Howard University
Adjunct Associate Professor
Intronn 1995 - 2004
Founder, Chief Executive Officer and Chief Strategy Officer
Retrotherapy 1995 - 2004
Chief Executive Officer and Chief Strategy Officer
Nih National Institute of Mental Health 1990 - 1992
Lieutenant Commander, Us Public Health Service
Nih Nimh 1988 - 1990
Senior Staff Fellow
Education:
The George Washington University School of Medicine and Health Sciences 1992 - 1994
University of South Florida 1984 - 1985
University of Maryland School of Medicine 1984 - 1984
Doctor of Medicine, Doctorates, Medicine
Georgetown University School of Medicine 1979 - 1980
Masters, Physiology
University of Maryland 1974 - 1978
Bachelors, Biochemistry
Skills:
Molecular Biology Biotechnology Drug Discovery Biochemistry Biopharmaceuticals Cell Culture Technology Transfer Lifesciences Commercialization R&D Life Sciences Pharmaceutical Industry Rna Trans Splicing Clinical Research Genetics Research and Development Medical Devices Gene Therapy Gene Editing Cell Biology Laboratory Medicine Science
The present invention provides methods and compositions for conferring selective death on cells expressing a specific target precursor messenger RNA (selective target pre-mRNA). The compositions of the invention include pre-trans-splicing molecules (PTMs) designed to interact with a target precursor messenger RNA molecule (target pre-mRNA) expressed within a cell and mediate a trans-splicing reaction resulting in the generation of a novel chimeric mRNA molecule (chimeric mRNA) capable of encoding a light producing protein or enzyme. Cell death is further mediated by the presence of a photosensitizer which upon photoactivation produces cytotoxicity.
Methods And Compositions For Determining The Purity Of Chemically Synthesized Nucleic Acids
Paul F. Agris - Raleigh NC, US Christopher D. J. Pearce - Surrey, GB Lloyd G. Mitchell - Durham NC, US
Assignee:
North Carolina State University - Raleigh NC
International Classification:
G01N 33/53
US Classification:
435 71, 435 6
Abstract:
This application describes an antibody that specifically binds to a synthetic oligomer (e. g. , an oligonucleotide or oligopeptide) having a organic protecting group covalently bound thereto, which antibody does not bind to that synthetic oligomer when the organic protecting group is not covalently bound thereto. Methods of making and using such antibodies are also disclosed, along with cells for making such antibodies and articles carrying immobilized oligomers that can be used in assay procedures with such antibodies.
Correction Of Alpha-1-Antitrypsin Genetic Defects Using Spliceosome Mediated Rna Trans Splicing
Madaiah Puttaraju - Germantown MD, US Edward Otto - Reston VA, US Mariano A. Garcia-Blanco - Durham NC, US Gerard J. McGarrity - Gaithersburgh MD, US Gary F. Temple - Washington Grove MD, US Lloyd G. Mitchell - Bethesda MD, US Colette Cote - Gaithersburgh MD, US S. Gary Mansfield - Montgomery Village MD, US
Assignee:
VIRxSYS Corporation - Gaithersburg MD
International Classification:
C12N 5/00 C12N 15/12 C12N 15/63 C12N 15/86
US Classification:
435325, 4353201
Abstract:
The present invention provides methods and compositions for generating novel nucleic acid molecules through targeted spliceosomal mediated RNA trans-splicing. The compositions of the invention include pre-trans-splicing molecules (PTMs) designed to interact with a SERPINA1 target precursor messenger RNA molecule (target pre-mRNA) and mediate a trans-splicing reaction resulting in the generation of a novel chimeric RNA molecule (chimeric RNA). In particular, the PTMs of the present invention include those genetically engineered to interact with SERPINA1 target pre-mRNA so as to result in correction of SERPINA1 genetic defects responsible for AAT deficiency. The PTMs of the invention may also comprise sequences that are processed out of the PTM to yield duplex siRNA molecules directed specifically to mutant SERPIN A1 mRNAs. Such duplexed siRNAs are designed to reduce the accumulation of toxic AAT protein in liver cells. The methods and compositions of the present invention can be used in gene therapy for correction of SERPINA1 disorders such as AAT deficiency.
Methods And Compositions For Determining The Purity Of And Purifying Chemically Synthesized Nucleic Acids
Christopher D. J. Pearce - Leatherhead, GB Lloyd G. Mitchell - Bethesda MD, US
Assignee:
Proteome Sciences PLC - Surrey
International Classification:
C07H 21/02 C07H 21/04
US Classification:
53038821, 435 61, 435 71, 536 231
Abstract:
An antibody microarray is described comprising a plurality of antibodies immobilized on a substrate, wherein each antibody specifically binds to a synthetic oligomer (e. g. , an oligonucleotide or oligopeptide) having an organic protecting group covalently bound thereto, which antibody does not bind to that synthetic oligomer when the organic protecting group is not covalently bound thereto. Methods of making and using such antibodies are disclosed, along with cells for making such antibodies. Methods of making and using such antibody microarrays are also disclosed.
Methods And Compositions For Determining The Purity Of Chemically Synthesized Nucleic Acids
Paul F. Agris - Raleigh NC, US Christopher D. J. Pearce - Surrey, GB Lloyd G. Mitchell - Durham NC, US
Assignee:
North Carolina State University - Raleigh NC
International Classification:
G01N 33/53
US Classification:
435 71, 435 72, 435518
Abstract:
This application describes an antibody that specifically binds to a synthetic oligomer (e. g. , an oligonucleotide or oligopeptide) having a organic protecting group covalently bound thereto, which antibody does not bind to that synthetic oligomer when the organic protecting group is not covalently bound thereto. Methods of making and using such antibodies are also disclosed, along with cells for making such antibodies and articles carrying immobilized oligomers that can be used in assay procedures with such antibodies.
Methods And Compositions For Determining The Purity Of Chemically Synthesized Nucleic Acids
Paul F. Agris - Raleigh NC, US Christopher D. J. Pearce - Surrey, GB Lloyd G. Mitchell - Durham NC, US
Assignee:
North Carolina State University - Raleigh NC
International Classification:
G01N 33/53
US Classification:
435 71, 436518
Abstract:
This application describes an antibody that specifically binds to a synthetic oligomer (e. g. , an oligonucleotide or oligopeptide) having a organic protecting group covalently bound thereto, which antibody does not bind to that synthetic oligomer when the organic protecting group is not covalently bound thereto. Methods of making and using such antibodies are also disclosed, along with cells for making such antibodies and articles carrying immobilized oligomers that can be used in assay procedures with such antibodies.
Methods And Compositions For Use In Spliceosome Mediated Rna Trans-Splicing
Lloyd Mitchell - Bethesda MD, US Mariano Garcia-Blanco - Durham NC, US Madaiah Puttaraju - Germantown MD, US
International Classification:
C07H021/02 C07H021/04
US Classification:
536/023100
Abstract:
The present invention provides methods and compositions for delivery of synthetic pre-trans-splicing molecules (synthetic PTMs) into a target cell. The compositions of the invention include synthetic pre-trans-splicing molecules (PTMs) with enhanced stability against chemical and enzymatic degradation. The synthetic PTMs are designed to interact with a natural target precursor messenger RNA molecule (target pre-mRNA) and mediate a trans-splicing reaction resulting in the generation of a novel chimeric RNA molecule (chimeric RNA).
Methods And Compositions For Use In Spliceosome Mediated Rna Trans-Splicing
Lloyd Mitchell - Bethesda MD, US Mariano Garcia-Blanco - Durham NC, US Madaiah Puttaraju - Germantown MD, US
International Classification:
C12P019/34 C12N005/00
US Classification:
435/091200, 435/375000
Abstract:
The present invention provides methods and compositions for delivery of synthetic pre-trans-splicing molecules (synthetic PTMs) into a target cell. The compositions of the invention include synthetic pre-trans-splicing molecules (PTMs) with enhanced stability against chemical and enzymatic degradation. The synthetic PTMs are designed to interact with a natural target precursor messenger RNA molecule (target pre-mRNA) and mediate a trans-splicing reaction resulting in the generation of a novel chimeric RNA molecule (chimeric RNA).
Name / Title
Company / Classification
Phones & Addresses
Lloyd Mitchell Owner
Mitchell Group Management Consulting Services
1816 11Th St Nw, Washington, DC 20001 Website: the-mitchellgroup.com
Lloyd Mitchell President
The Mitchell Group Inc Management Consulting Services
1816 11Th St Nw, Washington, DC 20001
Lloyd Mitchell Owner, President
The Mitchell Group Inc Management Consulting Services · Accountant · Process & Logistics Consulting Svcs
1816 11 St NW, Washington, DC 20001 1818 11 St NW, Washington, DC 20001 2027451919, 2024620789, 2022341697
Police at the scene of a double shooting in Ridgewood, Queens on May 9, 2022.Photo by Lloyd Mitchell Police cordoned off the block of Fresh Pond Road during a shooting investigation on May 9, 2022.Photo by Lloyd Mitchell