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LDR02176nmm uu200445 4500
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008181129s2018 |||||||||||||||||c||eng d
020 ▼a 9780438250314
035 ▼a (MiAaPQ)AAI10827863
035 ▼a (MiAaPQ)ucsf:11633
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 616.99
1001 ▼a Jahangiri, Arman.
24510 ▼a Cross-activating c-Met/beta1 Integrin Complex Drives Metastasis and Invasive Resistance in Cancer.
260 ▼a [S.l.] : ▼b University of California, San Francisco., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 144 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Advisers: Joseph F. Costello
5021 ▼a Thesis (Ph.D.)--University of California, San Francisco, 2018.
520 ▼a The molecular underpinnings of invasion, a hallmark of cancer, have been defined in terms of individual mediators but crucial interactions between these mediators remain undefined. In xenograft models and patient specimens, we identified a c-Met
520 ▼a Inducing c-Met/beta1 complex formation through an engineered inducible heterodimerization system promoted features crucial to overcoming stressors during metastases or antiangiogenic therapy: migration in the primary site, survival under hypoxia
520 ▼a Complex formation promoted ligand-independent receptor activation, with integrin-linked kinase phosphorylating c-Met and crystallography revealing the c-Met/beta1 complex to maintain the high-affinity beta1 integrin conformation. Site-directed m
590 ▼a School code: 0034.
650 4 ▼a Oncology.
650 4 ▼a Biochemistry.
650 4 ▼a Cellular biology.
690 ▼a 0992
690 ▼a 0487
690 ▼a 0379
71020 ▼a University of California, San Francisco. ▼b Biomedical Sciences.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0034
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999084 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자