D. J. Gruol

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Reversal of Multidrug Resistance by RU 4861

Joseph, Suzanne, D. J. Gruol, 2006 .

Profound differences in the transport of steroids by two mouse P-glycoproteins.

M. C. Zee, D. J. Gruol, Q. D. Vo, 1999, Biochemical pharmacology.

Chemosensitizing steroids: glucocorticoid receptor agonists capable of inhibiting P-glycoprotein function.

S. Bourgeois, D. J. Gruol, 1997, Cancer research.

Cyclic AMP-dependent protein kinase modulation of the glucocorticoid-induced cytolytic response in murine T-lymphoma cells.

S. Bourgeois, D. J. Gruol, F. Rajah, 1989, Molecular endocrinology.

Evidence for the locations of distinct steroid and Vinca alkaloid interaction domains within the murine mdr1b P-glycoprotein.

M. Kuehne, D. J. Gruol, M. N. King, 2002, Molecular pharmacology.

The use of a novel taxane-based P-glycoprotein inhibitor to identify mutations that alter the interaction of the protein with paclitaxel.

I. Ojima, R. Bernacki, D. J. Gruol, 2001, Molecular pharmacology.

Modulation of Glucocorticoid-Induced Responses by Cyclic AMP in Lymphoid Cell Lines

S. Bourgeois, Maureen T. Harrigan, D. J. Gruol, 1989 .

High-resolution anion exchange chromatography of the glucocorticoid receptor from WEHI-7 cells.

S. Bourgeois, N. F. Campbell, D. J. Gruol, 1988, Journal of steroid biochemistry.

Cyclic AMP-dependent protein kinase promotes glucocorticoid receptor function.

S. Bourgeois, N. F. Campbell, D. J. Gruol, 1986, The Journal of biological chemistry.

Transformation of glucocorticoid receptors bound to the antagonist RU 486: effects of alkaline phosphatase.

K. A. Wolfe, D. J. Gruol, 1990, Biochemistry.

The c-erb-A gene encodes a thyroid hormone receptor

R. Evans, R. Lebo, C. Weinberger, 1986, Nature.

Transformed glucocorticoid receptors consist of multiple subspecies with differing capacities to bind DNA-cellulose.

K. A. Wolfe, D. J. Gruol, 1989, Biochemistry.

Reversal of multidrug resistance by RU 486.

S. Bourgeois, J. Trotter, M. C. Zee, 1994, Cancer research.

Identification of P-glycoprotein Mutations Causing a Loss of Steroid Recognition and Transport*

D. J. Gruol, Q. D. Vo, 1999, The Journal of Biological Chemistry.

Reversal of multidrug resistance by RU 486.

S. Bourgeois, J. Trotter, M. C. Zee, 1994, Cancer research.

Structure-activity analysis of taxane-based broad-spectrum multidrug resistance modulators.

M. Baer, I. Ojima, R. Bernacki, 2004, Anticancer research.

Phenothiazines cause a shift in the cAMP dose‐response: Selection of resistant variants in a murine thymoma line

D. Dalton, D. Gruol, D. J. Gruol, 1984, Journal of cellular physiology.

Expression of an mdr gene is associated with a new form of resistance to dexamethasone-induced apoptosis.

S. Bourgeois, D. J. Gruol, R. Newby, 1993, Molecular endocrinology.

Isolation of new types of dexamethasone-resistant variants from a cAMP-resistant lymphoma.

S. Bourgeois, N. F. Campbell, M. Ashby, 1986, Journal of Steroid Biochemistry.

Nuclear interactions of wild type and variant glucocorticoid receptors.

S. Bourgeois, D. Dalton, D. J. Gruol, 1984, Journal of Steroid Biochemistry.

Characterization of the glucocorticoid receptor. Comparison of wild type and variant receptors.

S. Bourgeois, E. Kempner, D. J. Gruol, 1984, The Journal of biological chemistry.

Synergistic induction of apoptosis with glucocorticoids and 3',5'-cyclic adenosine monophosphate reveals agonist activity by RU 486.

J. Altschmied, D. Gruol, D. J. Gruol, 1993, Molecular endocrinology.

Expression of the mdr1 P-glycoprotein gene: a mechanism of escape from glucocorticoid-induced apoptosis.

S. Bourgeois, D. Gruol, D. J. Gruol, 1994, Biochemistry and cell biology = Biochimie et biologie cellulaire.