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Williams RNA-Seq Samples from Various Organ and Developmental Stages
PubMed Full text in PMC Similar studies SRA Run Selector
Clark RNA-Seq Sample from Immature Seed Coats
Mutations in Argonaute5 Illuminate Epistatic Interactions of the K1 and I Loci Leading to Saddle Seed Color Patterns in Glycine max
Endogenous, tissue-specific short-interfering RNAs silence the chalcone synthase gene family in Glycine max seed coats
Commonality in small RNA profiles between transgene-induced and naturally occurring RNA silencing of chalcone synthase-A gene in petunia
Tissue specific expression of chalcone synthase siRNAs
The Transition from Primary siRNAs to Amplified Secondary siRNAs that Regulate Chalcone Synthase During Development of Glycine max Seed Coat
Expression data from the seed coats of black (iRT) and brown (irT) soybean variant for alleles of the R locus
PubMed Full text in PMC Similar studies Analyze with GEO2R
Small RNA from Arabidopsis thaliana with RNA silencing directed to Chalcone Synthase (At5G13930) by a hairpin RNA, a 21-nt artificial miRNA and a 22-nt artificial miRNA in the pap1-D over-expressing background
Methylation Affects Transposition and Splicing of a Large CACTA Transposable Element From a MYB Transcription Factor Regulating Anthocyanin Synthase (ANS) Genes in Soybean Seed Coats
PubMed Full text in PMC Similar studies
Methylation Affects Transposition and Splicing of a Large CACTA Transposable Element From a MYB Transcription Factor Regulating Anthocyanin Synthase (ANS) Genes in Soybean Seed Coats (Bisulfite-Seq)
Methylation Affects Transposition and Splicing of a Large CACTA Transposable Element From a MYB Transcription Factor Regulating Anthocyanin Synthase (ANS) Genes in Soybean Seed Coats (RNA-Seq)
Single-Stranded Annealing Induced by Re-Initiation of Replication Origins Provides a Novel and Efficient Mechanism for Generating Copy Number Expansion via Non-Allelic Homologous Recombination.
Mapping of the HUWE1 duplication at Xp11.22 in eight unrelated XLID patients
CGH: NAM parent lines vs. Wm82-ISU-01
SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints
Array-CGH analysis of X chromosome of XLMR patient
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