Random Mutagenesis of β-Tubulin Defines a Set of Dispersed Mutations That Confer Paclitaxel Resistance
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Title
Random Mutagenesis of β-Tubulin Defines a Set of Dispersed Mutations That Confer Paclitaxel Resistance
Authors
Keywords
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Journal
PHARMACEUTICAL RESEARCH
Volume 29, Issue 11, Pages 2994-3006
Publisher
Springer Nature
Online
2012-06-05
DOI
10.1007/s11095-012-0794-5
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Note: Only part of the references are listed.- Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations
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- Discovery and Characterization of the Laulimalide-Microtubule Binding Mode by Mass Shift Perturbation Mapping
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- Tumoral and tissue-specific expression of the major human β-tubulin isotypes
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- Paclitaxel-Dependent Cell Lines Reveal a Novel Drug Activity
- (2010) A. Ganguly et al. MOLECULAR CANCER THERAPEUTICS
- Microtubule-binding agents: a dynamic field of cancer therapeutics
- (2010) Charles Dumontet et al. NATURE REVIEWS DRUG DISCOVERY
- Cancer Cells Acquire Mitotic Drug Resistance Properties Through Beta I-Tubulin Mutations and Alterations in the Expression of Beta-Tubulin Isotypes
- (2010) Chun Hei Antonio Cheung et al. PLoS One
- A mutation in β-tubulin and a sustained dependence on androgen receptor signalling in a newly established docetaxel-resistant prostate cancer cell line
- (2009) Takahito Hara et al. CELL BIOLOGY INTERNATIONAL
- Molecular Basis for Class V β-Tubulin Effects on Microtubule Assembly and Paclitaxel Resistance
- (2009) Rajat Bhattacharya et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria
- (2009) Xavier Hubert Jaglin et al. NATURE GENETICS
- Molecular Mechanisms of Patupilone Resistance
- (2008) S. Mozzetti et al. CANCER RESEARCH
- Microtubule dynamics as a target in oncology
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- A Unique Mode of Microtubule Stabilization Induced by Peloruside A
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- Class I β-tubulin mutations in 2-methoxyestradiol-resistant acute lymphoblastic leukemia cells: implications for drug-target interactions
- (2008) Tracy Y.E. Liaw et al. MOLECULAR CANCER THERAPEUTICS
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