USB1 is a miRNA deadenylase that regulates hematopoietic development
Published 2023 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
USB1 is a miRNA deadenylase that regulates hematopoietic development
Authors
Keywords
-
Journal
SCIENCE
Volume 379, Issue 6635, Pages 901-907
Publisher
American Association for the Advancement of Science (AAAS)
Online
2023-03-03
DOI
10.1126/science.abj8379
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Tailer: A Pipeline for Sequencing-Based Analysis of Non-Polyadenylated RNA 3’ End Processing
- (2022) Tim Nicholson-Shaw et al. RNA
- Chemical inhibition of PAPD5/7 rescues telomerase function and hematopoiesis in dyskeratosis congenita
- (2020) Siddharth Shukla et al. Blood Advances
- Neutrophils Derived from Genetically Modified Human Induced Pluripotent Stem Cells Circulate and Phagocytose Bacteria In Vivo
- (2019) Lisa R. Trump et al. Stem Cells Translational Medicine
- The RNase PARN Controls the Levels of Specific miRNAs that Contribute to p53 Regulation
- (2019) Siddharth Shukla et al. MOLECULAR CELL
- Posttranscriptional modulation of TERC by PAPD5 inhibition rescues hematopoietic development in dyskeratosis congenita
- (2019) Wilson Chun Fok et al. BLOOD
- MIENTURNET: an interactive web tool for microRNA-target enrichment and network-based analysis
- (2019) Valerio Licursi et al. BMC BIOINFORMATICS
- Structural and mechanistic basis for preferential deadenylation of U6 snRNA by Usb1
- (2018) Yuichiro Nomura et al. NUCLEIC ACIDS RESEARCH
- PAPD5/7 are novel host factors that are required for Hepatitis B virus RNA stabilization
- (2018) Henrik Mueller et al. HEPATOLOGY
- Salmon provides fast and bias-aware quantification of transcript expression
- (2017) Rob Patro et al. NATURE METHODS
- Usb1 controls U6 snRNP assembly through evolutionarily divergent cyclic phosphodiesterase activities
- (2017) Allison L. Didychuk et al. Nature Communications
- p53 Mediates Failure of Human Definitive Hematopoiesis in Dyskeratosis Congenita
- (2017) Wilson Chun Fok et al. Stem Cell Reports
- Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis
- (2016) A. J. Walne et al. HAEMATOLOGICA
- Directed differentiation of definitive hemogenic endothelium and hematopoietic progenitors from human pluripotent stem cells
- (2016) Andrea Ditadi et al. METHODS
- A new view of transcriptome complexity and regulation through the lens of local splicing variations
- (2016) Jorge Vaquero-Garcia et al. eLife
- Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis
- (2016) A. J. Walne et al. HAEMATOLOGICA
- Human Mpn1 promotes post-transcriptional processing and stability of U6atac
- (2015) Vadim Shchepachev et al. FEBS LETTERS
- A zebrafish model of Poikiloderma with Neutropenia recapitulates the human syndrome hallmarks and traces back neutropenia to the myeloid progenitor
- (2015) Elisa A. Colombo et al. Scientific Reports
- Trimmomatic: a flexible trimmer for Illumina sequence data
- (2014) Anthony M. Bolger et al. BIOINFORMATICS
- Wnt signaling controls the specification of definitive and primitive hematopoiesis from human pluripotent stem cells
- (2014) Christopher M Sturgeon et al. NATURE BIOTECHNOLOGY
- 3′ terminal diversity of MRP RNA and other human noncoding RNAs revealed by deep sequencing
- (2013) Katherine C Goldfarb et al. BMC MOLECULAR BIOLOGY
- STAR: ultrafast universal RNA-seq aligner
- (2012) Alexander Dobin et al. BIOINFORMATICS
- Aberrant 3' oligoadenylation of spliceosomal U6 small nuclear RNA in poikiloderma with neutropenia
- (2012) C. Hilcenko et al. BLOOD
- Dicer1 deletion in myeloid-committed progenitors causes neutrophil dysplasia and blocks macrophage/dendritic cell development in mice
- (2012) M. F. Alemdehy et al. BLOOD
- C16orf57, a gene mutated in poikiloderma with neutropenia, encodes a putative phosphodiesterase responsible for the U6 snRNA 3' end modification
- (2012) S. Mroczek et al. GENES & DEVELOPMENT
- Fast gapped-read alignment with Bowtie 2
- (2012) Ben Langmead et al. NATURE METHODS
- Mpn1, Mutated in Poikiloderma with Neutropenia Protein 1, Is a Conserved 3′-to-5′ RNA Exonuclease Processing U6 Small Nuclear RNA
- (2012) Vadim Shchepachev et al. Cell Reports
- Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia
- (2010) Akio Tanaka et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: Delineation of the phenotype
- (2010) D. Concolino et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome
- (2010) Amanda J. Walne et al. HUMAN MOLECULAR GENETICS
- MicroRNA miR-125a controls hematopoietic stem cell number
- (2010) S. Guo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene
- (2009) Ludovica Volpi et al. AMERICAN JOURNAL OF HUMAN GENETICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now