000 | 01462 a2200397 4500 | ||
---|---|---|---|
005 | 20250513093943.0 | ||
264 | 0 | _c19961010 | |
008 | 199610s 0 0 eng d | ||
022 | _a0893-228X | ||
024 | 7 |
_a10.1021/tx9501795 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aDeCorte, B L | |
245 | 0 | 0 |
_aImproved strategies for postoligomerization synthesis of oligodeoxynucleotides bearing structurally defined adducts at the N2 position of deoxyguanosine. _h[electronic resource] |
260 |
_bChemical research in toxicology _c |
||
300 |
_a630-7 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. | ||
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aChromatography, High Pressure Liquid |
650 | 0 | 4 |
_aDNA Adducts _xchemistry |
650 | 0 | 4 |
_aDeoxyguanosine _xchemistry |
650 | 0 | 4 | _aElectrophoresis, Capillary |
650 | 0 | 4 |
_aEpoxy Compounds _xchemistry |
650 | 0 | 4 |
_aInosine _xanalogs & derivatives |
650 | 0 | 4 | _aKinetics |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 |
_aOligonucleotides _xchemical synthesis |
650 | 0 | 4 |
_aTrimethylsilyl Compounds _xchemical synthesis |
700 | 1 | _aTsarouhtsis, D | |
700 | 1 | _aKuchimanchi, S | |
700 | 1 | _aCooper, M D | |
700 | 1 | _aHorton, P | |
700 | 1 | _aHarris, C M | |
700 | 1 | _aHarris, T M | |
773 | 0 |
_tChemical research in toxicology _gvol. 9 _gno. 3 _gp. 630-7 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1021/tx9501795 _zAvailable from publisher's website |
999 |
_c8725636 _d8725636 |