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Damage mechanisms of metallic HVOF-coatings for high heat flux application

Surface & coatings technology, 2017-04, Vol.316, p.219-225

2017

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Complete Genome Sequence and Analysis of Wolinella succinogenes

Proceedings of the National Academy of Sciences - PNAS, 2003-09, Vol.100 (20), p.11690-11695

2003

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The Cathelicidin LL-37 Activates Human Mast Cells and Is Degraded by Mast Cell Tryptase: Counter-Regulation by CXCL4

The Journal of immunology (1950), 2009-08, Vol.183 (4), p.2223-2231

2009

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Experimental Support for the "E Pathway Hypothesis" of Coupled Transmembrane e-and H+Transfer in Dihemic Quinol:Fumarate Reductase

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (52), p.18860-18865

2005

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Essential Role of Glu-C66 for Menaquinol Oxidation Indicates Transmembrane Electrochemical Potential Generation by Wolinella succinogenes Fumarate Reductase

Proceedings of the National Academy of Sciences - PNAS, 2000-11, Vol.97 (24), p.13051-13056

2000

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Characterization of the Menaquinone Reduction Site in the Diheme Cytochrome b Membrane Anchor of Wolinella succinogenes NiFe-hydrogenase

The Journal of biological chemistry, 2004-01, Vol.279 (1), p.274-281

2004

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Influence of the Temperature on Coccolith‐Containing Systems from Emiliania huxleyi Cultivations

Chemical engineering & technology, 2020-05, Vol.43 (5), p.904-912

2020

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The Ruhr Museums in the Capital of Culture Year 2010: Preliminary Conclusions

Museumskunde, 2010-01, Vol.75 (2), p.48-51

Gross, Roland

2010

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Site-directed modifications indicate differences in axial haem c iron ligation between the related NrfH and NapC families of multihaem c-type cytochromes

Biochemical journal, 2005-09, Vol.390 (Pt 3), p.689-693

2005

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Mast cells and neutrophils proteolytically activate chemokine precursor CTAP-III and are subject to counterregulation by PF-4 through inhibition of chymase and cathepsin G

Blood, 2006-03, Vol.107 (6), p.2234-2242

2006

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Fumarate respiration of Wolinella succinogenes: enzymology, energetics and coupling mechanism

BBA - Bioenergetics, 2002-01, Vol.1553 (1), p.23-38

2002

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Electron transport to periplasmic nitrate reductase (NapA) of Wolinella succinogenes is independent of a NapC protein

Molecular microbiology, 2003-07, Vol.49 (1), p.69-79

2003

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The hydE gene is essential for the formation of Wolinella succinogenes NiFe-hydrogenase

FEMS microbiology letters, 2003-10, Vol.227 (2), p.197-202

2003

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A NapC/NirT‐type cytochrome c (NrfH) is the mediator between the quinone pool and the cytochrome c nitrite reductase of Wolinella succinogenes

Molecular microbiology, 2000-02, Vol.35 (3), p.686-696

2000

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The nrfl gene is essential for the attachment of the active site haem group of Wolinella succinogenes cytochrome c nitrite reductase

Molecular microbiology, 2002-02, Vol.43 (3), p.763

2002

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The nrfI gene is essential for the attachment of the active site haem group of Wolinella succinogenes cytochrome c nitrite reductase

Molecular microbiology, 2002-02, Vol.43 (3), p.763-770

2002

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Transport of C 4 -Dicarboxylates in Wolinella succinogenes

Journal of bacteriology, 2000-10, Vol.182 (20), p.5757-5764

2000

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Modification of heme c binding motifs in the small subunit (NrfH) of the Wolinella succinogenes cytochrome c nitrite reductase complex

FEBS letters, 2002-07, Vol.522 (1), p.83-87

2002

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Transport of C4-dicarboxylates in Wolinella succinogenes

Journal of bacteriology, 2000-10, Vol.182 (20), p.5757-5764

2000

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FTIR Difference Spectra of Wolinella succinogenes Quinol:Fumarate Reductase Support a Key Role of Glu C180 within the “E-Pathway Hypothesis” of Coupled Transmembrane Electron and Proton Transfer

Biochemistry (Easton), 2005-10, Vol.44 (42), p.13949-13961

2005

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The hydE gene is essential for the formation of Wolinella succinogenes NiFe-hydrogenase

FEMS microbiology letters, 2003-10, Vol.227 (2), p.197-202

2003

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The role of the twin-arginine motif in the signal peptide encoded by the hydA gene of the hydrogenase from Wolinella succinogenes

Archives of microbiology, 1999-10, Vol.172 (4), p.227-232

1999

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Experimental support for the "E pathway hypothesis" of coupled transmembrane e super(-) and H super(+) transfer in dihemic quinol:fumarate reductase

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (52), p.18860-18865

2005

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Identification of histidine residues in Wolinella succinogenes hydrogenase that are essential for menaquinone reduction by H 2

Molecular microbiology, 1998-11, Vol.30 (3), p.639-646

1998

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Two membrane anchors of Wolinella succinogenes hydrogenase and their function in fumarate and polysulfide respiration

Archives of microbiology, 1998-07, Vol.170 (1), p.50-58

1998

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Damage mechanisms of metallic HVOF-coatings for high heat flux application

Complete Genome Sequence and Analysis of Wolinella succinogenes

The Cathelicidin LL-37 Activates Human Mast Cells and Is Degraded by Mast Cell Tryptase: Counter-Regulation by CXCL4

Experimental Support for the "E Pathway Hypothesis" of Coupled Transmembrane e-and H+Transfer in Dihemic Quinol:Fumarate Reductase

Essential Role of Glu-C66 for Menaquinol Oxidation Indicates Transmembrane Electrochemical Potential Generation by Wolinella succinogenes Fumarate Reductase

Characterization of the Menaquinone Reduction Site in the Diheme Cytochrome b Membrane Anchor of Wolinella succinogenes NiFe-hydrogenase

Influence of the Temperature on Coccolith‐Containing Systems from Emiliania huxleyi Cultivations

The Ruhr Museums in the Capital of Culture Year 2010: Preliminary Conclusions

Site-directed modifications indicate differences in axial haem c iron ligation between the related NrfH and NapC families of multihaem c-type cytochromes

Mast cells and neutrophils proteolytically activate chemokine precursor CTAP-III and are subject to counterregulation by PF-4 through inhibition of chymase and cathepsin G

Fumarate respiration of Wolinella succinogenes: enzymology, energetics and coupling mechanism

Electron transport to periplasmic nitrate reductase (NapA) of Wolinella succinogenes is independent of a NapC protein

The hydE gene is essential for the formation of Wolinella succinogenes NiFe-hydrogenase

A NapC/NirT‐type cytochrome c (NrfH) is the mediator between the quinone pool and the cytochrome c nitrite reductase of Wolinella succinogenes

The nrfl gene is essential for the attachment of the active site haem group of Wolinella succinogenes cytochrome c nitrite reductase

The nrfI gene is essential for the attachment of the active site haem group of Wolinella succinogenes cytochrome c nitrite reductase

Transport of C 4 -Dicarboxylates in Wolinella succinogenes

Modification of heme c binding motifs in the small subunit (NrfH) of the Wolinella succinogenes cytochrome c nitrite reductase complex

Transport of C4-dicarboxylates in Wolinella succinogenes

FTIR Difference Spectra of Wolinella succinogenes Quinol:Fumarate Reductase Support a Key Role of Glu C180 within the “E-Pathway Hypothesis” of Coupled Transmembrane Electron and Proton Transfer

The hydE gene is essential for the formation of Wolinella succinogenes NiFe-hydrogenase

The role of the twin-arginine motif in the signal peptide encoded by the hydA gene of the hydrogenase from Wolinella succinogenes

Experimental support for the "E pathway hypothesis" of coupled transmembrane e super(-) and H super(+) transfer in dihemic quinol:fumarate reductase

Identification of histidine residues in Wolinella succinogenes hydrogenase that are essential for menaquinone reduction by H 2

Two membrane anchors of Wolinella succinogenes hydrogenase and their function in fumarate and polysulfide respiration

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