摘要:
The present invention relates to a method for the in vitro diagnosis of bronchopulmonary carcinoma, in particular of non-small cell bronchial carcinoma, characterized in that it comprises the stage of detecting, in a biological sample derived from a patient suspected to be suffering from said bronchopulmonary carcinoma, at least one of the major alternative transcripts of the KLK8 gene encoding kallikrein 8. This method is particularly useful for the survival prognostication of patients suffering from bronchopulmonary carcinoma.
摘要:
Isolated HXHV virus having the following characteristics: (i) a DNA genome which is at least partially single-stranded, (ii) the said genome comprises one reading frame (ORF) encoding one protein or one polyprotein (iii) the said genome comprises a nucleotide sequence which exhibits, for any segment of at least 40 nucleotides belonging to the said sequence, at least 90% homology with SEQ ID NO: 1 or with its complementary sequence, nucleic material and peptide material and uses.
摘要翻译:具有以下特征的分离的HXHV病毒:(i)至少部分单链的DNA基因组,(ii)所述基因组包含编码一种蛋白质或一种多蛋白质的一个阅读框(ORF)(iii)所述基因组包含 核苷酸序列,对于属于所述序列的至少40个核苷酸的任何片段,其显示与SEQ ID NO:1至少90%的同源性,或其互补序列,核酸和肽材料和用途。
摘要:
Viral material, in the isolated or purified state, in which the genome comprises a nucleotide sequence chosen from the group including sequences SEQ ID NO:46, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:53 and SEQ ID NO:56, their complementary sequences and their equivalent sequences, in particular nucleotide sequences displaying, for any succession of 100 contiguous monomers, at least 50% and preferably at least 70% homology with the said sequences SEQ ID NO:46, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:53 and SEQ ID NO:56, respectively, and their complementary sequences.
摘要翻译:分离或纯化状态的病毒物质,其中基因组包含选自SEQ ID NO:46,SEQ ID NO:51,SEQ ID NO:52,SEQ ID NO:53和SEQ ID NO:53的核苷酸序列 SEQ ID NO:46,SEQ ID NO:56,其互补序列及其等同序列,特别是核苷酸序列,显示100个连续单体的任何连续序列,与所述序列SEQ ID NO:46,SEQ ID NO:至少50%,优选至少70% :51,SEQ ID NO:52,SEQ ID NO:53和SEQ ID NO:56及其互补序列。
摘要:
Isolated HXHV virus having the following characteristics: (i) a DNA genome which is at least partially single-stranded, (ii) the said genome comprises one reading frame (ORF) encoding one protein or one polyprotein (iii) the said genome comprises a nucleotide sequence which exhibits, for any segment of at least 40 nucleotides belonging to the said sequence, at least 90% homology with SEQ ID NO: 1 or with its complementary sequence, nucleic material and peptide material and uses.
摘要翻译:具有以下特征的分离的HXHV病毒:(i)至少部分单链的DNA基因组,(ii)所述基因组包含编码一种蛋白质或一种多蛋白质的一个阅读框(ORF)(iii)所述基因组包含 核苷酸序列,对于属于所述序列的至少40个核苷酸的任何片段,其显示与SEQ ID NO:1至少90%的同源性,或其互补序列,核酸和肽材料和用途。
摘要:
New conformational antibodies are directed against HCV and more particularly to monoclonal antibodies. Described compositions of particles are liable to be recognized by the antibodies, as are pharmaceutical compositions containing them. Also described are HCV enveloped subviral particles or purified HCV enveloped complete viral particles, and the processes for preparing them.
摘要:
New conformational antibodies are directed against HCV and more particularly to monoclonal antibodies. Described compositions of particles are liable to be recognized by the antibodies, as are pharmaceutical compositions containing them. Also described are HCV enveloped subviral particles or purified HCV enveloped complete viral particles, and the processes for preparing them.
摘要:
The invention concerns an artificial antigen specifically identified by the anti-filaggrin autoantibodies present in the serum of patients suffering from rheumatoid polyarthritis, and consisting of one polypeptide comprising all or part of the sequence of one filaggrin unit or of a related molecule, in which an arginine radical has been substituted by a citrulline radical. The invention also concerns the use of this antigen for diagnosing rheumatoid polyarthritis.
摘要:
Viral material, in the isolated or purified state, in which the genome comprises a nucleotide sequence chosen from the group including sequences SEQ ID NO:46, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:53 and SEQ ID NO:56, their complementary sequences and their equivalent sequences, in particular nucleotide sequences displaying, for any succession of 100 contiguous monomers, at least 50% and preferably at least 70% homology with the said sequences SEQ ID NO:46, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:53 and SEQ ID NO:56, respectively, and their complementary sequences.
摘要翻译:分离或纯化状态的病毒物质,其中基因组包含选自SEQ ID NO:46,SEQ ID NO:51,SEQ ID NO:52,SEQ ID NO:53和SEQ ID NO:53的核苷酸序列 SEQ ID NO:46,SEQ ID NO:56,其互补序列及其等同序列,特别是核苷酸序列,显示100个连续单体的任何连续序列,与所述序列SEQ ID NO:46,SEQ ID NO为至少50%,优选至少70% :51,SEQ ID NO:52,SEQ ID NO:53和SEQ ID NO:56及其互补序列。
摘要:
The invention relates to a polypeptide capable of reacting specifically with an anti-Toxoplasma gondii P30 protein antibody, and comprising a peptide sequence, in which any succession of 6 contiguous amino acids exhibits at most 67% homology with the peptide sequence of said P30 protein, identified by SEQ ID No.1, or comprising a sequence derived from said peptide sequence, and the applications of this polypeptide especially for detecting a Toxoplasma gondii infection, in a biological sample.
摘要翻译:本发明涉及能够与抗弓形体弓形体P30蛋白抗体特异性反应的多肽,并且包含肽序列,其中任何连续的6个连续氨基酸与所述P30蛋白的肽序列具有最多67%的同源性, 由SEQ ID No.1鉴定,或包含源自所述肽序列的序列,以及该多肽的应用,特别是用于检测生物样品中的弓形虫感染。
摘要:
The present invention relates to the use of at least one partner for binding to an aldehyde derivative resulting from the peroxidation of lipids in protein-bound form, for instance to 4-hydroxy-2-nonenal, to 4-hydroxy-2-hexenal or to malondialdehyde, for the detection of ischemia-modified albumin (IMA) in a biological sample.