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Molecular architecture of the human 17S U2 snRNP

Nature (London), 2020-07, Vol.583 (7815), p.310-313

2020

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SART3 associates with a post-splicing complex

Journal of cell science, 2023-01, Vol.136 (2)

2023

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Sequence-specific RNA recognition by an RGG motif connects U1 and U2 snRNP for spliceosome assembly

Proceedings of the National Academy of Sciences - PNAS, 2022-02, Vol.119 (6), p.1

2022

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Acute myeloid leukemia ontogeny is defined by distinct somatic mutations

Blood, 2015-02, Vol.125 (9), p.1367-1376

2015

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A prometastatic splicing program regulated by SNRPA1 interactions with structured RNA elements

Science (American Association for the Advancement of Science), 2021-05, Vol.372 (6543)

2021

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Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis

Blood, 2012-04, Vol.119 (14), p.3203-3210

2012

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Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma

Nature genetics, 2013-02, Vol.45 (2), p.133-135

2013

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Structural insights into branch site proofreading by human spliceosome

Nature structural & molecular biology, 2024-05, Vol.31 (5), p.835-845

2024

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SF3B1 mutations are associated with alternative splicing in uveal melanoma

Cancer discovery, 2013-10, Vol.3 (10), p.1122-1129

2013

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SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts

Blood, 2015-07, Vol.126 (2), p.233-241

2015

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Leukemia-Associated Somatic Mutations Drive Distinct Patterns of Age-Related Clonal Hemopoiesis

Cell reports (Cambridge), 2015-03, Vol.10 (8), p.1239-1245

2015

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HIF-driven SF3B1 induces KHK-C to enforce fructolysis and heart disease

Nature (London), 2015-06, Vol.522 (7557), p.444-449

2015

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SF3B1 mutations constitute a novel therapeutic target in breast cancer

The Journal of pathology, 2015-03, Vol.235 (4), p.571-580

2015

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Cancer-associated SF3B1 mutations affect alternative splicing by promoting alternative branchpoint usage

Nature communications, 2016-02, Vol.7 (1), p.10615-12, Article 10615

2016

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The splicing regulators RBM5 and RBM10 are subunits of the U2 snRNP engaged with intron branch sites on chromatin

Molecular cell, 2024-04, Vol.84 (8), p.1496-1511.e7

2024

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Phylogenetic Analysis of Spliceosome SF3a2 in Different Plant Species

International journal of molecular sciences, 2023-03, Vol.24 (6), p.5232

2023

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Structural basis for the interaction between the first SURP domain of the SF3A1 subunit in U2 snRNP and the human splicing factor SF1

Protein science, 2022-10, Vol.31 (10), p.e4437-n/a

2022

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Post-transcriptional spliceosomes are retained in nuclear speckles until splicing completion

Nature communications, 2012-08, Vol.3 (1), p.994-994, Article 994

2012

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Molecular basis for the activation of human spliceosome

Nature communications, 2024-07, Vol.15 (1), p.6348-10, Article 6348

2024

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Transcriptome and long noncoding RNA sequencing of three extracellular vesicle subtypes released from the human colon cancer LIM1863 cell line

Scientific reports, 2016-12, Vol.6 (1), p.38397-38397, Article 38397

2016

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Acetylation of PHF5A Modulates Stress Responses and Colorectal Carcinogenesis through Alternative Splicing-Mediated Upregulation of KDM3A

Molecular cell, 2019-06, Vol.74 (6), p.1250-1263.e6

2019

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Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

Nature genetics, 2013-08, Vol.45 (8), p.933-936

2013

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Cancer-Associated SF3B1 Hotspot Mutations Induce Cryptic 3′ Splice Site Selection through Use of a Different Branch Point

Molecular architecture of the human 17S U2 snRNP

SART3 associates with a post-splicing complex

Comprehensive genomic analysis of malignant pleural mesothelioma identifies recurrent mutations, gene fusions and splicing alterations

Sequence-specific RNA recognition by an RGG motif connects U1 and U2 snRNP for spliceosome assembly

Acute myeloid leukemia ontogeny is defined by distinct somatic mutations

A prometastatic splicing program regulated by SNRPA1 interactions with structured RNA elements

Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis

Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma

Structural insights into branch site proofreading by human spliceosome

SF3B1 mutations are associated with alternative splicing in uveal melanoma

SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts

Leukemia-Associated Somatic Mutations Drive Distinct Patterns of Age-Related Clonal Hemopoiesis

HIF-driven SF3B1 induces KHK-C to enforce fructolysis and heart disease

SF3B1 mutations constitute a novel therapeutic target in breast cancer

Cancer-associated SF3B1 mutations affect alternative splicing by promoting alternative branchpoint usage

The splicing regulators RBM5 and RBM10 are subunits of the U2 snRNP engaged with intron branch sites on chromatin

Gene mutations and treatment outcome in chronic lymphocytic leukemia: results from the CLL8 trial

Phylogenetic Analysis of Spliceosome SF3a2 in Different Plant Species

Structural basis for the interaction between the first SURP domain of the SF3A1 subunit in U2 snRNP and the human splicing factor SF1

Post-transcriptional spliceosomes are retained in nuclear speckles until splicing completion

Molecular basis for the activation of human spliceosome

Transcriptome and long noncoding RNA sequencing of three extracellular vesicle subtypes released from the human colon cancer LIM1863 cell line

Acetylation of PHF5A Modulates Stress Responses and Colorectal Carcinogenesis through Alternative Splicing-Mediated Upregulation of KDM3A

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

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