Department of Pathology and Immunology
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Reverse recruitment: the Nup84 nuclear pore subcomplex mediates Rap1/Gcr1/Gcr2 transcriptional activation.
Proceedings of the National Academy of Sciences of the United States of America Apr, 2005 | Pubmed ID: 15817685
Glucose-responsive regulators of gene expression in Saccharomyces cerevisiae function at the nuclear periphery via a reverse recruitment mechanism.
Genetics Mar, 2007 | Pubmed ID: 17237508
Dissection of the transformation of primary human hematopoietic cells by the oncogene NUP98-HOXA9.
PloS one , 2009 | Pubmed ID: 19696924
Inhibition of CRM1-mediated nuclear export of transcription factors by leukemogenic NUP98 fusion proteins.
The Journal of biological chemistry May, 2010 | Pubmed ID: 20233715
Amino-terminal enhancer of split (AES) interacts with the oncoprotein NUP98-HOXA9 and enhances its transforming ability.
The Journal of biological chemistry Nov, 2011 | Pubmed ID: 21937451
Identification of HLA-A24-restricted CD8(+) cytotoxic T-cell epitopes derived from mammaglobin-A, a human breast cancer-associated antigen.
Human immunology Jan, 2012 | Pubmed ID: 22074997
The nuclear pore complex mediates binding of the Mig1 repressor to target promoters.
PloS one , 2011 | Pubmed ID: 22110603
Washington University School of Medicine
Nayan J. Sarma1,
Akiko Takeda1,
Nabeel R. Yaseen1
1Department of Pathology and Immunology, Washington University School of Medicine
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