Search Results - "Messer, Jürg"
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1
In Vitro Binding Properties in Rat Brain of [3H]Ro 25‐6981, a Potent and Selective Antagonist of NMDA Receptors Containing NR2B Subunits
Published in Journal of neurochemistry (01-05-1998)“…: The in vitro binding of a new subtype‐selective NMDA receptor antagonist, [3H]Ro 25‐6981, to rat brain membranes and sections was characterized. The compound…”
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2
Gantenerumab: a novel human anti-Aβ antibody demonstrates sustained cerebral amyloid-β binding and elicits cell-mediated removal of human amyloid-β
Published in Journal of Alzheimer's disease (01-01-2012)“…The amyloid-β lowering capacity of anti-Aβ antibodies has been demonstrated in transgenic models of Alzheimer's disease (AD) and in AD patients. While the…”
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3
Characterization of (2S,2′R,3′R)‐2‐(2′,3′‐[3H]‐Dicarboxycyclopropyl)glycine Binding in Rat Brain
Published in Journal of neurochemistry (01-12-1998)“…: [(2S,2′R,3′R)‐2‐(2′,3′‐[3H]Dicarboxycyclopropyl)glycine ([3H]DCG IV) binding was characterized in vitro in rat brain cortex homogenates and rat brain…”
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4
Altered distribution of mGlu2 receptors in β-amyloid-affected brain regions of Alzheimer cases and aged PS2APP mice
Published in Brain research (06-12-2010)“…Abstract Altered glutamatergic synaptic transmission is among the key events defining the course of Alzheimer's disease (AD). mGlu2 receptors, a subtype of…”
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5
Distribution and abundance of metabotropic glutamate receptor subtype 2 in rat brain revealed by [3H]LY354740 binding in vitro and quantitative radioautography: Correlation with the sites of synthesis, expression, and agonist stimulation of [35S]GTPγs binding
Published in Journal of comparative neurology (1911) (20-06-2005)“…Until recently, there was a lack of selective radioligands for the subtypes of metabotropic glutamate (mGlu) receptors. [3H]LY354740…”
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6
A comparative study of binding properties of gantenerumab and aducanumab analog to aggregated amyloid-beta (P6.087)
Published in Neurology (18-04-2017)“…Abstract only…”
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7
Distribution and abundance of metabotropic glutamate receptor subtype 2 in rat brain revealed by [3H]LY354740 binding in vitro and quantitative radioautography: correlation with the sites of synthesis, expression, and agonist stimulation of [35S]GTPgammas binding
Published in Journal of comparative neurology (1911) (20-06-2005)“…Until recently, there was a lack of selective radioligands for the subtypes of metabotropic glutamate (mGlu) receptors. [(3)H]LY354740…”
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8
In vitro binding characteristics of a new selective group II metabotropic glutamate receptor radioligand, [3H]LY354740, in rat brain
Published in Molecular pharmacology (01-02-1998)“…The in vitro binding of [3H]LY354740, the first high affinity group II-selective metabotropic glutamate (mGlu) receptor radioligand, was characterized in rat…”
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9
Characterization of [3H]Quisqualate Binding to Recombinant Rat Metabotropic Glutamate 1a and 5a Receptors and to Rat and Human Brain Sections
Published in Journal of neurochemistry (01-12-2000)“…: We have investigated the binding properties of[3H]quisqualate to rat metabotropic glutamate (mGlu) 1a and 5areceptors and to rat and human brain sections…”
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10
Opposite effects of Zn on the in vitro binding of [3H]LY354740 to recombinant and native metabotropic glutamate 2 and 3 receptors
Published in Journal of neurochemistry (01-07-2005)“…We investigated the effect of Zn on agonist binding to both recombinant and native mGlu2 and mGlu3 receptors. Zn had a biphasic inhibitory effect on…”
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11
Binding Characteristics of a Potent AMPA Receptor Antagonist [3H]Ro 48‐8587 in Rat Brain
Published in Journal of neurochemistry (01-07-1998)“…: A new AMPA receptor antagonist, Ro 48‐8587, was characterized pharmacologically in vitro. It is highly potent and selective for AMPA receptors as shown by…”
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12
Characterization of behavioral response to amphetamine, tyrosine hydroxylase levels, and dopamine receptor levels in neurokinin 3 receptor knockout mice
Published in Behavioural pharmacology (01-09-2008)“…The neurokinin 3 (NK3) receptor is a novel target under investigation for improvement of symptoms of schizophrenia, because of its ability to modulate…”
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