Diagnosis and treatment for late onset neurodegenerative disorder
AssigneeThe Jackson Laboratory
InventorsJeffrey A. Klein, Susan L. Ackerman
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AssigneeThe Jackson Laboratory
InventorsJeffrey A. Klein, Susan L. Ackerman
Estimating the term…
Disclosed is a method for diagnosing the molecular basis for a late-onset neurodegenerative disorder in a mammal. In this method, a sample from the mammal is provided, the sample containing a nucleic acid sequence encoding the AIF. The sequence of nucleic acids in the nucleic acid sequence is determined by conventional techniques. This determined sequence of nucleic acids is then compared to a nucleic acid sequence encoding the wild-type AIF protein. Any difference between the sequence of nucleic acids determined from the two samples represents a candidate mutation. The candidate mutation is then further analyzed for an association with a decrease in expression of functional AIF protein. Such an association confirms a molecular basis for the late-onset neurodegenerative disorder in the mammal. Related methods and compositions are also disclosed.
A method for diagnosing the molecular basis for a late-onset neurodegenerative disorder in a mammal, the method comprising:
A method for diagnosing the molecular basis for a late-onset neurodegenerative disorder in a mammal, the method comprising:
A method for identifying a compound for mitigating ROS-induced damage associated with a late-onset neurodegenerative disorder in a mammal, the method comprising:
A method for treating oxidative stress in a cell of a mammal, the method comprising introducing an effective concentration of a wild-type AIF protein to the cell.
A method for making a mutant cell line sensitive to oxidative stress, the method comprising:
A mutant cell line sensitive to oxidative stress, the mutant cell line derived from a harlequin mouse.
A cell line according to claim 23 that is immortalized.
Dependencies are inferred from the claim text.