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RU 58668
Known as:
RU 58 668
, RU-58668
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Estradiol
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Systemic Magnetic Targeting of Pure-Antiestrogen-Loaded Superparamagnetic Nanovesicles for Effective Therapy of Hormone- Dependent Breast Cancers
V. Plassat
,
J. Renoir
,
+4 authors
S. Lesieur
2013
Corpus ID: 55971502
Systemic hormone therapy of breast cancer often suffers from severe side effects mainly due to non-specific drug delivery. To…
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2010
2010
Coadministration of nanosystems of short silencing RNAs targeting oestrogen receptor α and anti-oestrogen synergistically induces tumour growth inhibition in human breast cancer xenografts
C. Bouclier
,
V. Marsaud
,
+4 authors
J. Renoir
Breast Cancer Research and Treatment
2010
Corpus ID: 7841540
The suppression of oestrogen receptor α (ERα) functions by silencing RNAs in association with or not with anti-oestrogens (AEs…
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2009
2009
CO.77 In vitro, les ligands du récepteur beta aux estrogènes ont un effet pro-apoptotique dans des lignées cellulaires de cancer colique
B. Dupont
,
E. Longavenne
,
B. Sola
,
J. Reimund
2009
Corpus ID: 73359721
Highly Cited
2003
Highly Cited
2003
Polyester-Poly(Ethylene Glycol) Nanoparticles Loaded with the Pure Antiestrogen RU 58668: Physicochemical and Opsonization Properties
T. Ameller
,
V. Marsaud
,
P. Legrand
,
R. Gref
,
G. Barratt
,
J. Renoir
Pharmaceutical Research
2003
Corpus ID: 20249082
AbstractPurpose. The pure antiestrogen RU58668 (RU) was encapsulated within nanospheres (NS) and nanocapsules (NC) prepared from…
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2002
2002
Synthesis and cytotoxic activity of new 2,4-diaryl-4H,5H-pyrano[3,2-c]benzopyran-5-ones on MCF-7 cells.
Y. Jacquot
,
B. Refouvelet
,
L. Bermont
,
G. Adessi
,
G. Leclercq
,
A. Xicluna
Pharmazie
2002
Corpus ID: 38132358
A series of eight halogenated 2,4-diaryl-4H,5H-pyrano[3,2-c]benzopyran-5-ones have been synthesized, characterized and their…
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2001
2001
Dexamethasone blocks antioestrogen- and oxidant-induced death of pituitary tumour cells.
C. Newton
,
D. Bilko
,
S. Pappa
,
S. Atkin
Journal of Endocrinology
2001
Corpus ID: 16785937
The oestrogen receptor is fundamental to the growth and survival of the rat pituitary tumour cell line, GH(3). Our previous…
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1994
1994
RU 58 668 : profil des activités pharamcologiques d'un nouvel antiestrogène pur susceptible de traiter certains échappements au tamoxifène
P. V. D. Velde
,
F. Nique
,
+6 authors
G. Teutsch
1994
Corpus ID: 57328799
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