Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation
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Title
Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation
Authors
Keywords
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Journal
JCI Insight
Volume 8, Issue 10, Pages -
Publisher
American Society for Clinical Investigation
Online
2023-04-14
DOI
10.1172/jci.insight.167744
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Note: Only part of the references are listed.- Clinical findings in 39 individuals with Bohring–Opitz syndrome from a global patient‐driven registry with implications for tumor surveillance and recurrence risk
- (2023) Bianca E. Russell et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes
- (2022) Zain Awamleh et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Vangl2 Promotes Hematopoietic Stem Cell Expansion
- (2022) Sarah Bouali et al. Frontiers in Cell and Developmental Biology
- Asxl1 C-terminal mutation perturbs neutrophil differentiation in zebrafish
- (2021) Xiao Fang et al. LEUKEMIA
- Vangl2 promotes the formation of long cytonemes to enable distant Wnt/β-catenin signaling
- (2021) Lucy Brunt et al. Nature Communications
- BAP1/ASXL complex modulation regulates epithelial-mesenchymal transition during trophoblast differentiation and invasion
- (2021) Vicente Perez-Garcia et al. eLife
- Wnt10b promotes hair follicles growth and dermal papilla cells proliferation via Wnt/β-Catenin signaling pathway in Rex rabbits
- (2020) Zhenyu Wu et al. BIOSCIENCE REPORTS
- Characterization of the plant homeodomain (PHD) reader family for their histone tail interactions
- (2020) Kanishk Jain et al. Epigenetics & Chromatin
- Regulation of Wnt Signaling through Ubiquitination and Deubiquitination in Cancers
- (2020) Hong-Beom Park et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- WNT Signaling in Melanoma
- (2020) Anna Gajos-Michniewicz et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking
- (2020) Ahmed A. Z. Dawoud et al. LEUKEMIA
- An Adversarial DNA N6-Methyladenine-Sensor Network Preserves Polycomb Silencing
- (2019) Soo-Mi Kweon et al. MOLECULAR CELL
- Pathological ASXL1 Mutations and Protein Variants Impair Neural Crest Development
- (2019) Friederike Matheus et al. Stem Cell Reports
- Improved CUT&RUN chromatin profiling tools
- (2019) Michael P Meers et al. eLife
- Expression of mutant Asxl1 perturbs hematopoiesis and promotes susceptibility to leukemic transformation
- (2018) Reina Nagase et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Targeted in situ genome-wide profiling with high efficiency for low cell numbers
- (2018) Peter J Skene et al. Nature Protocols
- Targeting Wnt/β-Catenin Signaling for Cancer Immunotherapy
- (2018) Bojun Wang et al. TRENDS IN PHARMACOLOGICAL SCIENCES
- Mutant ASXL1 cooperates with BAP1 to promote myeloid leukaemogenesis
- (2018) Shuhei Asada et al. Nature Communications
- Mtf2-PRC2 control of canonical Wnt signaling is required for definitive erythropoiesis
- (2018) Janet L. Manias Rothberg et al. Cell Discovery
- Aberrant histone modifications induced by mutant ASXL1 in myeloid neoplasms
- (2018) Shuhei Asada et al. INTERNATIONAL JOURNAL OF HEMATOLOGY
- ASXL2mutations are frequently found in pediatric AML patients with t(8;21)/RUNX1-RUNX1T1and associated with a better prognosis
- (2017) Genki Yamato et al. GENES CHROMOSOMES & CANCER
- An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues
- (2017) M Ryan Corces et al. NATURE METHODS
- Histone H2A Monoubiquitination in Neurodevelopmental Disorders
- (2017) Anshika Srivastava et al. TRENDS IN GENETICS
- Non-canonical WNT/PCP signalling in cancer: Fzd6 takes centre stage
- (2017) G Corda et al. Oncogenesis
- De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
- (2016) Vandana Shashi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- DNA methylation and chromatin accessibility profiling of mouse and human fetal germ cells
- (2016) Hongshan Guo et al. CELL RESEARCH
- Truncation mutants of ASXL1 observed in myeloid malignancies are expressed at detectable protein levels
- (2016) Daichi Inoue et al. EXPERIMENTAL HEMATOLOGY
- The microtubule-associated protein PRC1 promotes early recurrence of hepatocellular carcinoma in association with the Wnt/β-catenin signalling pathway
- (2016) Jianxiang Chen et al. GUT
- BAP1/ASXL1 recruitment and activation for H2A deubiquitination
- (2016) Danny D. Sahtoe et al. Nature Communications
- The Role of Additional Sex Combs-Like Proteins in Cancer
- (2016) Jean-Baptiste Micol et al. Cold Spring Harbor Perspectives in Medicine
- Clinical management of patients withASXL1mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance
- (2015) Bianca Russell et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Functional proteomics of the epigenetic regulators ASXL1, ASXL2 and ASXL3: a convergence of proteomics and epigenetics for translational medicine
- (2015) Masaru Katoh Expert Review of Proteomics
- De novodominantASXL3mutations alter H2A deubiquitination and transcription in Bainbridge–Ropers syndrome
- (2015) Anshika Srivastava et al. HUMAN MOLECULAR GENETICS
- The stability of epigenetic factor ASXL1 is regulated through ubiquitination and USP7-mediated deubiquitination
- (2015) D Inoue et al. LEUKEMIA
- Cancer-associated ASXL1 mutations may act as gain-of-function mutations of the ASXL1–BAP1 complex
- (2015) Anand Balasubramani et al. Nature Communications
- Planar polarization of Vangl2 in the vertebrate neural plate is controlled by Wnt and Myosin II signaling
- (2015) O. Ossipova et al. Biology Open
- Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays
- (2014) Martin J. Aryee et al. BIOINFORMATICS
- Additional sex combs-likefamily genes are required for normal cardiovascular development
- (2014) Andrea L. McGinley et al. GENESIS
- Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
- (2014) Giulio Genovese et al. NEW ENGLAND JOURNAL OF MEDICINE
- Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
- (2014) Siddhartha Jaiswal et al. NEW ENGLAND JOURNAL OF MEDICINE
- Frizzled3 is required for the development of multiple axon tracts in the mouse central nervous system
- (2014) Z. L. Hua et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The planar cell polarity protein Vangl2 bidirectionally regulates dendritic branching in cultured hippocampal neurons
- (2014) Akari Hagiwara et al. Molecular Brain
- Vangl2-Regulated Polarisation of Second Heart Field-Derived Cells Is Required for Outflow Tract Lengthening during Cardiac Development
- (2014) Simon A. Ramsbottom et al. PLoS Genetics
- Loss of Asxl1 leads to myelodysplastic syndrome-like disease in mice
- (2013) J. Wang et al. BLOOD
- Myelodysplastic syndromes are induced by histone methylation–altering ASXL1 mutations
- (2013) Daichi Inoue et al. JOURNAL OF CLINICAL INVESTIGATION
- Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
- (2013) Omar Abdel-Wahab et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Wnt Stabilization of -Catenin Reveals Principles for Morphogen Receptor-Scaffold Assemblies
- (2013) S.-E. Kim et al. SCIENCE
- Expanding our knowledge of conditions associated with the ASXL gene family
- (2013) Bianca Russell et al. Genome Medicine
- De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
- (2013) Matthew N Bainbridge et al. Genome Medicine
- Frizzled3 controls axonal development in distinct populations of cranial and spinal motor neurons
- (2013) Zhong L Hua et al. eLife
- Wnt signaling in bone formation and its therapeutic potential for bone diseases
- (2013) Jeong Hwan Kim et al. Therapeutic Advances in Musculoskeletal Disease
- ASXL1 Mutations Promote Myeloid Transformation through Loss of PRC2-Mediated Gene Repression
- (2012) Omar Abdel-Wahab et al. CANCER CELL
- The HARE-HTH and associated domains
- (2012) L. Aravind et al. CELL CYCLE
- Stimulation of Histone Deacetylase Activity by Metabolites of Intermediary Metabolism
- (2012) Maria Vogelauer et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases
- (2012) Véronique Gelsi-Boyer et al. Journal of Hematology & Oncology
- clusterProfiler: an R Package for Comparing Biological Themes Among Gene Clusters
- (2012) Guangchuang Yu et al. OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY
- Alternative Wnt Pathways and Receptors
- (2012) R. van Amerongen Cold Spring Harbor Perspectives in Biology
- Tcf7 Is an Important Regulator of the Switch of Self-Renewal and Differentiation in a Multipotential Hematopoietic Cell Line
- (2012) Jia Qian Wu et al. PLoS Genetics
- Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value
- (2011) M. Pratcorona et al. HAEMATOLOGICA
- De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome
- (2011) Alexander Hoischen et al. NATURE GENETICS
- An Updated Overview on Wnt Signaling Pathways
- (2010) Tata Purushothama Rao et al. CIRCULATION RESEARCH
- Canonical and noncanonical Wnts use a common mechanism to activate completely unrelated coreceptors
- (2010) L. Grumolato et al. GENES & DEVELOPMENT
- The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation
- (2010) Laura L. Yates et al. HUMAN MOLECULAR GENETICS
- Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell Identities
- (2010) Sven Heinz et al. MOLECULAR CELL
- GREAT improves functional interpretation of cis-regulatory regions
- (2010) Cory Y McLean et al. NATURE BIOTECHNOLOGY
- VANGL2Mutations in Human Cranial Neural-Tube Defects
- (2010) Yun-Ping Lei et al. NEW ENGLAND JOURNAL OF MEDICINE
- Ezh2, the histone methyltransferase of PRC2, regulates the balance between self-renewal and differentiation in the cerebral cortex
- (2010) J. D. Pereira et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Wnt7a Activates the Planar Cell Polarity Pathway to Drive the Symmetric Expansion of Satellite Stem Cells
- (2009) Fabien Le Grand et al. Cell Stem Cell
- Towards an integrated view of Wnt signaling in development
- (2009) R. van Amerongen et al. DEVELOPMENT
- Additional sex combs-like 1 belongs to the enhancer of trithorax and polycomb group and genetically interacts with Cbx2 in mice
- (2009) C.L. Fisher et al. DEVELOPMENTAL BIOLOGY
- Proximal events in Wnt signal transduction
- (2009) Stephane Angers et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- GSK3: a multifaceted kinase in Wnt signaling
- (2009) Dianqing Wu et al. TRENDS IN BIOCHEMICAL SCIENCES
- A comprehensive functional analysis of tissue specificity of human gene expression
- (2008) Zoltan Dezso et al. BMC BIOLOGY
- Canonical Wnt pathway signaling suppresses VCAM-1 expression by marrow stromal and hematopoietic cells
- (2008) Sachin Malhotra et al. EXPERIMENTAL HEMATOLOGY
- Alternative Wnt Signaling Is Initiated by Distinct Receptors
- (2008) R. van Amerongen et al. Science Signaling
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