Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of integrin beta 3. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding integrin beta 3. Methods of using these compounds for modulation of integrin beta 3 expression and for treatment of diseases associated with expression of integrin beta 3 are provided.
Type:
Grant
Filed:
June 25, 1999
Date of Patent:
March 14, 2000
Assignee:
Isis Pharmaceuticals Inc.
Inventors:
C. Frank Bennett, Brett P. Monia, Lex M. Cowsert
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of Smad2. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Smad2. Methods of using these compounds for modulation of Smad2 expression and for treatment of diseases associated with expression of Smad2 are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of MAP kinase kinase 6. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding MAP kinase kinase 6. Methods of using these compounds for modulation of MAP kinase kinase 6 expression and for treatment of diseases associated with expression of MAP kinase kinase 6 are provided.
Abstract: Methods of modulating the activity of the TAR element of HIV are provided. Oligonucleotides having 6 to 50 bases and at least one 2'-O alkyl modification and selected sequences are disclosed.
Abstract: The present invention provides polymeric radio frequency resonant tags and methods of manufacturing these tags for use in detection of theft of article for sale.
Type:
Grant
Filed:
August 7, 1998
Date of Patent:
February 29, 2000
Assignee:
IRD/AS
Inventors:
Soren Jacobsen, John Engell, Jorgen Schjerning Lundsgaard, David Morgan Thomas
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of RhoC. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding RhoC. Methods of using these compounds for modulation of RhoC expression and for treatment of diseases associated with expression of RhoC are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of PEPCK-mitochondrial. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding PEPCK-mitochondrial. Methods of using these compounds for modulation of PEPCK-mitochondrial expression and for treatment of diseases associated with expression of PEPCK-mitochondrial are provided.
Type:
Grant
Filed:
August 3, 1999
Date of Patent:
February 29, 2000
Assignee:
Isis Pharmaceuticals Inc.
Inventors:
Robert McKay, Madeline M. Butler, Lex M. Cowsert
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of Ship-2. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Ship-2. Methods of using these compounds for modulation of Ship-2 expression and for treatment of diseases associated with expression of Ship-2 are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of PTEN. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding PTEN. Methods of using these compounds for modulation of PTEN expression and for treatment of diseases associated with expression of PTEN are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of RIP-1. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding RIP-1. Methods of using these compounds for modulation of RIP-1 expression and for treatment of diseases associated with expression of RIP-1 are provided.
Abstract: The present invention relates to the identification of biologically active transcription factors which are synthesized and modified in the dendritic compartment of neurons and uses thereof.
Type:
Grant
Filed:
September 16, 1998
Date of Patent:
February 1, 2000
Assignee:
The Trustees of the University of Pennsylvania
Abstract: Intercutaneous implant devices useful in intraluminal and extraluminal procedures for externalization of vessels are provided which have a hollow cylinder with an upper and lower end and an interior and exterior surface, said hollow cylinder having a central aperture which is greater in diameter than the exterior expanse of the access site and a length which provides for adequate annular separation of the externalized vessel at the exterior and interior surface of the implant to ensure adequate blood supply to the vessel; a flange extending from the upper end of the hollow cylinder which provides a platform onto which is attached a termination device; and a plane contacting surface extending from the lower end of the hollow cylinder which provides a means for fixation of the implant to the patient.
Type:
Grant
Filed:
June 24, 1998
Date of Patent:
January 25, 2000
Assignee:
Bio TAP A/S
Inventors:
Lasse Leif Hessel, Jorgen Scherning Lundsgaard, Carl Zimmermann-Neilsen, John Engell, Jesper Malling, David Morgan Thomas
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of FADD. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding FADD. Methods of using these compounds for modulation of FADD expression and for treatment of diseases associated with expression of FADD are provided.
Type:
Grant
Filed:
July 19, 1999
Date of Patent:
January 18, 2000
Assignee:
Isis Pharmaceuticals Inc.
Inventors:
Brett P. Monia, Brenda F. Baker, Hong Zhang, Lex M. Cowsert
Abstract: Compositions and methods are provided for the treatment and diagnosis of diseases amenable to treatment through modulation of the synthesis or metabolism of intercellular adhesion molecules. In accordance with preferred embodiments, oligonucleotides are provided which are specifically hybridizable with nucleic acids encoding intercellular adhesion molecule-1, vascular cell adhesion molecule-1, and endothelial leukocyte adhesion molecule-1. The oligonucleotide comprises nucleotide units sufficient in identity and number to effect said specific hybridization. In other preferred embodiments, the oligonucleotides are specifically hybridizable with a transcription initiation site, a translation initiation site, 5'-untranslated sequences, 3'-untranslated sequences, and intervening sequences.
Type:
Grant
Filed:
December 2, 1997
Date of Patent:
January 18, 2000
Assignee:
Isis Pharmaceuticals Inc.
Inventors:
C. Frank Bennett, Christopher K. Mirabelli
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of Smad1. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Smad1. Methods of using these compounds for modulation of Smad1 expression and for treatment of diseases associated with expression of Smad1 are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of Smad3. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Smad3. Methods of using these compounds for modulation of Smad3 expression and for treatment of diseases associated with expression of Smad3 are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of Smad4. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Smad4. Methods of using these compounds for modulation of Smad4 expression and for treatment of diseases associated with expression of Smad4 are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of Jun N-terminal Kinase Kinase-1. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Jun N-terminal Kinase Kinase-1. Methods of using these compounds for modulation of Jun N-terminal Kinase Kinase-1 expression and for treatment of diseases associated with expression of Jun N-terminal Kinase Kinase-1 are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of EGR-1. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding EGR-1. Methods of using these compounds for modulation of EGR-1 expression and for treatment of diseases associated with expression of EGR-1 are provided.
Abstract: Antisense compounds, compositions and methods are provided for modulating the expression of Phospholipase A2 Group IV. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Phospholipase A2 Group IV. Methods of using these compounds for modulation of Phospholipase A2 Group IV expression and for treatment of diseases associated with expression of Phospholipase A2 Group IV are provided.