Zobrazeno 1 - 10 of 10 pro vyhledávání: '"J. R. Moskal"'
1
STEM CELLS
Autor: L. Cheng, Z. Huang, W. Zhou, Q. Wu, J. Rich, S. Bao, P. Baxter, H. Mao, X. Zhao, Z. Liu, Y. Huang, H. Voicu, S. Gurusiddappa, J. M. Su, L. Perlaky, R. Dauser, H.-c. E. Leung, K. M. Muraszko, J. A. Heth, X. Fan, C. C. Lau, T.-K. Man, M. Chintagumpala, X.-N. Li, P. Clark, M. Zorniak, Y. Cho, X. Zhang, D. Walden, E. Shusta, J. Kuo, S. Sengupta, S. Goel-Bhattacharya, S. Kulkarni, B. Cochran, C. Cusulin, A. Luchman, S. Weiss, M. Wu, N. Fernandez, S. Agnihotri, R. Diaz, J. Rutka, M. Bredel, J. Karamchandani, S. Das, B. Day, B. Stringer, F. Al-Ejeh, M. Ting, J. Wilson, K. Ensbey, P. Jamieson, Z. Bruce, Y. C. Lim, C. Offenhauser, S. Charmsaz, L. Cooper, J. Ellacott, A. Harding, J. Lickliter, P. Inglis, B. Reynolds, D. Walker, M. Lackmann, A. Boyd, A. Berezovsky, L. Poisson, L. Hasselbach, S. Irtenkauf, A. Transou, T. Mikkelsen, A. C. deCarvalho, D. Emlet, C. Del Vecchio, P. Gupta, G. Li, S. Skirboll, A. Wong, J. Figueroa, T. Shahar, A. Hossain, F. Lang, S. Fouse, J. Nakamura, C. D. James, S. Chang, J. Costello, J. M. Frerich, S. Rahimpour, Z. Zhuang, J. D. Heiss, A. Golebiewska, D. Stieber, L. Evers, E. Lenkiewicz, N. H. C. Brons, N. Nicot, A. Oudin, S. Bougnaud, F. Hertel, R. Bjerkvig, M. Barrett, L. Vallar, S. P. Niclou, X. Hao, J. Rahn, E. Ujack, X. Lun, G. Cairncross, D. Senger, S. Robbins, J. Harness, R. Lerner, Y. Ihara, R. Santos, J. D. L. Torre, A. Lu, T. Ozawa, T. Nicolaides, D. James, C. Petritsch, D. Higgins, M. Schroeder, B. Ball, B. Milligan, F. Meyer, J. Sarkaria, J. Henley, W. Flavahan, M. Hitomi, N. Rahim, Y. Kim, A. Sloan, R. Weil, I. Nakano, M. Li, J. Lathia, A. Hjelmeland, M. Kaluzova, S. Platt, M. Kent, A. Bouras, R. Machaidze, C. Hadjipanayis, S.-G. Kang, S.-H. Kim, Y.-M. Huh, E.-H. Kim, E.-K. Park, J. H. Chang, S. H. Kim, Y. K. Hong, D. S. Kim, S.-J. Lee, E. H. Kim, S. G. Kang, L. Deleyrolle, M. Sinyuk, W. Goan, B. Otvos, M. Rohaus, M. Oli, V. Vedam-Mai, D. Schonberg, S.-T. Lee, K. Chu, S. K. Lee, M. Kim, J.-K. Roh, A. Griveau, B. Reichholf, M. McMahon, D. Rowitch, R. Nitta, S. Mitra, M. Agarwal, T. Bui, J. Lin, C. Adamson, J. Martinez-Quintanilla, S.-H. Choi, D. Bhere, P. Heidari, D. He, U. Mahmood, K. Shah, S. Gholamin, A. Feroze, A. Achrol, S. Kahn, I. Weissman, S. Cheshier, E. P. Sulman, Q. Wang, E. Mostovenko, H. Liu, C. F. Lichti, A. Shavkunov, R. A. Kroes, J. R. Moskal, C. A. Conrad, F. F. Lang, M. R. Emmett, C. L. Nilsson, S. Osuka, O. Sampetrean, T. Shimizu, I. Saga, N. Onishi, E. Sugihara, J. Okubo, S. Fujita, S. Takano, A. Matsumura, H. Saya, N. Saito, J. Fu, S. Wang, W. K. A. Yung, D. Koul, R. S. Schmid, D. M. Irvin, M. Vitucci, R. E. Bash, A. M. Werneke, C. R. Miller, N. Shinojima, T. Takezaki, J. Fueyo, J. Gumin, F. Gao, F. Nwajei, F. C. Marini, M. Andreeff, J.-I. Kuratsu, S. Singh, K. Burrell, E. Koch, S. Jalali, A. Vartanian, E. Sulman, B. Wouters, G. Zadeh, R. Spelat, E. Singer, L. Matlaf, S. McAllister, L. Soroceanu, S. Spiegl-Kreinecker, D. Loetsch, M. Laaber, C. Schrangl, A. Wohrer, J. Hainfellner, C. Marosi, J. Pichler, S. Weis, G. Wurm, G. Widhalm, E. Knosp, W. Berger, J.-i. Kuratsu, Q. Tam, S. Tanaka, M. Nakada, D. Yamada, T. Todo, Y. Hayashi, J.-i. Hamada, A. Hirao, J. Tilghman, M. Ying, J. Laterra, M. Venere, C. Chang, M. Summers, S. Rosenfeld, S. Luk, J. Iafrate, D. Cahill, R. Martuza, S. Rabkin, A. Chi, H. Wakimoto, H.-G. Wirsching, S. Krishnan, K. Frei, N. Krayenbuhl, G. Reifenberger, M. Weller, G. Tabatabai, J. Man, J. Shoemake, J. Yu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f94f7a03a17079a76eb686dc4535928
https://europepmc.org/articles/PMC3222962/
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2
Alpha2,6-sialylation of cell-surface N-glycans inhibits glioma formation in vivo
Autor: H, Yamamoto, A, Oviedo, C, Sweeley, T, Saito, J R, Moskal
Publikováno v: Cancer research. 61(18)
Human gliomas express very high levels of cell-surface alpha2,3-linked terminal sialic acids on glycoproteins bearing N-linked oligosaccharides, most notably on alpha3beta1 integrin, which is the predominant integrin found in these tumors. Alpha2,6-l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::28b7b3434278d7edb97c5029bcefefc1
https://pubmed.ncbi.nlm.nih.gov/11559557
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3
Beta1,6-N-acetylglucosamine-bearing N-glycans in human gliomas: implications for a role in regulating invasivity
Autor: H, Yamamoto, J, Swoger, S, Greene, T, Saito, J, Hurh, C, Sweeley, J, Leestma, E, Mkrdichian, L, Cerullo, A, Nishikawa, Y, Ihara, N, Taniguchi, J R, Moskal
Publikováno v: Cancer research. 60(1)
The metastatic potential of tumor cells has been shown to be correlated with the expression of tri- and tetra-antennary beta1,6-N-acetylglucosamine (beta1,6-GlcNAc)-bearing N-glycans, which are recognized by Phaseolus vulgaris leukoagglutinating lect
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::579be0ce9a8c91f46d162d52ddfe5207
https://pubmed.ncbi.nlm.nih.gov/10646865
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4
Sialidase gene transfection enhances epidermal growth factor receptor activity in an epidermoid carcinoma cell line, A431
Autor: E J, Meuillet, R, Kroes, H, Yamamoto, T G, Warner, J, Ferrari, B, Mania-Farnell, D, George, A, Rebbaa, J R, Moskal, E G, Bremer
Publikováno v: Cancer research. 59(1)
Glycosphingolipids expressed in cancer cells have been implicated in the modulation of tumor cell growth through their interaction with transmembrane signaling molecules such as growth factor receptors. For glycosphingolipids to interact with growth
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::283c87b4e16909ff3c8232595349efbc
https://pubmed.ncbi.nlm.nih.gov/9892212
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5
The expression of CMP-NeuAc: Gal beta 1,4GlcNAc alpha 2,6 sialyltransferase [EC 2.4.99.1] and glycoproteins bearing alpha 2,6-linked sialic acids in human brain tumours
Autor: H, Yamamoto, Y, Kaneko, D, Vandermulen, D, Kersey, E, Mkrdichian, L, Cerullo, J, Leestma, J R, Moskal
Publikováno v: Glycoconjugate journal. 12(6)
The expression of CMP-NeuAc: Gal beta 1,4GlcNAc alpha 2,6 sialyltransferase (alpha 2,6-ST) [EC 2.4.99.1] and glycoproteins bearing alpha 2,6-linked sialic acids were examined in primary human brain tumours and cell lines. 79% (19/24) of the meningiom
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::92dde282536d1b145bebb6f53ddcb49f
https://pubmed.ncbi.nlm.nih.gov/8748163
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6
Basic fibroblast growth factor-like activity and receptors are expressed in a human glioma cell line
Autor: R S, Morrison, J L, Gross, W F, Herblin, T M, Reilly, P A, LaSala, R L, Alterman, J R, Moskal, P L, Kornblith, D L, Dexter
Publikováno v: Cancer research. 50(8)
Basic fibroblast growth factor (bFGF), a potent mitogen and angiogenic peptide, has been examined as an autocrine regulator of glioma cell growth. The addition of purified bovine pituitary bFGF to an established human glioma cell line, SNB-19, double
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8283c3f8c8440ffdb86ffb84a0616c71
https://pubmed.ncbi.nlm.nih.gov/2156622
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9
Effect of retinoic acid and phorbol-12-myristate-13-acetate on glycosyltransferase activities in normal and transformed cells
Autor: J R, Moskal, M W, Lockney, C C, Marvel, J E, Trosko, C C, Sweeley
Publikováno v: Cancer research. 47(3)
Retinoic acid was found to increase the activity of cytidine monophosphosialic acid:lactosylceramide sialyltransferase activity in a nontransformed clonal hamster cell line, NIL 8, and a virally transformed clone, NIL 8-HSV. The potent tumor promoter
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f04c2fde922ce2820c94554582da496b
https://pubmed.ncbi.nlm.nih.gov/3100023
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