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Molecular genetic investigations of histone deacetylase inhibitors as potential neurotherapeutics for autosomal recessive proximal spinal muscular atrophy (SMA)

机译：组蛋白脱乙酰基酶抑制剂作为常染色体隐性遗传性近端脊髓性肌萎缩症（SMA）潜在神经疗法的分子遗传学研究

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Brichta Lars;
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年度 2006
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正文语种 {"code":"en","name":"English","id":9}
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1. Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs) [J] . EssawiM.L., Al-AttribiG.M., GaberK.R., Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function . 2012,第1期

机译：常染色体隐性儿童期脊髓性肌萎缩症（SMAs）的分子产前诊断。
2. Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy [J] . Jafar Mohseni, Teguh Haryo Sasongko, Z.a.m.h. Zabidi-hussin Genetics and molecular biology: publication of the Sociedade Brasileira de Genetica . 2013,第3期

机译：组蛋白脱乙酰基酶抑制剂可治疗脊髓性肌萎缩症
3. Histone Deacetylase Inhibition Activity and Molecular Docking of (E )-Resveratrol: Its Therapeutic Potential in Spinal Muscular Atrophy [J] . Dayangac-Erden D, Bora G, Ayhan P, Chemical biology and drug design . 2009,第3期

机译：组蛋白脱乙酰基酶抑制活性和（E）-白藜芦醇的分子对接：在脊髓性肌萎缩症中的治疗潜力。
4. Synthesis, Evaluation and Molecular Modeling Study of L-2-amino-7/8-Bromoalkanoic Acid Derivatives as Histone Deacetylase Inhibitors [C] . Dawei Huang, Xiaohui Li, Zhilong Xiu, Chinese international peptide symposium . 2011

机译：L-2-氨基-7 / 8-溴烷酸衍生物作为组蛋白脱乙酰酶抑制剂的合成，评价和分子建模研究
5. P27 as a molecular target for cancer therapeutics: Discovering small molecule inhibitors of p27 proteolysis and structure-activity relationship and mechanistic studies of largazole, a potent inhibitor of histone deacetylase . [D] . Ungermannova, Dana. 2010

机译：P27作为癌症治疗的分子靶标：发现p27蛋白水解和结构活性关系的小分子抑制剂以及组蛋白脱乙酰基酶的有效抑制剂largazole的机理研究。
6. Molecular genetics of autosomal recessive spinal muscular atrophy. [O] . N. R. Rodrigues, K. Talbot, K. E. Davies 1996

机译：常染色体隐性隐性脊髓性肌萎缩症的分子遗传学。
7. In vitro and in vivo characterization of histone deacetylase inhibitors as potential therapeutics for autosomal recessive proximal spinal muscular atrophy (SMA) [O] . Rießland Markus 2009

机译：组蛋白脱乙酰基酶抑制剂的体外和体内表征作为常染色体隐性隐性近端脊髓性肌萎缩症（SMA）的潜在疗法

Molecular genetic investigations of histone deacetylase inhibitors as potential neurotherapeutics for autosomal recessive proximal spinal muscular atrophy (SMA)

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