Citation: M. Montoya et al., TEMPERATURES AT THE LAST INTERGLACIAL SIMULATED BY A COUPLED OCEAN-ATMOSPHERE CLIMATE MODEL, Paleoceanography, 13(2), 1998, pp. 170-177
Authors:
PRABHAKAR SS
ZEBALLOS G
MONTOYA M
LEONARD C
Citation: Ss. Prabhakar et al., UREA INHIBITS INDUCIBLE NITRIC-OXIDE SYNTHESIS IN MURINE MACROPHAGES AT A POSTTRANSCRIPTIONAL LEVEL, Journal of the American Society of Nephrology, 8, 1997, pp. 112-112
Citation: Rd. Brinton et al., 17-BETA-ESTRADIOL ENHANCES THE OUTGROWTH AND SURVIVAL OF NEOCORTICAL NEURONS IN CULTURE, Neurochemical research, 22(11), 1997, pp. 1339-1351
Citation: Rd. Brinton et al., THE ESTROGEN REPLACEMENT PREMARIN IS NEUROTROPHIC FOR NEURONS DERIVEDFROM BRAIN-REGIONS INVOLVED IN COGNITION AND MEMORY FUNCTION, Journal of the American Geriatrics Society, 45(9), 1997, pp. 32-32
Authors:
KELNER MJ
BAGNELL R
MONTOYA M
ESTES L
UGLIK SF
CERUTTI P
Citation: Mj. Kelner et al., TRANSFECTION WITH HUMAN COPPER-ZINC SUPEROXIDE-DISMUTASE INDUCES BIDIRECTIONAL ALTERATIONS IN OTHER ANTIOXIDANT ENZYMES, PROTEINS, GROWTH-FACTOR RESPONSE, AND PARAQUAT RESISTANCE, Free radical biology & medicine, 18(3), 1995, pp. 497-506
Citation: M. Montoya et al., THE CALCULATION OF LIQUID-VAPOR-EQUILIBRIUM FOR GROUP IA AND GROUP IIA METALS, Physics and chemistry of liquids, 29(3), 1995, pp. 169-181
Authors:
KELNER MJ
MCMORRIS TC
ESTES L
STARR RJ
RUTHERFORD M
MONTOYA M
SAMSON KM
TAETLE R
Citation: Mj. Kelner et al., EFFICACY OF ACYLFULVENE ILLUDIN ANALOGS AGAINST A METASTATIC LUNG-CARCINOMA MV522 XENOGRAFT NONRESPONSIVE TO TRADITIONAL ANTICANCER AGENTS - RETENTION OF ACTIVITY AGAINST VARIOUS MDR PHENOTYPES AND UNUSUAL CYTOTOXICITY AGAINST ERCC2 AND ERCC3 DNA HELICASE-DEFICIENT CELLS, Cancer research, 55(21), 1995, pp. 4936-4940
Authors:
KELNER MJ
MCMORRIS TC
ESTES L
RUTHERFORD M
MONTOYA M
GOLDSTEIN J
SAMSON K
STARR R
TAETLE R
Citation: Mj. Kelner et al., CHARACTERIZATION OF ILLUDIN-S SENSITIVITY IN DNA REPAIR-DEFICIENT CHINESE-HAMSTER CELLS - UNUSUALLY HIGH-SENSITIVITY OF ERCC2 AND ERCC3 DNAHELICASE-DEFICIENT MUTANTS IN COMPARISON TO OTHER CHEMOTHERAPEUTIC-AGENTS, Biochemical pharmacology, 48(2), 1994, pp. 403-409