scholarly journals Changes in Nuclear Orientation Patterns of Chromosome 11 during Mouse Plasmacytoma Development

2015 ◽  
Vol 8 (5) ◽  
pp. 417-423 ◽  
Author(s):  
Ann-Kristin Schmälter ◽  
Christiaan H. Righolt ◽  
Alexandra Kuzyk ◽  
Sabine Mai
2014 ◽  
Vol 15 (1) ◽  
pp. 22 ◽  
Author(s):  
Ann-Kristin Schmälter ◽  
Alexandra Kuzyk ◽  
Christiaan H Righolt ◽  
Michaela Neusser ◽  
Ortrud K Steinlein ◽  
...  

Author(s):  
Fred E. Hossler

Preparation of replicas of the complex arrangement of blood vessels in various organs and tissues has been accomplished by infusing low viscosity resins into the vasculature. Subsequent removal of the surrounding tissue by maceration leaves a model of the intricate three-dimensional anatomy of the blood vessels of the tissue not obtainable by any other procedure. When applied with care, the vascular corrosion casting technique can reveal fine details of the microvasculature including endothelial nuclear orientation and distribution (Fig. 1), locations of arteriolar sphincters (Fig. 2), venous valve anatomy (Fig. 3), and vessel size, density, and branching patterns. Because casts faithfully replicate tissue vasculature, they can be used for quantitative measurements of that vasculature. The purpose of this report is to summarize and highlight some quantitative applications of vascular corrosion casting. In each example, casts were prepared by infusing Mercox, a methyl-methacrylate resin, and macerating the tissue with 20% KOH. Casts were either mounted for conventional scanning electron microscopy, or sliced for viewing with a confocal laser microscope.


1971 ◽  
Vol 32 (C1) ◽  
pp. C1-897-C1-898 ◽  
Author(s):  
N. J. STONE ◽  
R. A. FOX ◽  
F. HARTMANN-BOUTRON ◽  
D. SPANJAARD

1976 ◽  
Vol 37 (C6) ◽  
pp. C6-653-C6-655
Author(s):  
G. LANGOUCHE ◽  
B. B. TRIPLETT ◽  
N. S. DIXON ◽  
S. S. HANNA ◽  
P. BOOLCHAND

Diabetes ◽  
1996 ◽  
Vol 45 (3) ◽  
pp. 370-375 ◽  
Author(s):  
S. C. Elbein ◽  
K. L. Bragg ◽  
M. D. Hoffman ◽  
R. A. Mayorga ◽  
M. F. Leppert

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Vanessa Lakis ◽  
◽  
Rita T. Lawlor ◽  
Felicity Newell ◽  
Ann-Marie Patch ◽  
...  

AbstractHere we report the DNA methylation profile of 84 sporadic pancreatic neuroendocrine tumors (PanNETs) with associated clinical and genomic information. We identified three subgroups of PanNETs, termed T1, T2 and T3, with distinct patterns of methylation. The T1 subgroup was enriched for functional tumors and ATRX, DAXX and MEN1 wild-type genotypes. The T2 subgroup contained tumors with mutations in ATRX, DAXX and MEN1 and recurrent patterns of chromosomal losses in half of the genome with no association between regions with recurrent loss and methylation levels. T2 tumors were larger and had lower methylation in the MGMT gene body, which showed positive correlation with gene expression. The T3 subgroup harboured mutations in MEN1 with recurrent loss of chromosome 11, was enriched for grade G1 tumors and showed histological parameters associated with better prognosis. Our results suggest a role for methylation in both driving tumorigenesis and potentially stratifying prognosis in PanNETs.


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