STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion
about
Dissociation of cohesin from chromosome arms and loss of arm cohesion during early mitosis depends on phosphorylation of SA2.Characterization of vertebrate cohesin complexes and their regulation in prophaseSTAG2 and Rad21 mammalian mitotic cohesins are implicated in meiosis.Novel meiosis-specific isoform of mammalian SMC1Identification and characterization of SA/Scc3p subunits in the Xenopus and human cohesin complexesThe cohesin complex: sequence homologies, interaction networks and shared motifsSequential loading of cohesin subunits during the first meiotic prophase of grasshoppersMeiotic cohesin REC8 marks the axial elements of rat synaptonemal complexes before cohesins SMC1beta and SMC3Wapl is an essential regulator of chromatin structure and chromosome segregationSTAG3-mediated stabilization of REC8 cohesin complexes promotes chromosome synapsis during meiosisEvolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23Mutant Cohesin in Premature Ovarian FailureA meiotic chromosomal core consisting of cohesin complex proteins recruits DNA recombination proteins and promotes synapsis in the absence of an axial element in mammalian meiotic cells.Loss of Centromere Cohesion in Aneuploid Human Oocytes Correlates with Decreased Kinetochore Localization of the Sac Proteins Bub1 and Bubr1Corona is required for higher-order assembly of transverse filaments into full-length synaptonemal complex in Drosophila oocytesMeiosis genes in Daphnia pulex and the role of parthenogenesis in genome evolution.Comparative expression profiling of testis-enriched genes regulated during the development of spermatogonial cells.Prevalence of scoliosis in Williams-Beuren syndrome patients treated at a regional reference center.A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer.Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesionTissue-specific disallowance of housekeeping genes: the other face of cell differentiation.Characterization of the interaction between the cohesin subunits Rad21 and SA1/2.Activation of meiosis-specific genes is associated with depolyploidization of human tumor cells following radiation-induced mitotic catastrophe.Gain of chromosome band 7q11 in papillary thyroid carcinomas of young patients is associated with exposure to low-dose irradiationTelomere attachment, meiotic chromosome condensation, pairing, and bouquet stage duration are modified in spermatocytes lacking axial elements.The roles of cohesins in mitosis, meiosis, and human health and disease.Nuclear localization of PRDM9 and its role in meiotic chromatin modifications and homologous synapsis.Caenorhabditis elegans EVL-14/PDS-5 and SCC-3 are essential for sister chromatid cohesion in meiosis and mitosis.Telomere-independent homologue pairing and checkpoint escape of accessory ring chromosomes in male mouse meiosis.A conserved E2F6-binding element in murine meiosis-specific gene promoters.Regulation of the meiotic prophase I to metaphase I transition in mouse spermatocytesBiochemical reconstitution of topological DNA binding by the cohesin ring.Deregulation of polycomb repressor complex 1 modifier AUTS2 in T-cell leukemia.High density of REC8 constrains sister chromatid axes and prevents illegitimate synaptonemal complex formationSororin loads to the synaptonemal complex central region independently of meiotic cohesin complexes.The meiosis-specific modification of mammalian telomeres.Age-Related Loss of Cohesion: Causes and Effects.Synthetic lethality between the cohesin subunits STAG1 and STAG2 in diverse cancer contexts.Meiotic telomere clustering requires actin for its formation and cohesin for its resolution.
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P2860
STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion
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STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
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STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
@en
STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
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STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
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STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
@ast
STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
@en
STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
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STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
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prefLabel
STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
@ast
STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
@en
STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
@en-gb
STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
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STAG3, a novel gene encoding a ...... liams-Beuren syndrome deletion
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P2093
C Martínez-A
J Del Mazo
J L Barbero
L A Pérez Jurado
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P3181
P407
P577
2000-03-01T00:00:00Z