نتایج جستجو برای: copper 64

تعداد نتایج: 166299  

Journal: :Nanoscale 2015
Jin-Cheng Yu Fu-Gang Zhao Wei Shao Cong-Wu Ge Wei-Shi Li

Thanks to their outstanding properties and a wide range of promising applications, the development of a versatile and convenient preparation method for metallic copper nanocrystals with controllable shape is of primary significance. Different from the literature that utilized a capping agent bearing only one kind of Cu binding functionality, either an amino or a carboxylic unit, for their prepa...

Journal: :The Tohoku journal of experimental medicine 1983
T Chiba

Cu BA, T. Serum and Urine Amino Acid Analysis in Children with Biliary Atresia. Tohoku J. exp. Med., 1983, 139 (1), 61-66 Serum and urine amino acid levels were measured preoperatively and at varying time following successful hepatic portoenterostomy. All of the essential amino acids measured returned to normal levels during the late postoperative period over five years, whereas many of the non...

Journal: :Journal of the American Chemical Society 2007
Hein J Wijma Iain MacPherson Ole Farver Elitza I Tocheva Israel Pecht Martin Ph Verbeet Michael E P Murphy Gerard W Canters

Copper-containing nitrite reductase harbors a type-1 and a type-2 Cu site. The former acts as the electron acceptor site of the enzyme, and the latter is the site of catalytic action. The effect of the methionine ligand on the reorganization energy of the type-1 site was explored by studying the electron-transfer kinetics between NiR (wild type (wt) and the variants Met150Gly and Met150Thr) wit...

2011
Orit Jacobson Ido D. Weiss Lawrence P. Szajek Gang Niu Ying Ma Dale O. Kiesewetter Joshua M. Farber Xiaoyuan Chen

Expression of CXCR4 in cancer has been found to correlate with poor prognosis and resistance to chemotherapy. In this study we developed a derivative of the CXCR4 peptide antagonist, T140-2D, that can be labeled easily with the PET isotope copper-64, and thereby enable in vivo visualization of CXCR4 in tumors. T140 was conjugated to 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid mono ...

Journal: :Cancer biology & therapy 2011
Jeffrey N Bryan Fang Jia Huma Mohsin Geethapriya Sivaguru Carolyn J Anderson William H Miller Carolyn J Henry Michael R Lewis

BACKGROUND We previously described a two-antibody model of (64)Cu radioimmunotherapy to evaluate low-dose, solid-tumor response. This model was designed to test the hypothesis that cellular internalization is critical in causing tumor cell death by mechanisms in addition to radiation damage. The purpose of the present study was to estimate radiation dosimetry for both antibodies (mAbs) using po...

A.R. Jalilian, J. Moafian, M. Kamali-dehghan, M. Mirzaii, P. Rowshanfarzad,

Background: Copper-64 (T1/2=12.7 h) is an important radionuclide used both in PET imaging and therapy. [64Cu]-pyruvaldehyde-bis (N4-methylthiosemicarbazone) ([64Cu]-PTSM) is one of the most famous copper radiopharmaceuticals with unique specifications (suitable half life, stability, etc.). The wide range of 64Cu applications arouse great interest for its production. Materials and Methods: Cu-64...

2016
Thomas Sheppard Helen Daly Alex Goguet Jillian M Thompson

The mono(μ-oxo) dicopper cores present in the pores of Cu-ZSM-5 are active for the partial oxidation of methane to methanol. However, copper on the external surface reduces the ratio of active, selective sites to unselective sites. More efficient catalysts are obtained by controlling the copper deposition during synthesis. Herein, the external exchange sites of ZSM-5 samples were passivated by ...

Journal: :The Journal of biological chemistry 2004
Vicente Sancenón Sergi Puig Isabel Mateu-Andrés Eavan Dorcey Dennis J Thiele Lola Peñarrubia

Copper plays a dual role in aerobic organisms, as both an essential and a potentially toxic element. To ensure copper availability while avoiding its toxic effects, organisms have developed complex homeostatic networks to control copper uptake, distribution, and utilization. In eukaryotes, including yeasts and mammals, high affinity copper uptake is mediated by the Ctr family of copper transpor...

Journal: :Dalton transactions 2014
Brett M Paterson Peter Roselt Delphine Denoyer Carleen Cullinane David Binns Wayne Noonan Charmaine M Jeffery Roger I Price Jonathan M White Rodney J Hicks Paul S Donnelly

The use of copper radioisotopes in cancer diagnosis and radionuclide therapy is possible using chelators that are capable of binding Cu(II) with sufficient stability in vivo to provide high tumour-to-background contrast. Here we report the design and synthesis of a new bifunctional chelator, 5-(8-methyl-3,6,10,13,16,19-hexaaza-bicyclo[6.6.6]icosan-1-ylamino)-5-oxopentanoic acid (MeCOSar), that ...

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