Integrated miRNA–mRNA transcriptomic analysis reveals epigenetic-mediated embryonic muscle growth differences between Wuzhishan and Landrace pigs1
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Title
Integrated miRNA–mRNA transcriptomic analysis reveals epigenetic-mediated embryonic muscle growth differences between Wuzhishan and Landrace pigs1
Authors
Keywords
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Journal
JOURNAL OF ANIMAL SCIENCE
Volume 97, Issue 5, Pages 1967-1978
Publisher
Oxford University Press (OUP)
Online
2019-04-10
DOI
10.1093/jas/skz091
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- (2014) Francisco Hernandez-Torres et al. Biochimica et Biophysica Acta-Gene Regulatory Mechanisms
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- Integrative Analysis of Porcine microRNAome during Skeletal Muscle Development
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- (2013) Hana Velvarska et al. PLoS One
- Chd2 interacts with H3.3 to determine myogenic cell fate
- (2012) Akihito Harada et al. EMBO JOURNAL
- Identification of suitable endogenous control microRNA genes in normal pig tissues
- (2011) Yiren GU et al. ANIMAL SCIENCE JOURNAL
- Skeletal muscle proteomics in livestock production
- (2011) B. Picard et al. Briefings in Functional Genomics
- Comparative Analyses by Sequencing of Transcriptomes during Skeletal Muscle Development between Pig Breeds Differing in Muscle Growth Rate and Fatness
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- MicroRNAs in skeletal muscle: their role and regulation in development, disease and function
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- (2009) Andrew H Williams et al. CURRENT OPINION IN CELL BIOLOGY
- The Pig as an Experimental Model for Elucidating the Mechanisms Governing Dietary Influence on Mineral Absorption
- (2008) Jannine K. Patterson et al. EXPERIMENTAL BIOLOGY AND MEDICINE
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- (2008) Ali Mortazavi et al. NATURE METHODS
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