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Breast Cancer Research and Treatment
|
January 1, 1993
Modulators of cellular protein phosphorylation alter the trans-activation function of human progesterone receptor and the biological activity of progesterone antagonists
D P Edwards, N L Weigel, S K Nordeen, et al.
Endocrinology
|
April 7, 1998
The antagonists RU486 and ZK98299 stimulate progesterone receptor binding to deoxyribonucleic acid in vitro and in vivo, but have distinct effects on receptor conformation
E K Gass, S A Leonhardt, S K Nordeen, et al.
Cancer Research
|
November 1, 1981
Failure of estradiol immunofluorescence in MCF-7 breast cancer cells to detect estrogen receptors
W D Mercer, D P Edwards, G C Chamness, et al.
Biochemistry
|
November 3, 1992
Effects of the steroid antagonist RU486 on dimerization of the human progesterone receptor
A M DeMarzo, S A Oñate, S K Nordeen, et al.
Cancer Research
|
November 15, 1988
Immunocytochemical localization of progesterone receptors in breast cancer with anti-human receptor monoclonal antibodies
D Elashry-Stowers, D T Zava, W C Speers, et al.
Cancer Research
|
February 1, 1987
An immunotoxin cytotoxic for breast cancer cells in vitro
C F LeMaistre, D P Edwards, K A Krolick, et al.
Biofouling
|
November 26, 2011
The surface properties of silicone elastomers Exposed to seawater
T G Nevell, D P Edwards, A J Davis, et al.
Molecular Endocrinology (Baltimore, Md.)
|
April 1, 1993
The constitution of a progesterone response element
B A Lieberman, B J Bona, D P Edwards, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1991
Dimerization of mammalian progesterone receptors occurs in the absence of DNA and is related to the release of the 90-kDa heat shock protein
A M DeMarzo, C A Beck, S A Onate, et al.
Molecular and Cellular Biology
|
April 11, 2000
The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding
P H Giangrande, E A Kimbrel, D P Edwards, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 113) with videos related to
Sort By:
Page
of 12
Breast Cancer Research and Treatment
|
January 1, 1993
Modulators of cellular protein phosphorylation alter the trans-activation function of human progesterone receptor and the biological activity of progesterone antagonists
D P Edwards, N L Weigel, S K Nordeen, et al.
Endocrinology
|
April 7, 1998
The antagonists RU486 and ZK98299 stimulate progesterone receptor binding to deoxyribonucleic acid in vitro and in vivo, but have distinct effects on receptor conformation
E K Gass, S A Leonhardt, S K Nordeen, et al.
Cancer Research
|
November 1, 1981
Failure of estradiol immunofluorescence in MCF-7 breast cancer cells to detect estrogen receptors
W D Mercer, D P Edwards, G C Chamness, et al.
Biochemistry
|
November 3, 1992
Effects of the steroid antagonist RU486 on dimerization of the human progesterone receptor
A M DeMarzo, S A Oñate, S K Nordeen, et al.
Cancer Research
|
November 15, 1988
Immunocytochemical localization of progesterone receptors in breast cancer with anti-human receptor monoclonal antibodies
D Elashry-Stowers, D T Zava, W C Speers, et al.
Cancer Research
|
February 1, 1987
An immunotoxin cytotoxic for breast cancer cells in vitro
C F LeMaistre, D P Edwards, K A Krolick, et al.
Biofouling
|
November 26, 2011
The surface properties of silicone elastomers Exposed to seawater
T G Nevell, D P Edwards, A J Davis, et al.
Molecular Endocrinology (Baltimore, Md.)
|
April 1, 1993
The constitution of a progesterone response element
B A Lieberman, B J Bona, D P Edwards, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1991
Dimerization of mammalian progesterone receptors occurs in the absence of DNA and is related to the release of the 90-kDa heat shock protein
A M DeMarzo, C A Beck, S A Onate, et al.
Molecular and Cellular Biology
|
April 11, 2000
The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding
P H Giangrande, E A Kimbrel, D P Edwards, et al.
Page
of 12