While some patients had a hypertrophic pancreas at the last follow-up, which reflected the capacity for pancreatic regeneration and some factors were associated with a lower volume of the remnant pancreas, the volume of the remnant pancreas seem not to be associated with pancreatogenic diabetes. There were no clinicopathologic factors identified associated with the risk for pancreatogenic diabetes.
This paper describes two general methods: field map processing and NMR lineshape analysis, that we are currently using for the ongoing research of field improvement techniques specifically applied to our 700 MHz LTS/HTS NMR magnet. The validity of the methods is verified with comparison between calculations and experiments. Also, a simple but effective analysis has been used to identify the principal source of a remanent magnetic field measured in the bore of the 700 MHz LTS/HTS NMR magnet: the Screening Current induced Field (SCF) from the 100-MHz HTS insert, comprised of 48 double pancake coils, each wound with Bi2223 tape.
A 700-mm bore superconducting magnet was built and operated in our laboratory to demonstrate the feasibility of newly developed MgB(2) superconductor wire for fabricating MRI magnets. The magnet, an assembly of 10 coils each wound with a reacted and s-glass insulated wire ~1-km long, was immersed in solid nitrogen rather than in a bath of liquid cryogen. This MgB(2) magnet was designed to operate in the temperature range 10-15 K, maintained by a cryocooler. A combination of this "wide" temperature range and immersion of the winding in solid nitrogen enables this magnet to operate under conditions not possible with a low temperature superconductor (LTS) counterpart. Tested individually at 13 K, each coil could carry current up to 100 A. When assembled into the magnet, some coils, however, became resistive, causing the magnet to prematurely quench at currents ranging from 79 A to 88 A, at which point the magnet generated a center field of 0.54 T. Despite the presence of a large volume (50 liters) of solid nitrogen in the cold body, cooldown from 77 K to 10 K went smoothly.
Summary
The roles of Notch1 and Notch2 in T‐cell function have been well studied, but the functional roles of Notch in B cells have not been extensively investigated, except for Notch2 involvement in peripheral marginal zone B‐cell differentiation. This study examined the roles of Notch1 in murine primary B cells. During B‐cell activation by B‐cell receptor ligation, Notch1 was up‐regulated while Notch2 was not. In addition, Notch1 up‐regulation itself did not contribute to the further activation of B cells, but the Notch ligand was important for Notch1‐mediated further B‐cell activation. Moreover, Notch1 deficiency significantly decreased B‐cell activation and antibody secretion under the presence of Notch ligand. These data suggest that Notch1 is an important mediator for enhancing B‐cell activation and antibody secretion by Notch ligand.
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