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Exciton size and binding energy limitations in one-dimensional organic materials

The Journal of chemical physics, 2015-12, Vol.143 (24), p.244905-244905

2015

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Advances in organic solar cells

APL materials, 2023-08, Vol.11 (8), p.080401-080401-2

2023

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Dielectric function of a poly(benzimidazobenzophenanthroline) ladder polymer

Physical review. B, Condensed matter and materials physics, 2015-05, Vol.91 (19), Article 195202

2015

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Expression of a Constitutively Active Human Insulin Receptor in Hippocampal Neurons Does Not Alter VGCC Currents

Neurochemical research, 2019-01, Vol.44 (1), p.269-280

2019

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Harnessing the power of gene microarrays for the study of brain aging and Alzheimer's disease: statistical reliability and functional correlation

Ageing research reviews, 2005-11, Vol.4 (4), p.481-512

2005

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Loss of electrical excitability in an animal model of acute quadriplegic myopathy

Annals of neurology, 1998-02, Vol.43 (2), p.171-179

1998

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Organic and Hybrid Solar Cells

Second edition, 2022

Volltextzugriff (PDF)

Genes, BACs and artificial chromosomes

Xenotransplantation (Københaven), 2011-01, Vol.18 (1), p.66-66

2011

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REST: A mammalian silencer protein that restricts sodium channel gene expression to neurons

Cell, 1995-03, Vol.80 (6), p.949-957

1995

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PDGF-A promoter and enhancer elements provide efficient and selective antineoplastic gene therapy in multiple cancer types

Cancer gene therapy, 2009-04, Vol.16 (4), p.298-309

2009

Volltextzugriff (PDF)

Neuron-specific expression of the rat brain type II sodium channel gene is directed by upstream regulatory elements

Neuron (Cambridge, Mass.), 1990-02, Vol.4 (2), p.223-231

1990

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Altered Gene Expression in Steroid-Treated Denervated Muscle

Neurobiology of disease, 1999-12, Vol.6 (6), p.515-522

1999

Volltextzugriff (PDF)

Increased vulnerability of hippocampal neurons with age in culture: Temporal association with increases in NMDA receptor current, NR2A subunit expression and recruitment of L-type calcium channels

Brain research, 2007-06, Vol.1151, p.20-31

2007

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Inactivation and secondary structure in the D4/S4-5 region of the SkM1 sodium channel

The Journal of general physiology, 1998-06, Vol.111 (6), p.703-715

1998

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Congenital myasthenic syndrome of Brahman cattle in South Africa

Veterinary record, 2003-12, Vol.153 (25), p.779-781

2003

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Severe congenital myasthenic syndrome due to homozygosity of the 1293insG ε-acetylcholine receptor subunit mutation

Annals of neurology, 2000-09, Vol.48 (3), p.379-383

2000

Volltextzugriff (PDF)

Analysis of Local Structure in the D2/S1–S2 Region of the Rat Skeletal Muscle Type 1 Sodium Channel Using Insertional Mutagenesis

Journal of neurochemistry, 1998-04, Vol.70 (4), p.1628-1635

1998

Volltextzugriff (PDF)

Disruption of TrkB-Mediated Signaling Induces Disassembly of Postsynaptic Receptor Clusters at Neuromuscular Junctions

Neuron (Cambridge, Mass.), 1999-11, Vol.24 (3), p.567-583

1999

Volltextzugriff (PDF)

Escherichia coli-cloned CFTR loci relevant for human artificial chromosome therapy

Human gene therapy, 2010-09, Vol.21 (9), p.1077

2010

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Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene

European journal of neurology, 2002-11, Vol.9 (6), p.694-695

2002

Volltextzugriff (PDF)

Calcineurin Triggers Reactive/Inflammatory Processes in Astrocytes and Is Upregulated in Aging and Alzheimer's Models

The Journal of neuroscience, 2005-05, Vol.25 (18), p.4649-4658

2005

Volltextzugriff (PDF)

Purification and functional reconstitution of the voltage-sensitive sodium channel from rabbit T-tubular membranes

The Journal of biological chemistry, 1985-05, Vol.260 (10), p.6341-6347

1985

Volltextzugriff (PDF)

Two E-Boxes Are the Focal Point of Muscle-specific Skeletal Muscle Type 1 Na+ Channel Gene Expression

The Journal of biological chemistry, 1998-05, Vol.273 (18), p.11327-11334

1998

Volltextzugriff (PDF)

Interaction between the skeletal muscle type 1 Na+ channel promoter E-box and an upstream repressor element. Release of repression by myogenin

The Journal of biological chemistry, 1999-03, Vol.274 (12), p.8129

1999

Volltextzugriff (PDF)

Structural Inferences for the Native Skeletal Muscle Sodium Channel as Derived from Patterns of Endogenous Proteolysis

The Journal of biological chemistry, 1989-08, Vol.264 (22), p.13273-13280

1989

Volltextzugriff (PDF)

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Exciton size and binding energy limitations in one-dimensional organic materials

Advances in organic solar cells

Dielectric function of a poly(benzimidazobenzophenanthroline) ladder polymer

Expression of a Constitutively Active Human Insulin Receptor in Hippocampal Neurons Does Not Alter VGCC Currents

Harnessing the power of gene microarrays for the study of brain aging and Alzheimer's disease: statistical reliability and functional correlation

Loss of electrical excitability in an animal model of acute quadriplegic myopathy

Organic and Hybrid Solar Cells

Genes, BACs and artificial chromosomes

REST: A mammalian silencer protein that restricts sodium channel gene expression to neurons

PDGF-A promoter and enhancer elements provide efficient and selective antineoplastic gene therapy in multiple cancer types

Neuron-specific expression of the rat brain type II sodium channel gene is directed by upstream regulatory elements

Altered Gene Expression in Steroid-Treated Denervated Muscle

Increased vulnerability of hippocampal neurons with age in culture: Temporal association with increases in NMDA receptor current, NR2A subunit expression and recruitment of L-type calcium channels

Inactivation and secondary structure in the D4/S4-5 region of the SkM1 sodium channel

Congenital myasthenic syndrome of Brahman cattle in South Africa

Severe congenital myasthenic syndrome due to homozygosity of the 1293insG ε-acetylcholine receptor subunit mutation

Analysis of Local Structure in the D2/S1–S2 Region of the Rat Skeletal Muscle Type 1 Sodium Channel Using Insertional Mutagenesis

Disruption of TrkB-Mediated Signaling Induces Disassembly of Postsynaptic Receptor Clusters at Neuromuscular Junctions

Escherichia coli-cloned CFTR loci relevant for human artificial chromosome therapy

Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene

Calcineurin Triggers Reactive/Inflammatory Processes in Astrocytes and Is Upregulated in Aging and Alzheimer's Models

Purification and functional reconstitution of the voltage-sensitive sodium channel from rabbit T-tubular membranes

Two E-Boxes Are the Focal Point of Muscle-specific Skeletal Muscle Type 1 Na+ Channel Gene Expression

Interaction between the skeletal muscle type 1 Na+ channel promoter E-box and an upstream repressor element. Release of repression by myogenin

Structural Inferences for the Native Skeletal Muscle Sodium Channel as Derived from Patterns of Endogenous Proteolysis

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