Rodent model for Parkinson's Disease

Multicellular living organisms and unmodified parts thereof and – Nonhuman animal – The nonhuman animal is a model for human disease

Reexamination Certificate

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C800S008000, C424S009200, C514S04400A

Reexamination Certificate

active

06878858

ABSTRACT:
The present invention provides an animal model for Parkinson's Disease and a method for generating such a model. The method comprises the steps of transfecting dopaminergic neurons in the substantia nigra with a dominant negative mutant of FGFR1 with deleted tyrosine kinase domain. The animals are characterized by a reduction in the number of tyrosine hydroxylase neurons in the SNc area.

REFERENCES:
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Ekesbo, et al., (−)-OSU 6162 Inhibits Levodopa-indicued Dyskinesias in a Monkey Model of Parkinson's Disease, NeuroReport 8, (1997), pp. 2567-2570.
Pearce, et al., Chronic L-DOPA Administration Induced Dyskinesias in the 1-Methyl-4-phenyl-1,2,3,6-Tetrahydropyridine-Treated Common Marmoset (Callithrix jacchus), Movement Disorders, vol. 10, No. 6, 1995, pp. 731-740.
Peng, et al., Novel Nuclear Signaling Pathway Mediates Activation of Fibroblast Growth Factor-2 Gene by Type 1 and Type 2 Angiotensin II Receptors, Molecular Biology of the Cell, vol. 12, Feb. 2000, pp. 449-462.
Belluardo, et al.Comparative Localization of Fibroblast Growth Factor Receptor -1, -2, and -3 mRNAs in the Rat Brain: In Situ Hybridization Analysis, The Journal of Comparative Neurology, 1997, vol. 379, No. 2, pp. 226-246.
Gonzalez, et al.A Comprehensive Analysis of the Distribution of FGF-2 and FGFR1 in the Rat Brain, Brain Research, 1995, vol. 701, No. 1-2, pp. 201-226.
Stachowiak, et al.Nuclear Accumulation of Fibroblast Growth Factor Receptors is Regulated by Multiple Signals in Adrenal Medullary Cells, Molecular Biology of the Cell, 1996, vol. 7, No. 8, pp. 1299-1317.

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