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Norbert Topf

Researcher at Cornell University

Publications -  7
Citations -  2006

Norbert Topf is an academic researcher from Cornell University. The author has contributed to research in topics: Neural stem cell & Embryonic stem cell. The author has an hindex of 7, co-authored 7 publications receiving 1962 citations.

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Derivation of midbrain dopamine neurons from human embryonic stem cells

TL;DR: Conditions to direct hES cells into neurons of midbrain dopaminergic identity are described and high-yield DA neuron derivation was confirmed from three independent hES and two monkey embryonic stem cell lines.
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Neural subtype specification of fertilization and nuclear transfer embryonic stem cells and application in parkinsonian mice.

TL;DR: A set of coculture conditions is provided that allows rapid and efficient derivation of most central nervous system phenotypes and transplantation of ES and ntES cell–derived dopaminergic neurons corrected the phenotype of a mouse model of Parkinson disease, demonstrating an in vivo application of therapeutic cloning in neural disease.
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An Isoflurane- and Alcohol-Insensitive Mutant GABAA Receptor α1 Subunit with Near-Normal Apparent Affinity for GABA: Characterization in Heterologous Systems and Production of Knockin Mice

TL;DR: The double mutant α1(S270H,L277A)β2γ2S GABAAR was expressed in Xenopus laevis oocytes and human embryonic kidney (HEK)293 cells, and it had near-normal GABA sensitivity, but rapid application of a brief GABA pulse to receptors expressed in HEK293 cells revealed that the deactivation was faster in double mutant than in wild-type receptors.
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Impairment of hyperpolarization-activated, cyclic nucleotide- gated channel function by the intravenous general anesthetic propofol

TL;DR: The data suggest that propofol modulation of HCN channel gating is an important molecular mechanism that can contribute to the depression of central nervous system function and also lead to bradyarrhythmias in patients receiving prop ofol during surgical anesthesia.
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Selective Expansion of Alveolar Macrophages In Vivo by Adenovirus-Mediated Transfer of the Murine Granulocyte-Macrophage Colony-Stimulating Factor cDNA

TL;DR: It is feasible to genetically modify AM with Ad vectors and to use this strategy to modify the behavior of AM in vivo, and this strategy may be useful in enhancing pulmonary defenses in immunodeficiency states.