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
Unraveling the Genetic Basis of Hear...
~
O'Hearn, James David.
FindBook
Google Book
Amazon
博客來
Unraveling the Genetic Basis of Heart Failure via Systems Genetics.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Unraveling the Genetic Basis of Heart Failure via Systems Genetics./
作者:
O'Hearn, James David.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2017,
面頁冊數:
189 p.
附註:
Source: Dissertation Abstracts International, Volume: 78-08(E), Section: B.
Contained By:
Dissertation Abstracts International78-08B(E).
標題:
Molecular biology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10259664
ISBN:
9781369653137
Unraveling the Genetic Basis of Heart Failure via Systems Genetics.
O'Hearn, James David.
Unraveling the Genetic Basis of Heart Failure via Systems Genetics.
- Ann Arbor : ProQuest Dissertations & Theses, 2017 - 189 p.
Source: Dissertation Abstracts International, Volume: 78-08(E), Section: B.
Thesis (Ph.D.)--University of California, Los Angeles, 2017.
Heart failure (HF) is the leading cause of death worldwide. It is a complex disease involving multiple aspects of pathology affected by genetic pre-disposition, the aging process, and environmental stressors. Defining the genetic basis for HF can provide keys to the underlying mechanisms and lead to a better personalized diagnosis and therapy. A systems genetics approach was developed to perform functional characterization of 107 mouse strains from a Hybrid Mouse Diversity Panel (HMDP). Three categories were designated, sensitive, intermediate, and resistant, after beta-adrenergic stimulation using isoproterenol (ISO). Extremely resistant and sensitive strains were selected for angiotensin II (AngII) and transverse aortic constriction (TAC) treatment to study the contribution of genetic background on the pathogenesis of HF. ISO, AngII, and TAC share the hypertrophic and fibrotic responses in a strain and stressor specific manner. The contractility phenotype is common for sensitive and resistant strains. Itga1, the alpha subunit of integrin receptors was found to have significant association with left ventricular hypertrophy (LVH). Together, these results suggest that genetic variants significantly contribute to the development of heart failure and the genes implicated in the specific pathological features of heart failure can be revealed via systems genetics. In addition, we have identified a number of cardiac phenotypes implicated in diastolic dysfunction. More extensive studies using highly sensitive and resistant strains from the HMDP have shown differential responses and offer support for investigating HF using this mouse model which is suffering from Heart Failure with preserved Ejection Fraction (HFpEF). These results provide validation for our approach to unraveling the effects of genetic background associated with multiple cardiac phenotypic manifestations to pathological stressors and continue to generate hypotheses and analytical understanding in heart failure.
ISBN: 9781369653137Subjects--Topical Terms:
517296
Molecular biology.
Unraveling the Genetic Basis of Heart Failure via Systems Genetics.
LDR
:02972nmm a2200313 4500
001
2164263
005
20181106104110.5
008
190424s2017 ||||||||||||||||| ||eng d
020
$a
9781369653137
035
$a
(MiAaPQ)AAI10259664
035
$a
(MiAaPQ)ucla:15241
035
$a
AAI10259664
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
O'Hearn, James David.
$3
3352308
245
1 0
$a
Unraveling the Genetic Basis of Heart Failure via Systems Genetics.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2017
300
$a
189 p.
500
$a
Source: Dissertation Abstracts International, Volume: 78-08(E), Section: B.
500
$a
Adviser: Yibin Wang.
502
$a
Thesis (Ph.D.)--University of California, Los Angeles, 2017.
520
$a
Heart failure (HF) is the leading cause of death worldwide. It is a complex disease involving multiple aspects of pathology affected by genetic pre-disposition, the aging process, and environmental stressors. Defining the genetic basis for HF can provide keys to the underlying mechanisms and lead to a better personalized diagnosis and therapy. A systems genetics approach was developed to perform functional characterization of 107 mouse strains from a Hybrid Mouse Diversity Panel (HMDP). Three categories were designated, sensitive, intermediate, and resistant, after beta-adrenergic stimulation using isoproterenol (ISO). Extremely resistant and sensitive strains were selected for angiotensin II (AngII) and transverse aortic constriction (TAC) treatment to study the contribution of genetic background on the pathogenesis of HF. ISO, AngII, and TAC share the hypertrophic and fibrotic responses in a strain and stressor specific manner. The contractility phenotype is common for sensitive and resistant strains. Itga1, the alpha subunit of integrin receptors was found to have significant association with left ventricular hypertrophy (LVH). Together, these results suggest that genetic variants significantly contribute to the development of heart failure and the genes implicated in the specific pathological features of heart failure can be revealed via systems genetics. In addition, we have identified a number of cardiac phenotypes implicated in diastolic dysfunction. More extensive studies using highly sensitive and resistant strains from the HMDP have shown differential responses and offer support for investigating HF using this mouse model which is suffering from Heart Failure with preserved Ejection Fraction (HFpEF). These results provide validation for our approach to unraveling the effects of genetic background associated with multiple cardiac phenotypic manifestations to pathological stressors and continue to generate hypotheses and analytical understanding in heart failure.
590
$a
School code: 0031.
650
4
$a
Molecular biology.
$3
517296
650
4
$a
Cellular biology.
$3
3172791
650
4
$a
Physiology.
$3
518431
690
$a
0307
690
$a
0379
690
$a
0719
710
2
$a
University of California, Los Angeles.
$b
Molec, Cell, & Integ Physiology 0568.
$3
3181612
773
0
$t
Dissertation Abstracts International
$g
78-08B(E).
790
$a
0031
791
$a
Ph.D.
792
$a
2017
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10259664
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
W9363810
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