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STAG2
Mutational Inactivation of STAG2 Causes Aneuploidy in Human Cancer
The Mutational Landscape of Myeloid Leukaemia in Down Syndrome
Redundant and Specific Roles of Cohesin STAG Subunits in Chromatin Looping and Transcriptional Control
A Requirement for STAG2 in Replication Fork Progression Creates a Targetable Synthetic Lethality in Cohesin-Mutant Cancers
Loss of Cohesin Complex Components STAG2 Or STAG3 Confers Resistance to BRAF Inhibition in Melanoma
Low Tolerance for Transcriptional Variation at Cohesin Genes Is Accompanied by Functional Links to Disease-Relevant Pathways
Glioblastoma Cells Containing Mutations in the Cohesin Component STAG2 Are Sensitive to PARP Inhibition
Nonsense Variants of STAG2 Result in Distinct Congenital Anomalies
Redundant and Specific Roles of Cohesin STAG Subunits in Chromatin Looping and Transcriptional Control
Glioblastoma Cells Containing Mutations in the Cohesin Component STAG2 Are Sensitive to PARP Inhibition
Identification and Molecular Characterization of the Mammalian Α-Kleisin RAD21L
Loss of Stag2 Cooperates with EWS-FLI1 to Transform Murine Mesenchymal Stem Cells Marc El Beaino1†, Jiayong Liu2†, Amanda R
Cohesin Components Stag1 and Stag2 Differentially Influence Haematopoietic Mesoderm Development in Zebrafish Embryos
Low Tolerance for Transcriptional Variation at Cohesin Genes Is
Transposon Mutagenesis Identifies Genetic Drivers of Brafv600e Melanoma
Cohesin Mutations Alter DNA Damage Repair and Chromatin Structure and Create Therapeutic Vulnerabilities in MDS/AML
ARID1A Promotes Genomic Stability Through Protecting Telomere Cohesion
The Cohesin-Associated Protein Wapal Is Required for Proper Polycomb-Mediated Gene Silencing
Top View
SUPPLEMENTAL METHODS, FIGURES and TABLES Cohesin Mutations Alter DNA Damage Repair and Chromatin Structure and Create Therapeuti
Prioritization of Putatively Detrimental Variants in Euploid Miscarriages
Transient Abnormal Myelopoiesis and AML in Down Syndrome: an Update
Cohesin Mutations Alter DNA Damage Repair and Chromatin Structure and Create Therapeutic Vulnerabilities in MDS/AML
Cohesin Mutations Are Synthetic Lethal with Stimulation of WNT Signaling 2 3 4 Chue Vin Chin1,2, Jisha Antony1,2, Sarada Ketharnathan1, Gregory Gimenez1, Kate M
Identification and Molecular Characterization of the Mammalian Α-Kleisin RAD21L
Meiosis Made Simple: Mechanisms of Meiotic Chromosome Dynamics Elucidated in Somatic Cells
Combined Cohesin–RUNX1 Deficiency Synergistically Perturbs Chromatin Looping and Causes Myelodysplastic Syndromes
Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8 and RAD21L
Leukaemia Section Review
Chronic Loss of Stag2 Leads to Altered Chromatin Structure
Deep Phylogeny of Cancer Drivers and Compensatory Mutations ✉ Nash D
Loss of STAG2 Causes Aneuploidy in Normal Human Bladder Cells
STAG2 Cohesin Is Essential for Heart Morphogenesis
Transcriptional Regulation of RUNX1: an Informatics Analysis
Genetic Interactions Between the Meiosis-Specific Cohesin
Cohesin Mutations Are Synthetic Lethal with Stimulation of WNT Signaling
The Cohesin-Associated Protein Wapal Is Required for Proper Polycomb-Mediated Gene Silencing