نتایج جستجو برای: albumin adduct

تعداد نتایج: 49834  

Journal: :Chemical & pharmaceutical bulletin 2002
Naoko Morisaki Hisayoshi Kobayashi Yumiko Yamamura Masuo Morisaki Kazuo Nagasawa Yuichi Hashimoto

Steroidal allylic alcohols formed Na+ adduct ion peaks [M+Na]+ by the addition of NaCl in FAB mass spectrometry. A comparison of the intensities of the adduct ion peaks of allylic alcohols with those of the corresponding saturated alcohols and olefin suggested that the olefinic double bond and the proximal hydroxyl group had coordinated to Na+. The adduct ion was stable and did not undergo dehy...

Journal: :Cancer research 1988
A G Lurie D L Rozenski J E Coghill

Studies examined the in vivo binding of radiolabeled 7,12-dimethylbenz(a)anthracene (DMBA) to hamster cheek pouch epithelial DNA. Adduct formation was studied as functions of [3H]DMBA dose and of the time after single [3H]DMBA applications in mineral oil. Total DMBA-DNA adduct formation was determined by DNA-bound 3H activity, and qualitative binding characteristics were further studied by high...

2015
Marie Pedersen Michelle A. Mendez Bernadette Schoket Roger W. Godschalk Ana Espinosa Anette Landström Cristina M. Villanueva Domenico F. Merlo Eleni Fthenou Esther Gracia-Lavedan Frederik-J. van Schooten Gerard Hoek Gunnar Brunborg Helle M. Meltzer Jan Alexander Jeanette K. Nielsen Jordi Sunyer John Wright Katalin Kovács Kees de Hoogh Kristine B. Gutzkow Laura J. Hardie Leda Chatzi Lisbeth E. Knudsen Lívia Anna Matthias Ketzel Margaretha Haugen Maria Botsivali Mark J. Nieuwenhuijsen Marta Cirach Mireille B. Toledano Rachel B. Smith Sarah Fleming Silvia Agramunt Soterios A. Kyrtopoulos Viktória Lukács Jos C. Kleinjans Dan Segerbäck Manolis Kogevinas

BACKGROUND Bulky DNA adducts reflect genotoxic exposures, have been associated with lower birth weight, and may predict cancer risk. OBJECTIVE We selected factors known or hypothesized to affect in utero adduct formation and repair and examined their associations with adduct levels in neonates. METHODS Pregnant women from Greece, Spain, England, Denmark, and Norway were recruited in 2006-20...

Journal: :Carcinogenesis 1996
G Lévay D N Pathak W J Bodell

We have employed the P1-enhanced 32P-postlabeling procedure to detect the formation DNA of adducts in the white blood cells (WBC) of B6C3F1 mice treated by i.p. injection with benzene. Treatment twice a day with 440 mg/kg benzene for 1-7 days resulted in the formation of one major (adduct 1) and one minor (adduct 2) DNA adduct in the WBCs of mice. The same DNA adduct pattern was also found in t...

Journal: :Biochemistry 1976
A Schonbrunn R H Abeles C T Walsh S Ghisla H Ogata V Massey

2-Hydroxy-3-butynoic acid is a suicide substrate for Mycobacterium smegmatis lactate oxidase. Inactivation occurs by covalent modification of enzyme-bound FMN and does not involve labeling of the apoprotein. The spectrum of the enzyme bound adduct suggests that it is a 4a, 5-dihydroflavin derivative. When this adduct is released from the enzyme, a complex mixture of unstable compounds is obtain...

Journal: :Environmental Health Perspectives 1996
M J Meyer W E Bechtold

Covalent protein adducts formed after exposure to xenobiotics may provide readily measurable indicators of these exposures. After adequate characterization of the dose-dependent formation of a specific adduct, the adduct can often be used as a quantitative marker for exposure, DNA adduct formation, or, possibly, risk of disease. By elucidating the structure of an adduct and studying the conditi...

A.A Alameh M Mohammadi M.R Nori-Daloii

Benzo(a) pyrene is a carcinigen polycyclic aromatic hydrocarbon which diffuses into the environment from combustion of organic meterials.based on various epidemiological evidences it is related to lung,skin and liver cancer.mutagenicity,and immunosuppressivety are among important biological effects of Benzo(a) pyrene.after absorbtion and distribution in the body,it undergoes epoxidation by cyto...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1992
W G Humphreys F F Kadlubar F P Guengerich

Aromatic amines are bioactivated to electrophilic compounds that react with DNA, predominantly at the C8 position of guanine bases. This site is weakly nucleophilic and it has been proposed that the C8 adduct is the final product after initial N7-adduct formation. To consider this possibility, we reacted several C8-substituted guanine derivatives with N-acetoxy-2-aminofluorene, prepared in situ...

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