scholarly journals Oscillation Symmetry Applied to Nuclear Level Widths and Masses

2018 ◽  
Vol 2 (2) ◽  
pp. 5-22
Author(s):  
B. Tatischeff ◽  
Keyword(s):  
2021 ◽  
pp. 136173
Author(s):  
Deepak Pandit ◽  
Balaram Dey ◽  
Srijit Bhattacharya ◽  
T.K. Rana ◽  
Debasish Mondal ◽  
...  

2009 ◽  
Vol 79 (2) ◽  
Author(s):  
K. Van Houcke ◽  
S. M. A. Rombouts ◽  
K. Heyde ◽  
Y. Alhassid

1992 ◽  
Vol 293 (3-4) ◽  
pp. 282-286 ◽  
Author(s):  
D.S. Brenner ◽  
R.F. Casten ◽  
W.-T. Chou ◽  
J.-Y. Zhang ◽  
K. Heyde ◽  
...  
Keyword(s):  

2018 ◽  
Vol 115 (17) ◽  
pp. 4429-4434 ◽  
Author(s):  
Thies Gehrmann ◽  
Jordi F. Pelkmans ◽  
Robin A. Ohm ◽  
Aurin M. Vos ◽  
Anton S. M. Sonnenberg ◽  
...  

Many fungi are polykaryotic, containing multiple nuclei per cell. In the case of heterokaryons, there are different nuclear types within a single cell. It is unknown what the different nuclear types contribute in terms of mRNA expression levels in fungal heterokaryons. Each cell of the mushroomAgaricus bisporuscontains two to 25 nuclei of two nuclear types originating from two parental strains. Using RNA-sequencing data, we assess the differential mRNA contribution of individual nuclear types and its functional impact. We studied differential expression between genes of the two nuclear types, P1 and P2, throughout mushroom development in various tissue types. P1 and P2 produced specific mRNA profiles that changed through mushroom development. Differential regulation occurred at the gene level, rather than at the locus, chromosomal, or nuclear level. P1 dominated mRNA production throughout development, and P2 showed more differentially up-regulated genes in important functional groups. In the vegetative mycelium, P2 up-regulated almost threefold more metabolism genes and carbohydrate active enzymes (cazymes) than P1, suggesting phenotypic differences in growth. We identified widespread transcriptomic variation between the nuclear types ofA. bisporus. Our method enables studying nucleus-specific expression, which likely influences the phenotype of a fungus in a polykaryotic stage. Our findings have a wider impact to better understand gene regulation in fungi in a heterokaryotic state. This work provides insight into the transcriptomic variation introduced by genomic nuclear separation.


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Şeref Okuducu ◽  
Nisa N. Aktı ◽  
Sabahattin Akbaş ◽  
M. Orhan Kansu

The nuclear level density parameters of some deformed isotopes of target nuclei (Pb, Bi) used on the accelerator-driven subcritical systems (ADSs) have been calculated taking into consideration different collective excitation modes of observed nuclear spectra near the neutron binding energy. The method used in the present work assumes equidistant spacing of the collective coupled state bands of the considered isotopes. The present calculated results for different collective excitation bands have been compared with the compiled values from the literature for s-wave neutron resonance data, and good agreement was found.


1998 ◽  
Vol 111 (7) ◽  
pp. 985-994 ◽  
Author(s):  
J.M. Fayard ◽  
C. Tessier ◽  
J.F. Pageaux ◽  
M. Lagarde ◽  
C. Laugier

We have previously demonstrated that pancreatic PLA2 (PLA2-I) stimulates the proliferation of UIII cells, a stromal cell line derived from normal rat uterus. In order to gain further insight into the mechanism of action of PLA2-I, we have investigated the intracellular processing of PLA2-I. Either highly proliferative or growth arrested UIII cells were analyzed. Growth arrested cells were obtained from a contact inhibited monolayer or from aristolochic acid-treated cultures. Using cellular fractionation, western blotting, immunocytochemistry and confocal microscopy, we demonstrate that endogenous PLA2-I was mainly located in the nucleus in highly proliferative cells whereas its location was cytoplasmic in non proliferative cells. When non confluent UIII cells were incubated with nanomolar amounts of exogenous PLA2-I, the enzyme was internalized and, in the majority of cells, appeared within the nucleus. Both internalization and nuclear location of exogenous PLA2-I were suppressed by the addition of aristolochic acid to the culture medium. Binding experiments performed on purified nuclear preparations showed the presence of specific cooperative binding sites for PLA2-I. Collectively our data suggest that the proliferative effect exerted by pancreatic PLA2 in UIII cells is mediated by a direct interaction of the enzyme at the nuclear level. Putative mechanisms and targets are discussed.


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