摘要:
The invention relates to the use of a hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor and of a farnesyl-pyrophosphate synthase inhibitor, or of one of their associated physiologically acceptable salts, in the preparation of a composition, particularly a pharmaceutical composition, for use in the treatment of human or animal, pathological or nonpathological situations related to the accumulation and/or the persistence of prenylated proteins in cells, such as during progeria (Hutchinson-Gilford syndrome), restrictive dermopathy or physiological ageing.
摘要:
Described is the use of magnesium (Mg 2+ ) for the preparation of a therapeutic composition for the introduction of a polynucleotide into a cell in vivo.
摘要:
The invention concerns a combined product comprising at least a substance breaking up a cell extracellular matrix and at least a nucleic acid of interest, to be administered simultaneously, consecutively or spread over time, said nucleic acid being carried by an infectious viral particle or in the form of a synthetic vector. The invention also concerns the use of said product for therapeutic or vaccine purposes to prepare a medicine for treating the human or animal body using gene therapy and the use of a substance breaking up the extracellular matrix to improve the transfer and/or the expression of said nucleic acid of interest in a host cell or organism.
摘要:
The invention relates to a proteasome inhibitor for use for treating and/or preventing a disorder related to an accumulation of a non-degraded abnormal protein, particularly a premature ageing disorder. The invention also relates to the use of proteasome inhibitors for attenuating physiological ageing. The invention also relates to the use of proteasome inhibitors in the treatment and/or prevention of age-related disorders and their metabolic consequences. The invention also relates to the dermato logical, dermo cosmetic or cosmetic use of a proteasome inhibitor for preventing and/or attenuating skin ageing. The invention also relates to the use of proteasome inhibitors in the treatment of cancer.
摘要:
The invention relates to the use of fibromodulin and lumican, in particular the active fragments thereof, for increasing muscle mass, in particular in the treatment of muscular dystrophy.
摘要:
The invention concerns a method for obtaining cell populations derived from the muscular tissue and their use for preparing cell therapy products. It consists in particular in culturing cells previously removed by biopsy from skeletal muscular tissues, identifying the different types of cells present at different stages of culture, selecting the culture stage on the basis of the required cell population and collecting the selected culture stage for preparing a cell therapy product. The invention also concerns cell populations derived from muscular tissue obtained by implementing said method whereof the dominant cell type is CD34+, CD15+ or CD56+ or Class 1+ HLA, or comprises a doubly negative CD56-/CD15- cell type or may comprise more minority CD10+, Stro-1+ and CD117+ cell types.
摘要:
A nucleic acid sequence comprising: 1) the sequence represented in figure 8; or 2) the sequence represented in figure 2; or 3) a part of the sequence of figure 2 with the proviso that it is able to code for a protein having a calcium dependant protease activity involved in a LGMD2; or 4) a sequence derived from a sequence defined in 1), 2) or 3) by substitution, deletion or addition of one or more nucleotides with the proviso that said sequences still codes for said protease.