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郑二硕
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2023-03-05 加入
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Antisense oligonucleotide-mediated MSH3 suppression reduces somatic CAG repeat expansion in Huntington's disease iPSC-derived striatal neurons
10天前
已完结
Antisense oligonucleotide–mediated MSH3 suppression reduces somatic CAG repeat expansion in Huntington’s disease iPSC–derived striatal neurons
18天前
已完结
Next generation sequencing in children with unexplained epilepsy: A retrospective cohort study
1个月前
已完结
PCDH19-related female-limited epilepsy: further details regarding early clinical features and therapeutic efficacy
1个月前
已完结
PCDH19 mutation in Japanese females with epilepsy
1个月前
已完结
Autism spectrum disorder phenotype and intellectual disability in females with epilepsy and PCDH-19 mutations
1个月前
已完结
enOsCas12f1-mediated exon skipping for Duchenne muscular dystrophy therapy in humanized mouse model
2个月前
已完结
enOsCas12f1-mediated exon skipping for Duchenne muscular dystrophy therapy in humanized mouse model
2个月前
已完结
Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review
9个月前
已完结
Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model
9个月前
已完结
没有进行任何应助
感谢,点赞
18天前
感谢
2个月前
感谢,点赞
9个月前
感谢,帮大忙了,速度真快
1年前
已找到【积分已退回】
1年前
帮大忙了,感谢
1年前
感谢,速度真快
1年前
好的,感谢
1年前
也是内容不全
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文章内容不全
1年前
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