Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Laurence A Lasky"'
Autor:
Raffi Tonikian, Yingnan Zhang, Stephen L Sazinsky, Bridget Currell, Jung-Hua Yeh, Boris Reva, Heike A Held, Brent A Appleton, Marie Evangelista, Yan Wu, Xiaofeng Xin, Andrew C Chan, Somasekar Seshagiri, Laurence A Lasky, Chris Sander, Charles Boone, Gary D Bader, Sachdev S Sidhu
Publikováno v:
PLoS Biology, Vol 6, Iss 9, p e239 (2008)
PDZ domains are protein-protein interaction modules that recognize specific C-terminal sequences to assemble protein complexes in multicellular organisms. By scanning billions of random peptides, we accurately map binding specificity for approximatel
Externí odkaz:
https://doaj.org/article/4ed87eb30eb5451a85620aede5da754a
Publikováno v:
Stem Cells and Development. 14:105-110
Previous studies have demonstrated that mice null (-/-) for either CD34 or c-mpl are viable and have greatly decreased numbers of multipotential (CFU-Mix), erythroid (BFU-E), and granulocytemacrophage (CFU-GM) progenitor cells in the bone marrow (BM)
Autor:
Kerry Zobel, Wai Lee Wong, Sachdev S. Sidhu, Jian Ping Yin, Michael F. T. Koehler, Laurence A. Lasky, M. Theresa Pisabarro, Sherry Yeh, Nicholas J. Skelton
Publikováno v:
Journal of Biological Chemistry. 278:7645-7654
The LAP (leucine-rich repeatand PDZ-containing) family of proteins play a role in maintaining epithelial and neuronal cell size, and mutation of these proteins can have oncogenic consequences. The LAP protein Erbin has been implicated previously in a
Autor:
Laurence A. Lasky, Miranda Thomas, Charles L. Sawyers, Karin Hepner, Richard P. Laura, Lawrence Banks, Ernesto Guccione
Publikováno v:
Oncogene. 21:5088-5096
The E6 proteins from the high-risk human papillomavirus (HPV) types have previously been shown to target a number of PDZ domain-containing proteins for proteasome-mediated degradation. These include the hDlg tumour suppressor and the MAGI-1 protein.
Publikováno v:
Experimental Cell Research. 275:155-170
Tight junctions are apically localized structures that regulate the passage of small molecules and proteins through intercellular regions of epithelial or endothelial cells. These structures are complex multimolecular assemblages that contain both tr
Autor:
Lisa M. Toney, Laurence A. Lasky, Donald Dowbenko, Tracy Tang, Amanda Jackson, Alexander L. Dent, David A. Lewin
Publikováno v:
Journal of Biological Chemistry. 277:14255-14265
The activation of the AKT/protein kinase B kinases by mutation of the PTEN lipid phosphatase results in enhanced survival of a diversity of tumors. This resistance to apoptosis is partly accomplished by the inhibition of genetic programs induced by a
Publikováno v:
Journal of Biological Chemistry. 277:11352-11361
p21(Cip1/WAF1) (p21), a p53-inducible protein, is a critical regulator of cell cycle and cell survival. p21 binds to and inhibits both the DNA synthesis regulator proliferating cell nuclear antigen and cyclin A/E-CDK2 complexes. Recently, p21 has als
Publikováno v:
The American Journal of Pathology. 158:809-816
Prostate stem cell antigen (PSCA) is a GPI-anchored membrane protein whose expression is reportedly up-regulated in a majority of human prostate cancers, including advanced stages and metastases. In this study, we investigate the expression pattern o
Autor:
M. Teresa Pisabarro, Germaine Fuh, Sachdev S. Sidhu, Clifford Quan, Laurence A. Lasky, Ying Li
Publikováno v:
Journal of Biological Chemistry. 275:21486-21491
PDZ domains mediate protein-protein interactions at specialized subcellular sites, such as epithelial cell tight junctions and neuronal post-synaptic densities. Because most PDZ domains bind extreme carboxyl-terminal sequences, the phage display meth
Autor:
Yan Wu, Laurence A. Lasky, Qimin Gu, Richard P. Laura, Susan D. Spencer, James Lee, Donald Dowbenko
Publikováno v:
Journal of Biological Chemistry. 275:21477-21485
PTEN/MMAC is a phosphatase that is mutated in multiple human tumors. PTEN/MMAC dephosphorylates 3-phosphorylated phosphatidylinositol phosphates that activate AKT/protein kinase B (PKB) kinase activity. AKT/PKB is implicated in the inhibition of apop