ferrer, Subir Sarkar

Abstract:

Two ground-based experiments have recently independently detected TeV $\gamma$-rays from the direction of the Galactic center. The observations made by the VERITAS and CANGAROO collaborations are unexpected, although not impossible to interpret in terms of astrophysical sources. Here we examine in detail whether the observed $\gamma$-rays may arise from the more exotic alternative of annihilations of dark matter particles clustered in the center of the Galaxy.
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MeV Dark Matter: Has It Been Detected?

Physical Review Letters 92 (2004) 101301 4pp

Authors:

JI Silk, C. Boehm, D. Hooper, M. Casse
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The VITAL assay: a versatile fluorometric technique for assessing CTL- and NKT-mediated cytotoxicity against multiple targets in vitro and in vivo.

J Immunol Methods 285:1 (2004) 25-40

Authors:

Ian F Hermans, Jonathan D Silk, Jianping Yang, Michael J Palmowski, Uzi Gileadi, Corinna McCarthy, Mariolina Salio, Franca Ronchese, Vincenzo Cerundolo

Abstract:

Assessment of cell-mediated toxicity has traditionally been achieved by measuring the specific activity of enriched effector cell populations against antigen-loaded target cells labeled with radioactive isotopes in vitro. Fluorometric techniques are viewed as a promising alternative to the use of radioactive isotopes for these analyses. Direct assessment of cytotoxicity in vivo can be achieved by monitoring survival of injected fluorescent targets relative to a differentially labeled internal control population without specific antigen. We have developed this approach, incorporating the use of multiple target cell populations labeled with different dyes so that cytotoxicity can be assessed against titrated doses of a given antigen, or against a range of different antigens, simultaneously. We show that this assay, referred to as the VITAL assay, can be used to assess cytotoxic activity of CTL and iNKT cells in vivo and in vitro. CTL responses measured in vivo could be correlated with antigen doses used in immunization strategies, and also with the size of specific CTL populations enumerated in the blood with fluorescent MHC/peptide tetramers. The VITAL assay is, therefore, a sensitive technique allowing analysis of complex multi-epitope responses.
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An erupting classical nova in a globular cluster of M87

ASTROPHYSICAL JOURNAL 605:2 (2004) L117-L120

Authors:

MM Shara, DR Zurek, EA Baltz, TR Lauer, J Silk
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Are domain walls ruled out?

ASTROPARTICLE PHYSICS 21:4 (2004) 443-449

Authors:

L Conversi, A Melchiorri, L Mersini, J Silk
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