Abstract: The present disclosure relates to the manipulation of nucleic acids, and more particularly to systems and methods for nucleic acid mutagenesis.
Abstract: Genome editing systems, guide RNAs, dead guide RNAs, and CRISPR-mediated methods are provided for altering portions of a target nucleic acid.
Type:
Application
Filed:
November 8, 2019
Publication date:
May 21, 2020
Applicant:
Editas Medicine, Inc.
Inventors:
Edouard AUPEPIN DE LAMOTHE-DREUZY, Jack HEATH, Jennifer LEAH GORI, Luis BARRERA
Abstract: Disclosed herein are methods and compositions useful in targeting a payload to, or editing a target nucleic acid, where a governing gRNA molecule is used to target, optionally inactivate, a Cas9 molecule or a Cas9 molecule/gRNA complex.
Type:
Grant
Filed:
January 24, 2019
Date of Patent:
May 5, 2020
Assignees:
Editas Medicine, Inc., The Broad Institute Inc., Massachusetts Institute of Technology, University of Iowa Reseach Foundation
Abstract: Engineered nucleic acids encoding genome editing system components are provided, as are engineered RNA-guided nucleases that include inserts encoded in part by cellular genomic or other sequences recognized by guide RNAs.
Type:
Application
Filed:
October 29, 2019
Publication date:
February 20, 2020
Applicant:
EDITAS MEDICINE, INC.
Inventors:
Ari E. Friedland, Hariharan Jayaram, Barrett Ethan Steinberg
Abstract: Engineered nucleic acids encoding genome editing system components are provided, as are engineered RNA-guided nucleases that include inserts encoded in part by cellular genomic or other sequences recognized by guide RNAs.
Type:
Grant
Filed:
May 15, 2018
Date of Patent:
December 3, 2019
Assignee:
EDITAS MEDICINE, INC.
Inventors:
Ari E. Friedland, Hariharan Jayaram, Barrett Ethan Steinberg
Abstract: Disclosed herein are genome editing systems and genetic constructs that targets a herpes simplex virus (HSV) viral gene comprising one Cas9 molecule, and a gRNA molecule, and compositions and cells comprising such genome editing systems and genetic constructs. Also provided are methods for using the genome editing systems, genetic constructs, compositions and cells for genome engineering (e.g., altering a HSV viral gene), and for preventing, treating or reducing HSV infection.
Type:
Application
Filed:
April 26, 2019
Publication date:
August 15, 2019
Applicants:
EDITAS MEDICINE, INC., DUKE UNIVERSITY
Inventors:
Ari E. Friedland, Penrose O'Donnell, David A. Bumcrot, Bryan R. Cullen
Abstract: Disclosed herein are methods and compositions useful in targeting a payload to, or editing a target nucleic acid, where a governing gRNA molecule is used to target, optionally inactivate, a Cas9 molecule or a Cas9 molecule/gRNA complex.
Type:
Application
Filed:
January 24, 2019
Publication date:
June 6, 2019
Applicants:
EDITAS MEDICINE, INC., THE BROAD INSTITUTE INC., THE UNIVERSITY OF IOWA RESEARCH FOUNDATION, MASSACHUSETTS INSTITUITE OF TECHNOLOGY
Abstract: Provided are CRIS PR/CAS-related methods, compositions and components for editing a target nucleic acid sequence, or modulating expression of a target nucleic acid sequence, and applications thereof in connection with cancer immunotherapy comprising adoptive transfer of engineered T cells or T cell precursors.
Type:
Application
Filed:
May 6, 2017
Publication date:
May 9, 2019
Applicants:
Juno Therapeutics, Inc., Editas Medicine, Inc.
Inventors:
Blythe SATHER, G. Grant WELSTEAD, David A. BUMCROT, Ari E. FRIEDLAND, Jon JONES, Morgan L. MAEDER, Chris NYE, Eugenio Marco RUBIO, Ruth SALMON
Abstract: Disclosed herein are methods and compositions useful in targeting a payload to, or editing a target nucleic acid, where a governing gRNA molecule is used to target, optionally inactivate, a Cas9 molecule or a Cas9 molecule/gRNA complex.
Type:
Grant
Filed:
November 29, 2017
Date of Patent:
January 29, 2019
Assignees:
Editas Medicine, Inc., The Broad Institute Inc., Massachusetts Institute of Technology, University of Iowa Research Foundation
Abstract: This application provides improved methods of editing the genome of a target cell. Cas9 molecules can be used to create a break in a genomic region of interest. To increase the likelihood that the break is repaired by homology-directed repair (HDR), the cell can be contacted with an HDR-enhancer. The cell may be, e.g., a human cell, a non-human animal cell, a bacterial cell, or a plant cell.
Abstract: Engineered nucleic acids encoding genome editing system components are provided, as are engineered RNA-guided nucleases that include inserts encoded in part by cellular genomic or other sequences recognized by guide RNAs.
Type:
Application
Filed:
May 15, 2018
Publication date:
September 6, 2018
Applicant:
EDITAS MEDICINE, INC.
Inventors:
Ari E. Friedland, Hariharan Jayaram, Barrett Ethan Steinberg
Abstract: CRISPR/CAS-related systems, compositions and methods for editing RS1, RL2, and/or LAT genes in human cells are described, as are cells and compositions including cells edited according to the same.
Type:
Application
Filed:
April 30, 2018
Publication date:
September 6, 2018
Applicant:
EDITAS MEDICINE, INC.
Inventors:
Ari E. Friedland, Penrose O'Donnell, David A. Bumcrot
Abstract: Engineered nucleic acids encoding genome editing system components are provided, as are engineered RNA-guided nucleases that include inserts encoded in part by cellular genomic or other sequences recognized by guide RNAs.
Type:
Application
Filed:
March 23, 2018
Publication date:
July 19, 2018
Applicant:
EDITAS MEDICINE, INC.
Inventors:
Ari E. Friedland, Hariharan Jayaram, Barrett Ethan Steinberg
Abstract: Engineered nucleic acids encoding genome editing system components are provided, as are engineered RNA-guided nucleases that include inserts encoded in part by cellular genomic or other sequences recognized by guide RNAs.
Type:
Grant
Filed:
March 23, 2018
Date of Patent:
June 26, 2018
Assignee:
EDITAS MEDICINE, INC.
Inventors:
Ari E. Friedland, Hariharan Jayaram, Barrett Ethan Steinberg
Abstract: Disclosed herein are methods and compositions useful in targeting a payload to, or editing a target nucleic acid, where a governing gRNA molecule is used to target, optionally inactivate, a Cas9 molecule or a Cas9 molecule/gRNA complex.
Type:
Application
Filed:
November 29, 2017
Publication date:
May 10, 2018
Applicants:
EDITAS MEDICINE, INC., THE BROAD INSTITUTE INC., THE UNIVERSITY OF IOWA RESEARCH FOUNDATION, MASSACHUSETTS INSTITUITE OF TECHNOLOGY