US2007031395A1PendingUtilityA1
Repressor of skeletal muscle differentiation, nucleic acid coding therefor and the use thereof in diagnosis and therapy
Assignee: UNIVERSITAETSKLINIKUM FREIBURGPriority: Mar 20, 2002Filed: Mar 13, 2003Published: Feb 8, 2007
Est. expiryMar 20, 2022(expired)· nominal 20-yr term from priority
C07K 14/4716A61K 38/00C07K 14/4703C07K 16/18
45
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Claims
Abstract
Polypeptide sequences which play a part in the regulation of skeletal muscle differentiation, and nucleic acids coding therefor, and the use thereof in diagnosis and therapy are disclosed. Possible uses are also indicated for antibodies which are directed against corresponding epitopes of the GRIM1 polypeptide.
Claims
exact text as granted — not AI-modified1 . A polypeptide comprising at least 20 consecutive amino acids from the sequence of hsGRIM1 having the sequence ID No. 3.
2 . The polypeptide as claimed in claim 1 , comprising at least 40 consecutive amino acids.
3 . The polypeptide as claimed in claim 1 , comprising at least 80 consecutive amino acids.
4 . The polypeptide as claimed in claim 1 , comprising at least 120 consecutive amino acids.
5 . The polypeptide as claimed in claim 1 , comprising at least 200 consecutive amino acids.
6 . A polypeptide comprising at least 20 consecutive amino acids from the mmGRIM sequence having the sequence ID No. 4.
7 . The polypeptide comprising at least 40 consecutive amino acids.
8 . The polypeptide as claimed in claim 6 , comprising at least 120 consecutive amino acids.
9 . The polypeptide as claimed in claim 6 , comprising at least 200 consecutive amino acids.
10 . An antibody that binds specifically to an epitope of a polypeptide as claimed in any of claims 1 to 9 .
11 . A medicament comprising a polypeptide as claimed in any of claims 1 to 9 , and a pharmaceutically acceptable excipient.
12 . The medicament as claimed in claim 11 , that is employed for the treatment of disturbances of skeletal muscle differentiation.
13 . The medicament as claimed in claim 11 , characterized that is employed for the treatment of disturbances of fat cell differentiation.
14 . A method for identifying substances which influence the biological function of a polypeptide as claimed in any of claims 1 to 9 , comprising contacting the substance to be identified with said polypeptide in a test system.
15 . A cDNA which codes for hsGRIM1, comprising at least 1200 consecutive nucleotides from the sequence ID No.1.
16 . A cDNA which codes for mmGRIM, comprising at least 1200 consecutive nucleotides from the sequence ID No.2.
17 . A transfection vector comprising a cDNA as claimed in claim 15 or 16 .
18 . The transfection vector as claimed in claim 17 , which is an adenoviral vector.
19 . A cell transfected with a vector as claimed in claim 17 .
20 . The cell of claim 19 , wherein said vector is an adenovector.
21 . A method of treating a disturbance of skeletal muscle differentiation comprising administering to a subject in need thereof an effective amount of the medicament of claim 12 .
22 . A method of treating disturbances of fat cell differentiation comprising administering to a subject in need thereof an effective amount of the medicament of claim 13.Join the waitlist — get patent alerts
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