UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Chemical proteomics reveals new targets of cysteine sulfinic acid reductase

Nature chemical biology, 2018-11, Vol.14 (11), p.995-1004

2018

Volltextzugriff (PDF)

Novel hyperoxidation resistance motifs in 2-Cys peroxiredoxins

The Journal of biological chemistry, 2018-07, Vol.293 (30), p.11901-11912

2018

Volltextzugriff (PDF)

Reduction of cysteine sulfinic acid in eukaryotic, typical 2-Cys peroxiredoxins by sulfiredoxin

Antioxidants & redox signaling, 2011-07, Vol.15 (1), p.99-109

2011

Volltextzugriff (PDF)

Substrate specificity and membrane topologies of the iron-containing ω3 and ω6 desaturases from Mortierella alpina

Applied microbiology and biotechnology, 2018, Vol.102 (1), p.211-223

2018

Volltextzugriff (PDF)

Hydroxyproline Metabolism and Oxalate Synthesis in Primary Hyperoxaluria

Journal of the American Society of Nephrology, 2018-06, Vol.29 (6), p.1615-1623

2018

Volltextzugriff (PDF)

Cannabinoid Receptor Interacting Protein 1a (CRIP1a): Function and Structure

Molecules (Basel, Switzerland), 2019-10, Vol.24 (20), p.3672

2019

Volltextzugriff (PDF)

Molecular Basis for the Resistance of Human Mitochondrial 2-Cys Peroxiredoxin 3 to Hyperoxidation

The Journal of biological chemistry, 2013-10, Vol.288 (41), p.29714-29723

2013

Volltextzugriff (PDF)

Kinetic analysis of structural influences on the susceptibility of peroxiredoxins 2 and 3 to hyperoxidation

Biochemical journal, 2016-02, Vol.473 (4), p.411-421

2016

Volltextzugriff (PDF)

Metalloaminopeptidases: Common Functional Themes in Disparate Structural Surroundings

Chemical reviews, 2002-12, Vol.102 (12), p.4581-4608

2002

Volltextzugriff (PDF)

Proline dehydrogenase 2 (PRODH2) is a hydroxyproline dehydrogenase (HYPDH) and molecular target for treating primary hyperoxaluria

Biochemical journal, 2015-03, Vol.466 (2), p.273-281

2015

Volltextzugriff (PDF)

Hydroxyproline metabolism in a mouse model of Primary Hyperoxaluria Type 3

Biochimica et biophysica acta. Molecular basis of disease, 2015-12, Vol.1852 (12), p.2700-2705

2015

Volltextzugriff (PDF)

Crystal structure of the thioesterase domain of human fatty acid synthase inhibited by Orlistat

Nature structural & molecular biology, 2007-08, Vol.14 (8), p.704-709

2007

Volltextzugriff (PDF)

Mitochondrial peroxiredoxin 3 is more resilient to hyperoxidation than cytoplasmic peroxiredoxins

Biochemical journal, 2009-06, Vol.421 (1), p.51-58

2009

Volltextzugriff (PDF)

Structure of the sulphiredoxin-peroxiredoxin complex reveals an essential repair embrace

Nature, 2008-01, Vol.451 (7174), p.98-101

2008

Volltextzugriff (PDF)

Free methionine-(R)-sulfoxide reductase from Escherichia coli reveals a new GAF domain function

Proceedings of the National Academy of Sciences - PNAS, 2007-06, Vol.104 (23), p.9597-9602

2007

Volltextzugriff (PDF)

Discovery of Heteroaromatic Sulfones As a New Class of Biologically Compatible Thiol-Selective Reagents

ACS chemical biology, 2017-08, Vol.12 (8), p.2201-2208

2017

Volltextzugriff (PDF)

Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria

PloS one, 2011-10, Vol.6 (10), p.e26021-e26021

2011

Volltextzugriff (PDF)

Expression and purification of integral membrane fatty acid desaturases

PloS one, 2013-03, Vol.8 (3), p.e58139-e58139

2013

Volltextzugriff (PDF)

Disabling Mitochondrial Peroxide Metabolism via Combinatorial Targeting of Peroxiredoxin 3 as an Effective Therapeutic Approach for Malignant Mesothelioma

PloS one, 2015-05, Vol.10 (5), p.e0127310

2015

Volltextzugriff (PDF)

Cannabinoid Receptor Interacting Protein 1a (CRIP1a) in Health and Disease

Biomolecules (Basel, Switzerland), 2020-11, Vol.10 (12), p.1609

2020

Volltextzugriff (PDF)

Peroxiredoxins in Cancer and Response to Radiation Therapies

Antioxidants, 2019-01, Vol.8 (1), p.11

2019

Volltextzugriff (PDF)

Metabolism of [13C5]hydroxyproline in vitro and in vivo: implications for primary hyperoxaluria

American journal of physiology: Gastrointestinal and liver physiology, 2012-03, Vol.302 (6), p.G637-G643

2012

Volltextzugriff (PDF)

Reduction of Cysteine Sulfinic Acid in Peroxiredoxin by Sulfiredoxin Proceeds Directly through a Sulfinic Phosphoryl Ester Intermediate

The Journal of biological chemistry, 2008-08, Vol.283 (35), p.23846-23851

2008

Volltextzugriff (PDF)

Active Site and Loop 4 Movements within Human Glycolate Oxidase: Implications for Substrate Specificity and Drug Design

Biochemistry (Easton), 2008-02, Vol.47 (8), p.2439-2449

2008

Volltextzugriff (PDF)

Unique Cellular and Biochemical Features of Human Mitochondrial Peroxiredoxin 3 Establish the Molecular Basis for Its Specific Reaction with Thiostrepton

Antioxidants, 2021-01, Vol.10 (2), p.150

2021

Volltextzugriff (PDF)

1 – 25 von 87

Suche als RSS-Feed

Aktive Filter

SpracheEnglisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(84)
Mit Volltextzugriff
(76)

Publikationsform

Artikel
(86)
Buchkapitel
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Chemical proteomics reveals new targets of cysteine sulfinic acid reductase

Novel hyperoxidation resistance motifs in 2-Cys peroxiredoxins

Reduction of cysteine sulfinic acid in eukaryotic, typical 2-Cys peroxiredoxins by sulfiredoxin

Substrate specificity and membrane topologies of the iron-containing ω3 and ω6 desaturases from Mortierella alpina

Hydroxyproline Metabolism and Oxalate Synthesis in Primary Hyperoxaluria

Cannabinoid Receptor Interacting Protein 1a (CRIP1a): Function and Structure

Molecular Basis for the Resistance of Human Mitochondrial 2-Cys Peroxiredoxin 3 to Hyperoxidation

Kinetic analysis of structural influences on the susceptibility of peroxiredoxins 2 and 3 to hyperoxidation

Metalloaminopeptidases: Common Functional Themes in Disparate Structural Surroundings

Proline dehydrogenase 2 (PRODH2) is a hydroxyproline dehydrogenase (HYPDH) and molecular target for treating primary hyperoxaluria

Hydroxyproline metabolism in a mouse model of Primary Hyperoxaluria Type 3

Crystal structure of the thioesterase domain of human fatty acid synthase inhibited by Orlistat

Mitochondrial peroxiredoxin 3 is more resilient to hyperoxidation than cytoplasmic peroxiredoxins

Structure of the sulphiredoxin-peroxiredoxin complex reveals an essential repair embrace

Free methionine-(R)-sulfoxide reductase from Escherichia coli reveals a new GAF domain function

Discovery of Heteroaromatic Sulfones As a New Class of Biologically Compatible Thiol-Selective Reagents

Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria

Expression and purification of integral membrane fatty acid desaturases

Disabling Mitochondrial Peroxide Metabolism via Combinatorial Targeting of Peroxiredoxin 3 as an Effective Therapeutic Approach for Malignant Mesothelioma

Cannabinoid Receptor Interacting Protein 1a (CRIP1a) in Health and Disease

Peroxiredoxins in Cancer and Response to Radiation Therapies

Metabolism of [13C5]hydroxyproline in vitro and in vivo: implications for primary hyperoxaluria

Reduction of Cysteine Sulfinic Acid in Peroxiredoxin by Sulfiredoxin Proceeds Directly through a Sulfinic Phosphoryl Ester Intermediate

Active Site and Loop 4 Movements within Human Glycolate Oxidase: Implications for Substrate Specificity and Drug Design

Unique Cellular and Biochemical Features of Human Mitochondrial Peroxiredoxin 3 Establish the Molecular Basis for Its Specific Reaction with Thiostrepton

Aktive Filter

Suchergebnisse filtern