James Roberts - Seattle WA, US Fred Cross - Seattle WA, US Paul Warrener - Seattle WA, US Ernesto Javier Munoz - Seattle WA, US Martin Henry Lee - Seattle WA, US Khadidja Romari - Seattle WA, US Kimberly Marie Kotovic - Seattle WA, US Jason W. Hickman - Seattle WA, US
Assignee:
Matrix Genetics, LLC - Seattle WA
International Classification:
C12P 5/00 C12P 1/04 C12N 1/22
US Classification:
435170, 435 41, 435243, 4352521
Abstract:
This disclosure describes genetically modified photosynthetic microorganisms, including Cyanobacteria, that contain one or more exogenous genes encoding a diacylglycerol acyltransferase, a phosphatidate phosphatase, and/or an acetyl-CoA carboxylase, and which are capable of producing increased amounts of fatty acids and/or synthesizing triglycerides.
Modified Photosynthetic Microorganisms For Producing Triglycerides
James Roberts - Seattle WA, US Fred Cross - Seattle WA, US Paul Warrener - Seattle WA, US Ernesto Javier Munoz - Seattle WA, US Martin Henry Lee - Seattle WA, US Khadidja Romari - Seattle WA, US Kimberly Marie Kotovic - Seattle WA, US Jason W. Hickman - Seattle WA, US
Assignee:
Matrix Genetrics, LLC - Seattle WA
International Classification:
C12P 5/00 C12P 1/04 C12N 1/22
US Classification:
4352521, 435 41, 435170, 435243
Abstract:
This disclosure describes genetically modified photosynthetic microorganisms, including Cyanobacteria, that contain one or more exogenous genes encoding a diacylglycerol acyltransferase, a phosphatidate phosphatase, and/or an acetyl-CoA carboxylase, and which are capable of producing increased amounts of fatty acids and/or synthesizing triglycerides.
Modified Photosynthetic Microorganisms For Producing Triglycerides
MATRIX GENETICS, LLC - Seattle WA, US Fred Cross - Seattle WA, US Paul Warrener - Seattle WA, US Ernesto Javier Munoz - Seattle WA, US Martin Henry Lee - Seattle WA, US Khadidja Romari - Seattle WA, US Kimberly Marie Kotovic - Seattle WA, US Jason W. Hickman - Seattle WA, US
Assignee:
MATRIX GENETICS, LLC - Seattle WA
International Classification:
C12N 15/79
US Classification:
435134, 4352572, 435477
Abstract:
This disclosure describes genetically modified photosynthetic microorganisms, including Cyanobacteria, that contain one or more exogenous genes encoding a diacyglycerol acyltransferase, a phosphatidate phosphatase, and/or an acetyl-CoA carboxylase, and which are capable of producing increased amounts of fatty acids and/or synthesizing triglycerides.
Modified Photosynthetic Microorganisms For Producing Lipids
James Roberts - Seattle WA, US Fred Cross - New York NY, US Margaret Mary McCormick - Seattle WA, US Ernesto Javier Munoz - Seattle WA, US Brett K. Kaiser - Seattle WA, US Michael Carleton - Kirkland WA, US
Assignee:
Targeted Growth, Inc. - Seattle WA
International Classification:
C12P 7/64 C12N 15/82
US Classification:
435134, 4352572, 435471
Abstract:
This disclosure describes genetically modified photosynthetic microorganisms, e.g., Cyanobacteria, that overexpress an acyl carrier protein (ACP), an acyl-ACP synthase (Aas), or both, optionally in combination with one or more overexpressed or exogenous lipid biosynthesis proteins, and/or one or more overexpressed or exogenous glycogen breakdown proteins. Exemplary biosynthesis proteins include diacyglycerol acyltransferases, thioesterases, phosphatidate phosphatases, phospholipases, triacylglycerol (TAG) hydrolases, fatty acyl-CoA synthetases, and/or acetyl-CoA carboxylases, including combinations thereof. Also included are photosynthetic microorganisms comprising mutations or deletions in a glycogen biosynthesis or storage pathway, which accumulate a reduced amount of glycogen under reduced nitrogen conditions as compared to a wild type photosynthetic microorganism. The modified photosynthetic microorganisms provided herein are capable of producing increased amounts of lipids such as fatty acids and/or synthesizing triglycerides.
- Seattle WA, US Ernesto J. Munoz - Seattle WA, US
Assignee:
Kineta Chronic Pain, LLC - Seattle WA
International Classification:
C07K 14/435 A61K 47/54 A61K 47/60 A61P 29/00
Abstract:
The present disclosure describes analog conotoxin peptides of the α-conotoxin peptide RgIA. These analog conotoxin peptides block the α9α10 subtype of the nicotinic acetylcholine receptor (nAChR) and can be used for treating pain and inflammation including inflammatory pain, cancer related pain, and neuropathic pain. The RgIA analogs described in the present invention include a variety of sequence modifications and chemical modifications that are introduced to improve the drug-like characteristics of RgIA analogs and thereby increase their therapeutic value.
Sustained Release Depot Formulations Of Therapeutic Proteins, And Uses Thereof
- Seattle WA, US Ernesto J. MUNOZ - Seattle WA, US James CHESKO - Seattle WA, US Eric J. TARCHA - Seattle WA, US
Assignee:
KINETA ONE, LLC - Seattle WA
International Classification:
A61K 9/50 A61K 38/17 A61K 47/26 A61K 47/32
Abstract:
Depot formulations including therapeutic proteins are provided. The therapeutic proteins can be toxin-based therapeutic proteins. The depot formulations release the therapeutic protein within sustained effective levels for at least one month following a single administration. The toxin-based therapeutic proteins can include ShK-based proteins.
Methods Of Treating Ipex Syndrome Using Toxin-Based Pharmaceutical Compositions
Disclosed herein are methods of treating immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) comprising administering a toxin-based therapeutic peptide, such as an ShK-based peptide. The peptide can include an acid or amide at the C-terminus and/or the peptide can be attached to an organic or inorganic chemical entity that has an anionic charge.
- Seattle WA, US Kristin M. Bedard - Bellevue WA, US Ernesto J. Munoz - Seattle WA, US Myra Wang Imanaka - Seattle WA, US Kerry W. Fowler - Seattle WA, US
International Classification:
A61K 31/429 A61K 31/47 A61K 31/5377
Abstract:
Disclosed herein are compounds and related compositions for the treatment of viral infection, including RNA viral infection, and compounds that can modulate the RIG-I pathway in vertebrate cells, including compounds that can activate the RIG-I pathway.
Oct 2012 to Jan 2015 Assistant SuperintendentOAC Action Construction, Corp Miami, FL Feb 2010 to Sep 2012 Construction SuperintendentAmerican Contracting, Inc Miami, FL Jan 2003 to Dec 2009 Superintendent, Subcontractor
Education:
Miami Dade Community College Miami, FL 2000 to 2004 AA in English and Spanish
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