Zobrazeno 1 - 10
of 18
pro vyhledávání: '"James R. Bone"'
Autor:
Maxim I. Maron, Stephanie M. Lehman, Sitaram Gayatri, Joseph D. DeAngelo, Subray Hegde, Benjamin M. Lorton, Yan Sun, Dina L. Bai, Simone Sidoli, Varun Gupta, Matthew R. Marunde, James R. Bone, Zu-Wen Sun, Mark T. Bedford, Jeffrey Shabanowitz, Hongshan Chen, Donald F. Hunt, David Shechter
Publikováno v:
iScience, Vol 24, Iss 9, Pp 102971- (2021)
Summary: Protein arginine methyltransferases (PRMTs) catalyze the post-translational monomethylation (Rme1), asymmetric (Rme2a), or symmetric (Rme2s) dimethylation of arginine. To determine the cellular consequences of type I (Rme2a) and II (Rme2s) P
Externí odkaz:
https://doaj.org/article/c804eaefab6848b4b721da294a0ebcd5
Autor:
James R. Bone, Jeffrey Shabanowitz, Dina L. Bai, Matthew R. Marunde, Emmanuel S. Burgos, Zu-Wen Sun, Varun Gupta, Maxim I. Maron, David Shechter, Sitaram Gayatri, Simone Sidoli, Stephanie M. Lehman, Mark T. Bedford, Edward Nieves, Donald F. Hunt, Hongshan Chen
Arginine methylation is essential for both cellular viability and development and is also dysregulated in cancer. PRMTs catalyze the post translational monomethylation (Rme1/MMA, catalyzed by Type I-III), asymmetric (Rme2a/ADMA, Type I enzymes)-, or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84a25ee4fee537251be8b5c8680c19f6
https://doi.org/10.1101/2020.06.23.167601
https://doi.org/10.1101/2020.06.23.167601
Autor:
Varun Gupta, Benjamin M. Lorton, Simone Sidoli, Mark T. Bedford, Stephanie M. Lehman, Yan Sun, Matthew R. Marunde, Donald F. Hunt, David Shechter, James R. Bone, Joseph D. DeAngelo, Jeffrey Shabanowitz, Subray S. Hegde, Dina L. Bai, Sitaram Gayatri, Maxim I. Maron, Hongshan Chen, Zu-Wen Sun
Publikováno v:
iScience
iScience, Vol 24, Iss 9, Pp 102971-(2021)
iScience, Vol 24, Iss 9, Pp 102971-(2021)
Summary Protein arginine methyltransferases (PRMTs) catalyze the post-translational monomethylation (Rme1), asymmetric (Rme2a), or symmetric (Rme2s) dimethylation of arginine. To determine the cellular consequences of type I (Rme2a) and II (Rme2s) PR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57db5b6a4e5c207022129a55e66179cf
https://doi.org/10.1016/j.isci.2021.102971
https://doi.org/10.1016/j.isci.2021.102971
Publikováno v:
Current Biology. 14:481-487
MSL complexes bind hundreds of sites along the single male X chromosome to achieve dosage compensation in Drosophila. Previously, we proposed that approximately 35 "high-affinity" or "chromatin entry" sites (CES) might nucleate spreading of MSL compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::618296c005c85429afa61715e05df167
https://doi.org/10.1016/j.cub.2004.03.004
https://doi.org/10.1016/j.cub.2004.03.004
Publikováno v:
Cold Spring Harbor Symposia on Quantitative Biology. 69:81-88
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba3b45d3fd64e8b82d839c91d675e8ac
https://doi.org/10.1101/sqb.2004.69.81
https://doi.org/10.1101/sqb.2004.69.81
Autor:
Adel K. El-Naggar, Gary L. Clayman, James R. Bone, Sharon Y.R. Dent, Katrina Briggs, Madelene M. Coombes
Publikováno v:
Oncogene. 22:8902-8911
Head and neck squamous cell carcinoma (HNSCC) is the fifth most frequent cancer in the US. Several genetic and epigenetic alterations are associated with HNSCC tumorigenesis, including inactivation of CDKN2A, which encodes the p16 tumor suppressor, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45181cdc007691c9addec67e14d5e1e
https://doi.org/10.1038/sj.onc.1207050
https://doi.org/10.1038/sj.onc.1207050
Autor:
James R. Bone, Yaxin Yu, Wanting Xu, Wenzheng Zhang, Diane G. Edmondson, Sharon Y. Roth, David J. Stillman, A. Watson
Publikováno v:
Cold Spring Harbor Symposia on Quantitative Biology. 63:459-468
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbe15a1702357f79e0ebb7cebd28e3b3
https://doi.org/10.1101/sqb.1998.63.459
https://doi.org/10.1101/sqb.1998.63.459
Autor:
Mitzi I. Kuroda, James R. Bone
Publikováno v:
Genetics. 144:705-713
In the fruitfly Drosophila melanogaster, the four male-specific lethal (msl) genes are required to achieve dosage compensation of the male X chromosome. The MSL proteins are thought to interact with cis-acting sites that confer dosage compensation to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f9b3d6e9ebd0cca54ed0fa17ecb5fbe
https://doi.org/10.1093/genetics/144.2.705
https://doi.org/10.1093/genetics/144.2.705
Publikováno v:
Genes to Cells. 1:325-336
Background: Dosage compensation results in equivalent X-linked gene expression in males (XY) and females (XX). In Drosophila, both X chromosomes are active in females, and the single male X must double its transcriptional activity to allow male devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::796450684d5475f8056420cf632b6b78
https://doi.org/10.1046/j.1365-2443.1996.26027.x
https://doi.org/10.1046/j.1365-2443.1996.26027.x
Publikováno v:
Proceedings of the National Academy of Sciences. 89:10568-10572
Embryonic nuclear proteins from the sea urchin Strongylocentrotus purpuratus bind in vitro to a cis-acting element that lies upstream of the actin gene CyIIIb and consists of two direct repeats homologous to steroid hormone response elements. This se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25922d432b38455fca73dbb533645af7
https://doi.org/10.1073/pnas.89.22.10568
https://doi.org/10.1073/pnas.89.22.10568