Reza Talebi
Bu-Ali Sina University
10 Papers
10 Citations
Reza Talebi is an academic researcher from Bu-Ali Sina University. The author has contributed to research in topics: Gene & Luteal phase. The author has an hindex of 5, co-authored 10 publications.
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Papers
Runs of Homozygosity in Modern Chicken Revealed by Sequence Data.
TL;DR: Comparison of ROH landscape in sequencing resolution demonstrated that a sizable portion of genome of commercial lines segregates in homozygote state, reflecting many generations of assortative mating and intensive selection in their recent history.
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Transcriptome analysis of ovine granulosa cells reveals differences between small antral follicles collected during the follicular and luteal phases.
Reza Talebi,A. Ahmadi,Fazlollah Afraz,Julien Sarry,Florence Plisson-Petit,Carine Genet,Stéphane Fabre +6 more
TL;DR: This study provides new insights into the gene expression profile in ovine granulosa cells, and suggests that these molecular changes may have an implication at the time of follicle selection.
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Parkinson's disease and lactoferrin: Analysis of dependent protein networks
TL;DR: It was concluded that bovine LTF is one of the major proteins in initiation of signaling to PD-associated proteins as well as hub protein and high-degree protein for NDUFB4 and NDUFAB1, respectively.
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Analysis of protein-protein interaction network based on transcriptome profiling of ovine granulosa cells identifies candidate genes in cyclic recruitment of ovarian follicles
TL;DR: This study aimed to identify candidate genes in follicular cyclic recruitment via analysis of protein-protein interaction (PPI) network by identifying differentially expressed genes (DEGs) in ovine granulosa cells of small antral follicles between follicular and luteal phases.
A handmade DNA extraction kit using laundry powder; insights on simplicity, cost-efficiency, rapidity, safety and the quality of purified DNA.
TL;DR: An in-house kit for high throughput DNA extraction using laundry detergent successfully extracted clean DNA from all blood samples and discernably outperformed the commercial kits and the original salting-out procedure in the sense of the simplicity, cost-efficiency, quantity, and the quality of purified DNA.
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