摘要:
The invention concerns novel compounds and their uses, in particular pharmaceutical, diagnostic or as pharmacological targets. More particularly, the invention concerns a novel protein, called PAP1, and novel peptides and compounds capable of modulating at least partially parkin gene activity.
摘要:
The invention concerns a method for purifying G-CSF from a biological sample comprising steps which consist in: a) reducing the volume of the biological sample containing the G-CSF by hydrophobic interaction chromatography to obtain a concentrated, desalted and enriched fraction; b) passing the concentrated fraction over hydroxyapatite in conditions whereby the G-CSF is slightly bound to obtain a concentrated, desalted and enriched fraction containing the G-CSF; and c) collecting the G-CSF.
摘要:
The invention concerns the field of biology and the regulation of the cell cycle. More particularly, the invention concerns polypeptides derived from the human JNK3 protein, their variants, the corresponding nucleotide sequences, and their uses.
摘要:
The invention concerns novel methods and constructs for controlling nucleic acid expression, in particular methods and constructs using NRSE sequences for obtaining a targeted expression of transgenes in the nerve cells in vivo or ex vivo. The invention is particularly adapted for in vivo gene transfer applications, for instance for therapeutic or scientific approach.
摘要:
Antibodies are provided which specifically bind human and Macaca fascicularis lysosomal-associated membrane protein 1 (LAMP1) proteins and immunoconjugates comprising said antibodies conjugated or linked to a growth inhibitory agent. Pharmaceutical compositions comprising antibodies or immunoconjugates of the invention and use of the antibodies or immunoconjugates for the treatment of cancer are also provided, as well as LAMP1 antibodies, isolated nucleic acids, vectors and host cells comprising a sequence encoding said antibodies and the use of said antibody as a diagnostic tool. The application further provides for the detection of LAMP1 gene amplification or gain in cancer cells leading to the determination if patients with cancer are likely to respond to anti-LAMP1 therapy. Anti-LAMP1 therapeutic agent for use for treating cancer in a patient harboring LAMP1 gene copy number gain in cancer cells is further provided.
摘要:
Pharmaceutical composition comprising aflibercept, folinic acid, 5-fluorouracil (5-FU) and irinocetan (FOLFIRI) useful in the treatment of Colorectal cancer (CRC).
摘要:
The invention concerns the production of cholesterol in organisms of the Fungi kingdom. More particularly, the invention concerns genetically modified Fungus independently producing cholesterol from a simple carbon source. The invention also concerns the use of the inventive Fungus for producing non-marked and marked cholesterol.
摘要:
The invention relates to oligonucleotides which inhibit the expression of the OB-RGRP protein and use thereof for the prevention and/or treatment of diseases related to leptin. The invention further relates to a method for detection of compounds modifying the interaction between the proteins of the OB-RGRP family and the leptin receptor. Said detection can be achieved by means of the energy transfer between the fusion proteins comprising said proteins and proteins which are donors and acceptors of energy.
摘要:
The invention concerns novel peptide and nucleotide sequences, and their pharmaceutical use. More particularly, the invention concerns novel polypeptides capable of inhibiting at least partially the interaction between presenilin 1 or presenilin 2 and the β-amyloid peptide precursor and/or the β-amyloid peptide. The invention also concerns the preparation of in vitro tests for detecting molecules and in particular molecules capable of inhibiting said interaction.