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1  Par-4 and an induction in the expression of WT1 protein.
2 sence of a 17-amino-acid sequence within the WT1 protein.
3 peptides and antibody responses specific for WT1 protein.
4 vealed that this gel shift complex contained WT1 protein.
5 shion, implying a gain of function by mutant WT1 proteins.
6  wild-type and tumor-derived missense mutant WT1 proteins.
7 Both events result in a functionally changed WT1 protein and are potential mechanisms of altering nor
8  several oncogenic proteins, associates with WT1 protein and stabilizes its expression.
9           High levels of the Wilms' Tumor 1 (WT1) protein and mRNA had been associated with aggressiv
10               Finally, we detected Par-4 and WT1 proteins binding to a previously identified WT1-bind
11                                          The WT1 protein binds to the promoters of many genes through
12                                 Furthermore, WT1 protein bound to specific DNA-binding sites located
13                              Two recombinant WT1 proteins containing the DNA binding domain with or w
14 ern blot and FACS analysis which showed that WT1 protein expression was highest in S phase and almost
15        Our data strongly suggest that mutant WT1 proteins facilitate expression of these cell cycle g
16 findings show for the first time that mutant WT1 proteins have a gain-of-function and act as oncogene
17            Immunofluorescent staining of the WT1 protein in 3T3 and 293 cell clones, stably transfect
18             Aoc1 mRNA levels correlated with WT1 protein in several cell lines.
19 tected endogenous expression of Wt1 mRNA and Wt1 protein in the proepicardium and epicardium and also
20 rected against the N-terminus portion of the WT1 protein in the sera of 3 of 18 patients with acute m
21                                       Mutant WT1 proteins in Denys-Drash syndrome patients were unabl
22       We also expressed wild-type and mutant WT1 proteins in human mesenchymal stem cells and establi
23                                          The WT1 protein is normally expressed in the developing geni
24                                     Although WT1 protein is predominantly localized to the nucleus, t
25                      Decreased expression of WT1 protein led to cell cycle arrest at the G1 phase and
26 mab (Herceptintrade mark) antibody decreased WT1 protein levels in HER2/neu-overexpressing BT-474 and
27 e to healthy controls and non-trisomy 8 MDS; WT1 protein levels were also significantly elevated.
28 tutional WT1 mutations that encode truncated WT1 proteins may predispose to the development of crypto
29 ges Akt to increase WT1 expression, and that WT1 protein plays a vital role in regulating cell cycle
30  WT1 mRNA may regulate gene targeting of the WT1 protein through changes either in its regulatory or
31                                   Binding of WT1 protein to a cis-regulatory element in the AOC1 prom
32                                   Binding of Wt1 protein to these elements was verified by EMSA and C
33                      Antisense inhibition of WT1 protein translation strongly reduced Aoc1 transcript
34          Concordant with the other findings, WT1 protein was increased in juvenile DM muscle, with av
35              A significant decrease in total WT1 protein was observed by both immunocytochemistry and
36                Contrary to previous reports, WT1 protein was strongly expressed in primary carcinomas
37        To investigate the function of mutant WT1 proteins, we performed WT1 knockdown experiments in
38     Approximately threefold higher levels of WT1 protein were observed in MCF-7 breast cancer cells t
39     All are predicted to produce a truncated WT1 protein with absence or disruption of the zinc finge
40 nt to restore the functional properties of a WT1 protein with an amino-terminal deletion, an effect t
41                       Here, we show that the WT1 protein with and without the KTS tripeptide can repr

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