Study on the segregation behavior of Ce in CLYC crystals

2021 ◽  
pp. 126308
Author(s):  
Xianggang Zhang ◽  
Zhe Kang ◽  
Zhuochen Cai ◽  
Huiwen Zhai ◽  
Ziang Yin ◽  
...  
Keyword(s):  
Genetics ◽  
2000 ◽  
Vol 156 (2) ◽  
pp. 775-783 ◽  
Author(s):  
Renée LeMaire-Adkins ◽  
Patricia A Hunt

Abstract A fundamental principle of Mendelian inheritance is random segregation of alleles to progeny; however, examples of distorted transmission either of specific alleles or of whole chromosomes have been described in a variety of species. In humans and mice, a distortion in chromosome transmission is often associated with a chromosome abnormality. One such example is the fertile XO female mouse. A transmission distortion effect that results in an excess of XX over XO daughters among the progeny of XO females has been recognized for nearly four decades. Utilizing contemporary methodology that combines immunofluorescence, FISH, and three-dimensional confocal microscopy, we have readdressed the meiotic segregation behavior of the single X chromosome in oocytes from XO females produced on two different inbred backgrounds. Our studies demonstrate that segregation of the univalent X chromosome at the first meiotic division is nonrandom, with preferential retention of the X chromosome in the oocyte in ∼60% of cells. We propose that this deviation from Mendelian expectations is facilitated by a spindle-mediated mechanism. This mechanism, which appears to be a general feature of the female meiotic process, has implications for the frequency of nondisjunction in our species.


2021 ◽  
Vol 547 ◽  
pp. 152834
Author(s):  
Kun Wang ◽  
Chad M. Parish ◽  
Kevin G. Field ◽  
Lizhen Tan ◽  
Yutai Katoh

2013 ◽  
Vol 52 (15) ◽  
pp. 5489-5497 ◽  
Author(s):  
Yong Zhang ◽  
Wenqi Zhong ◽  
Baosheng Jin ◽  
Rui Xiao

Author(s):  
Hiroaki Nakade ◽  
Eita Tochigi ◽  
Bin Feng ◽  
Ryo Ishikawa ◽  
Hiromichi Ohta ◽  
...  

Author(s):  
Runjia Liu ◽  
Yong Zang ◽  
Rui Xiao

Abstract Detailed understanding the particle mixing and segregation dynamic is essential in successfully designing and reasonably operating multicomponent fluidized bed. In this work, a novel fluorescent tracer technique combining image processing method has been used to investigate the mixing and segregation behavior in a binary fluidized bed with wide size distributions. The particle number percentage in each layer for different gas velocities is obtained by an image processing method. Fluidization, mixing and segregation behavior has been discussed in terms of bed pressure drop, gas velocity and mixing index. Different types of binary particle systems, including the jetsam and the flotsam-rich system, are analyzed and compared. The mixing indexes at different minimum fluidization velocities are also analyzed and compared with other work. The results show that the theoretical minimum fluidization velocity calculated from the bed pressure drop cannot represent the whole fluidization for a wide size distribution binary particle system. The effect of a wide size distribution is an inflection point in the mixing index curve. There is also a dead region in the bottom of the bed that consists of particles with large size and a low degree of sphericity. The particles in the dead region are extraordinarily difficult to fluidize and should be considered in the design of fluidized beds in industrial applications.


1997 ◽  
Vol 17 (12) ◽  
pp. 7061-7068 ◽  
Author(s):  
A Ansari ◽  
M R Gartenberg

Circular plasmids containing telomeric TG1-3 arrays or the HMR E silencer segregate efficiently between dividing cells of the yeast Saccharomyces cerevisiae. Subtelomeric X repeats augment the TG1-3 partitioning activity by a process that requires the SIR2, SIR3, and SIR4 genes, which are also required for silencer-based partitioning. Here we show that targeting Sir4p to DNA directly via fusion to the bacterial repressor LexA confers efficient mitotic segregation to otherwise unstable plasmids. The Sir4p partitioning activity resides within a 300-amino-acid region (residues 950 to 1262) which precedes the coiled-coil dimerization motif at the extreme carboxy end of the protein. Using a topology-based assay, we demonstrate that the partitioning domain also retards the axial rotation of LexA operators in vivo. The anchoring and partitioning properties of LexA-Sir4p chimeras persist despite the loss of the endogenous SIR genes, indicating that these functions are intrinsic to Sir4p and not to a complex of Sir factors. In contrast, inactivation of the Sir4p-interacting protein Rap1p reduces partitioning by a LexA-Sir4p fusion. The data are consistent with a model in which the partitioning and anchoring domain of Sir4p (PAD4 domain) attaches to a nuclear component that divides symmetrically between cells at mitosis; DNA linked to Sir4p by LexA serves as a reporter of protein movement in these experiments. We infer that the segregation behavior of telomere- and silencer-based plasmids is, in part, a consequence of these Sir4p-mediated interactions. The assays presented herein illustrate two novel approaches to monitor the intracellular dynamics of nuclear proteins.


Vacuum ◽  
1990 ◽  
Vol 41 (1-3) ◽  
pp. 446-448 ◽  
Author(s):  
H Dreyssé ◽  
G Ceder ◽  
D de Fontaine ◽  
L.T. Wille

Silicon ◽  
2017 ◽  
Vol 10 (4) ◽  
pp. 1283-1290 ◽  
Author(s):  
Xiaolong Bai ◽  
Boyuan Ban ◽  
Jingwei Li ◽  
Zhiqiang Fu ◽  
Zhijian Peng ◽  
...  

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