scholarly journals The containment poset of type A Hessenberg varieties

2020 ◽  
Vol 29 (2) ◽  
pp. 195-210
Author(s):  
E. Drellich ◽  
Keyword(s):  
Type A ◽  
ISRN Geometry ◽  
2012 ◽  
Vol 2012 ◽  
pp. 1-34 ◽  
Author(s):  
Darius Bayegan ◽  
Megumi Harada

We develop the theory of poset pinball, a combinatorial game introduced by Harada-Tymoczko to study the equivariant cohomology ring of a GKM-compatible subspace X of a GKM space; Harada and Tymoczko also prove that, in certain circumstances, a successful outcome of Betti poset pinball yields a module basis for the equivariant cohomology ring of X. First we define the dimension pair algorithm, which yields a successful outcome of Betti poset pinball for any type A regular nilpotent Hessenberg and any type A nilpotent Springer variety, considered as GKM-compatible subspaces of the flag variety. The algorithm is motivated by a correspondence between Hessenberg affine cells and certain Schubert polynomials which we learned from Insko. Second, in a special case of regular nilpotent Hessenberg varieties, we prove that our pinball outcome is poset-upper-triangular, and hence the corresponding classes form a HS1*(pt)-module basis for the S1-equivariant cohomology ring of the Hessenberg variety.


10.37236/2126 ◽  
2012 ◽  
Vol 19 (1) ◽  
Author(s):  
Barry Dewitt ◽  
Megumi Harada

In this manuscript we study type $A$ nilpotent Hessenberg varieties equipped with a natural $S^1$-action using techniques introduced by Tymoczko, Harada-Tymoczko, and Bayegan-Harada, with a particular emphasis on a special class of nilpotent Springer varieties corresponding to the partition $\lambda= (n-2,2)$ for $n \geq 4$. First we define the adjacent-pair matrix corresponding to any filling of a Young diagram with $n$ boxes with the alphabet $\{1,2,\ldots,n\}$. Using the adjacent-pair matrix we make more explicit and also extend some statements concerning highest forms of linear operators in previous work of Tymoczko. Second, for a nilpotent operator $N$ and Hessenberg function $h$, we construct an explicit bijection between the $S^1$-fixed points of the nilpotent Hessenberg variety Hess$(N,h)$ and the set of $(h,\lambda_N)$-permissible fillings of the Young diagram $\lambda_N$. Third, we use poset pinball, the combinatorial game introduced by Harada and Tymoczko, to study the $S^1$-equivariant cohomology of type $A$ Springer varieties $\mathcal{S}_{(n-2,2)}$ associated to Young diagrams of shape $(n-2,2)$ for $n\geq 4$. Specifically, we use the dimension pair algorithm for Betti-acceptable pinball described by Bayegan and Harada to specify a subset of the equivariant Schubert classes in the $\mathbb{T}$-equivariant cohomology of the flag variety $\mathcal{F}\ell ags(\mathbb{C}^n) \cong GL(n,\mathbb{C})/B$ which maps to a module basis of $H^*_{S^1}(\mathcal{S}_{(n-2,2)})$ under the projection map $H^*_\mathbb{T}(\mathcal{F}\ell ags(\mathbb{C}^n)) \to H^*_{S^1}(\mathcal{S}_{(n-2,2)})$. Our poset pinball module basis is not poset-upper-triangular; this is the first concrete such example in the literature. A straightforward consequence of our proof is that there exists a simple and explicit change of basis which transforms our poset pinball basis to a poset-upper-triangular module basis for $H^*_{S^1}(\mathcal{S}_{(n-2,2)})$. We close with open questions for future work.


Author(s):  
S. Fujinaga ◽  
K. Maruyama ◽  
C.W. Williams ◽  
K. Sekhri ◽  
L. Dmochowski

Yumoto and Dmochowski (Cancer Res.27, 2098 (1967)) reported the presence of mature and immature type C leukemia virus particles in leukemic organs and tissues such as lymph nodes, spleen, thymus, liver, and kidneys of SJL/J strain mice with Hodgki's-like disease or reticulum cell neoplasm (type B). In an attempt to ascertain the possibility that this neoplasia may be of viral origin, experiments with induction and transmission of this neoplasm were carried out using cell-free extracts of leukemic organs from an SJL/J strain mouse with spontaneous disease.It has been possible to induce the disease in low-leukemia BALB/c and C3HZB strain mice and serially transfer the neoplasia by cell-free extracts of leukemic organs of these mice. Histological examination revealed the neoplasia to be of either reticulum cell-type A or type B. Serial transfer is now in its fifth passage. In addition leukemic spleen from another SJL/J strain mouse with spontaneous reticulum cell neoplasm (type A) was set up in tissue culture and is now in its 141st serial passage in vitro. Preliminary results indicate that cell-free material of 39th tissue culture passage can reproduce neoplasia in BALB/c mice.


Author(s):  
D.R. Jackson ◽  
J.H. Hoofnagle ◽  
A.N. Schulman ◽  
J.L. Dienstag ◽  
R.H. Purcell ◽  
...  

Using immune electron microscopy Feinstone et. al. demonstrated the presence of a 27 nm virus-like particle in acute-phase stools of patients with viral hepatitis, type A, These hepatitis A antigen (HA Ag) particles were aggregated by convalescent serum from patients with type A hepatitis but not by pre-infection serum. Subsequently Dienstag et. al. and Maynard et. al. produced acute hepatitis in chimpanzees by inoculation with human stool containing HA Ag. During the early acute disease, virus like particles antigenically, morphologically and biophysically identical to the human HA Ag particle were found in chimpanzee stool. Recently Hilleman et. al. have described similar particles in liver and serum of marmosets infected with hepatitis A virus (HAV). We have investigated liver, bile and stool from chimpanzees and marmosets experimentally infected with HAV. In an initial study, a chimpanzee (no.785) inoculated with HA Ag-containing stool developed elevated liver enzymes 21 days after exposure.


Author(s):  
Y. Ohtsuki ◽  
G. Seman ◽  
J. M. Bowen ◽  
M. Scanlon ◽  
L. Dmochowski

Recently, periodate-lysine-paraformaldehyde (PLP) fixation was reported for immunoelectron microscopy (1). In PLP fixation, carbohydrates are oxidized by periodate and cross-linked by lysine; paraformaldehyde stabilizes proteins and lipids. By using PLP fixation, intracytoplasmic type A viral antigens have been previously demonstrated by immunoperoxidase labeling (2). In the present study, PLP fixation has been applied for the detection of the same antigens in mouse mammary tumor culture cells by both immunoferritin and immunoperoxidase methods. Rabbit anti-intracytoplasmic type A virus serum (anti-A), kindly provided by Dr. M. Muller (3), rabbit anti-strain A mouse mammary tumor virus (anti-MMTV) and preimmune rabbit serum as control were used to detect viral antigens in cells of C3H/HeJ strain mouse mammary tumor culture. Attempts have been also made to demonstrate peroxidase labeling of type C virus particles in frozen sections of an SD-MSV-induced NZB rat bone tumor tissue by rabbit anti-MuLV serum.


1995 ◽  
Vol 40 (3) ◽  
pp. 272-272
Author(s):  
Lori A. Ingram ◽  
Gail M. Williamson
Keyword(s):  

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