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020 ▼a 9780438110045
035 ▼a (MiAaPQ)AAI10827605
035 ▼a (MiAaPQ)ucsd:17586
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 574
1001 ▼a Alvarez, Roberto, Jr.
24510 ▼a Cardiomyocyte Cell Cycle Revealed by FUCCI.
260 ▼a [S.l.] : ▼b University of California, San Diego., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 120 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
500 ▼a Adviser: Mark A. Sussman.
5021 ▼a Thesis (Ph.D.)--University of California, San Diego, 2018.
520 ▼a Rationale: Pre-existing cardiomyocytes and resident cardiac stem cells are limited in their capacity for substantial regeneration in postnatal endogenous mammalian myocardial repair. Evidence for adult cardiomyocyte proliferation remains inconcl
520 ▼a Objective: Authenticate fidelity of proliferative markers as indicators of de novo cardiomyogenesis and subsequently delineate the post-mitotic status of postnatal cardiomyocytes.
520 ▼a Methods and Results: Cardiomyocyte specific FUCCI expression driven by the alpha-myosin heavy chain (alphaMHC) promoter was utilized in conjunction with traditional proliferation markers to identify cell cycle status of postnatal murine cardiomy
520 ▼a Conclusions: Proliferation markers used to identify de novo cardiomyogenesis failed to distinguish cycling cardiomyocytes after injury. Adult cardiomyocytes upregulated cell cycle activity in response to sham injury but failed to complete regene
590 ▼a School code: 0033.
650 4 ▼a Biology.
650 4 ▼a Cellular biology.
650 4 ▼a Molecular biology.
690 ▼a 0306
690 ▼a 0379
690 ▼a 0307
71020 ▼a University of California, San Diego. ▼b Biology.
7730 ▼t Dissertation Abstracts International ▼g 79-11B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0033
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999048 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자