نتایج جستجو برای: mesoporous fdu 12

تعداد نتایج: 591126  

2009
Daman Kumari Valentina Somma Asako J. Nakamura William M. Bonner Ettoré D’Ambrosio Karen Usdin

FRAXA is one of a number of fragile sites in human chromosomes that are induced by agents like fluorodeoxyuridine (FdU) that affect intracellular thymidylate levels. FRAXA coincides with a >200 CGG*CCG repeat tract in the 5' UTR of the FMR1 gene, and alleles prone to fragility are associated with Fragile X (FX) syndrome, one of the leading genetic causes of intellectual disability. Using siRNA ...

2016
Yan Yan Xiangzi Han Yulan Qing Allison G. Condie Shashank Gorityala Shuming Yang Yan Xu Youwei Zhang Stanton L. Gerson

5-fluorodeoxyuridine (5-FdU, floxuridine) is active against multiple cancers through the inhibition of thymidylate synthase, which consequently introduces uracil and 5-FU incorporation into the genome. Uracil DNA glycosylase (UDG) is one of the main enzymes responsible for the removal of uracil and 5-FU. However, how exactly UDG mediates cellular sensitivity to 5-FdU, and if so whether it is th...

Journal: :Acta chimica Slovenica 2014
Rong Xing Lin Wu Zhenghao Fei

A versatile photocatalyst has been prepared by grafting palladium phthalocyaninesulfonate (PdPcS) onto the FDU-14 mesopolymer with 3-D cubic mesostructure (FDU-14-PdPcS) via multi-step chemical modification processes. The FDU-14-PdPcS was characterized by the X-ray diffraction (XRD), diffuse reflectance UV-vis spectroscopy and inductively coupled plasma (ICP) techniques. In the photodegradation...

Journal: :Cancer research 2005
Zhi-Yong Liao Olivier Sordet Hong-Liang Zhang Glenda Kohlhagen Smitha Antony William H Gmeiner Yves Pommier

FdUMP[10], a 10mer of 5-fluoro-2'-deoxyuridine 5'-monophosphate (FdUMP), the thymidylate synthase inhibitory metabolite of 5-fluorouracil (FU), is most closely correlated with the DNA topoisomerase I (Top1) inhibitor camptothecin in the National Cancer Institute COMPARE analysis, but not with FU. FdUMP[10] exhibits more potent antiproliferative activity than FdUMP or 5-fluoro-2'-deoxyuridine (F...

Journal: :Human molecular genetics 2014
Dmitry Yudkin Bruce E Hayward Mirit I Aladjem Daman Kumari Karen Usdin

Fragile X Syndrome (FXS) is a learning disability seen in individuals who have >200 CGG•CCG repeats in the 5' untranslated region of the X-linked FMR1 gene. Such alleles are associated with a fragile site, FRAXA, a gap or constriction in the chromosome that is coincident with the repeat and is induced by folate stress or thymidylate synthase inhibitors like fluorodeoxyuridine (FdU). The molecul...

Journal: :Thermal Science 2023

The present paper goal is to compile a comprehensive database of data on the pressure drop and flow distribution uniformity (FDU) utilizing CFD in network parallel tubes arranged Z configuration adopted for flat plate solar collectors. A 3D model implemented simulate such system as market, including two domains: tube materials fluid, besides entering exiting prolonged ports. specifications are ...

2011
Supratim Ghosh Freddie R. Salsbury David A. Horita William H. Gmeiner

We report, based on semi-empirical calculations, that Zn(2+) binds duplex DNA containing consecutive FdU-dA base pairs in the major groove with distorted trigonal bipyramidal geometry. In this previously uncharacterized binding motif, O4 and F5 on consecutive FdU are axial ligands while three water molecules complete the coordination sphere. NMR spectroscopy confirmed Zn(2+) complexation occurr...

Journal: :Anticancer research 2010
L Novotny P Rauko H Schott

The cytotoxic and antineoplastic potential of two new duplex drugs, ECyd-5-FdU and ECyd- lipid- 5-FdU, were compared with the activity of the parent single-nucleoside analogues, 3-C-ethynylcytidine (ECyd) and 5-fluorodeoxyuridine (5-FdU), either applied as monotherapy or simultaneously in equimolar concentrations simulating their ratio in a duplex drug. Murine leukaemia L1210 cells were used fo...

2013
Shao-yu Wu Tian-min Chen William H. Gmeiner Edward Chu John C. Schmitz

Therapeutic small interfering RNAs (siRNAs) are composed of chemically modified nucleotides, which enhance RNA stability and increase affinity in Watson-Crick base pairing. However, the precise fate of such modified nucleotides once the siRNA is degraded within the cell is unknown. Previously, we demonstrated that deoxythymidine release from degraded siRNAs reversed the cytotoxicity of thymidyl...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید