The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 15, 2021

Filed:

Jun. 28, 2019
Applicant:

Duke University, Durham, NC (US);

Inventors:

Michelle Winn, Durham, NC (US);

Margaret A. Pericak-Vance, Coral Gables, FL (US);

Jeffery M. Vance, Coral Gables, FL (US);

Assignee:

DUKE UNIVERSITY, Durham, NC (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/6883 (2018.01); C07K 14/705 (2006.01); G01N 33/68 (2006.01); A61K 31/4174 (2006.01); A61K 31/69 (2006.01); A61K 33/24 (2019.01); A61K 38/00 (2006.01);
U.S. Cl.
CPC ...
C12Q 1/6883 (2013.01); A61K 31/4174 (2013.01); A61K 31/69 (2013.01); A61K 33/24 (2013.01); C07K 14/705 (2013.01); G01N 33/6872 (2013.01); A61K 38/00 (2013.01); C12Q 2600/118 (2013.01); C12Q 2600/136 (2013.01); C12Q 2600/156 (2013.01); C12Q 2600/158 (2013.01); G01N 2333/705 (2013.01); G01N 2500/04 (2013.01); G01N 2800/347 (2013.01); G01N 2800/52 (2013.01);
Abstract

Focal and segmental glomerulosclerosis (FSGS) is a kidney disorder of unknown etiology and up to 20% of patients on dialysis have this diagnosis. A large family with hereditary FSGS carries a missense mutation in the TRPC6 gene on chromosome 11q, encoding the ion channel protein Transient Receptor Potential Cation Channel 6. The missense mutation is a P112Q substitution, which occurs in a highly conserved region of the protein, enhances TRPC6-mediated calcium signals in response to agonists such as angiotensin II, and alters the intracellular distribution of TRPC6 protein. Previous work has emphasized the importance of cytoskeletal and structural proteins in proteinuric kidney diseases. Our findings suggest a novel mechanism for glomerular disease pathogenesis.


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