Abstract: The present invention relates to anti-tumor vaccines comprising at least one type of tumor cell into each of which at least two genes encoding MHC proteins of different haplotypes have been inserted, or naturally expressed, said genes being expressed in said tumor cells and wherein at least one of said MHC proteins has the same haplotype as a haplotype of the individual to be vaccinated. The invention furthermore relates to a method of treating a patient suffering from a tumorous disease comprising administering a vaccine of the invention and to the use of a vaccine of the invention for the preparation of an anti-tumor vaccine.
Abstract: A fusion implant for insertion between opposing vertabrae includes a body having an inner surface defining a hollow inner chamber for containing a graft material therein. The body includes a stress transfer mechanism for transferring stress from the vertabrae surrounding the implant to the graft material contained within the implant. A method is provided for implanting the fusion implant between opposing vertabraes by the steps of inserting an implant into a collapsed disc space between adjacent vertabrae, the implant including a collapsed body, and expanding the body to spread the adjacent vertabrae apart.
Abstract: A DNA (SEQ ID No.:2) and amino acid (SEQ ID No.:4) sequences of Glycine .alpha.-D-galactosidase are provided as well as the DNA sequence (SEQ ID No:5) and mature length amino acid sequence (SEQ ID No:7) of Phaseolus.
Type:
Grant
Filed:
May 28, 1996
Date of Patent:
March 24, 1998
Assignee:
The Curators of the University of Missouri
Abstract: The salts are prepared by reacting a benzhydrylamine of the formula I (or a salt thereof) with clavulanic acid (or a salt thereof) in solvent, and isolating the resulting salt. In formula I, each of R.sup.1 and R.sup.2 is hydrogen (preferred) or an acceptable substituent. ##STR1## The clavulanic acid salts can be used in pharmaceutical formulations together with a pharmaceutically acceptable carrier, and, preferably, a beta-lactam antibiotic.
Abstract: The present invention is a protective guard for use during sports such as snowboarding. It comprises a substantially rigid dipartite sleeve adapted to receive the distal forearm, wrist and proximal portion of a hand; thumb receiving region at one end of the sleeve to receive and partially surround the base of the thumb of a user and retaining straps to hold the sleeve on the arm of a user.
Abstract: A compound of the formula ##STR1## wherein R.sub.1 is a straight or branched alkyl group having from 1 to 6 carbon atoms, phenyl, or cycloalkyl having from 3 to 6 carbon atoms; R.sub.2 is hydrogen or methyl; and R.sub.3 is hydrogen, methyl or carboxyl; which is useful in the treatment of seizure disorders. Processes are disclosed for the preparation of the compound. Intermediates prepared during the synthesis of the compound are also disclosed.
Type:
Grant
Filed:
October 16, 1996
Date of Patent:
January 20, 1998
Assignee:
Northwestern University
Inventors:
Richard B. Silverman, Ryszard Andruszkiewicz, Po-Wai Yuen, Denis Martin Sobieray, Lloyd Charles Franklin, Mark Alan Schwindt
Abstract: A method of generating in situ trophic factor production by transplanting Sertoli cells into the central nervous system of a mammal, the cells creating trophic factors in situ.
Type:
Grant
Filed:
March 13, 1995
Date of Patent:
December 30, 1997
Assignee:
University of South Florida
Inventors:
Paul R. Sanberg, Don F. Cameron, Cesario V. Borlongan
Abstract: A method of synthesizing multitier cascade polymers and the polymers made thereby are formed by reacting at least one tier of a polymer with a functionalized isocyanate having the following formula:O.dbd.C.dbd.N--C(CH.sub.2 --R).sub.3with R being selected from the group including:--(CH.sub.2).sub.n --CH.sub.2 --COOR' a)with R' being selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl- polycycloalkyl, adamantyl, n=0-10;--O--(CH.sub.2).sub.n --CH.sub.2 --COOR'--O--(CH.sub.2).sub.n --CH.sub.2 --CN b)with R' being selected from the group consisting of alkyl (c-1 to C(20), cycloalkyl (C-3 to C-10), aryl heteroaryl, polycycloalkyl, adamantyl, n=0-10; and--CH.sub.2 --(CH.sub.2).sub.
Abstract: This invention relates to a method to assess oxidative stress in vivo by quantification of prostaglandin F.sub.2 -like compounds and their metabolites produced by a noncyclooxygenase free radical catalyzed mechanism.
Abstract: A method of producing a natural nonrecombinant cytokine mixture is disclosed including the steps of immobilizing at least one mitogen in a tissue culture vessel. An isolated population of lymphocytes free of neutrophils and erythrocytes, is suspended in a serum-free media and placed in the vessel. The lymphocytes are cultured, the media removed, and characterized for the yield of cytokines.
Abstract: A method of selecting anti-aggregation molecules with chaperone-like activity that have characteristics including binding to a native target molecule epitope with a high binding constant and are non-inhibitory to the biological activity of the target molecule. The method molecules denaturating a target molecule in the presence of presumptative antiaggregation molecules to prevent the target molecules from self-or induced-aggregation. The nonaggregated target molecule coupled to the anti-aggregation molecule is then tested for bioactivity.
Type:
Grant
Filed:
December 16, 1994
Date of Patent:
November 18, 1997
Assignee:
RAMOT University Authority For Applied Research and Development Ltd.
Abstract: Regulation factors and a method for modulating bone forming cells including the steps of collecting regulation factors from bone stromal cells including marrow adipocytes and treating the bone forming cells with the regulation factors derived from stromal cells to modify the bone forming cells.
Type:
Grant
Filed:
December 23, 1994
Date of Patent:
November 18, 1997
Assignee:
Ramot University Authority for Applied Research and Industrial Development, Ltd.
Abstract: A method of forming an air bag which includes the steps of weaving on a loom an upper and lower fabric simultaneously, the two fabrics being combined in selected areas to define a seam of substantially circular shape. A bag is produced by cutting within the seam. The bag does not have an additional coating, but the permeability of the bag is determined by controlling the sett thereby utilizing the permeability of the weave itself.
Type:
Grant
Filed:
May 1, 1995
Date of Patent:
November 11, 1997
Assignee:
Airbags International Limited
Inventors:
Raymond Graham, Christopher Paul Kavanagh, Simon Valkenburg, Michael Gervase Litton
Abstract: A method of making a pharmaceutical composition is disclosed. The method includes the steps of contacting at least one pharmaceutical ingredient with a mixture consisting essentially of gelatin and lecithin to increase the dissolution rate of water-insoluble pharmaceutical ingredients. A pharmaceutical excipient coating for increasing the dissolution rate of water-insoluble pharmaceutical ingredients is also disclosed. The coating consists essentially of gelatin and lecithin.
Abstract: A compound of the formula ##STR1## wherein R.sub.1 is a straight or branched alkyl group having from 1 to 6 carbon atoms, phenyl, or cycloalkyl having from 3 to 6 carbon atoms; R.sub.2 is hydrogen or methyl; and R.sub.3 is hydrogen, methyl or carboxyl; which is useful in the treatment of seizure disorders. Processes are disclosed for the preparation of the compound. Intermediates prepared during the synthesis of the compound are also disclosed.
Type:
Grant
Filed:
April 12, 1995
Date of Patent:
November 4, 1997
Assignees:
Northwestern University, Warner-Lambert Company
Inventors:
Richard B. Silverman, Ryszard Andruszkiewicz, Po-Wai Yuen, Denis Martin Sobieray, Lloyd Charles Franklin, Mark Alan Schwindt
Abstract: Synthetic catalytic RNAs, i.e. ribozyme, including a hairpin portion, binding sites for binding to a human papilloma virus after viral base 419 and 434, respectively, and cleavage sites for cleaving the virus at the binding sites have been constructed.
Type:
Grant
Filed:
March 21, 1995
Date of Patent:
November 4, 1997
Assignees:
Northern Illinois University, United States of America as represented by the Department of Health and Human Services
Inventors:
Arnold Hampel, Joseph DiPaolo, Andrew M. Siwkowski, Scott C. Galasinski
Abstract: A method for increasing oligonucleotide selectivity comprising reversibly binding two oligonucleotides at adjacent positions to the bases on a complementary template and then spontaneously and irreversibly covalently joining said oligomers via two reactive groups brought into proximity of each other by the binding of the oligonucleotides, in the absence of added reagent or enzyme. By using a shorter, lower affinity, highly selective first oligonucleotide complementary which binds to the site of a point mutation combined, with a longer, high affinity, less selective second oligonucleotide, this method provides an effective way to identify the presence of absence of a point mutation.
Type:
Grant
Filed:
May 8, 1995
Date of Patent:
October 28, 1997
Assignee:
Northwestern University
Inventors:
Robert Lewis Letsinger, Sergei M. Gryaznov