US2014323408A1PendingUtilityA1
Method of inhibiting dopaminergic cell death
Est. expiryNov 16, 2027(~1.3 yrs left)· nominal 20-yr term from priority
Inventors:André Schrattenholz
A61P 43/00A61P 9/00A61P 9/10A61P 25/28A61P 25/16A61P 25/00A61P 25/08A61P 25/18A61P 25/24A61P 21/02A61P 21/00A61K 45/06A61K 38/1808A61K 31/5513C07K 14/485A61K 38/185A61K 38/1883C07K 14/4756
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Claims
Abstract
Soluble Neuregulin-1 isoforms representing Posttranslational Neuregulin-1 modifications for reducing dopaminergic cell death.
Claims
exact text as granted — not AI-modified1 . A method of reducing dopaminergic cell death in a subject in need thereof, comprising administering to said subject an effective amount of recombinant soluble Type I Neuregulin-1 β isoform which is an about 15 to about 35 kD N-terminal fragment of Type I Neuregulin-1 β.
2 . The method of claim 1 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 150 to 250 amino acids of Type I Neuregulin-1 β.
3 . The method of claim 1 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 245 to 250 amino acids of Type I Neuregulin-1 β.
4 . The method of claim 1 , wherein the Type I Neuregulin-1 β isoform has an isoelectric point (pI) of about 4 to about 10.
5 . The method of claim 1 , wherein the Type 1 Neuregulin-1 β isoform is a modified polypeptide, wherein the modifications are selected from phosphorylation, glycosylation, methylation, myristoylation, oxidation and any combination thereof.
6 . A method of promoting neuroprotection comprising administering a recombinant soluble Type I Neuregulin-1 β isoform which is an about 15 to about 35 kD N-terminal fragment of Type I Neuregulin-1 β to a subject in need thereof.
7 . The method of claim 6 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 150 to 250 amino acids of Type I Neuregulin-1 β.
8 . The method of claim 6 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 245 to 250 amino acids of Type I Neuregulin-1 β.
9 . The method of claim 6 , wherein the Type I Neuregulin-1 β isoform has an isoelectric point (pI) of about 4 to about 10.
10 . The method of claim 6 , wherein the Type I Neuregulin-1 β isoform is a modified polypeptide, wherein the modifications are selected from phosphorylation, glycosylation, methylation, myristoylation, oxidation and any combination thereof.
11 . A method of enhancing memory in a subject in need thereof comprising administering to said subject a recombinant soluble Type I Neuregulin-1 β isoform which is an about 15 to about 35 kD N-terminal fragment of Type I Neuregulin-1 β.
12 . The method of claim 11 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 150 to 250 amino acids of Type I Neuregulin-1 β.
13 . The method of claim 11 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 245 to 250 amino acids of Type I Neuregulin-1 β.
14 . The method of claim 11 , wherein the Type I Neuregulin-1 β isoform has an isoelectric point (pI) of about 4 to about 10.
15 . The method of claim 11 , wherein the Type I Neuregulin-1 β isoform is a modified polypeptide, wherein the modifications are selected from phosphorylation, glycosylation, methylation, myristoylation, oxidation and any combination thereof.
16 . A method of effecting antipsychotic activity in a subject in need thereof comprising administering to said subject a recombinant soluble Type I Neuregulin-1 β isoform which is an about 15 to about 35 kD N-terminal fragment of Type I Neuregulin-1 β.
17 . The method of claim 16 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 150 to 250 amino acids of Type I Neuregulin-1 β.
18 . The method of claim 16 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 245 to 250 amino acids of Type I Neuregulin-1 β.
19 . The method of claim 16 , wherein the Type I Neuregulin-1 β isoform has an isoelectric point (pI) of about 4 to about 10.
20 . The method of claim 16 , wherein the Type I Neuregulin-1 β isoform is a modified polypeptide, wherein the modifications are selected from phosphorylation, glycosylation, methylation, myristoylation, oxidation and any combination thereof.Cited by (0)
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