UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 383

Sortiert nach

Mechanisms and Consequences of Macromolecular Phase Separation

Cell, 2016-05, Vol.165 (5), p.1067-1079

2016

Volltextzugriff (PDF)

Mechanics, Structure and Function of Biopolymer Condensates

Journal of molecular biology, 2018-11, Vol.430 (23), p.4754-4761

2018

Volltextzugriff (PDF)

A Cell-Signaling Network Temporally Resolves Specific versus Promiscuous Phosphorylation

Cell reports (Cambridge), 2015-02, Vol.10 (7), p.1202-1214

2015

Volltextzugriff (PDF)

Cryo-EM reveals an unprecedented binding site for NaV1.7 inhibitors enabling rational design of potent hybrid inhibitors

eLife, 2023-03, Vol.12

2023

Volltextzugriff (PDF)

Endocytic proteins with prion-like domains form viscoelastic condensates that enable membrane remodeling

Proceedings of the National Academy of Sciences - PNAS, 2021-12, Vol.118 (50), p.1

2021

Volltextzugriff (PDF)

Antagonists of inhibitor of apoptosis proteins based on thiazole amide isosteres

Bioorganic & medicinal chemistry letters, 2010-04, Vol.20 (7), p.2229-2233

2010

Volltextzugriff (PDF)

Battling Btk Mutants With Noncovalent Inhibitors That Overcome Cys481 and Thr474 Mutations

ACS chemical biology, 2016-10, Vol.11 (10), p.2897-2907

2016

Volltextzugriff (PDF)

Structure- and Ligand-Based Discovery of Chromane Arylsulfonamide Nav1.7 Inhibitors for the Treatment of Chronic Pain

Journal of medicinal chemistry, 2019-04, Vol.62 (8), p.4091-4109

2019

Volltextzugriff (PDF)

Development of a Potent, Specific CDK8 Kinase Inhibitor Which Phenocopies CDK8/19 Knockout Cells

ACS medicinal chemistry letters, 2016-03, Vol.7 (3), p.223-228

2016

Volltextzugriff (PDF)

Flagellin produced in plants is a potent adjuvant for oral immunization

Vaccine, 2011-09, Vol.29 (38), p.6695-6703

2011

Volltextzugriff (PDF)

Discovery of Acyl-sulfonamide Nav1.7 Inhibitors GDC-0276 and GDC-0310

Journal of medicinal chemistry, 2021-03, Vol.64 (6), p.2953-2966

2021

Volltextzugriff (PDF)

Design and Development of a Series of Potent and Selective Type II Inhibitors of CDK8

ACS medicinal chemistry letters, 2016-06, Vol.7 (6), p.595-600

2016

Volltextzugriff (PDF)

Discovery of Acyl-sulfonamide Na v 1.7 Inhibitors GDC-0276 and GDC-0310

Journal of medicinal chemistry, 2021-03, Vol.64 (6), p.2953-2966

2021

Volltextzugriff (PDF)

Identification of C‑2 Hydroxyethyl Imidazopyrrolopyridines as Potent JAK1 Inhibitors with Favorable Physicochemical Properties and High Selectivity over JAK2

Journal of medicinal chemistry, 2013-06, Vol.56 (11), p.4764-4785

2013

Volltextzugriff (PDF)

Dynamic FLNa and FilGAP Binding Is Required for Contractile Mechanotransduction Response to Shear-Stress

Biophysical journal, 2021-02, Vol.120 (3), p.169a-169a

2021

Volltextzugriff (PDF)

Structure- and Ligand-Based Discovery of Chromane Arylsulfonamide Na v 1.7 Inhibitors for the Treatment of Chronic Pain

Journal of medicinal chemistry, 2019-04, Vol.62 (8), p.4091-4109

2019

Volltextzugriff (PDF)

A hit to lead discovery of novel N-methylated imidazolo-, pyrrolo-, and pyrazolo-pyrimidines as potent and selective mTOR inhibitors

Bioorganic & medicinal chemistry letters, 2013-09, Vol.23 (18), p.5097-5104

2013

Volltextzugriff (PDF)

Cryo-EM reveals an unprecedented binding site for Na V 1.7 inhibitors enabling rational design of potent hybrid inhibitors

eLife, 2023-03, Vol.12

2023

Volltextzugriff (PDF)

An integrated suite of modeling tools that empower scientists in structure- and property-based drug design

Journal of computer-aided molecular design, 2015-06, Vol.29 (6), p.511-523

2015

Volltextzugriff (PDF)

Discovery and Optimization of C-2 Methyl Imidazopyrrolopyridines as Potent and Orally Bioavailable JAK1 Inhibitors with Selectivity over JAK2

Journal of medicinal chemistry, 2012-07, Vol.55 (13), p.6176-6193

2012

Volltextzugriff (PDF)

Potent, Selective, and Orally Bioavailable Inhibitors of the Mammalian Target of Rapamycin Kinase Domain Exhibiting Single Agent Antiproliferative Activity

Journal of medicinal chemistry, 2012-12, Vol.55 (24), p.10958-10971

2012

Volltextzugriff (PDF)

L’intégration socioprofessionnelle des personnes en situation d’itinérance : état de la question et proposition d’un modèle conceptualisé à partir de l’institutionnalisme pragmatiste de John Rogers Commons

Interventions économiques, 2014-09 (50)

2014

Volltextzugriff (PDF)

L’intégration socioprofessionnelle des personnes en situation d’itinérance : état de la question et proposition d’un modèle conceptualisé à partir de l’institutionnalisme pragmatiste de John Rogers Commons

Revue interventions économiques, 2014-07

2014

Volltextzugriff (PDF)

Production of Human Rotavirus and Salmonella Antigens in Plants and Elicitation of fljB-Specific Humoral Responses in Mice

Molecular biotechnology, 2011-02, Vol.47 (2), p.157-168

2011

Volltextzugriff (PDF)

Structure-Guided Rescaffolding of Selective Antagonists of BCL-X L

ACS medicinal chemistry letters, 2014-06, Vol.5 (6), p.662-667

2014

Volltextzugriff (PDF)

1 – 25 von 383

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(339)
Mit Volltextzugriff
(357)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Mechanisms and Consequences of Macromolecular Phase Separation

Mechanics, Structure and Function of Biopolymer Condensates

A Cell-Signaling Network Temporally Resolves Specific versus Promiscuous Phosphorylation

Cryo-EM reveals an unprecedented binding site for NaV1.7 inhibitors enabling rational design of potent hybrid inhibitors

Endocytic proteins with prion-like domains form viscoelastic condensates that enable membrane remodeling

Antagonists of inhibitor of apoptosis proteins based on thiazole amide isosteres

Battling Btk Mutants With Noncovalent Inhibitors That Overcome Cys481 and Thr474 Mutations

Structure- and Ligand-Based Discovery of Chromane Arylsulfonamide Nav1.7 Inhibitors for the Treatment of Chronic Pain

Development of a Potent, Specific CDK8 Kinase Inhibitor Which Phenocopies CDK8/19 Knockout Cells

Flagellin produced in plants is a potent adjuvant for oral immunization

Discovery of Acyl-sulfonamide Nav1.7 Inhibitors GDC-0276 and GDC-0310

Design and Development of a Series of Potent and Selective Type II Inhibitors of CDK8

Discovery of Acyl-sulfonamide Na v 1.7 Inhibitors GDC-0276 and GDC-0310

Identification of C‑2 Hydroxyethyl Imidazopyrrolopyridines as Potent JAK1 Inhibitors with Favorable Physicochemical Properties and High Selectivity over JAK2

Dynamic FLNa and FilGAP Binding Is Required for Contractile Mechanotransduction Response to Shear-Stress

Structure- and Ligand-Based Discovery of Chromane Arylsulfonamide Na v 1.7 Inhibitors for the Treatment of Chronic Pain

A hit to lead discovery of novel N-methylated imidazolo-, pyrrolo-, and pyrazolo-pyrimidines as potent and selective mTOR inhibitors

Cryo-EM reveals an unprecedented binding site for Na V 1.7 inhibitors enabling rational design of potent hybrid inhibitors

An integrated suite of modeling tools that empower scientists in structure- and property-based drug design

Discovery and Optimization of C-2 Methyl Imidazopyrrolopyridines as Potent and Orally Bioavailable JAK1 Inhibitors with Selectivity over JAK2

Potent, Selective, and Orally Bioavailable Inhibitors of the Mammalian Target of Rapamycin Kinase Domain Exhibiting Single Agent Antiproliferative Activity

L’intégration socioprofessionnelle des personnes en situation d’itinérance : état de la question et proposition d’un modèle conceptualisé à partir de l’institutionnalisme pragmatiste de John Rogers Commons

L’intégration socioprofessionnelle des personnes en situation d’itinérance : état de la question et proposition d’un modèle conceptualisé à partir de l’institutionnalisme pragmatiste de John Rogers Commons

Production of Human Rotavirus and Salmonella Antigens in Plants and Elicitation of fljB-Specific Humoral Responses in Mice

Structure-Guided Rescaffolding of Selective Antagonists of BCL-X L

Suchergebnisse filtern