語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Expression of neuronal proteins in a...
~
Chen, Ya.
FindBook
Google Book
Amazon
博客來
Expression of neuronal proteins in a differentiating human neuroblastoma cell line (IMR32): Insights into neuronal development and disease.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Expression of neuronal proteins in a differentiating human neuroblastoma cell line (IMR32): Insights into neuronal development and disease./
作者:
Chen, Ya.
面頁冊數:
199 p.
附註:
Source: Dissertation Abstracts International, Volume: 66-10, Section: B, page: 5251.
Contained By:
Dissertation Abstracts International66-10B.
標題:
Biology, Neuroscience. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3193556
ISBN:
0542369877
Expression of neuronal proteins in a differentiating human neuroblastoma cell line (IMR32): Insights into neuronal development and disease.
Chen, Ya.
Expression of neuronal proteins in a differentiating human neuroblastoma cell line (IMR32): Insights into neuronal development and disease.
- 199 p.
Source: Dissertation Abstracts International, Volume: 66-10, Section: B, page: 5251.
Thesis (Ph.D.)--Case Western Reserve University, 2006.
The acquisition of a neuronal phenotype by exposure to specific intrinsic and extrinsic signals is a property of neuroblasts, adult neural stem cells, and the IMR32 human neuroblastoma cell line. As several complex psychiatric, cognitive, and neurological human disorders such as schizophrenia, autism, and some epilepsies are now being approached as neurodevelopmental disorders, it is critical to understand the normal course of neuronal differentiation with the long term goal of strategic intervention and management of the chronic and debilitating diseases. In my thesis, we explore the use of IMR32 cells as a simplified and accessible model system for studying neuronal differentiation and exploring the expression of proteins with synaptic functions; specifically, secretory proteins, voltage-dependent calcium channels, and proteins implicated in growth cone formation and neurite formation. We also explore the expression of MeCP2 and use a novel antibody to neural cell adhesion molecule (NCAM) 180 kDa isoform to monitor the acquisition of a neuronal phenotype in parallel to other markers of synaptic function. The biochemical analyses of VDCC assembly in IMR32 cells and expression of VDCC subunits have identified how alpha 1 and beta subunits are assembled in a single cell type. Thus, the use of differentiated IMR32 cells as a cell model offers a unique cell population for future study on neuronal differentiation and neuronal proteins involved with neurodevelopmental disorders in vitro.
ISBN: 0542369877Subjects--Topical Terms:
1017680
Biology, Neuroscience.
Expression of neuronal proteins in a differentiating human neuroblastoma cell line (IMR32): Insights into neuronal development and disease.
LDR
:02537nmm 2200289 4500
001
1817916
005
20060829133403.5
008
130610s2006 eng d
020
$a
0542369877
035
$a
(UnM)AAI3193556
035
$a
AAI3193556
040
$a
UnM
$c
UnM
100
1
$a
Chen, Ya.
$3
1907261
245
1 0
$a
Expression of neuronal proteins in a differentiating human neuroblastoma cell line (IMR32): Insights into neuronal development and disease.
300
$a
199 p.
500
$a
Source: Dissertation Abstracts International, Volume: 66-10, Section: B, page: 5251.
500
$a
Advisers: Maureen W. McEnery; Rolfe G. Petschek.
502
$a
Thesis (Ph.D.)--Case Western Reserve University, 2006.
520
$a
The acquisition of a neuronal phenotype by exposure to specific intrinsic and extrinsic signals is a property of neuroblasts, adult neural stem cells, and the IMR32 human neuroblastoma cell line. As several complex psychiatric, cognitive, and neurological human disorders such as schizophrenia, autism, and some epilepsies are now being approached as neurodevelopmental disorders, it is critical to understand the normal course of neuronal differentiation with the long term goal of strategic intervention and management of the chronic and debilitating diseases. In my thesis, we explore the use of IMR32 cells as a simplified and accessible model system for studying neuronal differentiation and exploring the expression of proteins with synaptic functions; specifically, secretory proteins, voltage-dependent calcium channels, and proteins implicated in growth cone formation and neurite formation. We also explore the expression of MeCP2 and use a novel antibody to neural cell adhesion molecule (NCAM) 180 kDa isoform to monitor the acquisition of a neuronal phenotype in parallel to other markers of synaptic function. The biochemical analyses of VDCC assembly in IMR32 cells and expression of VDCC subunits have identified how alpha 1 and beta subunits are assembled in a single cell type. Thus, the use of differentiated IMR32 cells as a cell model offers a unique cell population for future study on neuronal differentiation and neuronal proteins involved with neurodevelopmental disorders in vitro.
590
$a
School code: 0042.
650
4
$a
Biology, Neuroscience.
$3
1017680
650
4
$a
Health Sciences, Pathology.
$3
1017854
690
$a
0317
690
$a
0571
710
2 0
$a
Case Western Reserve University.
$3
1017714
773
0
$t
Dissertation Abstracts International
$g
66-10B.
790
1 0
$a
McEnery, Maureen W.,
$e
advisor
790
1 0
$a
Petschek, Rolfe G.,
$e
advisor
790
$a
0042
791
$a
Ph.D.
792
$a
2006
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3193556
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9208779
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入