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020 ▼a 9780438125643
035 ▼a (MiAaPQ)AAI10902957
035 ▼a (MiAaPQ)umichrackham:001165
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 574.191
1001 ▼a Woldemichael, Tehetina B.
24510 ▼a Exploring Drug Bioaccumulation and Stabilization with Respect to Endolysosomal Ion Homeostasis Using a Systems-Based Mathematical Modeling Approach.
260 ▼a [S.l.] : ▼b University of Michigan., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 216 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Advisers: Gustavo Rosania
5021 ▼a Thesis (Ph.D.)--University of Michigan, 2018.
520 ▼a Even though most of the FDA approved drugs currently out in the market and in the process of development are weakly basic drugs, the bioaccumulation and stabilization of these drugs are not well understood. For this purpose, we use a model drug,
520 ▼a To test our hypothesis, we adapt a systems-based mathematical lysosomal ion regulation model, which consists of lysosomal membrane proteins, such as the proton-pump known as Vacuolar ATPase (V-ATPase), Cl-/H + antiporter known as CLC7, and membr
520 ▼a Collectively, our computational results as well as the CFZ-H+ Cl- physicochemical properties in relation to the ion contents and pH of the microenvironment suggest that the physiological and preferential phase-transition-dependent accumulation a
590 ▼a School code: 0127.
650 4 ▼a Biophysics.
690 ▼a 0786
71020 ▼a University of Michigan. ▼b Biophysics.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0127
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T15000466 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자