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Title
TUBB1 variants and human platelet traits
Authors
Keywords
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Journal
PLATELETS
Volume 29, Issue 2, Pages 209-211
Publisher
Informa UK Limited
Online
2018-01-15
DOI
10.1080/09537104.2017.1411587
References
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Related references
Note: Only part of the references are listed.- Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
- (2017) José M. Bastida et al. HAEMATOLOGICA
- The tubulin code at a glance
- (2017) Sudarshan Gadadhar et al. JOURNAL OF CELL SCIENCE
- Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
- (2017) José M. Bastida et al. HAEMATOLOGICA
- The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
- (2016) William J. Astle et al. CELL
- A new mutation in TUBB1 associated with thrombocytopenia confirms that C-terminal part of β1-tubulin plays a role in microtubule assembly
- (2016) M. Fiore et al. CLINICAL GENETICS
- Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects
- (2016) B. Johnson et al. HAEMATOLOGICA
- Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects
- (2016) B. Johnson et al. HAEMATOLOGICA
- β-1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia
- (2015) P. A. Basciano et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits
- (2014) Paul L Auer et al. NATURE GENETICS
- TUBB1mutation disrupting microtubule assembly impairs proplatelet formation and results in congenital macrothrombocytopenia
- (2013) Shinji Kunishima et al. EUROPEAN JOURNAL OF HAEMATOLOGY
- The beta 1 tubulin R307H single nucleotide polymorphism is associated with treatment failures in immune thrombocytopenia (ITP)
- (2012) Paul A. Basciano et al. BRITISH JOURNAL OF HAEMATOLOGY
- Hematologic -Tubulin VI Isoform Exhibits Genetic Variability That Influences Paclitaxel Toxicity
- (2012) L. J. Leandro-Garcia et al. CANCER RESEARCH
- Mutation of the 1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly
- (2008) S. Kunishima et al. BLOOD
- Mutation inβ1-TubulinCorrelates with Macrothrombocytopenia in Cavalier King Charles Spaniels
- (2008) B. Davis et al. JOURNAL OF VETERINARY INTERNAL MEDICINE
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