Method for treating or preventing a neural disorder with a neurotrophic growth factor
Abstract
There is disclosed an isolated nucleic acid molecule encoding a human neurotrophic growth factor designated enovin and having the amino acid sequence illustrated in FIG. 1, 21, 23 or 24 or encoding a functional equivalent, derivative or bioprecursor of said growth factor. The growth factor preferably comprises the amino acid sequence from position 27 to 139 of the sequence illustrated in FIG. 1 , or a functional equivalent, derivative or bioprecursor thereof. The nucleic acid molecule encoding enovin can be used to transform a host cell, tissue or organism by including it in an appropriate vector. The host cell, tissue or organism and the vector also form part of the invention.
Claims
exact text as granted — not AI-modified1 - 57 . (canceled)
58 . A method for treating or preventing a neural disorder in a subject the method comprising administering to the subject an amount of a human neurotrophic growth factor polypeptide comprising the amino acid sequence of SEQ ID NO:3, or a functional equivalent derivative thereof, in a sufficient concentration to reduce or prevent the symptoms of the neural disorder.
59 . A method according to claim 58 , wherein the neural disorder is selected from the group consisting of: Parkinson's disease, Alzheimer's disease, neuronal disorders associated with expanded polyglutamine sequences such as Huntington's disease, peripheral neuropathy, neuropathic pain; acute brain injury, nervous system tumors, multiple sclerosis, amyotrophic lateral sclerosis, peripheral nerve trauma, injury exposure to neurotoxins, multiple endocrine neoplasia, familial Hirschsprung disease, prion associated diseases, Creutzfeld-Jacob disease, cancer or stroke.
60 . A method according to claim 58 , wherein the functional equivalent derivative comprises an amino acid sequence having at least 90% homology to SEQ ID NO:3.
61 . A method according to claim 60 , wherein the functional equivalent derivative comprises SEQ ID NO:9 or SEQ ID NO:10.Join the waitlist — get patent alerts
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