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RAD21
Insights Into Hp1a-Chromatin Interactions
Suppression of RAD21 Gene Expression Decreases Cell Growth and Enhances Cytotoxicity of Etoposide and Bleomycin in Human Breast Cancer Cells
The Mutational Landscape of Myeloid Leukaemia in Down Syndrome
RAD21 Gene RAD21 Cohesin Complex Component
Gene Regulation by Cohesin in Cancer: Is the Ring an Unexpected Party to Proliferation?
Cohesin Mutations in Cancer: Emerging Therapeutic Targets
Enhanced RAD21 Cohesin Expression Confers Poor Prognosis and Resistance to Chemotherapy in High Grade Luminal, Basal and HER2 Br
Redundant and Specific Roles of Cohesin STAG Subunits in Chromatin Looping and Transcriptional Control
Clinical Impact of Genomic Characterization of 15 Patients with Acute Megakaryoblastic Leukemia Related Malignancies
Suppressor Mutation Analysis Combined with 3D Modeling
Rad21 Haploinsufficiency Prevents ALT-Associated Phenotypes In
Identification and Molecular Characterization of the Mammalian Α-Kleisin RAD21L
A Novel RAD21 Mutation in a Boy with Mild Cornelia De Lange Presentation Further Delineation of the Phenotype
The Cohesin-Associated Protein Wapal Is Required for Proper Polycomb-Mediated Gene Silencing
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
Microrna-155-5P Plays a Critical Role in Transient Leukemia of Down Syndrome by Targeting Tumor Necrosis Factor Receptor Superfamily Members
Top View
Identification and Molecular Characterization of the Mammalian Α-Kleisin RAD21L
Mutations in SGOL1 Cause a Novel Cohesinopathy Affecting Heart And
A Novel RAD21 P.(Gln592del) Variant Expands the Clinical Description of Cornelia De Lange Syndrome Type 4
Leukaemia Section Review
Chromatin Landscapes and Genetic Risk in Systemic Lupus Joyce S
Delineation of Phenotypes and Genotypes Related to Cohesin Structural Protein RAD21
Mouse Tryptase Gene Expression Is Coordinately Regulated by GATA1 and GATA2 in Bone Marrow-Derived Mast Cells
Cohesin Mutations Are Synthetic Lethal with Stimulation of WNT Signaling
Down Syndrome-Like Acute Megakaryoblastic Leukemia in A
GATA-1-Dependent Histone H3k27ac Mediates Erythroid Cell-Specific Interaction Between CTCF Sites
The Cohesin-Associated Protein Wapal Is Required for Proper Polycomb-Mediated Gene Silencing
Clinical Impact of Genomic Characterization of 15 Patients with Acute Megakaryoblastic Leukemia– Related Malignancies
The Cohesin Complex and Its Roles in Chromosome Biology
Oncology Gene List
LDB1-Mediated Enhancer Looping Can Be Established Independent of Mediator and Cohesin Ivan Krivega and Ann Dean*
RAD21 Cohesin Overexpression Is a Prognostic and Predictive Marker Exacerbating Poor Prognosis in KRAS Mutant Colorectal Carcinomas
CTCF) and Cohesin in the SEE COMMENTARY Generation of Single-Cell Diversity of Protocadherin-Α Gene Expression
Sequence Conservation of the Rad21 Schizosaccharomyces Pombe DNA Double-Strand Break Repair Gene in Human and Mouse
RAD21 Overexpression Is Frequently Observed in BRCA-X Prostate Cancers
Overexpression of the Cohesin-Core Subunit SMC1A Contributes To
Separase Cleaves the Kinetochore Protein Meikin to Direct the Meiosis I/II Transition Nolan K Maier1,2, Jun Ma3, Michael a Lamps
Rad21 Is Involved in Corneal Stroma Development by Regulating Neural Crest Migration
PDS5A and PDS5B in Cohesin Function and Human Disease
Cornelia De Lange Syndrome
Synthetic Lethality Between the Cohesin Subunits STAG1 and STAG2 in Diverse Cancer Contexts
NIPBL SMC1A HDAC8 SMC3 RAD21 Heart 1,00 1,00 1,00 1,00 1
Disruption of NIPBL/Scc2 in Cornelia De Lange Syndrome Provokes
Shugoshin-2 Is Essential for the Completion of Meiosis but Not for Mitotic Cell Division in Mice
Rad21 (B-2): Sc-271601