Automated Author Profile

A. S. Daptare

Current S-Index

0.5

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.2

Average Dataset Index per dataset

Total Datasets

2

Total datasets for this author

Average FAIR Score

84.6%

Average FAIR Score per dataset

Total Citations

0

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

PREPRATON AND CHARACTERIZATION OF STEROID-LINKED DERIVATIVES AS ANTICANCER AGENTS"

of a variety of regulatory function such as ovulation, development of corpusluteum, and maintenance of
uterine quiescence during pregnancy. It is also involved in proliferation and differentiation of mammary
glands. The biological activity of progesterone is mediated by the progesterone receptor [PR], a member
of the large gene family of nuclear receptors, which induces a cascade of transcriptional events after
binding with the hormone. PR contains three functional domains including the N-terminus, a centrally
located DNA binding domain (DBD) and C-terminal ligand binging domain (LBD) respectively. The
binding of progesterone induces of conformational change in PR that promotes dissociation from a
multi-protein complex followed by homo dimerization and binding to specific progesterone response
elements (PRE) within the promoter genes. The hormone activated PR recruits co-activators throug

Authors

  • M.D. Sangale ;
  • A. S. Daptare
0 Citations0 Mentions85% FAIR0.1 Dataset Index
10.6084/m9.figshare.9134882014

PREPRATON AND CHARACTERIZATION OF STEROID-LINKED DERIVATIVES AS ANTICANCER AGENTS"

of a variety of regulatory function such as ovulation, development of corpusluteum, and maintenance of
uterine quiescence during pregnancy. It is also involved in proliferation and differentiation of mammary
glands. The biological activity of progesterone is mediated by the progesterone receptor [PR], a member
of the large gene family of nuclear receptors, which induces a cascade of transcriptional events after
binding with the hormone. PR contains three functional domains including the N-terminus, a centrally
located DNA binding domain (DBD) and C-terminal ligand binging domain (LBD) respectively. The
binding of progesterone induces of conformational change in PR that promotes dissociation from a
multi-protein complex followed by homo dimerization and binding to specific progesterone response
elements (PRE) within the promoter genes. The hormone activated PR recruits co-activators throug

Authors

  • M.D. Sangale ;
  • A. S. Daptare
0 Citations0 Mentions85% FAIR0.3 Dataset Index
10.6084/m9.figshare.913488.v12014