摘要:
Bacterial cells genetically modified to improve their tolerance to certain commodity chemicals, such as isobutyric acid and related compounds, and methods of preparing and using such bacterial cells for production of isobutyric acid and related compounds.
摘要翻译:细菌细胞通过基因改造以提高它们对某些商品化学品如异丁酸和相关化合物的耐受性,以及制备和使用这些细菌细胞生产异丁酸及相关化合物的方法。 p >
摘要:
The present invention relates to an anticancer composition containing full-length GRS proteins or fragments thereof, or a nucleic acid encoding the GRS proteins or fragments as active ingredients. The GRS proteins or fragments thereof are useful for specifically inducing cancer cell death. Therefore, the composition of the present invention containing the GRS proteins or fragments thereof, or a nucleic acid encoding the GRS proteins or fragments can be used for an anticancer treatment.
摘要:
The present invention relates to an anticancer composition containing full-length GRS proteins or fragments thereof, or a nucleic acid encoding the GRS proteins or fragments as active ingredients. The GRS proteins or fragments thereof are useful for specifically inducing cancer cell death. Therefore, the composition of the present invention containing the GRS proteins or fragments thereof, or a nucleic acid encoding the GRS proteins or fragments can be used for an anticancer treatment.
摘要:
본 발명은 전체길이의 GRS 단백질 또는 이의 단편, 상기 GRS 단백질 또는 이의 단편을 암호화하는 핵산을 유효성분으로 함유하는 것을 특징으로 하는 항암용 조성물에 관한 것이다. 상기 GRS 단백질 또는 이의 단편은 특이적으로 암세포 사멸을 유도하는 활성이 우수하므로 이를 함유하거나 상기 GRS 단백질 또는 이의 단편을 암호화하는 핵산을 함유하는 본 발명의 조성물은 항암용으로 유용하게 사용될 수 있다.
摘要:
본 발명은 아미노아실 티알엔에이 합성효소를 포함하는 나노파티클 및 이를 포함하는 항암용 조성물에 관한 것으로, 구체적으로는 글라이실 티알엔에이 합성효소 (Glycyl-tRNA synthetase, GRS), 류신 티알엔에이 합성효소 (Leucyl-tRNA synthetase, LRS) 및 이소류신 티알엔에이 합성효소 ( Isoleucyl-tRNA synthetase, IRS)를 포함하며, 항암 또는 면역증강 활성이 있는 나노파티클, 상기 나노파티클을 유효성분으로 포함하는 암 예방 또는 치료용 약학적 조성물, 면역 증강용 조성물 및 상기 나노파티클의 제조방법에 관한 것이다.
摘要:
The present invention provides compositions comprising peptidyl inhibitors of CD40L- dependent signaling that are not derived from a natural binding partner of CD40L such as CD40, or from a native CD40-CD40L interface. More particularly, the peptidyl inhibitors of the present invention are derived from natural sources that do not express CD40-Cd40L costimulatory pathways. The invention also provides synthetic derivatives and analogs of the peptidyl inhibitors having enhanced binding affinity for CD40L or enhanced inhibitory activity relative to their parent molecules.
摘要:
Provided are compositions comprising newly identified protein fragments of aminoacyl-tRNA synthetases, polynucleotides that encode them and complements thereof, related agents, and methods of use thereof in diagnostic, drug discovery, research, and therapeutic applications.
摘要:
Provided are compositions comprising newly identified protein fragments of aminoacyl-tRNA synthetases, polynucleotides that encode them and complements thereof, related agents, and methods of use thereof in diagnostic, drug discovery, research, and therapeutic applications.
摘要:
Isolated glycyl-tRNA synthetase polypeptides and polynucleotides having non-canonical biological activities are provided, as well as compositions and methods related thereto.