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Specificity of Induction of the vanA and vanB Operons in Vancomycin-Resistant Enterococci by Telavancin

Antimicrobial Agents and Chemotherapy, 2010-07, Vol.54 (7), p.2814-2818

2010

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Enhanced Degradation of Chemical Warfare Agents through Molecular Engineering of the Phosphotriesterase Active Site

Journal of the American Chemical Society, 2003-07, Vol.125 (30), p.8990-8991

2003

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Catalytic properties of the PepQ prolidase from Escherichia coli

Archives of biochemistry and biophysics, 2004-09, Vol.429 (2), p.224-230

2004

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Demonstration of a fast-reconfigurable silicon CMOS optical lattice filter

Optics express, 2011-07, Vol.19 (14), p.13245-13256

2011

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Concomitant Angiotensin AT1 Receptor Antagonism and Neprilysin Inhibition Produces Omapatrilat-like Antihypertensive Effects Without Promoting Tracheal Plasma Extravasation in the Rat

Journal of cardiovascular pharmacology, 2011-04, Vol.57 (4), p.495-504

2011

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Discovery of TD-0212, an Orally Active Dual Pharmacology AT 1 Antagonist and Neprilysin Inhibitor (ARNI)

ACS medicinal chemistry letters, 2019-01, Vol.10 (1), p.86-91

2019

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Purification of Escherichia coli acetohydroxyacid synthase isoenzyme II and reconstitution of active enzyme from its individual pure subunits

Biochemical journal, 1997-11, Vol.327 ( Pt 3) (3), p.891-898

1997

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Discovery of TD-0212, an Orally Active Dual Pharmacology AT1 Antagonist and Neprilysin Inhibitor (ARNI)

ACS medicinal chemistry letters, 2019-01, Vol.10 (1), p.86-91

2019

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CMOS-Compatible Si-Ring-Assisted Mach-Zehnder Interferometer With Internal Bandwidth Equalization

IEEE journal of selected topics in quantum electronics, 2010-01, Vol.16 (1), p.45-52

2010

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Enzymatic Synthesis of Chiral Organophosphothioates from Prochiral Precursors

Journal of the American Chemical Society, 2002-04, Vol.124 (14), p.3498-3499

2002

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A multivalent approach towards linked dual-pharmacology prostaglandin F receptor agonist/carbonic anhydrase-II inhibitors for the treatment of glaucoma

Bioorganic & medicinal chemistry letters, 2013-02, Vol.23 (4), p.939-943

2013

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Peptide Ketobenzoxazole Inhibitors Bound to Cathepsin K

Biochemistry (Easton), 2003-12, Vol.42 (51), p.15018-15028

2003

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The ITK Inhibitor Cpi-818 Blocks Activation of T Cells from Autoimmune Lymphoproliferative Syndrome (ALPS) Patients and Is Active in a Murine Model of ALPS

Blood, 2020-11, Vol.136 (Supplement 1), p.36-37

2020

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Preliminary Clinical Data from a Phase 1 Trial with CPI-818, a Selective ITK Inhibitor That Preferentially Blocks the Growth of T Lymphoma Cells

Blood, 2019-11, Vol.134 (Supplement_1), p.1571-1571

2019

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Cpi-818, an Oral Interleukin-2-Inducible T-Cell Kinase Inhibitor, Is Well-Tolerated and Active in Patients with T-Cell Lymphoma

Blood, 2020-11, Vol.136 (Supplement 1), p.19-20

2020

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Abstract 1313: CPI-818: A selective inhibitor of interleukin-2-inducible T-cell kinase (ITK) that inhibits T-cell receptor signaling, promotes Th1 skewing, and achieves objective tumor responses when administered to dogs with T cell lymphomas

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.1313-1313

2019

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Stereochemical Specificity of Organophosphorus Acid Anhydrolase toward p-Nitrophenyl Analogs of Soman and Sarin

Bioorganic chemistry, 2001-02, Vol.29 (1), p.27-35

2001

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CMOS-Compatible Si-Ring-Assisted MachaZehnder Interferometer With Internal Bandwidth Equalization

IEEE journal of selected topics in quantum electronics, 2010-01, Vol.16 (1), p.45-52

2010

Volltextzugriff (PDF)

Mutagenesis of Escherichia coli acetohydroxyacid synthase isoenzyme II and characterization of three herbicide-insensitive forms

Biochemical journal, 1998-11, Vol.335 ( Pt 3) (3), p.653-661

1998

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Substrate and stereochemical specificity of the organophosphorus acid anhydrolase from Alteromonas sp. JD6.5 toward p-nitrophenyl phosphotriesters

Bioorganic & medicinal chemistry letters, 2000-06, Vol.10 (11), p.1285-1288

2000

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Purified RecombinantEscherichia coliKetol-Acid Reductoisomerase Is Unsuitable for Use in a Coupled Assay of Acetohydroxyacid Synthase Activity due to an Unexpected Side Reaction

Protein expression and purification, 1999-02, Vol.15 (1), p.57-61

1999

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Purified recombinant Escherichia coli ketol-acid reductoisomerase is unsuitable for use in a coupled assay of acetohydroxyacid synthase activity due to an unexpected side reaction

Protein expression and purification, 1999-02, Vol.15 (1), p.57-61

1999

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Increasing Cropping System Diversity Balances Productivity, Profitability and Environmental Health

PloS one, 2012-10, Vol.7 (10), p.e47149

2012

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GWAS on family history of Alzheimer's disease

Translational psychiatry, 2018-05, Vol.8 (1), p.99-7, Article 99

2018

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Liver health in adults with Fontan circulation: A multicenter cross-sectional study

The Journal of thoracic and cardiovascular surgery, 2017-03, Vol.153 (3), p.656-664

2017

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Specificity of Induction of the vanA and vanB Operons in Vancomycin-Resistant Enterococci by Telavancin

Enhanced Degradation of Chemical Warfare Agents through Molecular Engineering of the Phosphotriesterase Active Site

Catalytic properties of the PepQ prolidase from Escherichia coli

Demonstration of a fast-reconfigurable silicon CMOS optical lattice filter

Concomitant Angiotensin AT1 Receptor Antagonism and Neprilysin Inhibition Produces Omapatrilat-like Antihypertensive Effects Without Promoting Tracheal Plasma Extravasation in the Rat

Discovery of TD-0212, an Orally Active Dual Pharmacology AT 1 Antagonist and Neprilysin Inhibitor (ARNI)

Purification of Escherichia coli acetohydroxyacid synthase isoenzyme II and reconstitution of active enzyme from its individual pure subunits

Discovery of TD-0212, an Orally Active Dual Pharmacology AT1 Antagonist and Neprilysin Inhibitor (ARNI)

CMOS-Compatible Si-Ring-Assisted Mach-Zehnder Interferometer With Internal Bandwidth Equalization

Enzymatic Synthesis of Chiral Organophosphothioates from Prochiral Precursors

A multivalent approach towards linked dual-pharmacology prostaglandin F receptor agonist/carbonic anhydrase-II inhibitors for the treatment of glaucoma

Peptide Ketobenzoxazole Inhibitors Bound to Cathepsin K

The ITK Inhibitor Cpi-818 Blocks Activation of T Cells from Autoimmune Lymphoproliferative Syndrome (ALPS) Patients and Is Active in a Murine Model of ALPS

Preliminary Clinical Data from a Phase 1 Trial with CPI-818, a Selective ITK Inhibitor That Preferentially Blocks the Growth of T Lymphoma Cells

Cpi-818, an Oral Interleukin-2-Inducible T-Cell Kinase Inhibitor, Is Well-Tolerated and Active in Patients with T-Cell Lymphoma

Abstract 1313: CPI-818: A selective inhibitor of interleukin-2-inducible T-cell kinase (ITK) that inhibits T-cell receptor signaling, promotes Th1 skewing, and achieves objective tumor responses when administered to dogs with T cell lymphomas

Stereochemical Specificity of Organophosphorus Acid Anhydrolase toward p-Nitrophenyl Analogs of Soman and Sarin

CMOS-Compatible Si-Ring-Assisted MachaZehnder Interferometer With Internal Bandwidth Equalization

Mutagenesis of Escherichia coli acetohydroxyacid synthase isoenzyme II and characterization of three herbicide-insensitive forms

Substrate and stereochemical specificity of the organophosphorus acid anhydrolase from Alteromonas sp. JD6.5 toward p-nitrophenyl phosphotriesters

Purified RecombinantEscherichia coliKetol-Acid Reductoisomerase Is Unsuitable for Use in a Coupled Assay of Acetohydroxyacid Synthase Activity due to an Unexpected Side Reaction

Purified recombinant Escherichia coli ketol-acid reductoisomerase is unsuitable for use in a coupled assay of acetohydroxyacid synthase activity due to an unexpected side reaction

Increasing Cropping System Diversity Balances Productivity, Profitability and Environmental Health

GWAS on family history of Alzheimer's disease

Liver health in adults with Fontan circulation: A multicenter cross-sectional study

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