語系:
繁體中文
English
說明(常見問題)
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Characterizing the Role of ice1 in M...
~
University of Toronto (Canada).
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
紀錄類型:
書目-語言資料,手稿 : Monograph/item
正題名/作者:
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells./
作者:
D'Amata, Cassandra Marie.
面頁冊數:
1 online resource (95 pages)
附註:
Source: Masters Abstracts International, Volume: 57-02.
標題:
Cellular biology. -
電子資源:
click for full text (PQDT)
ISBN:
9780355449556
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
D'Amata, Cassandra Marie.
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
- 1 online resource (95 pages)
Source: Masters Abstracts International, Volume: 57-02.
Thesis (M.Sc.)--University of Toronto (Canada), 2017.
Includes bibliographical references
Maintenance of neural stem cell (NSC) niches is required for the continued growth of the zebrafish retina and forebrain after embryogenesis. The zebrafish mutant kess564, which maps to the ice1 locus, exhibits reduced NSC niches. RNA polymerase II-dependent snRNA transcription requires the little elongation complex (LEC) for which ICE1 is an essential scaffolding component. Mutant NSCs which are normally active no longer express markers of cycling cells and become apoptotic. Furthermore, quiescent NSCs of the mutant retina are unable to dedifferentiate in response to UV lesion. Whole-transcriptome analysis of ice1 mutant larvae show a decrease in CNS and cell cycle levels, and an increase in splicing genes indicative of a possible compensatory mechanism. snRNA transcript levels appear to be unaffected in a subset of NSCs but reduced in differentiated neurons. This work demonstrates that ice1 is essential for NSC maintenance in an in vivo loss of function model.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2018
Mode of access: World Wide Web
ISBN: 9780355449556Subjects--Topical Terms:
1148666
Cellular biology.
Index Terms--Genre/Form:
554714
Electronic books.
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
LDR
:02144ntm a2200337K 4500
001
913360
005
20180618102637.5
006
m o u
007
cr mn||||a|a||
008
190606s2017 xx obm 000 0 eng d
020
$a
9780355449556
035
$a
(MiAaPQ)AAI10637149
035
$a
(MiAaPQ)toronto:16706
035
$a
AAI10637149
040
$a
MiAaPQ
$b
eng
$c
MiAaPQ
100
1
$a
D'Amata, Cassandra Marie.
$3
1186170
245
1 0
$a
Characterizing the Role of ice1 in Maintaining Zebrafish Neural Stem Cells.
264
0
$c
2017
300
$a
1 online resource (95 pages)
336
$a
text
$b
txt
$2
rdacontent
337
$a
computer
$b
c
$2
rdamedia
338
$a
online resource
$b
cr
$2
rdacarrier
500
$a
Source: Masters Abstracts International, Volume: 57-02.
500
$a
Adviser: Vincent Tropepe.
502
$a
Thesis (M.Sc.)--University of Toronto (Canada), 2017.
504
$a
Includes bibliographical references
520
$a
Maintenance of neural stem cell (NSC) niches is required for the continued growth of the zebrafish retina and forebrain after embryogenesis. The zebrafish mutant kess564, which maps to the ice1 locus, exhibits reduced NSC niches. RNA polymerase II-dependent snRNA transcription requires the little elongation complex (LEC) for which ICE1 is an essential scaffolding component. Mutant NSCs which are normally active no longer express markers of cycling cells and become apoptotic. Furthermore, quiescent NSCs of the mutant retina are unable to dedifferentiate in response to UV lesion. Whole-transcriptome analysis of ice1 mutant larvae show a decrease in CNS and cell cycle levels, and an increase in splicing genes indicative of a possible compensatory mechanism. snRNA transcript levels appear to be unaffected in a subset of NSCs but reduced in differentiated neurons. This work demonstrates that ice1 is essential for NSC maintenance in an in vivo loss of function model.
533
$a
Electronic reproduction.
$b
Ann Arbor, Mich. :
$c
ProQuest,
$d
2018
538
$a
Mode of access: World Wide Web
650
4
$a
Cellular biology.
$3
1148666
650
4
$a
Developmental biology.
$3
669036
650
4
$a
Molecular biology.
$3
583443
655
7
$a
Electronic books.
$2
local
$3
554714
690
$a
0379
690
$a
0758
690
$a
0307
710
2
$a
ProQuest Information and Learning Co.
$3
1178819
710
2
$a
University of Toronto (Canada).
$b
Cell and Systems Biology.
$3
1186171
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10637149
$z
click for full text (PQDT)
筆 0 讀者評論
多媒體
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼[密碼必須為2種組合(英文和數字)及長度為10碼以上]
登入