A method for magnetic resonance imaging (MRI) is provided. A magnetic resonance excitation is provided. A magnetic field is read out through k-space using winders, wherein some of the winders overlap for a length of the winders.
An apparatus for use in a magnetic resonance (MR) system, which generates an external MR magnetic field, is provided. A rotor comprises a rotor shaft with an axis along a length of the rotor shaft and a plurality of coils on the rotor shaft.
A method for imaging unknown objects in a computed tomography (CT) system, comprising determining ray gain for a known object is provided. A CT reconstruction is performed with the known object to obtain reconstructed values.
In tensor MRI, a set of k-space MRI data points is acquired that includes one or more k-space subsets of MRI data points. An object orientation (or spatial transformation) corresponding to each of the k-space subsets is determined.
A method of providing selective spectral suppression in balanced SSFP magnetic resonance imaging for a first and second species is provided. A plurality of balanced SSFP images are acquired.
A computer implemented method for designing a spectral-spatial pulse for exciting at least one passband and minimally exciting at least one stopband is provided. A uniform shaped spectral envelope is generated.
We have recently shown that rab9 plays a key role in the transport of proteins between late endosomes and the trans Golgi network. Purified, recombinant, rab9 protein stimulated transport in a cell free system that reconstitutes this event.
RNKp30 monoclonal antibodies were generated by immunizing BALB/c mice with rNKp30-Fc fusion protein. The rNKp30-Fc fusion protein is a soluble protein consisting of the extracellular domain of rNKp30 fused to the Fc domain of human IgG1.
Stanford and IBM researchers have recently patented methods for making a new class of multi-branched macromolecules with well-defined molecular weights and surface structures.
Researchers in Prof. Liqun Luo's laboratory have developed a mouse model system for in vivo, non-invasive, spatially- and temporally-controlled labeling of individual synapses.