Zobrazeno 1 - 10 of 16 pro vyhledávání: '"S G, Wong"'
1
Limits on Active to Sterile Neutrino Oscillations from Disappearance Searches in the MINOS, Daya Bay, and Bugey-3 Experiments
Autor: Adamson, P. An, F. P. Anghel, I. Aurisano, A. and Balantekin, A. B. Band, H. R. Barr, G. Bishai, M. Blake, A. Blyth, S. Bock, G. J. Bogert, D. Cao, D. Cao, G. F. Cao, J. Cao, S. V. Carroll, T. J. Castromonte, C. M. and Cen, W. R. Chan, Y. L. Chang, J. F. Chang, L. C. and Chang, Y. Chen, H. S. Chen, Q. Y. Chen, R. Chen, S. M. and Chen, Y. Chen, Y. X. Cheng, J. Cheng, J. -H. Cheng, Y. P. Cheng, Z. K. Cherwinka, J. J. Childress, S. Chu, M. C. Chukanov, A. Coelho, J. A. B. Corwin, L. and Cronin-Hennessy, D. Cummings, J. P. de Arcos, J. De Rijck, S. Deng, Z. Y. Devan, A. V. Devenish, N. E. Ding, X. F. and Ding, Y. Y. Diwan, M. V. Dolgareva, M. Dove, J. and Dwyer, D. A. Edwards, W. R. Escobar, C. O. Evans, J. J. and Falk, E. Feldman, G. J. Flanagan, W. Frohne, M. V. and Gabrielyan, M. Gallagher, H. R. Germani, S. Gill, R. and Gomes, R. A. Gonchar, M. Gong, G. H. Gong, H. Goodman, M. C. Gouffon, P. Graf, N. Gran, R. Grassi, M. and Grzelak, K. Gu, W. Q. Guan, M. Y. Guo, L. Guo, R. P. and Guo, X. H. Guo, Z. Habig, A. Hackenburg, R. W. Hahn, S. R. Han, R. Hans, S. Hartnell, J. Hatcher, R. He, M. and Heeger, K. M. Heng, Y. K. Higuera, A. Holin, A. Hor, Y. K. Hsiung, Y. B. Hu, B. Z. Hu, T. Hu, W. Huang, E. C. Huang, H. X. Huang, J. Huang, X. T. Huber, P. and Huo, W. Hussain, G. Hylen, J. Irwin, G. M. Isvan, Z. and Jaffe, D. E. Jaffke, P. James, C. Jen, K. L. Jensen, D. and Jetter, S. Ji, X. L. Ji, X. P. Jiao, J. B. Johnson, R. A. de Jong, J. K. Joshi, J. Kafka, T. Kang, L. and Kasahara, S. M. S. Kettell, S. H. Kohn, S. Koizumi, G. and Kordosky, M. Kramer, M. Kreymer, A. Kwan, K. K. Kwok, M. W. Kwok, T. Lang, K. Langford, T. J. Lau, K. and Lebanowski, L. Lee, J. Lee, J. H. C. Lei, R. T. Leitner, R. Leung, J. K. C. Li, C. Li, D. J. Li, F. Li, G. S. and Li, Q. J. Li, S. Li, S. C. Li, W. D. Li, X. N. and Li, Y. F. Li, Z. B. Liang, H. Lin, C. J. Lin, G. L. and Lin, S. Lin, S. K. Lin, Y. -C. Ling, J. J. Link, J. M. and Litchfield, P. J. Littenberg, L. Littlejohn, B. R. Liu, D. W. Liu, J. C. Liu, J. L. Loh, C. W. Lu, C. Lu, H. Q. Lu, J. S. Lucas, P. Luk, K. B. Lv, Z. Ma, Q. M. and Ma, X. B. Ma, X. Y. Ma, Y. Q. Malyshkin, Y. Mann, W. A. Marshak, M. L. Caicedo, D. A. Martinez Mayer, N. and McDonald, K. T. McGivern, C. McKeown, R. D. Medeiros, M. M. and Mehdiyev, R. Meier, J. R. Messier, M. D. Miller, W. H. and Mishra, S. R. Mitchell, I. Mooney, M. Moore, C. D. and Mualem, L. Musser, J. Nakajima, Y. Naples, D. and Napolitano, J. Naumov, D. Naumova, E. Nelson, J. K. and Newman, H. B. Ngai, H. Y. Nichol, R. J. Ning, Z. Nowak, J. A. O'Connor, J. Ochoa-Ricoux, J. P. Olshevskiy, A. and Orchanian, M. Pahlka, R. B. Paley, J. Pan, H. -R. Park, J. Patterson, R. B. Patton, S. Pawloski, G. Pec, V. and Peng, J. C. Perch, A. Pfuetzner, M. M. Phan, D. D. and Phan-Budd, S. Pinsky, L. Plunkett, R. K. Poonthottathil, N. and Pun, C. S. J. Qi, F. Z. Qi, M. Qian, X. Qiu, X. and Radovic, A. Raper, N. Rebel, B. Ren, J. Rosenfeld, C. and Rosero, R. Roskovec, B. Ruan, X. C. Rubin, H. A. and Sail, P. Sanchez, M. C. Schneps, J. Schreckenberger, A. and Schreiner, P. Sharma, R. Sher, S. Moed Sousa, A. and Steiner, H. Sun, G. X. Sun, J. L. Tagg, N. Talaga, R. L. and Tang, W. Taychenachev, D. Thomas, J. Thomson, M. A. and Tian, X. Timmons, A. Todd, J. Tognini, S. C. Toner, R. and Torretta, D. Treskov, K. Tsang, K. V. Tull, C. E. and Tzanakos, G. Urheim, J. Vahle, P. Viaux, N. Viren, B. and Vorobel, V. Wang, C. H. Wang, M. Wang, N. Y. Wang, R. G. Wang, W. Wang, X. Wang, Y. F. Wang, Z. Wang, Z. M. Webb, R. C. Weber, A. Wei, H. Y. Wen, L. J. and Whisnant, K. White, C. Whitehead, L. Whitehead, L. H. and Wise, T. Wojcicki, S. G. Wong, H. L. H. Wong, S. C. F. and Worcester, E. Wu, C. -H. Wu, Q. Wu, W. J. Xia, D. M. and Xia, J. K. Xing, Z. Z. Xu, J. L. Xu, J. Y. Xu, Y. and Xue, T. Yang, C. G. Yang, H. Yang, L. Yang, M. S. and Yang, M. T. Ye, M. Ye, Z. Yeh, M. Young, B. L. Yu, Z. Y. Zeng, S. Zhan, L. Zhang, C. Zhang, H. H. and Zhang, J. W. Zhang, Q. M. Zhang, X. T. Zhang, Y. M. and Zhang, Y. X. Zhang, Z. J. Zhang, Z. P. Zhang, Z. Y. and Zhao, J. Zhao, Q. W. Zhao, Y. B. Zhong, W. L. Zhou, L. and Zhou, N. Zhuang, H. L. Zou, J. H. Daya Bay Collaboration and MINOS Collaboration
Searches for a light sterile neutrino have been performed independently by the MINOS and the Daya Bay experiments using the muon (anti) neutrino and electron antineutrino disappearance channels, respectively. In this Letter, results from both experim
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::3035079e6ec6b9f562bea0e1eed936c6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3171600
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2
Isolation of regioisomers of N-alkylprotoporphyrin IX from chick embryo liver after treatment with porphyrinogenic xenobiotics
Autor: S M, Kobus, S G, Wong, G S, Marks
Publikováno v: Canadian journal of physiology and pharmacology. 79(9)
Several porphyrinogenic xenobiotics cause mechanism-based inactivation of cytochrome P450 (P450) isozymes with concomitant formation of a mixture of four N-alkylprotoporphyrin IX (N-alkylPP) regioisomers, which have ferrochelatase inhibitory properti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::22b580ef78a61f6ff9efe7510966a8f4
https://pubmed.ncbi.nlm.nih.gov/11599783
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3
Use of recombinant human ferrochelatase as a sensitive bioassay for N-alkylprotoporphyrin IX formed after interaction of porphyrinogenic xenobiotics with rat liver microsomes
Autor: J T, Gamble, S G, Wong, H A, Dailey, G S, Marks
Publikováno v: Canadian journal of physiology and pharmacology. 78(7)
Several porphyrinogenic xenobiotics elicit mechanism-based inactivation of cytochrome P450 (CYP) isozymes, leading to the formation of N-alkylprotoporphyrin IX (N-alkylPP), a potent inhibitor of ferrochelatase, the terminal enzyme in heme biosynthesi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cc542ecf74ab61be8845aec5a0711f52
https://pubmed.ncbi.nlm.nih.gov/10926165
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4
Cytochrome CYP sources of N-alkylprotoporphyrin IX after administration of porphyrinogenic xenobiotics to rats
Autor: S G, Wong, E H, Lin, G S, Marks
Publikováno v: Drug metabolism and disposition: the biological fate of chemicals. 27(9)
Cytochrome P-450 (CYP) 3A2 and CYP2C11 are sources of 70 and 30%, respectively, of N-vinylprotoporphyrin IX (N-vinylPP) formation after administration of 3-[(arylthio)ethyl]sydnone (TTMS) to rats. Female rats receiving TTMS were pretreated with dexam
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::307cd31641eb163bd9404e285ff7e839
https://pubmed.ncbi.nlm.nih.gov/10460791
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5
Gender differences in N-alkyl protoporphyrin IX production in rats after the administration of porphyrinogenic xenobiotics
Autor: S G, Wong, S M, Kobus, J P, McNamee, G S, Marks
Publikováno v: Drug metabolism and disposition: the biological fate of chemicals. 26(8)
The porphyrinogenicity of 3-[(arylthio)ethyl]sydnone (TTMS) and 3, 5-diethoxycarbonyl-1,4-dihydro-2,6-dimethyl-4-ethylpyridine (4-ethylDDC) in rats is dependent on mechanism-based inactivation of selected isozymes of hepatic cytochrome P450 (P450), n
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::522fbecb8a0aa6e7e703bd2d8a1cbac1
https://pubmed.ncbi.nlm.nih.gov/9698287
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6
Surgical management of giant nonmelanoma skin neoplasia
Autor: R Harrington, C N Harris, William O. Thomas, James A. Parker, B Murphy, L L Harper, S G Wong, J Abernethy
Publikováno v: Southern medical journal. 91(2)
Background Management of advanced integumentary malignancy has been controversial. We have evaluated and treated 10 patients with giant nonmelanoma skin neoplasias more than 8 cm in diameter. Methods Aggressive surgical ablation was prospectively rec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7883764ad6073797d1b3121a8717f02
https://pubmed.ncbi.nlm.nih.gov/9634130
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7
Human c-FES is a nuclear tyrosine kinase
Autor: K E, Yates, M R, Lynch, S G, Wong, D J, Slamon, J C, Gasson
Publikováno v: Oncogene. 10(6)
FES is a non-receptor protein tyrosine kinase expressed in hematopoietic progenitors and differentiated myeloid cells. It has recently been implicated in granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-3 (IL-3) and erythropoiet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6ab42304b40cda6a437e8297f4b30358
https://pubmed.ncbi.nlm.nih.gov/7700650
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8
Identification of conserved amino acids in the human granulocyte-macrophage colony-stimulating factor receptor alpha subunit critical for function. Evidence for formation of a heterodimeric receptor complex prior to ligand binding
Autor: L V, Ronco, S L, Silverman, S G, Wong, D J, Slamon, L S, Park, J C, Gasson
Publikováno v: The Journal of biological chemistry. 269(1)
A superfamily of growth factor and cytokine receptors has recently been identified, which is characterized by four spatially conserved cysteine residues, a tryptophan-serine motif (WSXWS) in the extracellular domain, and a proline-rich cytoplasmic do
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::74ea6a38f78f5386bed96aa5a8703bf0
https://pubmed.ncbi.nlm.nih.gov/8276807
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9
Molecular analysis of adrenocortical carcinoma (ACC) tumors
Autor: M. G. Yeh, T. Frew, M. C. Pastor, S. G. Wong
Publikováno v: Journal of Clinical Oncology. 29:e21174-e21174
e21174 Background: Personalized medicine has become increasingly important in the management of oncology patients. Traditional approaches require a large numbers of unselected patients to enroll on...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::915e7d9d40304fe4d2a3264d701804e6
https://doi.org/10.1200/jco.2011.29.15_suppl.e21174
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10
Phase I clinical trial of gemcitabine (GEM) in combination with PF-00477736 (PF-736), a selective inhibitor of CHK1 kinase
Autor: A. Blasina, N. Brega, J. Gallo, A. N. Tse, S. G. Wong, C. Britten, K. D. Wilner, Grant A. McArthur, G. K. Schwartz, E. Wang
Publikováno v: Journal of Clinical Oncology. 28:3062-3062
3062 Background: The S-phase and G2-checkpoints are critical mediators of the cell cycle response to cytotoxic therapy. PF-736 is a selective inhibitor of the S/G2-checkpoint kinase CHK1, displayin...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fcc7d8ac80dfe33a19c0ca096ca6584d
https://doi.org/10.1200/jco.2010.28.15_suppl.3062
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