Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kathryn A. Grako"'
Publikováno v:
Developmental Dynamics. 222:218-227
Immunofluorescence mapping demonstrates that the NG2 proteoglycan is invariably expressed by the mural cell component of mouse neovascular structures. This pattern is independent of the developmental mechanism responsible for formation of the vascula
Publikováno v:
Journal of Cellular Physiology. 177:299-312
The human homologue of NG2, the human melanoma proteoglycan (HMP), is expressed on most human melanomas. To investigate the role of this proteoglycan in melanoma progression, we have attempted to identify functionally important molecular ligands for
Autor:
Zaza Gomurashvili, Huashi Zhang, Jane Da, Turner D. Jenkins, Jonathan Hughes, Mark Wu, Leanne Lambert, Kathryn A. Grako, Kristin M. DeFife, Kassandra MacPherson, Vassil Vassilev, Ramaz Katsarava, William G. Turnell
Publikováno v:
ACS Symposium Series ISBN: 9780841239661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e93b145b67a771b9448e2254fa93dec3
https://doi.org/10.1021/bk-2008-0977.ch002
https://doi.org/10.1021/bk-2008-0977.ch002
Autor:
Philip D.G. Miles, Christen M. Anderson, Claes B. Wollheim, Leonardo Vargas, Kathryn A. Grako, Yulia Kushnareva, Susan Glasco, Pierre Maechler, Bumsup Lee, Elisabeth S. Kornbrust, Peng Luan, Jerrold M. Olefsky
Publikováno v:
Diabetes. 52(4)
The mitochondrial Na(+)-Ca(2+) exchanger (mNCE) mediates efflux of Ca(2+) from mitochondria in exchange for influx of Na(+). We show that inhibition of the mNCE enhances mitochondrial oxidative metabolism and increases glucose-stimulated insulin secr
Publikováno v:
The Journal of biological chemistry. 274(24)
NG2 is a transmembrane chondroitin sulfate proteoglycan that is expressed by immature progenitor cells in several developmental lineages and by some types of malignant cells. In vitro studies have suggested that NG2 participates in growth factor acti
Publikováno v:
Journal of cell science. 112
A line of null mice has been produced which fails to express the transmembrane chondroitin sulfate proteoglycan NG2. Homozygous NG2 null mice do not exhibit gross phenotypic differences from wild-type mice, suggesting that detailed analyses are requi
Autor:
Ankur S. Kulshrestha, Anil Mahapatro, Zaza Gomurashvili, Huashi Zhang, Jane Da, Turner D. Jenkins, Jonathan Hughes, Mark Wu, Leanne Lambert, Kathryn A. Grako, Kristin M. DeFife, Kassandra MacPherson, Vassil Vassilev, Ramaz Katsarava, William G. Turnell, Suwabun Chirachanchai, Juthathip Fangkangwanwong, Boyd A. Laurent, Dawanne M. Eugene, Scott M. Grayson, Kevin Cooper, Angelo Scopelianos, Julien Nicolas, Veronica San Miguel, Giuseppe Mantovani, David M. Haddleton, Cassandra L. Fraser, Gina L. Fiore, Lori A. Henderson, Matt J. Kipper, Martin Y. M. Chiang, Mohammad K. Hassan, Jeffrey S. Wiggins, Robson F. Storey, Kenneth A. Mauritz, E. Peter Maziarz, X. Michael Liu, Troy D. Wood, Louise E. Smith, Stephen Collins, Zuifang Liu, Sheila Mac Neil, Rachel Williams, Stephen Rimmer, Rajesh Kumar, Mukesh K. Pandey, Rahul Tyagi, Virinder S. Parmar, Arthur C. Watterson, Jayant Kumar, Aijun Gong, Fanqing Meng, Jean R. Starkey, Britney L. Moss, Aleksandre Rebane, Mikhail Drobizhev, Charles W. Spangler, S. Rahima Benhabbour, Alex Adronov, Fredrik Nederberg, Bj
Publikováno v:
Molecular biology of the cell. 7(12)
The transmembrane proteoglycan NG2 is able to interact both with components of the extracellular matrix and with the actin cytoskeleton. An examination of the distribution of NG2 during cell spreading suggests that NG2 can associate with two distinct
Autor:
Kathryn A. Grako, William B. Stallcup
Publikováno v:
Experimental cell research. 221(1)
Through immunohistochemical studies we have identified the cell-surface proteoglycan, NG2, on blood vessels throughout the rat embryo. The particular cell type expressing this chondroitin sulfate proteoglycan, however, is dependent upon tissue locati
Publikováno v:
Molecular endocrinology (Baltimore, Md.). 8(6)
Swiss Mouse 3T3-L1 cells provide a unique model for insulin-sensitive primary fat cells. Under defined conditions this fibroblast cell line can be converted to fully differentiated adipocytes, characterized by increased insulin receptor number and in