Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies - Test2 - elhamkhani - TriplyDB

Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Cohesin mutations in myeloid malignancies: underlying mechanisms Disorders of Transcriptional Regulation: An Emerging Category of Multiple Malformation Syndromes A neural crest origin for cohesinopathy heart defects Complex elaboration: making sense of meiotic cohesin dynamics Drosophila TDP-43 RNA-Binding Protein Facilitates Association of Sister Chromatid Cohesion Proteins with Genes, Enhancers and Polycomb Response Elements.Measuring Sister Chromatid Cohesion Protein Genome Occupancy in Drosophila melanogaster by ChIP-seq.Drosophila Nipped-B Mutants Model Cornelia de Lange Syndrome in Growth and Behavior.Double SMCHD1 variants in FSHD2: the synergistic effect of two SMCHD1 variants on D4Z4 hypomethylation and disease penetrance in FSHD2.The role of structural disorder in cell cycle regulation, related clinical proteomics, disease development and drug targeting.Crossed wires: 3D genome misfolding in human disease.How many roads lead to cohesinopathies?Emancipation from transcriptional latency: unphosphorylated STAT5 as guardian of hematopoietic differentiation.The cohesin complex prevents Myc-induced replication stress.The effect of Nipped-B-like (Nipbl) haploinsufficiency on genome-wide cohesin binding and target gene expression: modeling Cornelia de Lange syndrome.Zebrafish as a Model to Study Cohesin and Cohesinopathies.Cohesin facilitates zygotic genome activation in zebrafish.The Opposing Actions of Arabidopsis CHROMOSOME TRANSMISSION FIDELITY7 and WINGS APART-LIKE1 and 2 Differ in Mitotic and Meiotic Cells.DNA Topoisomerase II modulates acetyl-regulation of cohesin-mediated chromosome dynamics.Analysis of Cohesin Function in Gene Regulation and Chromatin Organization in Interphase.De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies.

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

http://www.wikidata.org/entity/Q26861558

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2014 թուականի Մարտին հրատարակուած գիտական յօդուած

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2014 թվականի մարտին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年论文

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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label

Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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prefLabel

Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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J.BBAGRM.2013.11.002

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Biochimica et Biophysica Acta

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Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies

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Alexander R. Ball

http://www.w3.org/2001/XMLSchema#string

Kyoko Yokomori

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Yen-Yun Chen

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The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2

Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene

Transcriptional dysregulation in NIPBL and cohesin mutant human cells

Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance

Characterization of vertebrate cohesin complexes and their regulation in prophase

A potential role for human cohesin in mitotic spindle aster assembly

SMC1 is a downstream effector in the ATM/NBS1 branch of the human S-phase checkpoint

NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

Human SMC5/6 complex promotes sister chromatid homologous recombination by recruiting the SMC1/3 cohesin complex to double-strand breaks

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10.1016/J.BBAGRM.2013.11.002

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3951616

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