Modulating SMN2 exon7 splicing by increasing Tra2-??1 protein expression in neuron cells
碩士 === 高雄醫學大學 === 生物醫學暨環境生物學研究所 === 100 === Spinal muscular atrophy (SMA) is a neuromuscular disorder caused by homozygous mutations of the survival motor neuron 1 (SMN1) gene. All SMA patients have at least one or more copies of a highly homologous SMN2 gene, which produces insufficient levels of f...
Main Authors: | Wei-Che Hsiao, 蕭瑋哲 |
---|---|
Other Authors: | Chung-Yee You |
Format: | Others |
Language: | zh-TW |
Published: |
2012
|
Online Access: | http://ndltd.ncl.edu.tw/handle/48759436629916889188 |
Similar Items
-
High expression level of Tra2-β1 is responsible for increased SMN2 exon 7 inclusion in the testis of SMA mice.
by: Yu-Chia Chen, et al.
Published: (2015-01-01) -
Absence of an intron splicing silencer in porcine Smn1 intron 7 confers immunity to the exon skipping mutation in human SMN2.
by: Thomas Koed Doktor, et al.
Published: (2014-01-01) -
Temporally inducible SMN expression and splicing modulation of the SMN2 gene in SMA mouse models
by: Bebee, Thomas Wayne
Published: (2012) -
Enhancement of SMN2 exon 7 inclusion by antisense oligonucleotides targeting the exon.
by: Yimin Hua, et al.
Published: (2007-04-01) -
Colorimetric Assay for Exon 7 SMN1/SMN2 Single Nucleotide Polymorphism Using Gold Nanoprobes
by: Hossein Ahmadpour-Yazdi, et al.
Published: (2013-12-01)