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Title
Somatic SF3B1 hotspot mutation in prolactinomas
Authors
Keywords
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Journal
Nature Communications
Volume 11, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-05-19
DOI
10.1038/s41467-020-16052-8
References
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Note: Only part of the references are listed.- Recurrent hotspot SF3B1 mutations at codon 625 in vulvovaginal mucosal melanoma identified in a study of 27 Australian mucosal melanomas
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- Transcriptomic Characterization of SF3B1 Mutation Reveals Its Pleiotropic Effects in Chronic Lymphocytic Leukemia
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- Cryptic splicing events in the iron transporter ABCB7 and other key target genes in SF3B1-mutant myelodysplastic syndromes
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- Role of Estrogen Response Element in the Human Prolactin Gene: Transcriptional Response and Timing
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- Cancer-associated SF3B1 mutations affect alternative splicing by promoting alternative branchpoint usage
- (2016) Samar Alsafadi et al. Nature Communications
- Mutations in the deubiquitinase gene USP8 cause Cushing's disease
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- Splicing factor mutations and cancer
- (2014) Kenichi Yoshida et al. Wiley Interdisciplinary Reviews-RNA
- The functional consequences of intron retention: Alternative splicing coupled to NMD as a regulator of gene expression
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- Evolution and Impact of Subclonal Mutations in Chronic Lymphocytic Leukemia
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- A compendium of RNA-binding motifs for decoding gene regulation
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- Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma
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- Pre-mRNA splicing in disease and therapeutics
- (2012) Ravi K. Singh et al. TRENDS IN MOLECULAR MEDICINE
- SomaticSF3B1Mutation in Myelodysplasia with Ring Sideroblasts
- (2011) E. Papaemmanuil et al. NEW ENGLAND JOURNAL OF MEDICINE
- Gender-related Differences in Pituitary Adenomas
- (2009) B. D. Arasho et al. EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
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