Patents Represented by Attorney, Agent or Law Firm LeeAnn Gorthey
  • Patent number: 6541655
    Abstract: Complexes of a selected class of chiral ligands with molybdenum, tungsten or chromium, preferably molybdenum, are effective as catalysts in highly enantioselective and regioselective alkylation of allylic substrates.
    Type: Grant
    Filed: September 7, 2001
    Date of Patent: April 1, 2003
    Assignee: The Board of Trustees of the Leland Stanford Junior University
    Inventors: Barry M. Trost, Iwao Hachiya
  • Patent number: 6541486
    Abstract: Compounds, pharmaceutical compositions, and methods of use are described which are effective in inhibiting cell death, particularly apoptotic cell death. The compositions may be used for prevention and treatment of injuries associated with cell death, including ischemia, such as results from stroke or myocardial infarction, trauma, neurodegeneration, and inflammation.
    Type: Grant
    Filed: June 2, 2000
    Date of Patent: April 1, 2003
    Assignee: Elan Pharma International Ltd.
    Inventors: Catherine M. Bitler, Paul L. Wood, Duran T. Anstine, Anke Meyer-Franke, Qi Zhao, Mohamed A. Khan
  • Patent number: 6537814
    Abstract: The invention relates to a new and improved pharmaceutical composition and method for delivery of therapeutic agents. The methods and composition of the invention can be used with several therapeutic agents and can achieve site specific delivery of a therapeutic or diagnostic substance. This can allow for lower doses and for improved efficacy with drugs which traditionally reach targeted sites and can result in improved utility for agents such as oligonucleotides and polynucleotides which are plagued with problems with biodistribution.
    Type: Grant
    Filed: June 9, 2000
    Date of Patent: March 25, 2003
    Assignee: The Board of Regents of the University of Nebraska
    Inventors: Thomas R. Porter, Patrick L. Iversen
  • Patent number: 6518023
    Abstract: The invention provides a method for constructing a high resolution physical map of a polynucleotide. In accordance with the invention, the polynucleotide is digested successively with at least two different restriction endonucleases and the ends of the restriction fragments are sequenced after each digestion. In this manner, restriction fragments having sequenced ends are produced that can be aligned by their sequences to give a physical map of the polynucleotide. Preferably, restriction fragment ends are sequenced by massively parallel signature sequencing (MPSS), or a like parallel sequencing technique.
    Type: Grant
    Filed: March 27, 2000
    Date of Patent: February 11, 2003
    Assignee: Lynx Therapeutics, Inc.
    Inventor: Sydney Brenner
  • Patent number: 6511802
    Abstract: The invention provides a method and materials for monitoring and isolating differentially expressed genes. In accordance with the method of the invention, differently labeled populations of DNAs from sources to be compared are competitively hybridized with reference DNA cloned on solid phase supports, e.g. microparticles, to provide a differential expression library which, in the preferred embodiment, may be manipulated by fluorescence-activated cell sorting (FACS). Monitoring the relative signal intensity of the different fluorescent labels on the microparticles permits quantitative analysis of expression levels relative to the reference DNA. The invention also provides a method for identifying and isolating rare genes. Populations of microparticles having relative signal intensities of interest can be isolated by FACS and the attached DNAs identified by sequencing, such as with massively parallel signature sequencing (MPSS), or with conventional DNA sequencing protocols.
    Type: Grant
    Filed: January 8, 1999
    Date of Patent: January 28, 2003
    Assignee: Lynx Therapeutics, Inc.
    Inventors: Glenn Albrecht, Sydney Brenner, Robert B. DuBridge
  • Patent number: 6468986
    Abstract: This invention relates compositions and methods for increasing the uptake of polynucleotides into cells. Specifically, the invention relates to vectors, targeting ligands, and polycationic agents. The polycationic agents are capable of (1) increasing the frequency of uptake of polynucleotides into a cell, (2) condensing polynucleotides; and (3) inhibiting serum and/or nuclease degradation of polynucleotides.
    Type: Grant
    Filed: July 21, 2000
    Date of Patent: October 22, 2002
    Assignee: Chiron Corporation
    Inventors: Ronald N. Zuckermann, Nathalie Dubois-Stringfellow, Varavani Dwarki, Michael A. Innis, John E. Murphy, Fred E. Cohen, Tetsuo Uno
  • Patent number: 6451828
    Abstract: Compounds are disclosed which efficiently inhibit glutaminase but which have no effect, at higher levels, on various mechanistically and functionally related enzymes. The compounds, which are useful for neuroprotection and in treatment of hepatic encephalopathy, have the general formula I: as defined further herein.
    Type: Grant
    Filed: August 10, 2001
    Date of Patent: September 17, 2002
    Assignee: Elan Pharmaceuticals, Inc.
    Inventor: Robert W. Newcomb
  • Patent number: 6431370
    Abstract: Detergent formulations are prepared by directly agglomerating a fermentation broth extract, containing a detergent-type enzyme and a nonionic detergent-type surfactant, with a suitable detergent base mixture, without need for prior isolation of the enzyme.
    Type: Grant
    Filed: June 8, 2000
    Date of Patent: August 13, 2002
    Assignee: Genencor International, Inc.
    Inventors: Edit L. Braunstein, Nathaniel T. Becker, Thomas P. Graycar
  • Patent number: 6420109
    Abstract: Methods for determining the relative binding affinities of various ligands to various nucleic acid sequences are described. In a direct binding assay, the effect of adding increasing amounts of a ligand on a signal generated by two “indicator” oligonucleotides is observed. Also described is a competitive binding assay, in which a competitor oligonucleotide is added to an indicator duplex having a ligand bound thereto. The assays allow the rapid and convenient determination of nucleic acid binding specificities and base pair determinants of specificity of particular ligands.
    Type: Grant
    Filed: September 11, 1998
    Date of Patent: July 16, 2002
    Assignee: Genelabs Technologies, Inc.
    Inventors: Gary P. Schroth, Thomas Wayne Bruice, Young J. Suh
  • Patent number: 6416712
    Abstract: Effective corrosion inhibitors having minimal organic content, particularly suitable for use in municipal drinking water systems, are described. The corrosion inhibiting additive is a stannous salt of a non-carbon acid.
    Type: Grant
    Filed: December 19, 2000
    Date of Patent: July 9, 2002
    Assignee: A.S. Incorporated
    Inventor: Olen L. Riggs, Jr.
  • Patent number: 6406848
    Abstract: An apparatus and system are provided for simultaneously analyzing a plurality of analytes anchored to microparticles. Microparticles each having a uniform population of a single kind of analyte attached are disposed as a substantially immobilized planar array inside of a flow chamber where steps of an analytical process are carried out by delivering a sequence of processing reagents to the microparticles by a fluidic system under microprocessor control. In response to such process steps, an optical signal is generated at the surface of each microparticle which is characteristic of the interaction between the analyte carried by the microparticle and the delivered processing reagent. The plurality of analytes are simultaneously analyzed by collecting and recording images of the optical signals generated by all the microparticles in the planar array.
    Type: Grant
    Filed: November 16, 1999
    Date of Patent: June 18, 2002
    Assignee: Lynx Therapeutics, Inc.
    Inventors: John Bridgham, Kevin Corcoran, George Golda, Michael C. Pallas, Sydney Brenner
  • Patent number: 6365577
    Abstract: Antisense oligonucleotides useful for treating a disease state characterized by p53 induction, such as proliferative cell disorders, e.g. cancer, or a hypoxic state induced by an ischemic attack, such as stroke, are described. The antisense agents are preferably of the class known as “steric blocker” type oligonucleotides, including morpholino oligonucleotides, peptide nucleic acids, 2′-O-allyl or 2′-O-alkyl modified oligonucleotides, or N3′→P5′ phosphoramidate oligonucleotides.
    Type: Grant
    Filed: October 22, 1999
    Date of Patent: April 2, 2002
    Assignee: AVI BioPharma, Inc.
    Inventor: Patrick L. Iversen
  • Patent number: 6358636
    Abstract: Protective overlayers for magnetic recording media are described. The overlayers, composed of a transition metal-silicon or transition metal-germanium interlayer and a carbon overcoat, provide good wear resistance and corrosion resistance at thicknesses of less than 100 Å.
    Type: Grant
    Filed: January 20, 1999
    Date of Patent: March 19, 2002
    Assignee: HMT Technology Corporation
    Inventors: Ming M. Yang, Zhangmin Wang, James L. Chao, Michael A. Russak
  • Patent number: 6355428
    Abstract: Methods for determining the relative binding affinities of various ligands to various nucleic acid sequences, particularly in double stranded form, are described. In a direct binding assay, the effect of adding increasing amounts of a ligand on a signal generated by two “indicator” oligonucleotides is observed. Also described is a competitive binding assay, in which a competitor oligonucleotide is added to an indicator duplex having a ligand bound thereto. The assays allow the rapid and convenient determination of nucleic acid binding specificities and base pair determinants of specificity of particular ligands.
    Type: Grant
    Filed: September 10, 1999
    Date of Patent: March 12, 2002
    Assignee: Genelabs Technologies, Inc.
    Inventors: Gary P. Schroth, Thomas Wayne Bruice, Young J. Suh
  • Patent number: 6310093
    Abstract: Disclosed is a method for preventing neuronal cell death subsequent to an injury to neuronal tissue, particularly central nervous tissue exposed to an ischemic or hypoxic event, to trauma or to a chronic neurodegenerative disorder. The method includes exposing the cells to a glutaminase inhibitor that is relatively impermeant to healthy, intact cell membranes, and which is preferably a specific inhibitor of the form of glutaminase that is widely present in brain tissue.
    Type: Grant
    Filed: August 27, 1998
    Date of Patent: October 30, 2001
    Assignee: Elan Pharmaceuticals, Inc.
    Inventor: Robert Newcomb
  • Patent number: 6306597
    Abstract: The present invention includes, in one aspect, a kit comprising one or more sets of oligonucleotide probes whose perfectly matched duplexes with complementary sequences have similar or substantially the same free energy of duplex formation.
    Type: Grant
    Filed: March 29, 1999
    Date of Patent: October 23, 2001
    Assignee: Lynx Therapeutics, Inc.
    Inventor: Stephen C. Macevicz
  • Patent number: 6307067
    Abstract: Nucleophilic oxygen species, such as primary alcohols, carboxylates, and water, are added to vinyl epoxides in a highly regioselective and enantioselective manner, providing a convenient route to enantiomerically enriched 1,2-diols and oxygen-containing heterocycles. The reaction employs a chiral Pd(0) complex and a borane or borate as co-catalysts Also described are similar additions of nitrogen nucleophiles, and the addition of carbonates to vinyl epoxides using a chiral Pd(0) catalyst.
    Type: Grant
    Filed: September 7, 1999
    Date of Patent: October 23, 2001
    Assignee: The Board of Trustees of the Leland Stanford Junior University
    Inventors: Ernest John McEachern, Francisco Dean Toste, Barry Martin Trost
  • Patent number: 6274063
    Abstract: Polishing slurries for use in polishing substrates having a nickel or nickel-containing surface, such as those used for magnetic media, are described. The slurries include, in addition to a chemical etchant such as aluminum nitrate and suspended abrasive particles, an oxidizer which converts nickel metal at the surface to nickel oxide, but does not solubilize the nickel oxide in the aqueous medium to any significant degree. Preferred oxidizers include hydrogen peroxide, ferric nitrate and potassium iodate.
    Type: Grant
    Filed: January 15, 1999
    Date of Patent: August 14, 2001
    Assignee: HMT Technology Corporation
    Inventors: Jiangning Li, Ming M. Yang
  • Patent number: 6251433
    Abstract: This invention relates compositions and methods for increasing the uptake of polynucleotides into cells. Specifically, the invention relates to vectors, targeting ligands, and polycationic agents. The polycationic agents are capable of (1) increasing the frequency of uptake of polynucleotides into a cell, (2) condensing polynucleotides; and (3) inhibiting serum and/or nuclease degradation of polynucleotides.
    Type: Grant
    Filed: August 13, 1997
    Date of Patent: June 26, 2001
    Assignee: Chiron Corporation
    Inventors: Ronald N. Zuckermann, Nathalie Dubois-Stringfellow, Varavani Dwarki, Michael A. Innis, John E. Murphy, Fred E. Cohen, Tetsuo Uno
  • Patent number: 6245747
    Abstract: The invention relates to a new and improved pharmaceutical composition and method for delivery of therapeutic agents. The methods and composition of the invention can be used with several therapeutic agents and can achieve site specific delivery of a therapeutic substance. This can allow for lower doses and for improved efficacy with drugs which traditionally reach targeted sites and can result in utility for agents such as oligonucleotides which are plagued with problems in reaching targeted sites in necessary therapeutic levels. The delivery system includes gas-filled microbubbles formed in a nitrogen-free environment. Microbubbles formed through sonication in a nitrogen-free environment are smaller and more stable than microbubbles sonicated in the presence of room air.
    Type: Grant
    Filed: July 13, 1998
    Date of Patent: June 12, 2001
    Assignee: The Board of Regents of the University of Nebraska
    Inventors: Thomas R. Porter, Patrick L. Iversen, Gary D. Meyer