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Functional hotspots revealed by mutational, evolutionary, and structural characterization of ABC transporters.

机译：通过ABC转运蛋白的突变，进化和结构表征揭示了功能性热点。

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作者
Kelly, Libusha.;
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作者单位

University of California, San Francisco.;

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授予单位 University of California, San Francisco.;
学科 Bioinformatics.
学位 Ph.D.
年度 2008
页码 123 p.
总页数 123
原文格式 PDF
正文语种 eng
中图分类
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1. Kinetic and mutational analysis of the Trypanosoma brucei NBT1 nucleobase transporter expressed in Saccharomyces cerevisiae reveals structural similarities between ENT and MFS transporters. [J] . Papageorgiou I, De-Koning HP, Soteriadou K, International Journal for Parasitology . 2008,第6期

机译：在啤酒酵母中表达的布鲁氏锥虫NBT1核碱基转运蛋白的动力学和突变分析揭示了ENT和MFS转运蛋白之间的结构相似性。
2. Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations [J] . FaletraF., SniderK., ShyngS.-L., Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function . 2013,第1期

机译：导致无反应的先天性高胰岛素血症的两个ABCC8突变的共同遗传：两个新的ABCC8突变的临床和功能表征
3. Functional characterization of activating mutations in the sulfonylurea receptor 1 ( ABCC8 ABCC8 ) causing neonatal diabetes mellitus in Asian Indian children [J] . Balamurugan Kandasamy, Kavitha Babu, Yang Zhongying, Pediatric diabetes. . 2019,第4期

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4. Interwound Structural and Functional Difference Between Preterm and Term Infant Brains Revealed by Multi-view CCA [C] . Zhibin He, Shu Zhang, Songyao Zhang, International Workshop on Machine Learning in Medical Imaging;International Conference on Medical Image Computing and Computer-Assisted Intervention . 2020

机译：多视图CCA揭示早产和术语婴儿大脑之间的间歇结构和功能差异
5. Functional Characterization of the Mammalian TRPV4 Channel: Yeast Screen Reveals Gain-of-Function Mutations. [D] . Doyle, Christina A. 2012

机译：哺乳动物TRPV4通道的功能表征：酵母菌筛选揭示了功能增益突变。
6. Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations [O] . Flavio Faletra, Kara Snider, Show-Ling Shyng, -1

机译：两种ABCC8突变的共同遗传导致无响应先天性高胰岛素主义：两种新型ABCC8突变的临床和功能性
7. Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations [O] . Faletra F, Snider K, Shyng SL, 2013

机译：导致无反应的先天性高胰岛素血症的两个ABCC8突变的共同遗传：两个新的ABCC8突变的临床和功能表征

Functional hotspots revealed by mutational, evolutionary, and structural characterization of ABC transporters.

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