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Results for “spatial localization”

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At least 73 records · Page 4Linked to original sources
PubMed1984

Depth pulse sequences for surface coils: spatial localization and T1 measurements.

The depth pulse sequences theta;[2 theta(+/- x, +/- y)]2 and 2 theta;theta(+/- x);[2 theta(+/- x, +/- y)]2 have been implemented with a 20 mm diameter two-turn surface coil operating at 31P resonance (89.96 MHz). In these sequences theta refers to the pi/2 rf pulse at the center of the sensitive region of the coil, +/- x and +/- y denote the four orthogonal phases of the rf pulses, and ";" represents an optional brief delay (e.g., 4 microseconds) between pulses to facilitate switching between different phases. Localization of the sensitive region was demonstrated with phantom samples by in vivo monitoring of rat livers and detection of necrotic regions of subcutaneously implanted tumors. The inversion-recovery pulse sequence, 2 theta-tau-theta(+/- x);[2 theta(+/- x, +/- y)]2, where tau is a variable delay, was employed to measure the spin-lattice relaxation time of a selected region, which could be varied by changing the pulse width and the size of the surface coil.

Animals↗
PubMed1985

SHARP NMR biomedical spatial localization.

An application of the Slepian-Pollak-Landau "time and band limited functions" is found in NMR imaging. The precise context is best described by the rotating-frame dynamics of the Bloch equations, where an analogy is made to the problem of simultaneously concentrating a function in time and frequency. The appropriately modulated rf fields are found to yield excellent response characteristics when used in numerical simulations of the Bloch equations.

Magnetic Resonance Spectroscopy↗
PubMed1990

A homonuclear shift correlated and spatially localized spectroscopy using stimulated echoes.

A new method which combines localized high-resolution proton NMR spectroscopy with two-dimensional correlated spectroscopy using stimulated echoes is presented. Stimulated-echo correlated spectroscopy (STECSY) is a straightforward extension of the STEAM method. Experiments with phantoms illustrate the efficacy of STECSY. An in situ application on rat adipose tissue demonstrates that STECSY is a helpful tool with which to select and assign resonances in complex 1H NMR spectra.

Adipose Tissue↗
PubMed1995

Spatial localization: tests of a two-process model.

The present study examined the recently proposed two-process model of localization performance in which a shift of attention, providing coarse location information, is followed by a saccadic eye movement, providing fine location information. In experiment 1 the nature of the localization response was manipulated. In contrast to the indirect response mode used in the study by Adam et al., i.e., manipulating the "arrow" keys to move the cursor to the target location, experiment 1 required subjects to point to the target location. The high degree of similarity between the pattern of results obtained with the pointing and cursor response indicated that performance in the localization paradigm was not differentially affected by the nature of the required response. In experiment 2 the characteristics of the backward masking stimulus was manipulated by employing three masking conditions: (1) a long-duration mask; (2) a short-duration mask (100 ms); and (3) a no-mask condition. Results showed that the long-duration mask caused interference at short and facilitation at long intervals between onset of target and mask; the short-duration mask caused interference only at short intervals. Overall the findings were consistent with the two-process model of localization performance.

Adult↗
PubMed1994

Temporal and spatial localization of type I and II collagens in human thyroid cartilage.

Thyroid cartilages of various ages were investigated by immunofluorescence staining for localization of the fibrillar collagen types I and II in order to understand the tissue remodeling occurring during the mineralization and ossification of thyroid cartilage. In fetal and juvenile thyroid cartilages, type I collagen was restricted to the inner and outer perichondrium, while type II collagen was localized in the matrix of hyaline cartilage. However, in advanced ages, type I collagen was also localized in the pericellular and in the interterritorial matrix of intermediate and central chondrocytes of thyroid cartilage. The matrix of peripheral chondrocytes was negative for type I collagen. This suggest that some chondrocytes in thyroid cartilage undergo a differentiation to type I collagen-producing chondrocytes. At the beginning of ossification, bone-related type I collagen was chiefly detected in the central cartilage layer, but was never deposited first from the perichondrium in the direction to the subperichondrial cartilage. This observation confirmed previous findings showing that osteogenesis mainly follows an endochondral ossification pattern. Interterritorial matrix failed to react with the type II collagen antibody in men from the beginning of the third decade, and later still in women, even after treatment with hyaluronidase. These observations indicate that major matrix changes occur faster in male than in female thyroid cartilage.

Adolescent↗
PubMed1985

Colliding targets: evidence for spatial localization within the motion system.

The ability to judge the relative location of moving targets is seriously degraded if the targets move in different directions. The vernier acuity for a target in which the two components move in the same direction is not impaired until target velocity exceeds about 4 deg/sec. If the components are moving along trajectories which differ in direction by more than 15 deg, vernier thresholds rise significantly at target speeds greater than 1 deg/sec. The conditions which affect stationary vernier acuity, i.e. separation of target components, duration, and orientation, do not account for the loss in acuity. Our results suggest that localization for moving targets depends on directionally-selective motion detectors.

Female↗
PubMed1985

Accuracy of spatial localizations near the time of saccadic eye movements.

Two-dimensional eye movements were recorded while subjects used a hammer to strike targets that were flashed-on briefly before, during or up to 750 msec after a horizontal saccade. Mean position of hammer blows was 20 min arc (SD = 67 min arc) from the target when the only cue to target location was eye position. Position of responses varied slightly with time of target exposure relative to the saccade. These results show that observers can closely monitor small changes in eye position during and near the time of saccadic eye movements.

Eye Movements↗
PubMed1993

Spatially localized neuronal cell lineages in the developing mammalian forebrain.

The role of cell lineage in the organization of the cerebral cortex and striatum of the developing rat forebrain was analysed using retroviral-mediated gene transfer to mark the progeny of individual progenitors. Injections around the onset of neurogenesis (embryonic day 14) produced neuronal- and glial-specific clones in the striatum and cortex. The majority of the neuronal clones were restricted to either the deep or superficial layers of the cortex and to either the striatal patch or matrix compartments of the striatum. Moreover, modeling the distributions of the neuronal clones in various ways revealed that grouping the clones into deep vs superficial cortical compartments and patch vs matrix striatal compartments best accounted for the clone distributions. These results suggest that at the onset of neurogenesis there is a heterogeneity of neuronal progenitors within the proliferative ventricular zone.

Animals↗
PubMed1990

Distinct spatial localization of specific mRNAs in cultured sympathetic neurons.

We examined the subcellular distribution of specific mRNAs in cultured sympathetic neurons. Under appropriate conditions, sympathetic neurons extend both axons and dendrites that are distinguishable by light microscopic and immunocytochemical criteria. In situ hybridization revealed a differential localization of mRNA within dendrites. mRNA encoding MAP2 was abundant in cell bodies and distributed nonhomogeneously throughout the dendritic compartment, but was not detected in axons. In contrast, mRNAs encoding GAP-43 and alpha-tubulin were restricted to the cell body and largely excluded from dendrites as well as axons. Detergent extraction revealed that most dendrite-associated mRNA encoding MAP2 was associated with the Triton X-100 insoluble fraction of the cell. The subset of mRNAs present in the dendritic compartment may encode proteins involved in the morphogenesis and remodeling of dendrites.

Animals↗
PubMed1994

Spatial localization of pre-mRNA transcription and processing within the nucleus.

The organization of transcription, processing, and transport of pre-mRNA within the nucleus is a major unsolved problem in cell biology. Several recent studies have helped to define the localization of specific DNAs, RNAs, and proteins within the nucleus and have led to various models for higher level organization of pre-mRNA metabolism.

Animals↗