Varying susceptibility to myocardial infarction among C57BL/6 mice of different genetic background

2003 ◽  
Vol 35 (6) ◽  
pp. 705-708 ◽  
Author(s):  
D Gorog
2015 ◽  
Vol 11 (7) ◽  
pp. 781-793 ◽  
Author(s):  
Lei Sheng ◽  
Wenbo Chai ◽  
Xuefeng Gong ◽  
Lingyan Zhou ◽  
Ronghao Cai ◽  
...  

Cryobiology ◽  
2010 ◽  
Vol 60 (2) ◽  
pp. 129-137 ◽  
Author(s):  
Kuo-Yu Huang ◽  
Suzanna A. de Groot ◽  
Henri Woelders ◽  
Gijsbertus T.J. van der Horst ◽  
Axel P.N. Themmen ◽  
...  

2020 ◽  
Author(s):  
Alena Moudra ◽  
Veronika Niederlova ◽  
Jiri Novotny ◽  
Lucie Schmiedova ◽  
Jan Kubovciak ◽  
...  

AbstractAntigen-inexperienced memory-like T (AIMT) cells are functionally unique T cells representing one of the two largest subsets of murine CD8+ T cells. However, differences between laboratory inbred strains, insufficient data from germ-free mice, a complete lack of data from feral mice, and unclear relationship between AIMT cells formation during aging represent major barriers for better understanding of their biology. We performed a thorough characterization of AIMT cells from mice of different genetic background, age, and hygienic status by flow cytometry and multi-omics approaches including analyses of gene expression, TCR repertoire, and microbial colonization. Our data showed that AIMT cells are steadily present in mice independently of their genetic background and hygienic status. Despite differences in their gene expression profiles, young and aged AIMT cells originate from identical clones. We identified that CD122 discriminates two major subsets of AIMT cells in a strain-independent manner. Whereas thymic CD122LOW AIMT cells (innate memory) prevail only in young animals with high thymic IL-4 production, peripheral CD122HIGH AIMT cells (virtual memory) dominate in aged mice. Co-housing with feral mice changed the bacterial colonization of laboratory strains, but had only minimal effects on the CD8+ T-cell compartment including AIMT cells.


2011 ◽  
pp. 113-120
Author(s):  
Kouichi Ozaki ◽  
Toshihiro Tanaka

1987 ◽  
Vol 7 (9) ◽  
pp. 3168-3177
Author(s):  
M G Schechtman

The most distal known gene on Neurospora crassa linkage group VR, his-6, was cloned. A genomic walk resulted in isolation of the telomere at VR. It was obtained from a library in which the endmost nucleotides of the chromosome had not been removed by nuclease treatment before being cloned, and mapping indicates that the entire chromosome end has probably been cloned. Sequences homologous to the terminal 2.5 kilobases of DNA from VR from these Oak Ridge N. crassa strains are found at other sites in the genome. To characterize these sites, I crossed an Oak Ridge-derived his-6 strain with a wild-type strain of different genetic background (Mauriceville) and characterized the hybridization patterns seen in the progeny. It appears that the sequences homologous to the VR terminus are found at genetically different sites in the two parental strains, and no hybridization to the VR telomere from Mauriceville was detected. The other genomic copies identified in the Oak Ridge parent were not telomeres. I suggest that any repeating sequence blocks found immediately adjacent to the VR terminus in Oak Ridge strains must be small and that the repeating element identified in that background may be an N. crassa transposable element integrated near the the chromosome end at VR.


2019 ◽  
Vol 7 (35) ◽  
pp. 5376-5391 ◽  
Author(s):  
Christian Seca ◽  
Alessandra Ferraresi ◽  
Suratchanee Phadngam ◽  
Chiara Vidoni ◽  
Ciro Isidoro

Polystyrene NH2-NPs induce toxicity through a differential impact on autophagy machinery in ovarian cancer cells with a different genetic background.


2007 ◽  
Vol 41 (5) ◽  
pp. 534-547 ◽  
Author(s):  
Dasha A. Koroteeva ◽  
Valentina I. Kiseleva ◽  
Aleksey V. Krivandin ◽  
Olga V. Shatalova ◽  
Wioletta Błaszczak ◽  
...  

1972 ◽  
Vol 14 (2) ◽  
pp. 199-208 ◽  
Author(s):  
R. S. Barber ◽  
R. Braude ◽  
K. G. Mitchell ◽  
R. J. Pittman

SUMMARY1. Twelve blocks of six enzootic-pneumonia-free Large White litter-mate pigs were individually fed, wet, from 20 to 92 kg live weight on six different levels of feed intake. Four groups were fed according to scales based on live weight and two were fed on a ‘semi-ad libitum’ system. One of the scales used was based on the ARC (1967) recommendations.2. Pigs on ‘semi-ad libitum’ feeding grew significantly faster than those on scale feeding although the feed: gain ratios were similar. Differences in performance between the four scale-fed groups were relatively small.3. Although treatment differences in carcass measurements were in the main small, the commercial grading results favoured the carcasses from the scale-fed pigs. The firmness of backfat assessed by thumb pressure was reduced as the level of feeding was increased.4. The results were compared with those obtained in a similar trial carried out at Shinfield in 1957 using pigs of a completely different genetic background. The general conclusions reached were similar in the two trials, that to obtain the most satisfactory overall results some form of controlled scale-feeding was necessary.


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