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Real-time RT-PCR quantification of p...
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Aad, Pauline Youssef.
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Real-time RT-PCR quantification of pregnancy-associated plasma protein-A gene expression in granulosa and theca cells: Effects of hormones in vitro.
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Real-time RT-PCR quantification of pregnancy-associated plasma protein-A gene expression in granulosa and theca cells: Effects of hormones in vitro./
Author:
Aad, Pauline Youssef.
Description:
98 p.
Notes:
Adviser: Leon J. Spicer.
Contained By:
Masters Abstracts International43-05.
Subject:
Biology, Animal Physiology. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1431126
ISBN:
9780542038785
Real-time RT-PCR quantification of pregnancy-associated plasma protein-A gene expression in granulosa and theca cells: Effects of hormones in vitro.
Aad, Pauline Youssef.
Real-time RT-PCR quantification of pregnancy-associated plasma protein-A gene expression in granulosa and theca cells: Effects of hormones in vitro.
- 98 p.
Adviser: Leon J. Spicer.
Thesis (M.S.)--Oklahoma State University, 2005.
Ovarian follicular growth and dominance is controlled by a series of hormonal events including a decrease in intrafollicular IGF-binding proteins-2, -4 and -5 levels. Proteolytic enzymes such as pregnancy-associated plasma protein-A (PAPP-A) degrade IGFBPs and increase availability of IGF-I and -II during follicular development. The objective of this study was to determine the effect of IGF-I, IGF-II, insulin (INS), LH, FSH, estradiol (E), leptin or cortisol on ovarian PAPP-A mRNA levels. Granulosa (GC) from small (SM) (<5 mm) and large (LG) (>7.9 mm) follicles as well as theca cells (TC) from LG follicles were collected from bovine ovaries and cultured for 48 h in medium containing 10% FCS and then treated with various hormones in serum-free medium for an additional 12 or 24 h. LG-GC and LG-TC were cultured for either 12 or 24 h with 0 or 100 ng/mL of IGF-I or -II (exp 1 and 2). In all other experiments, SM-GC LG-GC and LG-TC were treated with various combinations of IGF-I, IGF-II, FSH, LH, E, INS, leptin and (or) cortisol for 24 h (exp 3 through 12). PAPP-A mRNA expression levels quantified using quantitative real-time RT-PCR. (Abstract shortened by UMI.)
ISBN: 9780542038785Subjects--Topical Terms:
1017835
Biology, Animal Physiology.
Real-time RT-PCR quantification of pregnancy-associated plasma protein-A gene expression in granulosa and theca cells: Effects of hormones in vitro.
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Real-time RT-PCR quantification of pregnancy-associated plasma protein-A gene expression in granulosa and theca cells: Effects of hormones in vitro.
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98 p.
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Adviser: Leon J. Spicer.
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Source: Masters Abstracts International, Volume: 43-05, page: 1651.
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Thesis (M.S.)--Oklahoma State University, 2005.
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Ovarian follicular growth and dominance is controlled by a series of hormonal events including a decrease in intrafollicular IGF-binding proteins-2, -4 and -5 levels. Proteolytic enzymes such as pregnancy-associated plasma protein-A (PAPP-A) degrade IGFBPs and increase availability of IGF-I and -II during follicular development. The objective of this study was to determine the effect of IGF-I, IGF-II, insulin (INS), LH, FSH, estradiol (E), leptin or cortisol on ovarian PAPP-A mRNA levels. Granulosa (GC) from small (SM) (<5 mm) and large (LG) (>7.9 mm) follicles as well as theca cells (TC) from LG follicles were collected from bovine ovaries and cultured for 48 h in medium containing 10% FCS and then treated with various hormones in serum-free medium for an additional 12 or 24 h. LG-GC and LG-TC were cultured for either 12 or 24 h with 0 or 100 ng/mL of IGF-I or -II (exp 1 and 2). In all other experiments, SM-GC LG-GC and LG-TC were treated with various combinations of IGF-I, IGF-II, FSH, LH, E, INS, leptin and (or) cortisol for 24 h (exp 3 through 12). PAPP-A mRNA expression levels quantified using quantitative real-time RT-PCR. (Abstract shortened by UMI.)
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1431126
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