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UnknownAssessing Pubertal Timing, Duration, and Related Characteristics in ASXL-Related Disorders: A Cross-Sectional Caregiver Survey Analysis.
Not available
S-EPMC12671694 | biostudies-literature
UnknownASXL gain-of-function truncation mutants: defective and dysregulated forms of a natural ribosomal frameshifting product?
Not available
S-EPMC5644247 | biostudies-literature
UnknownUnderstanding the phenotypic spectrum of ASXL-related disease: Ten cases and a review of the literature.
Not available
S-EPMC8842511 | biostudies-literature
UnknownDNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes.
Not available
S-EPMC9177544 | biostudies-literature
UnknownIdentification of differential microRNAs and messenger RNAs resulting from ASXL transcriptional regulator 3 knockdown during during heart development.
Not available
S-EPMC9161854 | biostudies-literature
UnknownIntegrative analysis of ASXL family genes reveals ASXL2 as an immunoregulatory molecule in head and neck squamous cell carcinoma.
Not available
S-EPMC11682168 | biostudies-literature
GenomicsBAP1/ASXL complex modulation regulates Epithelial-Mesenchymal Transition during trophoblast differentiation and invasion
BAP1/ASXL complex modulation regulates Epithelial-Mesenchymal Transition during trophoblast differentiation and invasion
PRJNA666166 | ENA
ProteomicsBAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation
In Drosophila, a complex consisting of Calypso and ASX catalyzes H2A deubiquitination and has been reported to act as part of the Polycomb machinery in transcriptional silencing. The mammalian homologs of these proteins (BAP1 and ASXL1/2/3, respectively), are frequently mutated in various cancer typ...
ORGANISM(S): Homo sapiens (Human) 
2019-01-28 | PXD011808 | Pride
Bap Asxl Prc1 
GenomicsGenome wide binding sites of BAP1, HCF1 and OGT
We report the genome wide binding sites of BAP1, HCF1 and OGT in bone marrow derived macrophages. De-ubiquitinating enzyme BAP1 is mutated in a hereditary cancer syndrome with increased risk of mesothelioma and uveal melanoma. Somatic BAP1 mutations occur in various malignancies. We show that mouse ...
ORGANISM(S): Mus musculus 
2012-11-07 | E-GEOD-40723 | biostudies-arrayexpress
ProteomicsPervasive Roles of Ubiquitination in Orchestrating the Deubiquitinase Activity and Function of the BAP1/ASXL2 Tumor Suppressor Complex
The tumor suppressor and deubiquitinase (DUB) BAP1 regulates chromatin-associated processes and is frequently mutated in various malignancies. BAP1 and its drosophila orthologue Calypso assemble DUB complexes with ASXL-1, -2, -3 paralogues and ASX respectively, and these cofactors are required for s...
ORGANISM(S): Homo sapiens (Human) 
2018-09-28 | PXD011124 | Pride
Histone h2ak119ub  deubiquitination Polycomb group proteins  bap1  calypso  asxl  cell proliferation 
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