An apparatus and method are provided for transmitting control information and data in an SC-FDMA communication system. The method includes placing a reference signal onto one middle symbol among a plurality of symbols in one slot, wherein the one slot is one of two slots in one subframe; placing CQI information onto at least one symbol of other symbols except for the one middle symbol; placing the data onto the other symbols except for the one middle symbol; placing a HARQ-ACK onto two symbols, wherein the two symbols are directly adjacent to the one middle symbol; and transmitting a signal including the reference signal, the data, the CQI information, and the HARQ-ACK. The HARQ-ACK is placed onto a position of at least part of the data. The symbols are SC-FDMA symbols, the one middle symbol is a 4th symbol, the two symbols are a 3rd symbol and a 5th symbol.

Methods and systems for producing a magnetic resonance (MR) image of a subject include acquiring a first physiological monitoring signal related to a first physiological process of the subject and acquiring a second physiological monitoring signal related to a second physiological process of the subject. The method also includes analyzing the first physiological monitoring signal and the second physiological monitoring signal to identify at least a first trigger point and a second trigger point and, upon identifying the first trigger point, applying a radiofrequency (RF) saturation module at a selected frequency to saturate a selected spin species in the subject. Upon identifying the second trigger point, the method includes performing a chemical exchange striation transfer (CEST) readout to acquire CEST data and then reconstructing the CEST data to produce a CEST image of the subject.

CEST imaging technique and MR scanning are used as an MRI method for detecting levels of lactate in vivo by exploiting the exchange of —OH protons on lactate with bulk water. In accordance with this method, one first obtains a lactate CEST MRI map of a slice of the body of a patient. A contrast agent such as pyruvate, glucose or glutamine is administered and a post-administration CEST MRI map is obtained. The difference in the spatial maps indicates the level of expression of lactate in the tissue of interest.

In a method of performing magnetic resonance (MR) imaging, an MR apparatus, and a computer-readable medium during a first cardiac cycle of a subject, a first imaging sequence is generated for application to a subject. The first imaging sequence has a preparatory pulse and an inversion recovery pulse following the preparatory pulse. First signals emitted from the subject in response to the first imaging sequence are detected, and first image data are generated based on the first signals. During a second cardiac cycle following the first cardiac cycle, a second imaging sequence is generated for application to the subject. The second imaging sequence has a preparatory pulse. Second signals emitted from the subject in response to the second imaging sequence are detected, and second image data are generated based on the second signals.

A magnetic resonance CEST imaging sequence and device based on a frequency stabilization module are provided. It includes following steps: first, in the frequency stabilization module, exciting a target slice with a small-flip-angle radio frequency pulse, and collecting three lines of non-phase-encoded k-space data; second, obtaining an estimated value of the frequency drift of the main magnetic field by calculating the phase difference between the three lines of non-phase encoded k-space data; third, adjusting a center frequency of the radio frequency pulse based on the calculation result of the frequency drift of the main magnetic field, to realize a real-time correction of the frequency drift of the main magnetic field; and fourth, performing conventional magnetic resonance CEST imaging.

A magnetic resonance imaging apparatus according to an embodiment includes sequence controlling circuitry and processing circuitry. The sequence controlling circuitry is configured to execute a first pulse sequence including application of a Magnetization Transfer (MT) pulse and to subsequently execute a second pulse sequence including application of an MT pulse after an action that causes a change in a physiological state of a patient. The processing circuitry is configured to generate a first Z-spectrum based on data obtained by executing the first pulse sequence, to generate a second Z-spectrum based on data obtained by executing the second pulse sequence, and to generate data by performing an analysis based on the first Z-spectrum and the second Z-spectrum.

A method to detect transient binding of a substrate molecule of interest in solution to a molecular target includes selecting the substrate molecule of interest and the molecular target such that the substrate molecule of interest can transiently bind to the molecular target; placing one of a sample or a subject of interest in a magnetic resonance (MR) apparatus, the sample or the subject of interest containing the substrate molecule of interest so as to be in contact with the molecular target; providing magnetic labelling of non-exchangeable or slowly exchangeable MR sensitive nuclei of the substrate molecule of interest; receiving an MR signal from the MR sensitive nuclei of the solvent molecules using the MR apparatus; and analyzing the MR signal to obtain a quantity associated with the transient binding of the substrate molecule of interest to the molecular target.

The invention relates to a method of CEST or APT MR imaging of at least a portion of a body (10) placed in a main magnetic field B.sub.0 within the examination volume of a MR device. The method of the invention comprises the following steps: •a) subjecting the portion of the body (10) to a saturation RF pulse at a saturation frequency offset; •b) subjecting the portion of the body (10) to an imaging sequence comprising at least one excitation/refocusing RF pulse and switched magnetic field gradients, whereby MR signals are acquired from the portion of the body (10) as spin echo signals; •c) repeating steps a) and b) two or more times, wherein the saturation frequency offset and/or a echo time shift in the imaging sequence are varied, such that a different combination of saturation frequency offset and echo time shift is applied in two or more of the repetitions; •d) reconstructing a MR image and/or B.sub.0 field homogeneity corrected APT/CEST images from the acquired MR signals. Moreover, the invention relates to a MR device (1) for carrying out the method of the invention and to a computer program to be run on a MR device.

Thermography of an ablation site is carried out by navigating a probe into contact with target tissue in the heart, obtaining a first position of a position sensor in the probe and acquiring a first magnetic resonance thermometry image of the target tissue. The method is further carried out during ablation by iteratively reading the position sensor to obtain second positions, and acquiring a new magnetic resonance thermometry image of the target tissue when the distance between the first position and one of the second positions is less than a predetermined distance. The images are analyzed to determine the temperature of the target tissue.

The disclosure relates to techniques for perming chemical exchange saturation transfer (CEST) imaging correction. The present disclosure improves the speed of correcting CEST images.