scholarly journals In vivo lung morphometry with hyperpolarized 3 He diffusion MRI: Reproducibility and the role of diffusion-sensitizing gradient direction

2014 ◽  
Vol 73 (3) ◽  
pp. 1252-1257 ◽  
Author(s):  
James D. Quirk ◽  
Yulin V. Chang ◽  
Dmitriy A. Yablonskiy
2014 ◽  
Vol 73 (4) ◽  
pp. 1609-1614 ◽  
Author(s):  
Yulin V. Chang ◽  
James D. Quirk ◽  
Dmitriy A. Yablonskiy

Author(s):  
Jason C. Woods ◽  
Wei Wang ◽  
Dmitriy A. Yablonskiy ◽  
Rodney Kowalewski ◽  
Nguyet M. Nguyen

Author(s):  
A.S. Bdaiwi ◽  
M.M. Hossain ◽  
M.M. Willmering ◽  
H. Wang ◽  
N. Gupta ◽  
...  

2017 ◽  
Vol 79 (5) ◽  
pp. 2738-2744 ◽  
Author(s):  
Fernando Calamante ◽  
Ben Jeurissen ◽  
Robert E. Smith ◽  
Jacques‐Donald Tournier ◽  
Alan Connelly

2020 ◽  
Author(s):  
Raquel Garcia-Hernandez ◽  
Alejandro Trouve Carpena ◽  
Mark Drakesmith ◽  
Kristen Koller ◽  
Derek K. Jones ◽  
...  

AbstractWe present a strategy to image neuroinflammation in grey matter using diffusion-weighted MRI. We demonstrate that the MRI signal carries the fingerprint of microglia and astrocytes activation, and that specific signatures from each glia population can be extracted in vivo. In addition, we prove the translational value of the approach in a cohort of healthy humans. This framework will aid basic and clinical research to clarify the role of inflammation during lifespan.


Author(s):  
W.A. Jacob ◽  
R. Hertsens ◽  
A. Van Bogaert ◽  
M. De Smet

In the past most studies of the control of energy metabolism focus on the role of the phosphorylation potential ATP/ADP.Pi on the regulation of respiration. Studies using NMR techniques have demonstrated that the concentrations of these compounds for oxidation phosphorylation do not change appreciably throughout the cardiac cycle and during increases in cardiac work. Hence regulation of energy production by calcium ions, present in the mitochondrial matrix, has been the object of a number of recent studies.Three exclusively intramitochondnal dehydrogenases are key enzymes for the regulation of oxidative metabolism. They are activated by calcium ions in the low micromolar range. Since, however, earlier estimates of the intramitochondnal calcium, based on equilibrium thermodynamic considerations, were in the millimolar range, a physiological correlation was not evident. The introduction of calcium-sensitive probes fura-2 and indo-1 made monitoring of free calcium during changing energy metabolism possible. These studies were performed on isolated mitochondria and extrapolation to the in vivo situation is more or less speculative.


2020 ◽  
Vol 64 (2) ◽  
pp. 251-261
Author(s):  
Jessica E. Fellmeth ◽  
Kim S. McKim

Abstract While many of the proteins involved in the mitotic centromere and kinetochore are conserved in meiosis, they often gain a novel function due to the unique needs of homolog segregation during meiosis I (MI). CENP-C is a critical component of the centromere for kinetochore assembly in mitosis. Recent work, however, has highlighted the unique features of meiotic CENP-C. Centromere establishment and stability require CENP-C loading at the centromere for CENP-A function. Pre-meiotic loading of proteins necessary for homolog recombination as well as cohesion also rely on CENP-C, as do the main scaffolding components of the kinetochore. Much of this work relies on new technologies that enable in vivo analysis of meiosis like never before. Here, we strive to highlight the unique role of this highly conserved centromere protein that loads on to centromeres prior to M-phase onset, but continues to perform critical functions through chromosome segregation. CENP-C is not merely a structural link between the centromere and the kinetochore, but also a functional one joining the processes of early prophase homolog synapsis to late metaphase kinetochore assembly and signaling.


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