Chemistry Reference
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Boudaiffa B, Cloutier P, Hunting D, Huels MA, Sanche L (2002) Cross sections for low-energy (10−50
eV) electron damage to DNA. Radiat Res 157:227−234
Bourdat A-G, Douki T, Frelon S, Gasparutto D, Cadet J (2000) Tandem base lesions are gene-
rated by hydroxyl radical within isolated DNA in aerated aqueous solution. J Am Chem Soc
122:4549−4556
Box HC, Patrzyc HB, Dawidzik JB, Wallace JC, Freund HG, Iijima H, Budzinski EE (2000) Double base
lesions in X-irradiated DNA in the presence or absence of oxygen. Radiat Res 153:442−446
Bradley MO, Erickson LC (1981) Comparison of the effect of hydrogen peroxide and X-ray irradiation
on toxicity, mutation and DNA damage/repair in mammalian cells (V-79). Biochim Biophys Acta
654:135−141
Brady LW (1980) Radiation sensitizers: their use in the clinical management of cancer. Masson Pub-
lishers, New York
Braunlin WH, Strick TJ, Record MT (1982) Equilibrium dialysis studies of polyamine binding to DNA.
Biopolymers 21:1301−1314
Breen AP, Murphy JA (1995) Reactions of oxyl radicals with DNA. Free Radical Biol Med
18:1033−1077
Bremner I (1987) Interactions between metallothionein and trace elements. Progr Food Nutr Sci
11:1− 37
Brenner DJ, Ward JF (1992) Constraints on energy deposition and target size of multiply damaged
sites associated with DNA double-strand breaks. Int J Radiat Biol 61:737−748
Breusegem SY, Clegg RM, Loontiens FG (2002) Base-sequence specificity of Hoechst 33258 and
DAPI binding to five (A/T) 4 sites with kinetic evidence for more than one highly-affinic Hoechst
33258-AATT complex. J Mol Biol 315:1049−1061
Bridges BA (1969) Sensitization of organisms to radiation by sulfhydryl-binding agents. Adv Radiat
Biol 3:123−176
Brooks PJ, Wise DS, Berry DA, Kosmoski JV, Smerdon MJ, Somers RL, Mackie H, Spoonde AY, Acker-
man EJ, Coleman K, Tarone RE, Robbins JH (2000) The oxidative DNA lesion 8,5 -(S)-cyclo-2 -de-
oxyadenosine is repaired by the nucleotide excision repair pathway and blocks gene expressi-
on in mammalian cells. J Biol Chem 275:22355−22362
Brown AU, Todd AR (1952) Nucleotides 10. Some observations on the structure and chemical beha-
viour of the nucleic acids. J Chem Soc 52−58
Brown JM (1990) Redox activation of benzotriazine N-oxides: mechanisms and potential as antican-
cer drugs. In: Adams GE (ed) Selective activation of druges by redox processes; NATO ASI Series
A 19. Plenum Press, New York, pp 137−148
Brown JM (1993) SR 4233 (Tirapazamin): a new anticancer drug exploiting hypoxia in solid tumors.
Br J Cancer 67:1163−1170
Brown JM, Wang L-H (1998) Tirapazamine: laboratory data relevant to clinical activity. Anti-Cancer
Drug Design 13:529−539
Bruckmann E, Wojcik A, Obe G (1999) X-irradiation of G1 CHO cells induces SCE which are both true
and false in BrdU-substituted cells but only false in biotin-dUTP-substituted cells. Chromosome
Res 7:277−288
Brun AM, Harriman A (1994) Energy- and electron-transfer processes involving palladium porphy-
rins bound to DNA. J Am Chem Soc 116:10383−10393
Brustad T, Wold E (1976) Long-lived species in irradiated N 2 O-flushed saline phosphate buffer, with
toxic effect upon E. coli K-12. Radiat Res 66:215−230
Bump EA, Yu NY, Brown JM (1982) The use of drugs which deplete intracellular glutathione in hypo-
xic cell radiosensitization. Int J Radiat Oncol Biol Phys 8:439−442
Burger RM (1998) Cleavage of nucleic acids by bleomycin. Chem Rev 98:1153−1169
Burger RM (2000) Nature of activated bleomycin. Struct Bonding 97:288−289
Burger RM, Drlica K (1996) Bleomycin reaction pathways: kinetic approaches. In: Meunier B (ed) DNA
cleavers and chemotherapy of cancer or viral disease. Kluver, Dordercht, pp 91−106
Burger RM, Horwitz SB, Peisach J, Wittenberg JB (1979) Oxygenated iron bleomycin. A short-lived
intermediate in the reaction of ferrous bleomycin with O 2 . J Biol Chem 254:12299−12302
Burger RM, Berkowitz AR, Peisach J, Horwitz SB (1980) Origin of malondialdehyde from DNA de-
graded by Fe(II) . bleomycin. J Biol Chem 255:11832−11838
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