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Xeno Amino Acids: A Look into Biochemistry as We Do Not Know It

Life (Basel, Switzerland), 2023-11, Vol.13 (12), p.2281

2023

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Neuronal Hyperpolarization-Activated Pacemaker Channels Drive Neuropathic Pain

The Journal of neuroscience, 2003-02, Vol.23 (4), p.1169-1178

2003

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Biochemical and Biological Properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a Mechanism-Based Inhibitor of Fatty Acid Amide Hydrolase

Anesthesia and analgesia, 2009, Vol.108 (1), p.316-329

2009

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What Would an Alien Amino Acid Alphabet Look Like and Why?

Astrobiology, 2023-05, Vol.23 (5), p.536

2023

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Fetal cardiomyocyte phenotype, ketone body metabolism, and mitochondrial dysfunction in the pathology of atrial fibrillation

Molecular and cellular biochemistry, 2021-02, Vol.476 (2), p.1165-1178

2021

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Cloning and molecular characterization of the rat CB2 cannabinoid receptor

Biochimica et biophysica acta, 2002-07, Vol.1576 (3), p.255-264

2002

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Female song is structurally different from male song in Orchard Orioles, a temperate-breeding songbird with delayed plumage maturation

Journal of field ornithology, 2022-03, Vol.93 (1), p.3, Article art3

2022

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Heteroarylureas with spirocyclic diamine cores as inhibitors of fatty acid amide hydrolase

Bioorganic & medicinal chemistry letters, 2014-02, Vol.24 (3), p.737-741

2014

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Beta-adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca2+-activated K+ channel

American Journal of Physiology - Renal Physiology, 2008-10, Vol.295 (4), p.F1149-F1157

2008

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Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure–mutagenicity relationships for arylamine metabolites

Bioorganic & medicinal chemistry letters, 2012-12, Vol.22 (24), p.7357-7362

2012

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Stimulation of β3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

American Journal of Physiology: Cell Physiology, 2008-11, Vol.295 (5), p.C1344-C1353

2008

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Acetylcholinesterase and butyrylcholinesterase are expressed in the spinal meninges of monkeys and pigs

Anesthesiology (Philadelphia), 1998-05, Vol.88 (5), p.1259-1265

1998

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The Role of Pacemaker Currents in Neuropathic Pain

Pain practice, 2004-09, Vol.4 (3), p.182-193

2004

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Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structureamutagenicity relationships for arylamine metabolites

Bioorganic & medicinal chemistry letters, 2012-12, Vol.22 (24), p.7357-7362

2012

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Stimulation of {beta}3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

American Journal of Physiology: Cell Physiology, 2008-11, Vol.295 (5), p.C1344

2008

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Stimulation of beta3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

American Journal of Physiology: Cell Physiology, 2008-11, Vol.295 (5), p.C1344

2008

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Stimulation of [beta]3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca^sup 2+^-activated K+ channels

American Journal of Physiology: Cell Physiology, 2008-11, Vol.295 (5), p.C1344

2008

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Stimulation of β3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca 2+ -activated K + channels

American Journal of Physiology: Cell Physiology, 2008-11, Vol.295 (5), p.C1344-C1353

2008

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Stimulation of β3–adrenoceptors activates spontaneous transient outward BK currents and causes relaxation in rat urinary bladder smooth muscle

The FASEB journal, 2008-03, Vol.22 (S1)

2008

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Stimulation of β3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

American Journal of Physiology: Cell Physiology, 2008, Vol.64 (5)

2008

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Large conductance voltage‐ and Ca2+‐activated K+ (BK) channels mediate the β‐adrenergic relaxation of mouse urinary bladder smooth muscle

The FASEB journal, 2007, Vol.21 (6), p.LB102-LB102

2007

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Inhibitory mechanism of BRL37344, a specific β3‐adrenoceptor agonist, on guinea pig urinary bladder smooth muscle contractions: Role of the BK channel

The FASEB journal, 2007, Vol.21 (6), p.LB102-LB102

2007

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β-Adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca 2+ -activated K + channel

American journal of physiology. Renal physiology, 2008-10, Vol.295 (4), p.F1149-F1157

2008

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[beta]-Adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca^sup 2+^-activated K+ channel

American journal of physiology. Renal physiology, 2008-10, Vol.295 (4), p.F1149

2008

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Β-Adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca2+-activated K+ channel

American journal of physiology. Renal physiology, 2008, Vol.64 (4)

2008

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Xeno Amino Acids: A Look into Biochemistry as We Do Not Know It

Neuronal Hyperpolarization-Activated Pacemaker Channels Drive Neuropathic Pain

Biochemical and Biological Properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a Mechanism-Based Inhibitor of Fatty Acid Amide Hydrolase

What Would an Alien Amino Acid Alphabet Look Like and Why?

Fetal cardiomyocyte phenotype, ketone body metabolism, and mitochondrial dysfunction in the pathology of atrial fibrillation

Cloning and molecular characterization of the rat CB2 cannabinoid receptor

Female song is structurally different from male song in Orchard Orioles, a temperate-breeding songbird with delayed plumage maturation

Heteroarylureas with spirocyclic diamine cores as inhibitors of fatty acid amide hydrolase

Beta-adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca2+-activated K+ channel

Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure–mutagenicity relationships for arylamine metabolites

Stimulation of β3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

Acetylcholinesterase and butyrylcholinesterase are expressed in the spinal meninges of monkeys and pigs

The Role of Pacemaker Currents in Neuropathic Pain

Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structureamutagenicity relationships for arylamine metabolites

Stimulation of {beta}3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

Stimulation of beta3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

Stimulation of [beta]3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca^sup 2+^-activated K+ channels

Stimulation of β3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca 2+ -activated K + channels

Stimulation of β3–adrenoceptors activates spontaneous transient outward BK currents and causes relaxation in rat urinary bladder smooth muscle

Stimulation of β3-adrenoceptors relaxes rat urinary bladder smooth muscle via activation of the large-conductance Ca2+-activated K+ channels

Large conductance voltage‐ and Ca2+‐activated K+ (BK) channels mediate the β‐adrenergic relaxation of mouse urinary bladder smooth muscle

Inhibitory mechanism of BRL37344, a specific β3‐adrenoceptor agonist, on guinea pig urinary bladder smooth muscle contractions: Role of the BK channel

β-Adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca 2+ -activated K + channel

[beta]-Adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca^sup 2+^-activated K+ channel

Β-Adrenergic relaxation of mouse urinary bladder smooth muscle in the absence of large-conductance Ca2+-activated K+ channel

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