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.
Patent No.:
Date of Patent:
Sep. 26, 2023
Filed:
Nov. 01, 2019
Regeneron Pharmaceuticals, Inc., Tarrytown, NY (US);
Yale University, New Haven, CT (US);
Institute for Research IN Biomedicine (Irb), Belinzona, CH;
Andrew J. Murphy, Croton-on-Hudson, NY (US);
Sean Stevens, San Francisco, CA (US);
Richard Flavell, Guilford, CT (US);
Markus Gabriel Manz, Bellinzona, CH;
Liang Shan, New Haven, CT (US);
Regeneron Pharmaceuticals, Inc., Tarrytown, NY (US);
Yale University, New Haven, CT (US);
Institute for Research in Biomedicine (IRB), Bellinzona, CH;
Abstract
Genetically modified non-human animals expressing human EPO from the animal genome are provided. Also provided are methods for making non-human animals expressing human EPO from the non-human animal genome, and methods for using non-human animals expressing human EPO from the non-human animal genome. These animals and methods find many uses in the art, including, for example, in modeling human erythropoiesis and erythrocyte function; in modeling human pathogen infection of erythrocytes; in in vivo screens for agents that modulate erythropoiesis and/or erythrocyte function, e.g. in a healthy or a diseased state; in in vivo screens for agents that are toxic to erythrocytes or erythrocyte progenitors; in in vivo screens for agents that prevent against, mitigate, or reverse the toxic effects of toxic agents on erythrocytes or erythrocyte progenitors; in in vivo screens of erythrocytes or erythrocyte progenitors from an individual to predict the responsiveness of an individual to a disease therapy.