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Investigation of TRPV1 loss-of-function phenotypes in transgenic shRNA expressing and knockout mice

Molecular and cellular neuroscience, 2008-03, Vol.37 (3), p.579-589

2008

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Pyrazole C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists

Bioorganic & medicinal chemistry letters, 2017-09, Vol.27 (18), p.4383-4388

2017

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Quantitative trait loci for obesity and insulin resistance (Nob1, Nob2) and their interaction with the leptin receptor allele (LeprA720T/T10441) in New Zealand obese mice

Diabetologia, 2000-12, Vol.43 (12), p.1565-1572

2000

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A hydrophobic residue in position 15 of the rP2X3 receptor slows desensitization and reveals properties beneficial for pharmacological analysis and high-throughput screening

Neuropharmacology, 2014-04, Vol.79, p.603-615

2014

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4-Aminophenyl acetamides and propanamides as potent transient receptor potential vanilloid 1 (TRPV1) ligands

Bioorganic & medicinal chemistry, 2018-08, Vol.26 (15), p.4509-4517

2018

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Discovery of 2-(3,5-difluoro-4-methylsulfonaminophenyl)propanamides as potent TRPV1 antagonists

Bioorganic & medicinal chemistry letters, 2018-08, Vol.28 (14), p.2539-2542

2018

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(223) Evidence for a combined mode of action underlying the broad efficacy profile of tapentadol, a novel centrally acting analgesic

The journal of pain, 2008, Vol.9 (4), p.31-31

2008

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RNA interference-based functional knockdown of the voltage-gated potassium channel Kv7.2 in dorsal root ganglion neurons after in vitro and in vivo gene transfer by adeno-associated virus vectors

Molecular pain, 2018-01, Vol.14, p.1744806917749669-1744806917749669

2018

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t-Butyl pyridine and phenyl C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists

Bioorganic & medicinal chemistry, 2017-04, Vol.25 (8), p.2451-2462

2017

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Molecular determinants of potent P2X2 antagonism identified by functional analysis, mutagenesis, and homology docking

Molecular pharmacology, 2011-04, Vol.79 (4), p.649-661

2011

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Salt bridge switching from Arg290/Glu167 to Arg290/ATP promotes the closed-to-open transition of the P2X2 receptor

Molecular pharmacology, 2013-01, Vol.83 (1), p.73-84

2013

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GLUT8, a Novel Member of the Sugar Transport Facilitator Family with Glucose Transport Activity

The Journal of biological chemistry, 2000-05, Vol.275 (21), p.16275-16280

2000

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Pyridine C-region analogs of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists

European journal of medicinal chemistry, 2015-03, Vol.93, p.101-108

2015

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Structure activity relationships of benzyl C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists

Bioorganic & medicinal chemistry, 2015-11, Vol.23 (21), p.6844-6854

2015

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2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists

Bioorganic & medicinal chemistry letters, 2014-08, Vol.24 (16), p.4039-4043

2014

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α-Substituted 2-(3-fluoro-4-methylsulfonamidophenyl)acetamides as potent TRPV1 antagonists

Bioorganic & medicinal chemistry letters, 2015-06, Vol.25 (11), p.2326-2330

2015

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Antinociceptive effect of antisense oligonucleotides against the vanilloid receptor VR1/TRPV1

Neurochemistry international, 2007, Vol.50 (1), p.281-290

2007

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2-Aryl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists

Bioorganic & medicinal chemistry letters, 2014-08, Vol.24 (16), p.4044-4047

2014

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6,6-Fused heterocyclic ureas as highly potent TRPV1 antagonists

Bioorganic & medicinal chemistry letters, 2015-02, Vol.25 (4), p.803-806

2015

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Reduced Expression of PSCA, a Member of the LY-6 Family of Cell Surface Antigens, in Bladder, Esophagus, and Stomach Tumors

Biochemical and biophysical research communications, 2000-09, Vol.275 (3), p.783-788

2000

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Globalisierung und Regionalisierung : die Enträumlichung der Region: Wirtschaftsgeographie

Geographische Zeitschrift, 2002, Vol.90 (1), p.52-63

BAHRENBERG, G

2002

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Unsinn und Sinn des Regionalismus in der Geographie (Non-sens et sens du concept de régionalisme en géographie)

Geographische Zeitschrift, 1987, Vol.75 (3), p.149-160

BAHRENBERG, G

1987

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Differential Regulation of Endogenous Glucose-6-Phosphatase and Phosphoenolpyruvate Carboxykinase Gene Expression by the Forkhead Transcription Factor FKHR in H4IIE-Hepatoma Cells

Biochemical and biophysical research communications, 2001-07, Vol.285 (4), p.897-902

2001

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Identification of the critical sequence elements in the cytoplasmic domain of leptin receptor isoforms required for Janus kinase/signal transducer and activator of transcription activation by receptor heterodimers

Molecular endocrinology (Baltimore, Md.), 2002-04, Vol.16 (4), p.859

2002

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A New Class of Spiegelmers Containing 2′-Fluoro-nucleotides

Nucleosides, nucleotides & nucleic acids, 2003-10, Vol.22 (5-8), p.1035-1038

2003

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Investigation of TRPV1 loss-of-function phenotypes in transgenic shRNA expressing and knockout mice

Pyrazole C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists

Quantitative trait loci for obesity and insulin resistance (Nob1, Nob2) and their interaction with the leptin receptor allele (LeprA720T/T10441) in New Zealand obese mice

A hydrophobic residue in position 15 of the rP2X3 receptor slows desensitization and reveals properties beneficial for pharmacological analysis and high-throughput screening

4-Aminophenyl acetamides and propanamides as potent transient receptor potential vanilloid 1 (TRPV1) ligands

Discovery of 2-(3,5-difluoro-4-methylsulfonaminophenyl)propanamides as potent TRPV1 antagonists

(223) Evidence for a combined mode of action underlying the broad efficacy profile of tapentadol, a novel centrally acting analgesic

RNA interference-based functional knockdown of the voltage-gated potassium channel Kv7.2 in dorsal root ganglion neurons after in vitro and in vivo gene transfer by adeno-associated virus vectors

t-Butyl pyridine and phenyl C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists

Molecular determinants of potent P2X2 antagonism identified by functional analysis, mutagenesis, and homology docking

Salt bridge switching from Arg290/Glu167 to Arg290/ATP promotes the closed-to-open transition of the P2X2 receptor

GLUT8, a Novel Member of the Sugar Transport Facilitator Family with Glucose Transport Activity

Pyridine C-region analogs of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists

Structure activity relationships of benzyl C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists

2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists

α-Substituted 2-(3-fluoro-4-methylsulfonamidophenyl)acetamides as potent TRPV1 antagonists

Antinociceptive effect of antisense oligonucleotides against the vanilloid receptor VR1/TRPV1

2-Aryl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists

6,6-Fused heterocyclic ureas as highly potent TRPV1 antagonists

Reduced Expression of PSCA, a Member of the LY-6 Family of Cell Surface Antigens, in Bladder, Esophagus, and Stomach Tumors

Globalisierung und Regionalisierung : die Enträumlichung der Region: Wirtschaftsgeographie

Unsinn und Sinn des Regionalismus in der Geographie (Non-sens et sens du concept de régionalisme en géographie)

Differential Regulation of Endogenous Glucose-6-Phosphatase and Phosphoenolpyruvate Carboxykinase Gene Expression by the Forkhead Transcription Factor FKHR in H4IIE-Hepatoma Cells

Identification of the critical sequence elements in the cytoplasmic domain of leptin receptor isoforms required for Janus kinase/signal transducer and activator of transcription activation by receptor heterodimers

A New Class of Spiegelmers Containing 2′-Fluoro-nucleotides

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