MARC보기
LDR02008nmm uu200397 4500
001000000330952
00520240805163132
008181129s2018 |||||||||||||||||c||eng d
020 ▼a 9780438115552
035 ▼a (MiAaPQ)AAI10830418
035 ▼a (MiAaPQ)wisc:15448
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 574
1001 ▼a Jones, Elaina K.
24514 ▼a The Role of D52 in Acinar Homeostasis.
260 ▼a [S.l.] : ▼b The University of Wisconsin - Madison., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 123 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
500 ▼a Adviser: Guy E. Groblewski.
5021 ▼a Thesis (Ph.D.)--The University of Wisconsin - Madison, 2018.
520 ▼a D52 is a cytosolic, peripheral membrane associated protein that binds a number of membrane trafficking associated proteins and is highly expressed in pancreatic acinar cells. Work by the Groblewski lab has identified a role for D52 in regulating
520 ▼a Pancreatitis induces acinar cell dedifferentiation to a duct-like exocrine progenitor state as a mechanism of recovery. The dedifferentiated progenitors proliferate to repopulate the gland before differentiating back into acinar cells under the
520 ▼a In Chapter four, we utilized an inducible model of acinar specific D52 deletion (D52--/--) to investigate the impact of losing D52 expression, an early event in the onset of pancreatitis. Loss of D52 alone caused significant acinar cell damage,
590 ▼a School code: 0262.
650 4 ▼a Cellular biology.
690 ▼a 0379
71020 ▼a The University of Wisconsin - Madison. ▼b Nutritional Sciences.
7730 ▼t Dissertation Abstracts International ▼g 79-11B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0262
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999431 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자