UB Paderborn / Katalog / Suche / in CDI

Discovery of the Selective CYP17A1 Lyase Inhibitor BMS-351 for the Treatment of Prostate Cancer

ACS medicinal chemistry letters, 2016-01, Vol.7 (1), p.40-45

2016

Volltextzugriff (PDF)

[2.2.1]-Bicyclic sultams as potent androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2016-12, Vol.26 (23), p.5707-5711

2016

Volltextzugriff (PDF)

The synthesis and evaluation of [2.2.1]-bicycloazahydantoins as androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2004-12, Vol.14 (24), p.6107-6111

2004

Volltextzugriff (PDF)

Discovery of BMS-641988, a Novel and Potent Inhibitor of Androgen Receptor Signaling for the Treatment of Prostate Cancer

Cancer research (Chicago, Ill.), 2009-08, Vol.69 (16), p.6522-6530

2009

Volltextzugriff (PDF)

Multiorgan inflammation and hematopoietic abnormalities in mice with a targeted disruption of RelB, a member of the NF-κB/Rel family

Cell, 1995-01, Vol.80 (2), p.331-340

1995

Volltextzugriff (PDF)

The androgen receptor can signal through Wnt/beta-Catenin in prostate cancer cells as an adaptation mechanism to castration levels of androgens

BMC cell biology, 2008-01, Vol.9, p.4

2008

Volltextzugriff (PDF)

Structure based approach to the design of bicyclic-1H-isoindole-1,3(2H)-dione based androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2005-01, Vol.15 (2), p.271-276

2005

Volltextzugriff (PDF)

Identification and optimization of a novel series of [2.2.1]-oxabicyclo imide-based androgen receptor antagonists

Bioorganic & medicinal chemistry, 2008-03, Vol.18 (6), p.1910-1915

2008

Volltextzugriff (PDF)

Design and synthesis of 4-[3,5-dioxo-11-oxa-4,9-diazatricyclo[5.3.1.02,6]undec-4-yl]-2-trifluoromethyl-benzonitriles as androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (15), p.4491-4495

2010

Volltextzugriff (PDF)

Identification of a novel class of androgen receptor antagonists based on the bicyclic-1H-isoindole-1,3(2H)-dione nucleus

Bioorganic & medicinal chemistry letters, 2005-01, Vol.15 (2), p.389-393

2005

Volltextzugriff (PDF)

Identification of novel functional inhibitors of 17β-hydroxysteroid dehydrogenase type III (17β-HSD3)

The Prostate, 2005-10, Vol.65 (2), p.159-170

2005

Volltextzugriff (PDF)

Nuclear factor (NF)-kappa B2 (p100/p52) is required for normal splenic microarchitecture and B cell-mediated immune responses

The Journal of experimental medicine, 1998-01, Vol.187 (2), p.185-196

1998

Volltextzugriff (PDF)

Design and synthesis of 4-[3,5-dioxo-11-oxa-4,9-diazatricyclo[5.3.1.02,6]undec4-yl]-2-trifluoromethyl-benzonitriles as androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (15), p.4491-4495

2010

Volltextzugriff (PDF)

The v‐rel oncogene promotes malignant T‐cell leukemia/lymphoma in transgenic mice

The EMBO journal, 1996-07, Vol.15 (14), p.3640-3650

1996

Volltextzugriff (PDF)

Identification of novel functional inhibitors of 17beta-hydroxysteroid dehydrogenase type III (17beta-HSD3)

The Prostate, 2005-10, Vol.65 (2), p.159-170

2005

Volltextzugriff (PDF)

Expression of FosB during mouse development: normal development of FosB knockout mice

Oncogene, 1996-05, Vol.12 (10), p.2177-2185

1996

Volltextzugriff (PDF)

Both products of the fosB gene, FosB and its short form, FosB/SF, are transcriptional activators in fibroblasts

Molecular and Cellular Biology, 1991-11, Vol.11 (11), p.5470-5478

1991

Volltextzugriff (PDF)

Structure based approach to the design of bicyclic-1 H-isoindole-1,3(2 H)-dione based androgen receptor antagonists

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (2), p.271-276

2005

Volltextzugriff (PDF)

Both Products of the fos B Gene, FosB and Its Short Form, FosB/SF, Are Transcriptional Activators in Fibroblasts

Molecular and cellular biology, 1991-11, Vol.11 (11), p.5470-5478

1991

Volltextzugriff (PDF)

Both Products of the fosB Gene, FosB and Its Short Form, FosB/SF, Are Transcriptional Activators in Fibroblasts

Molecular and cellular biology, 1991-11, Vol.11 (11), p.5470-5478

1991

Volltextzugriff (PDF)

Multiple origins of downy mildews and mito-nuclear discordance within the paraphyletic genus Phytophthora

PloS one, 2018-03, Vol.13 (3), p.e0192502-e0192502

2018

Volltextzugriff (PDF)

Gerontological Social Work and the Grand Challenges: Focusing on Policy and Practice

1st ed. 2019., 2019

Volltextzugriff (PDF)

Temporal Patterns of Influenza A and B in Tropical and Temperate Countries: What Are the Lessons for Influenza Vaccination?

PloS one, 2016-03, Vol.11 (3), p.e0152310-e0152310

2016

Volltextzugriff (PDF)

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

Molecular psychiatry, 2017-06, Vol.22 (6), p.836-849

2017

Volltextzugriff (PDF)

Post-Embedding Immunogold Detection of GABA-Labeling Using Large Area, High Resolution SEM Backscatter Imaging

Microscopy and microanalysis, 2018-08, Vol.24 (S1), p.1386-1387

2018

Volltextzugriff (PDF)

Menü

Weitere Dienste

Einstellungen

Discovery of the Selective CYP17A1 Lyase Inhibitor BMS-351 for the Treatment of Prostate Cancer

[2.2.1]-Bicyclic sultams as potent androgen receptor antagonists

The synthesis and evaluation of [2.2.1]-bicycloazahydantoins as androgen receptor antagonists

Discovery of BMS-641988, a Novel and Potent Inhibitor of Androgen Receptor Signaling for the Treatment of Prostate Cancer

Multiorgan inflammation and hematopoietic abnormalities in mice with a targeted disruption of RelB, a member of the NF-κB/Rel family

The androgen receptor can signal through Wnt/beta-Catenin in prostate cancer cells as an adaptation mechanism to castration levels of androgens

Structure based approach to the design of bicyclic-1H-isoindole-1,3(2H)-dione based androgen receptor antagonists

Identification and optimization of a novel series of [2.2.1]-oxabicyclo imide-based androgen receptor antagonists

Design and synthesis of 4-[3,5-dioxo-11-oxa-4,9-diazatricyclo[5.3.1.02,6]undec-4-yl]-2-trifluoromethyl-benzonitriles as androgen receptor antagonists

Identification of a novel class of androgen receptor antagonists based on the bicyclic-1H-isoindole-1,3(2H)-dione nucleus

Identification of novel functional inhibitors of 17β-hydroxysteroid dehydrogenase type III (17β-HSD3)

Nuclear factor (NF)-kappa B2 (p100/p52) is required for normal splenic microarchitecture and B cell-mediated immune responses

Design and synthesis of 4-[3,5-dioxo-11-oxa-4,9-diazatricyclo[5.3.1.02,6]undec4-yl]-2-trifluoromethyl-benzonitriles as androgen receptor antagonists

The v‐rel oncogene promotes malignant T‐cell leukemia/lymphoma in transgenic mice

Identification of novel functional inhibitors of 17beta-hydroxysteroid dehydrogenase type III (17beta-HSD3)

Expression of FosB during mouse development: normal development of FosB knockout mice

Both products of the fosB gene, FosB and its short form, FosB/SF, are transcriptional activators in fibroblasts

Structure based approach to the design of bicyclic-1 H-isoindole-1,3(2 H)-dione based androgen receptor antagonists

Both Products of the fos B Gene, FosB and Its Short Form, FosB/SF, Are Transcriptional Activators in Fibroblasts

Both Products of the fosB Gene, FosB and Its Short Form, FosB/SF, Are Transcriptional Activators in Fibroblasts

Multiple origins of downy mildews and mito-nuclear discordance within the paraphyletic genus Phytophthora

Gerontological Social Work and the Grand Challenges: Focusing on Policy and Practice

Temporal Patterns of Influenza A and B in Tropical and Temperate Countries: What Are the Lessons for Influenza Vaccination?

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

Post-Embedding Immunogold Detection of GABA-Labeling Using Large Area, High Resolution SEM Backscatter Imaging

Suchergebnisse filtern