Results 71 to 80 of about 875,624 (353)
Probing M-theory with tetrahedron instantons
The duality between type IIA superstring theory and M-theory enables us to lift bound states of D0-branes and n parallel D6-branes to M-theory compactified on an n-centered multi-Taub-NUT space TN $$ \mathbbm{TN} $$ n .
Elli Pomoni, Wenbin Yan, Xinyu Zhang
doaj +1 more source
Ten dimensional type IIA and IIB theories with p-branes are compactified to 8-dimensions. It is shown that resulting branes can be classified according to the representations of $\bf {SL(3,Z) \times SL(2,Z)}$.
Maharana, Jnanadeva
core +2 more sources
Dynamics of M-theory vacua [PDF]
At very early times, the universe was not in a vacuum state. Under the assumtion that the deviation from equillibrium was large, in particular that it is higher than the scale of inflation, we analyse the conditions for local transitions between states ...
Donoghue, John F.
core +3 more sources
The Hydrodynamics of M-Theory [PDF]
We consider the low energy limit of a stack of N M-branes at finite temperature. In this limit, the M-branes are well described, via the AdS/CFT correspondence, in terms of classical solutions to the eleven dimensional supergravity equations of motion.
openaire +3 more sources
Holographic Superconductivity in M Theory [PDF]
Using seven-dimensional Sasaki-Einstein spaces we construct solutions of D=11 supergravity that are holographically dual to superconductors in three spacetime dimensions. Our numerical results indicate a new zero temperature solution dual to a quantum critical point.
Toby Wiseman+2 more
openaire +3 more sources
M theory fivebrane and SQCD [PDF]
Talk presented at Strings `97 in Amsterdam (June 16 - 21, 1997)
Hirosi Ooguri, Hirosi Ooguri
openaire +6 more sources
The dual nature of TDC – bridging dendritic and T cells in immunity
TDC are hematopoietic cells combining dendritic and T cell features. They reach secondary lymphoid organs (SLOs) and peripheral organs (liver and lungs) after FLT3‐dependent development in the bone marrow and maturation in the thymus. TDC are activated and enriched in SLOs upon viral infection, suggesting that they might play unique immune roles, since
Maria Nelli, Mirela Kuka
wiley +1 more source
The Lin, Lunin, Maldacena (LLM) ansatz in D = 11 supports two independent Killing directions when a general Killing spinor ansatz is considered. Here we show that these directions always commute, identify when the Killing spinors are charged, and show ...
A Donos+42 more
core +2 more sources
In vivo IL‐10 produced by tissue‐resident tolDC is involved in maintaining/inducing tolerance. Depending on the agent used for ex vivo tolDC generation, cells acquire common features but prime T cells towards anergy, FOXP3+ Tregs, or Tr1 cells according to the levels of IL‐10 produced. Ex vivo‐induced tolDC were administered to patients to re‐establish/
Konstantina Morali+3 more
wiley +1 more source