Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Kelly Y"'
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Repositório da Produção Científica e Intelectual da Unicamp
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Repositório Institucional da Unicamp
Universidade de São Paulo (USP)
instacron:USP
Repositório da Produção Científica e Intelectual da Unicamp
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Repositório Institucional da Unicamp
Agradecimentos: This study was part of the research program "Programa de Monitoramento de Longa Duração das Comunidades Recifais de Ilhas Oceânicas - PELD" (441241/2016-6, Carlos E.L. Ferreira-PI). K.Y.I. received scholarships from Coordination fo
Autor:
Andre Valcour, Thomas Rogge, Alex Katayev, Kelly Y. Chun, Etienne Cavalier, Sven Diederich, Martin Bidlingmaier, Katharina Schilbach, Tim Kühnle
Publikováno v:
Journal of the Endocrine Society
Background: IGF-I is the most widely used biomarker for management of GH related diseases. Reproducible assays and method-specific reference intervals (RIs) are crucial determinants of its clinical utility. Assay validation and RIs based on >15,000 s
Autor:
Julie Y.J. Ang, Kelly Y. Li, Danny Leung, Qinghong Jiang, Ah Young Lee, Kevin Y. Yip, Qin Cao
Publikováno v:
Cell reports. 33(4)
G9a is a lysine methyltransferase that regulates epigenetic modifications, transcription, and genome organization. However, whether these properties are dependent on one another or represent distinct functions of G9a remains unclear. In this study, w
Autor:
Sue S. Yom, Haja Sittana El Mubarak, Miriam Sander, K.C. Allen Chan, Quynh-Thu Le, Benjamin A. Pinsky, Kelly Y. Kim, Raymond H.W. Ng, Barbara A. Conley, Scott V. Bratman
Publikováno v:
Journal of the National Cancer Institute, vol 109, iss 4
Clinical studies have shown plasma Epstein-Barr virus (EBV) DNA level to be an independent prognostic biomarker for nasopharyngeal carcinoma (NPC). However, the proportion of NPC patients whose tumors are associated with EBV vary with geographic loca
Autor:
Arjun Srinivasan, Suzanne F. Beavers, Linda Goss, Timothy L. Wiemken, Andrew Wong, Malkanthie McCormick, Douglas Thoroughman, Kelly Y. Kawaoka, David B. Blossom
Publikováno v:
Public Health Reports. 124:868-874
Objectives. Acinetobacter baumannii ( A. baumannii) is a well-described cause of nosocomial outbreaks and can be highly resistant to antimicrobials. We investigated A. baumannii outbreaks at two Kentucky hospitals to find risk factors for Acinetobact
Autor:
Priscilla M.K. Poon, Stephen T.S. Lam, Chun-Kwok Wong, Chi Pui Pang, Kelly Y. C. Lai, Nan Zhong, Qian L. Chen
Publikováno v:
Clinical Biochemistry. 39:244-248
To study the AGG interspersion pattern in mentally retarded patients of unspecified cause.FMR1 CGG substructure in 104 normal and 232 mentally retarded (MR) males was determined by CGG repeat and AGG interspersion analyses. Genomic DNA of the study s
Publikováno v:
Biochemistry. 39:14670-14681
Inactivation of HMG-CoA synthase by a carboxyl-directed reagent, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), in a concentration-dependent and substrate-protectable manner suggested that the active site contains reactive acidic amino acids. T
Publikováno v:
Journal of Biological Chemistry. 275:17946-17953
Replacement of 3-hydroxy-3-methylglutaryl-CoA synthase's glutamate 95 with alanine diminishes catalytic activity by over 5 orders of magnitude. The structural integrity of E95A enzyme is suggested by the observation that this protein contains a full
Publikováno v:
Journal of General Virology. 81:695-700
The effects of interferon (IFN)-alpha, IFN-beta and IFN-gamma on human papillomavirus (HPV) oncogene expression were studied in various cervical carcinoma cell lines containing integrated copies of either HPV type 16 or HPV type 18. The levels of E6
Autor:
Chun-Kwok Wong, Chi Pui Pang, Nan Zhong, W. Ted Brown, C.H. Lau, Qian L. Chen, Kelly Y. C. Lai, Priscilla M.K. Poon
Publikováno v:
American Journal of Medical Genetics. 84:208-213
The fragile X syndrome is the most common inherited form of mental retardation. Haplotype studies using FRAXAC1 and DXS548 polymorphic markers flanking the fragile site have demonstrated linkage disequilibrium at the FMR1 locus. We investigated the a