UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 31

Sortiert nach

Galectin-3 Regulates Myofibroblast Activation and Hepatic Fibrosis

Proceedings of the National Academy of Sciences - PNAS, 2006-03, Vol.103 (13), p.5060-5065

2006

Volltextzugriff (PDF)

Critical role of c-jun (NH2) terminal kinase in paracetamol- induced acute liver failure

Gut, 2007-07, Vol.56 (7), p.982-990

2007

Volltextzugriff (PDF)

C. elegans PAT-4/ILK Functions as an Adaptor Protein within Integrin Adhesion Complexes

Current biology, 2002-05, Vol.12 (10), p.787-797

2002

Volltextzugriff (PDF)

Extracellular matrix proteins protect small cell lung cancer cells against apoptosis: A mechanism for small cell lung cancer growth and drug resistance in vivo

Nature medicine, 1999-06, Vol.5 (6), p.662-668

1999

Volltextzugriff (PDF)

MRI FINDINGS IN ACUTE WERNICKE'S ENCEPHALOPATHY

Journal of neurology, neurosurgery and psychiatry, 2012-11, Vol.83 (Suppl 2), p.A3-A3

2012

Volltextzugriff (PDF)

Sphingosine Kinase: A Point of Convergence in the Action of Diverse Neutrophil Priming Agents

The Journal of immunology (1950), 2002-12, Vol.169 (11), p.6394-6400

2002

Volltextzugriff (PDF)

TYMS and ERCC1 expression in naive and neoadjuvant-treated pancreatic cancer

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2013-03, Vol.13 (2), p.e83-e83

2013

Volltextzugriff (PDF)

Bombesin and substance P analogues differentially regulate G-protein coupling to the bombesin receptor. Direct evidence for biased agonism

The Journal of biological chemistry, 2001-07, Vol.276 (30), p.28083-28091

2001

Volltextzugriff (PDF)

Increased gastrin-releasing peptide (GRP) receptor expression in tumour cells confers sensitivity to [Arg , -Trp , Phe ]-substance P (6-11)-induced growth inhibition

British journal of cancer, 2003-06, Vol.88 (11), p.1808-1816

2003

Volltextzugriff (PDF)

[Arg ,D-Trp ,N Phe ]-substance P (6-11) activates JNK and induces apoptosis in small cell lung cancer cells via an oxidant-dependent mechanism

British Journal of Cancer, 1999-06, Vol.80 (7), p.1026-1034

1999

Volltextzugriff (PDF)

[Arg , D-Trp , N Phe ]-substance P (6-11) (antagonist G) induces AP-1 transcription and sensitizes cells to chemotherapy

British journal of cancer, 2000-10, Vol.83 (7), p.941-948

2000

Volltextzugriff (PDF)

Alpha 2-adrenoceptor subtypes and imidazoline-like binding sites in the rat brain

British journal of pharmacology, 1990-04, Vol.99 (4), p.803-809

1990

Volltextzugriff (PDF)

α2‐Adrenoceptor subtypes and imidazoline‐like binding sites in the rat brain

British journal of pharmacology, 1990-04, Vol.99 (4), p.803-809

1990

Volltextzugriff (PDF)

[ 3 H]‐RS‐45041‐190: a selective high‐affinity radioligand for I 2 imidazoline receptors

British journal of pharmacology, 1995-09, Vol.116 (2), p.1729-1736

1995

Volltextzugriff (PDF)

[ 3H]p-Aminoclonidine and [ 3H]idazoxan label different populations of imidazoline sites on rat kidney

European journal of pharmacology, 1993-02, Vol.232 (1), p.79-87

1993

Volltextzugriff (PDF)

Neuropeptides stimulate tyrosine phosphorylation and tyrosine kinase activity in small cell lung cancer cell lines

Peptides (New York, N.Y. : 1980), 1996, Vol.17 (4), p.665-673

1996

Volltextzugriff (PDF)

[3H]‐lifarizine, a high affinity probe for inactivated sodium channels

British journal of pharmacology, 1995-07, Vol.115 (6), p.1103-1109

1995

Volltextzugriff (PDF)

RS‐45041‐190: a selective, high‐affinity ligand for I 2 imidazoline receptors

British journal of pharmacology, 1995-09, Vol.116 (2), p.1737-1744

1995

Volltextzugriff (PDF)

[3H]-RS-15385-197, a selective and high affinity radioligand for alpha 2-adrenoceptors: implications for receptor classification

British journal of pharmacology, 1992-08, Vol.106 (4), p.1011-1018

1992

Volltextzugriff (PDF)

The pharmacology of RS-15385-197, a potent and selective alpha 2-adrenoceptor antagonist

British journal of pharmacology, 1993-02, Vol.108 (2), p.516-525

1993

Volltextzugriff (PDF)

Heterogeneity of alpha 2-adrenoceptors in rat cortex but not human platelets can be defined by 8-OH-DPAT, RU 24969 and methysergide

British journal of pharmacology, 1990-03, Vol.99 (3), p.481-486

1990

Volltextzugriff (PDF)

Development of a Coupled VanA/VanX Assay: Screening for Inhibitors of Glycopeptide Resistance

SLAS discovery, 1997-06, Vol.2 (4), p.241-247

1997

Volltextzugriff (PDF)

1,9-Alkano-bridged 2,3,4,5-tetrahydro-1H-3-benzazepines with affinity for the alpha 2-adrenoceptor and the 5-HT1A receptor

Journal of medicinal chemistry, 1990-02, Vol.33 (2), p.633-641

1990

Volltextzugriff (PDF)

Modulation of central noradrenergic function by RS‐15385‐197

British journal of pharmacology, 1993-02, Vol.108 (2), p.526-533

1993

Volltextzugriff (PDF)

Structure-affinity relationships of 12-sulfonyl derivatives of 5,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1,6]naphthyridines at .alpha.-adrenoceptors

Journal of medicinal chemistry, 1991-02, Vol.34 (2), p.705-717

1991

Volltextzugriff (PDF)

1 – 25 von 31

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(31)
Mit Volltextzugriff
(30)

Publikationsform

Artikel
(31)

Sprache

Englisch
(31)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

Science & Technology
(28)
Life Sciences & Biomedicine
(27)
Animals
(18)
Humans
(13)
Pharmacology & Pharmacy
(13)
Rats
(13)
Biological And Medical Sciences
(11)
Male
(11)
Medical Sciences
(10)
In Vitro Techniques
(8)
Biochemistry & Molecular Biology
(6)
Cerebral Cortex - Metabolism
(6)
Pharmacology. Drug Treatments
(6)
Receptors, Adrenergic, Alpha - Metabolism
(6)
Signal Transduction
(6)
Tumor Cells, Cultured
(6)
Adrenergic Alpha-Antagonists - Pharmacology
(5)
Mice
(5)
Radioligand Assay
(5)
Rats, Inbred Strains
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Galectin-3 Regulates Myofibroblast Activation and Hepatic Fibrosis

Critical role of c-jun (NH2) terminal kinase in paracetamol- induced acute liver failure

C. elegans PAT-4/ILK Functions as an Adaptor Protein within Integrin Adhesion Complexes

Extracellular matrix proteins protect small cell lung cancer cells against apoptosis: A mechanism for small cell lung cancer growth and drug resistance in vivo

MRI FINDINGS IN ACUTE WERNICKE'S ENCEPHALOPATHY

Sphingosine Kinase: A Point of Convergence in the Action of Diverse Neutrophil Priming Agents

TYMS and ERCC1 expression in naive and neoadjuvant-treated pancreatic cancer

Bombesin and substance P analogues differentially regulate G-protein coupling to the bombesin receptor. Direct evidence for biased agonism

Increased gastrin-releasing peptide (GRP) receptor expression in tumour cells confers sensitivity to [Arg , -Trp , Phe ]-substance P (6-11)-induced growth inhibition

[Arg ,D-Trp ,N Phe ]-substance P (6-11) activates JNK and induces apoptosis in small cell lung cancer cells via an oxidant-dependent mechanism

[Arg , D-Trp , N Phe ]-substance P (6-11) (antagonist G) induces AP-1 transcription and sensitizes cells to chemotherapy

Alpha 2-adrenoceptor subtypes and imidazoline-like binding sites in the rat brain

α2‐Adrenoceptor subtypes and imidazoline‐like binding sites in the rat brain

[ 3 H]‐RS‐45041‐190: a selective high‐affinity radioligand for I 2 imidazoline receptors

[ 3H]p-Aminoclonidine and [ 3H]idazoxan label different populations of imidazoline sites on rat kidney

Neuropeptides stimulate tyrosine phosphorylation and tyrosine kinase activity in small cell lung cancer cell lines

[3H]‐lifarizine, a high affinity probe for inactivated sodium channels

RS‐45041‐190: a selective, high‐affinity ligand for I 2 imidazoline receptors

[3H]-RS-15385-197, a selective and high affinity radioligand for alpha 2-adrenoceptors: implications for receptor classification

The pharmacology of RS-15385-197, a potent and selective alpha 2-adrenoceptor antagonist

Heterogeneity of alpha 2-adrenoceptors in rat cortex but not human platelets can be defined by 8-OH-DPAT, RU 24969 and methysergide

Development of a Coupled VanA/VanX Assay: Screening for Inhibitors of Glycopeptide Resistance

1,9-Alkano-bridged 2,3,4,5-tetrahydro-1H-3-benzazepines with affinity for the alpha 2-adrenoceptor and the 5-HT1A receptor

Modulation of central noradrenergic function by RS‐15385‐197

Structure-affinity relationships of 12-sulfonyl derivatives of 5,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1,6]naphthyridines at .alpha.-adrenoceptors

Suchergebnisse filtern