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The genetics of splicing in neuroblastoma
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创建时间：
2015-04-03
相关数据集
SNP data from Neuroblastoma samples. Homo sapiens
Neuroblastoma in advanced stages is among the most intractable pediatric cancers, even with the recent therapeutic advances. Neruroblastoma harbours a variety of genetic changes, including a high freq
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ERRβ splice variants differentially regulate cell cycle progression
Orphan receptors comprise nearly half of all members of the nuclear receptor superfamily. Despite having broad structural similarities to the classical estrogen receptors, estrogen-related receptors (
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Identification of novel fusion transcripts in neuroblastoma
Detection of novel chimeric transcripts by paired-end RNA-seq in neuroblastoma cell lines Overall design: Identification of novel fusion transcripts in 8 neuroblastoma cells available in our lab via p
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Chromosome 17/17q gain and unaltered profiles in high resolution array-CGH are prognostically informative in neuroblastoma
Oligonucleotide aCGH profiles from 37 neuroblastoma tumor samples were generated using 44K or 105K microarrays. Two-color array-based comparative genome hybridization (aCGH)
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Chronic kidney disease and splicing events
Renal failure is associated with accumulation of various solutes called Uremic toxins. Post transcriptional regulation related to Chronic kidney disease (CKD) have already been described as RNA based
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