UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 25

Sortiert nach

Protein Expression in Insect and Mammalian Cells Using Baculoviruses in Wave Bioreactors

Methods in molecular biology (Clifton, N.J.), 2016, Vol.1350, p.263

2016

Volltextzugriff (PDF)

The characterization of novel, dual ErbB-2/EGFR, tyrosine kinase inhibitors: Potential therapy for cancer

Cancer research (Chicago, Ill.), 2001-10, Vol.61 (19), p.7196-7203

2001

Volltextzugriff (PDF)

Agouti protein is an antagonist of the melanocyte-stimulating-hormone receptor

Nature (London), 1994-10, Vol.371 (6500), p.799-802

1994

Volltextzugriff (PDF)

Discovery of Novel Quinoline-Based Estrogen Receptor Ligands Using Peptide Interaction Profiling

Journal of medicinal chemistry, 2005-03, Vol.48 (6), p.2243-2247

2005

Volltextzugriff (PDF)

Structure of the Tie2 RTK Domain: Self-Inhibition by the Nucleotide Binding Loop, Activation Loop, and C-Terminal Tail

Structure (London), 2000-11, Vol.8 (11), p.1105-1113

2000

Volltextzugriff (PDF)

Production of baculovirus-expressed recombinant proteins in wave bioreactors

Methods in molecular biology (Clifton, N.J.), 2007, Vol.388, p.247

2007

Volltextzugriff (PDF)

Correlation between in Vitro Peptide Binding Profiles and Cellular Activities for Estrogen Receptor-Modulating Compounds

Molecular endocrinology (Baltimore, Md.), 2004-05, Vol.18 (5), p.1064-1081

2004

Volltextzugriff (PDF)

Field performance of elite transgenic maize plants expressing an insecticidal protein derived from Bacillus thuringiensis

Bio/technology (New York, N.Y. 1983), 1993-02, Vol.11 (2), p.194-200

1993

Volltextzugriff (PDF)

Comparison of the biochemical and kinetic properties of the type 1 receptor tyrosine kinase intracellular domains. Demonstration of differential sensitivity to kinase inhibitors

The Journal of biological chemistry, 2002-01, Vol.277 (2), p.1576-1585

2002

Volltextzugriff (PDF)

Expression Cloning and Receptor Pharmacology of Human Calcitonin Receptors from MCF-7 Cells and Their Relationship to Amylin Receptors

Molecular pharmacology, 1997-12, Vol.52 (6), p.1164-1175

1997

Volltextzugriff (PDF)

Human Recombinant Phosphodiesterase 4B2B Binds (R)-Rolipram at a Single Site with Two Affinities

Biochemistry (Easton), 1997-11, Vol.36 (46), p.14250-14261

1997

Volltextzugriff (PDF)

Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5α-reductases : determinants for different in vivo activities of GI198745 and finasteride in the rat

Biochemical pharmacology, 2001-10, Vol.62 (7), p.933-942

2001

Volltextzugriff (PDF)

Inhibition of Human Steroid 5α Reductases type I and II by 6-Aza-Steroids: Structural Determinants of One-Step vs Two-Step Mechanism

Biochemistry (Easton), 1996-03, Vol.35 (11), p.3457-3464

1996

Volltextzugriff (PDF)

Cloning and characterization of a maize pollen-specific calcium-dependent calmodulin-independent protein kinase

Proceedings of the National Academy of Sciences - PNAS, 1994-09, Vol.91 (19), p.8837-8841

1994

Volltextzugriff (PDF)

Comparison of the Biochemical and Kinetic Properties of the Type 1 Receptor Tyrosine Kinase Intracellular Domains

The Journal of biological chemistry, 2002-01, Vol.277 (2), p.1576-1585

2002

Volltextzugriff (PDF)

Agouti regulation of intracellular calcium: role in the insulin resistance of viable yellow mice

Proceedings of the National Academy of Sciences - PNAS, 1995-05, Vol.92 (11), p.4733-4737

1995

Volltextzugriff (PDF)

Production and characterization of an estrogen receptor beta subtype-specific mouse monoclonal antibody

Hybridoma, 2000-12, Vol.19 (6), p.481

2000

Volltextzugriff (PDF)

CYP3A4 Expressed by Insect Cells Infected with a Recombinant Baculovirus Containing Both CYP3A4 and Human NADPH-Cytochrome P450 Reductase Is Catalytically Similar to Human Liver Microsomal CYP3A4

Archives of biochemistry and biophysics, 1995-05, Vol.319 (1), p.157-167

1995

Volltextzugriff (PDF)

17.beta.-(N-tert-Butylcarbamoyl)-4-aza-5.alpha.-androstan-1-en-3-one Is an Active Site-Directed Slow Time-Dependent Inhibitor of Human Steroid 5.alpha.-Reductase 1

Biochemistry (Easton), 1994-03, Vol.33 (8), p.2291-2296

1994

Volltextzugriff (PDF)

Cyclic AMP signaling pathways are important in IL-1 beta transcriptional regulation

The Journal of immunology (1950), 1995-11, Vol.155 (10), p.4535

1995

Volltextzugriff (PDF)

Expression, Purification, and Characterization of the Human Receptor Activator of NF-κB Ligand (RANKL) Extracellular Domain

Protein expression and purification, 2000-10, Vol.20 (1), p.48-57

2000

Volltextzugriff (PDF)

17β-(N-tert-butylcarbamoyl)-4-aza-5α-androstan-1-en-3-one is an active site-directed slow time-dependent inhibitor of human steroid 5α-reductase 1

Biochemistry (Easton), 1994-03, Vol.33 (8), p.2291-2296

1994

Volltextzugriff (PDF)

Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5α-reductases: determinants for different in vivo activities of GI198745 and finasteride in the rat 3 3Abbreviations: r5AR1, rat 5α-reductase 1; r5AR2, rat 5α-reductase 2; and DHT, dihydrotestosterone

Biochemical pharmacology, 2001-10, Vol.62 (7), p.933-942

2001

Volltextzugriff (PDF)

Structure of the Tie2 RTK Domain

Structure (London), 2000-11, Vol.8 (11), p.1105-1113

2000

Volltextzugriff (PDF)

Characterization of human E4BP4, a phosphorylated bZIP factor

Biochimica et biophysica acta, 1995-12, Vol.1264 (3), p.388-396

1995

Volltextzugriff (PDF)

1 – 25 von 25

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(23)
Mit Volltextzugriff
(21)

Publikationsform

Artikel
(25)

Sprache

Englisch
(25)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Protein Expression in Insect and Mammalian Cells Using Baculoviruses in Wave Bioreactors

The characterization of novel, dual ErbB-2/EGFR, tyrosine kinase inhibitors: Potential therapy for cancer

Agouti protein is an antagonist of the melanocyte-stimulating-hormone receptor

Discovery of Novel Quinoline-Based Estrogen Receptor Ligands Using Peptide Interaction Profiling

Structure of the Tie2 RTK Domain: Self-Inhibition by the Nucleotide Binding Loop, Activation Loop, and C-Terminal Tail

Production of baculovirus-expressed recombinant proteins in wave bioreactors

Correlation between in Vitro Peptide Binding Profiles and Cellular Activities for Estrogen Receptor-Modulating Compounds

Field performance of elite transgenic maize plants expressing an insecticidal protein derived from Bacillus thuringiensis

Comparison of the biochemical and kinetic properties of the type 1 receptor tyrosine kinase intracellular domains. Demonstration of differential sensitivity to kinase inhibitors

Expression Cloning and Receptor Pharmacology of Human Calcitonin Receptors from MCF-7 Cells and Their Relationship to Amylin Receptors

Human Recombinant Phosphodiesterase 4B2B Binds (R)-Rolipram at a Single Site with Two Affinities

Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5α-reductases : determinants for different in vivo activities of GI198745 and finasteride in the rat

Inhibition of Human Steroid 5α Reductases type I and II by 6-Aza-Steroids: Structural Determinants of One-Step vs Two-Step Mechanism

Cloning and characterization of a maize pollen-specific calcium-dependent calmodulin-independent protein kinase

Comparison of the Biochemical and Kinetic Properties of the Type 1 Receptor Tyrosine Kinase Intracellular Domains

Agouti regulation of intracellular calcium: role in the insulin resistance of viable yellow mice

Production and characterization of an estrogen receptor beta subtype-specific mouse monoclonal antibody

CYP3A4 Expressed by Insect Cells Infected with a Recombinant Baculovirus Containing Both CYP3A4 and Human NADPH-Cytochrome P450 Reductase Is Catalytically Similar to Human Liver Microsomal CYP3A4

17.beta.-(N-tert-Butylcarbamoyl)-4-aza-5.alpha.-androstan-1-en-3-one Is an Active Site-Directed Slow Time-Dependent Inhibitor of Human Steroid 5.alpha.-Reductase 1

Cyclic AMP signaling pathways are important in IL-1 beta transcriptional regulation

Expression, Purification, and Characterization of the Human Receptor Activator of NF-κB Ligand (RANKL) Extracellular Domain

17β-(N-tert-butylcarbamoyl)-4-aza-5α-androstan-1-en-3-one is an active site-directed slow time-dependent inhibitor of human steroid 5α-reductase 1

Pharmacokinetic parameters and mechanisms of inhibition of rat type 1 and 2 steroid 5α-reductases: determinants for different in vivo activities of GI198745 and finasteride in the rat 3 3Abbreviations: r5AR1, rat 5α-reductase 1; r5AR2, rat 5α-reductase 2; and DHT, dihydrotestosterone

Structure of the Tie2 RTK Domain

Characterization of human E4BP4, a phosphorylated bZIP factor

Suchergebnisse filtern