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Mitochondrial permeability transition in CNS trauma: Cause or effect of neuronal cell death?

Journal of neuroscience research, 2005-01, Vol.79 (1-2), p.231-239

2005

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Strongyle faecal egg counts in Swiss horses: a retrospective analysis after the introduction of a selective treatment strategy

Veterinary parasitology, 2023-11, Vol.323, p.110027-110027, Article 110027

2023

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NIM811, a Mitochondrial Permeability Transition Inhibitor, Prevents Mitochondrial Depolarization in Small‐for‐Size Rat Liver Grafts

American journal of transplantation, 2007-05, Vol.7 (5), p.1103-1111

2007

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Interrupting apoptosis in neurodegenerative disease: potential for effective therapy?

Drug Discovery Today, 2004-03, Vol.9 (5), p.210-218

2004

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An orally active anti‐apoptotic molecule (CGP 3466B) preserves mitochondria and enhances survival in an animal model of motoneuron disease

British journal of pharmacology, 2000-10, Vol.131 (4), p.721-728

2000

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Transgenic Activation of Ras in Neurons Promotes Hypertrophy and Protects from Lesion-Induced Degeneration

The Journal of cell biology, 2000-12, Vol.151 (7), p.1537-1548

2000

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CGP 3466 protects dopaminergic neurons in lesion models of Parkinson's disease

Naunyn-Schmiedeberg's archives of pharmacology, 2000-12, Vol.362 (6), p.526-537

2000

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Similar potency of carbamazepine, oxcarbazepine, and lamotrigine in inhibiting the release of glutamate and other neurotransmitters

Neurology, 1995-10, Vol.45 (10), p.1907

1995

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Graduate nursing online orientation course: transitioning for success

The Journal of nursing education, 2010-12, Vol.49 (12), p.687

2010

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Dibenzoxepines as treatments for neurodegenerative diseases

Pure and applied chemistry, 1999-11, Vol.71 (11), p.2039-2046

1999

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Effect of carbamazepine, oxcarbazepine and lamotrigine on the increase in extracellular glutamate elicited by veratridine in rat cortex and striatum

Naunyn-Schmiedeberg's archives of pharmacology, 1996-07, Vol.354 (2), p.164-172

1996

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GABA and glutamate release affected by GABAB receptor antagonists with similar potency: no evidence for pharmacologically different presynaptic receptors

British journal of pharmacology, 1994-12, Vol.113 (4), p.1515-1521

1994

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Specific gamma-hydroxybutyrate-binding sites but loss of pharmacological effects of gamma-hydroxybutyrate in GABA(B)(1)-deficient mice

The European journal of neuroscience, 2003-11, Vol.18 (10), p.2722

2003

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Cyclophilin D as a drug target

Current medicinal chemistry, 2003-08, Vol.10 (16), p.1485

2003

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Efficient Enantioselective Synthesis of the NMDA 2B Receptor Antagonist Ro 67-8867

Organic process research & development, 2003-05, Vol.7 (3), p.418-425

2003

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Neurorescuing effects of the GAPDH ligand CGP 3466B

Journal of neural transmission. Supplementum, 2000 (60), p.197

2000

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Prospects for antiapoptotic drug therapy of neurodegenerative diseases

Progress in neuro-psychopharmacology & biological psychiatry, 2003-04, Vol.27 (2), p.303-321

Waldmeier, Peter C.

2003

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Inhibition of the Mitochondrial Permeability Transition by the Nonimmunosuppressive Cyclosporin Derivative NIM811

Molecular pharmacology, 2002-07, Vol.62 (1), p.22-29

2002

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Efficient Synthesis of Novel NK1 Receptor Antagonists: Selective 1,4-Addition of Grignard Reagents to 6-Chloronicotinic Acid Derivatives

Journal of organic chemistry, 2006-03, Vol.71 (5), p.2000-2008

2006

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The nonimmunosuppressive cyclosporin analogs NIM811 and UNIL025 display nanomolar potencies on permeability transition in brain-derived mitochondria

Journal of bioenergetics and biomembranes, 2004-08, Vol.36 (4), p.407-413

2004

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Inhibition of catechol- O-methyltransferase (COMT) as well as tyrosine and tryptophan hydroxylase by the orally active iron chelator, 1,2-dimethyl-3-hydroxypyridin-4-one (L1, CP20), in rat brain in vivo

Biochemical pharmacology, 1993-06, Vol.45 (12), p.2417-2424

1993

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Efficient Synthesis of a 5-HT2C Receptor Agonist Precursor

Organic process research & development, 2005-07, Vol.9 (4), p.508-512

2005

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Amine oxidases and their endogenous substrates (with special reference to monoamine oxidase and the brain)

Journal of neural transmission. Supplementum, 1987, Vol.23, p.55

Waldmeier, P C

1987

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Glyceraldehyde-3-phosphate Dehydrogenase, the Putative Target of the Antiapoptotic Compounds CGP 3466 and R-(−)-Deprenyl

The Journal of biological chemistry, 1998-03, Vol.273 (10), p.5821-5828

1998

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Is There a Common Denominator for the Antimanic Effect of Lithium and Anticonvulsants?

Pharmacopsychiatry, 1987-03, Vol.20 (2), p.37-47

Waldmeier, P. C.

1987

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Mitochondrial permeability transition in CNS trauma: Cause or effect of neuronal cell death?

Strongyle faecal egg counts in Swiss horses: a retrospective analysis after the introduction of a selective treatment strategy

NIM811, a Mitochondrial Permeability Transition Inhibitor, Prevents Mitochondrial Depolarization in Small‐for‐Size Rat Liver Grafts

Interrupting apoptosis in neurodegenerative disease: potential for effective therapy?

An orally active anti‐apoptotic molecule (CGP 3466B) preserves mitochondria and enhances survival in an animal model of motoneuron disease

Transgenic Activation of Ras in Neurons Promotes Hypertrophy and Protects from Lesion-Induced Degeneration

CGP 3466 protects dopaminergic neurons in lesion models of Parkinson's disease

Similar potency of carbamazepine, oxcarbazepine, and lamotrigine in inhibiting the release of glutamate and other neurotransmitters

Graduate nursing online orientation course: transitioning for success

Dibenzoxepines as treatments for neurodegenerative diseases

Effect of carbamazepine, oxcarbazepine and lamotrigine on the increase in extracellular glutamate elicited by veratridine in rat cortex and striatum

GABA and glutamate release affected by GABAB receptor antagonists with similar potency: no evidence for pharmacologically different presynaptic receptors

Specific gamma-hydroxybutyrate-binding sites but loss of pharmacological effects of gamma-hydroxybutyrate in GABA(B)(1)-deficient mice

Cyclophilin D as a drug target

Efficient Enantioselective Synthesis of the NMDA 2B Receptor Antagonist Ro 67-8867

Neurorescuing effects of the GAPDH ligand CGP 3466B

Prospects for antiapoptotic drug therapy of neurodegenerative diseases

Inhibition of the Mitochondrial Permeability Transition by the Nonimmunosuppressive Cyclosporin Derivative NIM811

Efficient Synthesis of Novel NK1 Receptor Antagonists: Selective 1,4-Addition of Grignard Reagents to 6-Chloronicotinic Acid Derivatives

The nonimmunosuppressive cyclosporin analogs NIM811 and UNIL025 display nanomolar potencies on permeability transition in brain-derived mitochondria

Inhibition of catechol- O-methyltransferase (COMT) as well as tyrosine and tryptophan hydroxylase by the orally active iron chelator, 1,2-dimethyl-3-hydroxypyridin-4-one (L1, CP20), in rat brain in vivo

Efficient Synthesis of a 5-HT2C Receptor Agonist Precursor

Amine oxidases and their endogenous substrates (with special reference to monoamine oxidase and the brain)

Glyceraldehyde-3-phosphate Dehydrogenase, the Putative Target of the Antiapoptotic Compounds CGP 3466 and R-(−)-Deprenyl

Is There a Common Denominator for the Antimanic Effect of Lithium and Anticonvulsants?

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