Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D P McDonnell

Showing results (31-40 of 99) with videos related to

Pageof 10
Sort By:
Gene Expression|January 1, 1992
Identification of novel steroid-response elementsZ Nawaz, M J Tsai, D P McDonnell, et al.
Molecular Carcinogenesis|January 1, 1993
Creation of an active estrogen-responsive element by a single base change in the flanking sequence of a cellular oncogene: a possible mechanism for hormonal carcinogenesis?Z Nawaz, G M Stancel, D P McDonnell, et al.
Vitamins and Hormones|January 1, 1996
The molecular pharmacology of ovarian steroid receptorsE Vegeto, B L Wagner, M O Imhof, et al.
The Journal of Biological Chemistry|April 18, 1998
Enhancement of estrogen receptor transcriptional activity by the coactivator GRIP-1 highlights the role of activation function 2 in determining estrogen receptor pharmacologyJ D Norris, D Fan, M R Stallcup, et al.
Molecular Endocrinology (Baltimore, Md.)|June 1, 1997
Identification of a third autonomous activation domain within the human estrogen receptorJ D Norris, D Fan, S A Kerner, et al.
The Journal of Biological Chemistry|September 25, 1991
Transactivation functions facilitate the disruption of chromatin structure by estrogen receptor derivatives in vivoT A Pham, Y P Hwung, D P McDonnell, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Definition of the critical cellular components which distinguish between hormone and antihormone activated progesterone receptorD L Clemm, B L Macy, D Santiso-Mere, 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 bindingP H Giangrande, E A Kimbrel, D P Edwards, et al.
Biochemistry|February 11, 1992
Modulation of progesterone receptor binding to progesterone response elements by positioned nucleosomesT A Pham, D P McDonnell, M J Tsai, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Vitamin D receptor interaction with specific DNA requires a nuclear protein and 1,25-dihydroxyvitamin D3J Liao, K Ozono, T Sone, et al.
Pageof 10

Showing results (31-40 of 99) with videos related to

Sort By:
Pageof 10
Gene Expression|January 1, 1992
Identification of novel steroid-response elementsZ Nawaz, M J Tsai, D P McDonnell, et al.
Molecular Carcinogenesis|January 1, 1993
Creation of an active estrogen-responsive element by a single base change in the flanking sequence of a cellular oncogene: a possible mechanism for hormonal carcinogenesis?Z Nawaz, G M Stancel, D P McDonnell, et al.
Vitamins and Hormones|January 1, 1996
The molecular pharmacology of ovarian steroid receptorsE Vegeto, B L Wagner, M O Imhof, et al.
The Journal of Biological Chemistry|April 18, 1998
Enhancement of estrogen receptor transcriptional activity by the coactivator GRIP-1 highlights the role of activation function 2 in determining estrogen receptor pharmacologyJ D Norris, D Fan, M R Stallcup, et al.
Molecular Endocrinology (Baltimore, Md.)|June 1, 1997
Identification of a third autonomous activation domain within the human estrogen receptorJ D Norris, D Fan, S A Kerner, et al.
The Journal of Biological Chemistry|September 25, 1991
Transactivation functions facilitate the disruption of chromatin structure by estrogen receptor derivatives in vivoT A Pham, Y P Hwung, D P McDonnell, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Definition of the critical cellular components which distinguish between hormone and antihormone activated progesterone receptorD L Clemm, B L Macy, D Santiso-Mere, 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 bindingP H Giangrande, E A Kimbrel, D P Edwards, et al.
Biochemistry|February 11, 1992
Modulation of progesterone receptor binding to progesterone response elements by positioned nucleosomesT A Pham, D P McDonnell, M J Tsai, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Vitamin D receptor interaction with specific DNA requires a nuclear protein and 1,25-dihydroxyvitamin D3J Liao, K Ozono, T Sone, et al.
Pageof 10