Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Melissa Mattia"'
Autor:
James J. Manfredi, Ella Freulich, Andrew Zupnick, Tamar Kahan, Inbal Shamir, Itamar Simon, Oleg Laptenko, Melissa Mattia, William A. Freed-Pastor, Idit Shiff, Noam Kadouri, Carol Prives
Publikováno v:
Molecular Cell. 57:1034-1046
DNA binding by numerous transcription factors including the p53 tumor suppressor protein constitutes a vital early step in transcriptional activation. While the role of the central core DNA binding domain (DBD) of p53 in site-specific DNA binding has
Autor:
Rachel Beckerman, Susan Keezer, Andrew Zupnick, Kathryn E. Yoh, Oleg Laptenko, Jinwoo Ahn, Melissa Mattia-Sansobrino, Orit Karni-Schmidt, Carol Prives, In-Ja L. Byeon
Functional in a tetrameric state, the protein product of the p53 tumor suppressor gene confers its tumor-suppressive activity by transactivating genes which promote cell-cycle arrest, senescence, or programmed cell death. How p53 distinguishes betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee0c331c84cac63290674eedfde3cee4
Autor:
Maria Lokshin, Oleg Laptenko, Assaf Friedler, Masha V. Poyurovsky, Rachel Beckerman, Chen Katz, Melissa Mattia, Lewis M. Brown, Carol Prives, Ronen Gabizon, In-Ja L. Byeon, Andrew Zupnick, Jinwoo Ahn
Publikováno v:
Nature structural & molecular biology
The p53 tumor suppressor interacts with its negative regulator Mdm2 via the former’s N-terminal region and core domain. Yet the extreme p53 C-terminal region contains lysine residues ubiquitinated by Mdm2 and can bear post-translational modificatio
Autor:
Lois Resnick-Silverman, Wen Jun Liu, Melissa Mattia, James J. Manfredi, Andrea DaCosta, Jayasri Dastidar, Abhilash Padi, Shohreh Varmeh-Ziaie, Selvon St. Clair, Luciana E. Giono
Publikováno v:
Molecular Cell. 16:725-736
The Cdc25C phosphatase mediates cellular entry into mitosis. The cdc25C gene is a target for transcriptional downregulation by the tumor suppressor protein p53, and this repression can be shown to contribute to p53-dependent cell cycle arrest. Two in
Autor:
Xiangyuan Wang, Melissa Mattia, Jochen Buck, Marco Conti, Lonny R. Levin, Meeghan L. Sinclair, Debra J. Wolgemuth
Publikováno v:
Molecular Reproduction and Development. 56:6-11
The cAMP signaling pathway is an important mediator of extracellular signals in organisms from prokaryotes to higher eukaryotes. In mammals two types of adenylyl cyclase synthesize cAMP; a ubiquitous family of transmembrane isoforms regulated by G pr
Autor:
Melissa J. Peart, James L. Manley, Carol Prives, Rachel Beckerman, Melissa Mattia, Joaquín M. Espinosa, Aaron J Donner
We reported previously that when cells are arrested in S phase, a subset of p53 target genes fails to be strongly induced despite the presence of high levels of p53. When DNA replication is inhibited, reduced p21 mRNA accumulation is correlated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ee339159ea01a553b207fc1553b8ca
https://europepmc.org/articles/PMC2701578/
https://europepmc.org/articles/PMC2701578/
Autor:
Jinwoo Ahn, Carol Prives, Masha V. Poyurovsky, Rachel Beckerman, Nicole Baptiste, Melissa Mattia, Jianmin Zhou, Andrew Zupnick, Christine Cain, Kristine McKinney, Vanesa Gottifredi
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Scopus-Elsevier
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Scopus-Elsevier
Both sequence-specific DNA binding and exonuclease activities have been mapped to the central conserved core domain of p53. To gain more information about these two activities a series of mutants were generated that changed core domain histidine resi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06e741908264c2bb127a851ae26516e5
http://www.tandfonline.com/doi/abs/10.4161/cc.8.10.8548
http://www.tandfonline.com/doi/abs/10.4161/cc.8.10.8548
Autor:
Kristine McKinney, Alan R. Fersht, Michael P. Sheetz, Rachel Beckerman, Andrew Zupnick, Orit Karni-Schmidt, Philippe Bouvet, Assaf Friedler, Melissa Mattia, Carol Prives
Publikováno v:
Oncogene
Oncogene, Nature Publishing Group, 2007, 26, pp.3878-3891. ⟨10.1038/sj.onc.1210162⟩
Oncogene, 2007, 26, pp.3878-3891. ⟨10.1038/sj.onc.1210162⟩
Oncogene, Nature Publishing Group, 2007, 26, pp.3878-3891. ⟨10.1038/sj.onc.1210162⟩
Oncogene, 2007, 26, pp.3878-3891. ⟨10.1038/sj.onc.1210162⟩
The p53 tumor suppressor is a nucleocytoplasmic shuttling protein that is found predominantly in the nucleus of cells. In addition to mutation, abnormal p53 cellular localization is one of the mechanisms that inactivate p53 function. To further under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e7a4fabe5f83eabc959752d9b6fd7cf
https://hal.archives-ouvertes.fr/hal-00378604
https://hal.archives-ouvertes.fr/hal-00378604
We have previously reported that when DNA replication is blocked in some human cell lines, p53 is impaired in its ability to induce a subset of its key target genes, including p21(WAF1/CIP1). Here, we investigated the reason for this impairment by co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::264069d1befd744e965e97fbb6c32d8a
http://mcb.asm.org/content/27/4/1309
http://mcb.asm.org/content/27/4/1309
Publikováno v:
Molecular cell. 16(3)
In cells, sequence-specific transcription factors must search through an entire genome to find their target sites in promoters. Such sites may be identified by using one-dimensional (linear diffusion) and/or three-dimensional (association/dissociatio