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HnRNP C1/C2 May Regulate Exon 7 Splicing in the Spinal Muscular Atrophy Gene SMN1

机译：HnRNP C1 / C2可能规管脊髓肌萎缩基因SMN1中的外显子7剪接。

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Spinal muscular atrophy (SMA) is caused by loss of SMN1. A nearly identical gene,SMN2, fails to compensate for the loss of SMN1 because SMN2 produces mainly anexon 7-skipped product. The +6C in SMN1 exon 7 proceeds to include exon 7 intomRNA, while the +6

机译：脊髓肌萎缩症（SMA）是由SMN1丢失引起的。几乎相同的基因SMN2无法弥补SMN1的损失，因为SMN2主要产生anexon 7跳过的产物。 SMN1外显子7中的+ 6C继续将外显子7纳入mRNA，而+6

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Irimura Sanae; Kitamura Keiko; Kato Nozomu; Saiki Kayoko; Takeuchi Atsuko; GUNADI; Matsuo Masafumi; Nishio Hisahide; LEE MYEONG　JIN;
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年度 2008
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1. Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2. [J] . Cartegni L, Hastings ML, Calarco JA, The American Journal of Human Genetics . 2006,第1期

机译：脊柱肌肉萎缩基因SMN1和SMN2中剪接的外显子7的决定因素。
2. A rare variant (c.863G > T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy [J] . Qu Yu-jin, Bai Jin-li, Cao Yan-yan, European journal of human genetics: EJHG . 2016,第6期

机译：SMN1外显子7中的一种罕见变体（c.863G> T）破坏了mRNA剪接并导致脊髓性肌萎缩
3. A leaky splicing mutation affecting SMN1 exon 7 inclusion explains an unexpected mild case of spinal muscular atrophy [J] . Human mutation . 2011,第9期

机译：一个泄漏的剪接突变影响SMN1外显子7包涵体解释了脊髓肌萎缩的意外轻度病例
4. A Motor Imagery-based Brain-Computer Interface Scheme for a Spinal Muscular Atrophy Subject in CYBATHLON Race [C] . Shi-Chun Bao, Kai Yuan, Cheng Chen, International IEEE/EMBS Conference on Neural Engineering . 2021

机译：基于电机图像的脑电电脑界面方案，用于Cybathlon Race中的脊柱肌肉萎缩课程
5. Characterizing the effect of mutations within exon 7 of the murine survival motor neuron gene to model spinal muscular atrophy in the mouse. [D] . Hammond, Suzan Michelle. 2010

机译：表征小鼠存活运动神经元基因外显子7内突变对小鼠脊髓性肌萎缩模型的影响。
6. Determinants of Exon 7 Splicing in the Spinal Muscular Atrophy Genes SMN1 and SMN2 [O] . Luca Cartegni, Michelle L. Hastings, John A. Calarco, 2006

机译：脊髓肌萎缩基因SMN1和SMN2剪接的外显子7的决定因素。
7. Determinants of Exon 7 Splicing in the Spinal Muscular Atrophy Genes, SMN1 and SMN2 [O] . Cartegni, Luca, Hastings, Michelle L., Calarco, John A., 2006

机译：脊髓肌萎缩基因，SMN1和SMN2剪接的外显子7的决定因素。

HnRNP C1/C2 May Regulate Exon 7 Splicing in the Spinal Muscular Atrophy Gene SMN1

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