Abstract: The invention relates to the individualization of therapy on the basis of a phenotypic profile of an individual. More specifically, the present invention relates to the use of metabolic phenotyping for the individualization of treatment with ED agents.
Abstract: The invention relates to the individualization of therapy on the basis of a phenotypic profile of an individual. More specifically, the present invention relates to the use of metabolic phenotyping for the individualization of treatment with immunosuppressants.
Abstract: The complete genomic structure of the peroxisome proliferator-activated receptor alpha gene is described. Also described are the identification of novel single nucleotide polymorphisms and association with higher plasma LDL-cholesterol and total and LDL-apolipoprotein B concentrations.
Type:
Grant
Filed:
September 14, 2000
Date of Patent:
April 8, 2003
Assignees:
McGill University, Complexe Hospitalier de la Sagamie
Inventors:
Thomas J. Hudson, Marie-Claude Vohl, Carl Brewer, Kenneth Morgan, Daniel Gaudet
Abstract: Cyclic peptides comprising a cadherin cell adhesion recognition sequence HAV, and compositions comprising such cyclic peptides, are provided. Methods for using such peptides for modulating cadherin-mediated cell adhesion in a variety of contexts are also provided.
Type:
Application
Filed:
March 22, 2002
Publication date:
April 3, 2003
Applicant:
McGill University
Inventors:
Orest W. Blaschuk, Barbara J. Gour, Riaz Farookhi, Anmar Ali
Abstract: The invention relates to the individualization of therapy on the basis of a phenotypic profile of an individual. More specifically, the present invention relates to the use of metabolic phenotyping for the individualization of treatment with hyperlipidemia agents.
Abstract: The thermal degradation of the biodegradable bacterial polyesters poly(3-hydroxybutyrate), PHB, and poly(3-hydroxybutyrate-co-3-hydroxyvalerate), PHB/V produces a macromer, especially a 1000-6000 g/mol macromolecule, which contains an unsaturated end group as well as a carboxylic acid end group. The macromers may be polymerized to produce homopolymers and copolymers for different applications in which amphiphilic and biocompatible properties are required, for example, drug delivery systems.
Type:
Grant
Filed:
August 15, 2001
Date of Patent:
March 18, 2003
Assignee:
McGill University
Inventors:
Robert H. Marchessault, Sophie Nguyen, Ga-Er Yu
Abstract: Cellular sensitivity to DNA damaging agents and progression through cell cycle is modulated through manipulation of T cell protein tyrosine phosphatase (TC-PTP) activity. Phenotypic characterization of cells lacking TC-PTP demonstrates a defective progression through the cell cycle, and sensitivity to DNA damaging agents. Screening assays are provided for selecting agents that affect the activity of TC-PTP, including assays relating to the interaction of TC-PTP with its substrate, p62dok.
Type:
Grant
Filed:
December 10, 1999
Date of Patent:
March 18, 2003
Assignee:
McGill University
Inventors:
Michel L. Tromblay, Maria De Jesus Ibarra Sanchez, Paul Daniel Simoncic
Abstract: The present invention relates to a novel DNA assay for the diagnosis and/or prediction of autoimmune diabetes. The present invention relates to a DNA assay for the prediction of autoimmune diabetes in human subjects, which comprises the steps of a) obtaining a DNA sample from the subject and amplifying at least one class III allele of variable number of tandem repeats (VNTR) located upstream of the insulin gene (INS) which is associated with silencing of thymic insulin mRNA expression; and b) subjecting the sample to electrophoresis to identify the silencing class III allele.
Type:
Grant
Filed:
July 23, 2001
Date of Patent:
March 18, 2003
Assignee:
McGill University
Inventors:
Constantin Polychronakos, Petros Vafiadis, Rosemarie Grabs, Houria Ounissi-Benkalha
Abstract: The invention relates to the individualization of therapy on the basis of a phenotypic profile of an individual. More specifically, the present invention relates to the use of metabolic phenotyping for the individualization of treatment with GERD agents.
Abstract: Provided herein is a heretofore unknown isolated nucleic acid molecule which encodes human methylenetetrahydrofolate reducatase, along with an amino acid sequence of methylenetetrahydrofolate reductase, and a cDNA probe for human methylenetetrahydrofolate reductase. Also provided are a molecule description of mutations in humans resulting in a phenotype having reduced levels of methylenetetrahydrofolate reductase, and methods of diagnosing methylenetetrahydrofolate reductase deficiency in a human.
Abstract: A hydrogen storage composition has a hydrogenated state and a dehydrogenated state; the hydrogenated state comprises a hydrided composition of lithium and an element M which forms a hydride, for example Be or Mg, an element E which forms a compound or solid solution with lithium, e.g. C, B or Zn, or a mixture thereof; there are thus provided reversible Li-based hydrides of high hydrogen capacity.
Type:
Grant
Filed:
March 30, 2001
Date of Patent:
February 4, 2003
Assignee:
McGill University
Inventors:
Alicja Zaluska, Leszek Zaluski, John Olaf Strom-Olsen
Abstract: In recent years, much effort has been placed on improving the performance of timing and jitter measurement devices using Delay Locked Loop (DLL) and Vernier Delay Line (VDL) techniques. However, these approaches require highly matched elements in order to reduce differential non-linearity timing errors. In an attempt to reduce the requirement on element matching, a component-invariant VDL technique is disclosed that enables the measurement device to be synthesized from an RTL description. The present invention is based on a single-stage VDL structure, which is used to mimic the behavior of a complete VDL. Furthermore, as test time is an important consideration during a production test, a method and system is provided that reduces test time at the expense of additional hardware.
Abstract: The present invention relates to a screening method to identify individuals at risk of developing diseases associated with different polymorphic forms of wildtype p53; which comprises the steps of: a) obtaining a biological sample from said patients; and b) determining the presence of p53pro or p53arg wildtype alleles in said sample; wherein the allele pattern of patients selected from the group consisting of p53pro/p53pro, p53arg/p53arg and p53pro/p53arg are indicative of a risk factor for developing disease associated with different polymorphic forms of wildtype p53. Notably, individuals who are p53arg/arg are at greater risk of developing pathologies associated with human papillomavirus infections, including cervical cancer.
Type:
Grant
Filed:
March 1, 2000
Date of Patent:
December 3, 2002
Assignees:
McGill University, Imperial Cancer Research Technology, International Center for Genetic Engineering and
Biotechnology
Inventors:
Greg J. Matlashewski, Lawrence Banks, Alan Storey
Abstract: The present invention provides alkylphosphonate dimers and oligonucleotides prepared therefrom. The invention further provides novel methods for the preparation of these alkylphosphonate dimers. Methods for the preparation of substantially diastereomerically pure alkylphosphonate dimers are also provided.
Type:
Grant
Filed:
February 18, 1999
Date of Patent:
November 26, 2002
Assignees:
ISIS Pharmaceuticals, Inc., McGill University
Inventors:
Muthiah Manoharan, George Just, Andrei Guzaev, Arlène Roland, Jianchao Wang, Michael E. Jung
Abstract: A mobile robot comprising a body and at least six compliant legs each having only one actuator. The compliant legs are mounted to the body for movement relative thereto in a single degree of freedom. A controller is operably coupled to the actuator of each compliant leg, the controller selectively actuates the actuators to drive the compliant legs in an alternating tripod gait.
Type:
Grant
Filed:
March 14, 2001
Date of Patent:
November 19, 2002
Assignees:
McGill University, The Regents of the University of Michigan
Inventors:
Martin Buehler, Daniel E. Koditschek, Uluc Saranli
Abstract: A biosensor apparatus for detecting a binding event between a ligand and receptor. The apparatus includes a biosensor surface and surface-bound two-subunit heterodimer complexes composed of first and second, preferably oppositely charged peptides that together form an &agr;-helical coiled-coil heterodimer. The first peptide is attached to the biosensor surface, and the second peptide carries the ligand, accessible for binding by a ligand-binding agent. Binding of anti-ligand binding agent to the surface-bound ligand is detected by a suitable detector. A ligand-specific biosensor surface can be readily prepared from a universal template containing the first charged peptide, by addition of a selected ligand attached to the second peptide.
Type:
Grant
Filed:
May 24, 2000
Date of Patent:
November 12, 2002
Assignees:
Pence, Inc., McGill University
Inventors:
R. Bruce Lennox, Robert S. Hodges, Randall T. Irvin
Abstract: Polymorphic nucleic acid molecules encoding the very low density lipoprotein receptor are described, as well as gene products encoded by these nucleic acid molecules. Allele-specific primers and probes hybridizing to regions flanking or containing these sites are also described, along with methods of use therefor.
Type:
Application
Filed:
March 8, 2001
Publication date:
October 24, 2002
Applicant:
McGill University
Inventors:
James Engert, Marie-Claude Vohl, Carl Brewer, Kenneth Morgan, Daniel Gaudet, Thomas J. Hudson
Abstract: The present invention relates to diblock copolymers and more particularly to polycaprolactone-b-polyethylene oxide (PCL-b-PEO) diblock copolymers used in micellar systems, for delivering a biologically active agent to a site. There is provided a diblock copolymer compound comprising a hydrophilic block and a hydrophobic block, the hydrophilic block comprising a polyethylene oxide (PEO) polymer, the hydrophobic block comprising a polycaprolactone (PCL) polymer, the PCL polymer comprising a number of caprolactone monomers selected from 5 to 150, the PEO polymer comprising a number of ethylene oxide monomers selected from 30 to 100. The diblock copolymer compound of the present invention may be used to form a micellar delivery system for delivering biologically active agents such as lipophilic drugs to sites such as the central nervous system.
Type:
Grant
Filed:
May 3, 2000
Date of Patent:
October 22, 2002
Assignee:
McGill University
Inventors:
Adi Eisenberg, Dusica Maysinger, Christine Allen
Abstract: Cyclic peptides and compositions comprising such cyclic peptides are provided. The cyclic peptides comprise a cadherin cell adhesion recognition sequence HAV. Methods for using such peptides and compositions for modulating cadherin-mediated cell adhesion in a variety of contexts are also provided.