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Biao Liu

Researcher at Roswell Park Cancer Institute

Publications -  30
Citations -  1578

Biao Liu is an academic researcher from Roswell Park Cancer Institute. The author has contributed to research in topics: RNA & Nucleic acid secondary structure. The author has an hindex of 19, co-authored 28 publications receiving 1439 citations. Previous affiliations of Biao Liu include University of Science and Technology of China & University of Rochester.

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General Synthesis of Single-Crystal Tungstate Nanorods/Nanowires: A Facile, Low-Temperature Solution Approach

TL;DR: In this article, a large-scale synthesis of a family of single-crystalline transition metal tungstate nanorods/nanowires is easily realized by a hydrothermal crystallization technique under mild conditions using cheap and simple inorganic salts as precursors.
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Nanorod-direct oriented attachment growth and promoted crystallization processes evidenced in case of ZnWO4

TL;DR: In this article, single-crystal ZnWO4 nanorods can direct the self-aggregation of amorphous nanoparticulates and promote the crystallization and transformation process of the amorphized nanopartsiculates derived from a simple supersaturation precipitation reaction in a nanorod/amorphous nanoparticle coexisting system under refluxing conditions or mild hydrothermal conditions.
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Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges.

TL;DR: This review aims to provide a guide to the analytic tools used in NGS-based cancer CNV studies, and to discuss the important factors that researchers need to consider when analyzing NGS data for somatic CNV detections.
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A small molecule that targets r(CGG)(exp) and improves defects in fragile X-associated tremor ataxia syndrome.

TL;DR: A bioactive small molecule probe that targets expanded r(CGG) repeats, or r( CGG)(exp), that causes Fragile X-associated Tremor Ataxia Syndrome (FXTAS) is described and is efficacious in FXTAS model cellular systems as evidenced by its ability to improve FXTas-associated pre-mRNA splicing defects and to reduce the size and number of r (C GG)(exp)-containing nuclear foci.