about
Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatinDicentric chromosomes: unique models to study centromere function and inactivationHistone modifications within the human X centromere region.Telomere disruption results in non-random formation of de novo dicentric chromosomes involving acrocentric human chromosomes.Structural and functional dynamics of human centromeric chromatin.Centromeres of human chromosomes.Determining centromere identity: cyclical stories and forking paths.Neocentromeres: a place for everything and everything in its placeNucleolar organization, ribosomal DNA array stability, and acrocentric chromosome integrity are linked to telomere function.Human centromeric chromatin is a dynamic chromosomal domain that can spread over noncentromeric DNARegulation of mitotic chromosome cohesion by Haspin and Aurora B.Functional epialleles at an endogenous human centromere.Control of gene expression and assembly of chromosomal subdomains by chromatin regulators with antagonistic functions.Centromere identity in Drosophila is not determined in vivo by replication timing.Application of FISH to complex chromosomal rearrangements associated with chronic myelogenous leukemia.Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.Inheritance of the CENP-A chromatin domain is spatially and temporally constrained at human centromeresHuman gamma-satellite DNA maintains open chromatin structure and protects a transgene from epigenetic silencing.DNMT3B interacts with constitutive centromere protein CENP-C to modulate DNA methylation and the histone code at centromeric regions.Genomic variation within alpha satellite DNA influences centromere location on human chromosomes with metastable epialleles.The past, present, and future of human centromere genomics.Epigenomics of centromere assembly and function.Conserved organization of centromeric chromatin in flies and humans.α satellite DNA variation and function of the human centromere.Genomic size of CENP-A domain is proportional to total alpha satellite array size at human centromeres and expands in cancer cells.MYC activity mitigates response to rapamycin in prostate cancer through eukaryotic initiation factor 4E-binding protein 1-mediated inhibition of autophagy.Regulation of nuclear Prointerleukin-16 and p27(Kip1) in primary human T lymphocytes.RNA-dependent stabilization of SUV39H1 at constitutive heterochromatin.Histone H3K4 methylation keeps centromeres open for business.Expanded Satellite Repeats Amplify a Discrete CENP-A Nucleosome Assembly Site on Chromosomes that Drive in Female Meiosis.Human Centromeres Produce Chromosome-Specific and Array-Specific Alpha Satellite Transcripts that Are Complexed with CENP-A and CENP-C.Human centromere repositioning within euchromatin after partial chromosome deletion.Stable dicentric X chromosomes with two functional centromeres.Unusual chromosome architecture and behaviour at an HSRForeword: the centromere and kinetochore in creatures great and smallCentromeres Poised En Pointe: CDKs Put a Hold on CENP-A AssemblyhBub1 negatively regulates p53 mediated early cell death upon mitotic checkpoint activationCentromere round-up at the heterochromatin corralIdentification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeresAnalysis of centromeric activity in Robertsonian translocations: implications for a functional acrocentric hierarchy
P50
Q24537593-9D5AAC19-62C3-4425-B347-B0F613DB96D0Q26824800-7467E5B5-3868-4D89-A5EF-28000B2E370CQ33492759-C63E2E1A-AD8D-4C5B-A4C7-67E28C15D4C1Q33658678-A40B4F2C-7BF9-4C1E-BFE7-B25B26DF2C5AQ33996546-EE65C58B-3A16-4757-AAF0-9B5697BF8092Q34063608-55F2820D-E40E-4AB5-9403-1931A8FF8030Q34325316-7E837082-E4F7-4DFB-85F9-963D20EE52DDQ34392191-024D85AC-2C2B-48BC-9CEC-7DAD251D5ADAQ34411779-583447D3-BCEF-457D-A52A-FD13D4DF805BQ34573024-D9D2A512-505E-4772-A853-CD9A2F9B2CE3Q34579183-F8828038-AF03-4805-97F0-120635F57C3DQ36187287-379D18E1-7F16-4C1A-91FE-C230BC6F3079Q36192038-9CCB016E-FEF2-4965-BD7A-C6AA2AFF0D37Q36377636-083E1F7B-3C5B-4A7F-9162-570FA0CBBB67Q36693349-1CC00B4C-4805-4940-9387-917654F0DAC9Q36876661-F0A82A41-C7FC-4C7B-ADF9-030F051985E4Q36955138-B1E2BC32-2CBE-4FEC-BAB4-8AB40F019E62Q37150852-13BEAA7D-02A6-434F-868A-27B3547E9324Q37295052-7BCE6168-163A-4A0F-853B-E28082A02D90Q37313724-812F0212-9005-49A6-A168-362A2DBA5153Q37665277-936E5413-6806-45CA-9675-481EC760351EQ37776921-E8A5FCC2-3A92-40A7-997C-E5AEE19896EEQ38692366-91BC3F75-68FD-49D1-8D2D-772890A9C1E6Q38730809-A2B9019A-D560-4FC7-9154-4BA2317CA4ADQ39560198-D99069CB-688B-4954-BF09-E61854647EBBQ39796361-43241E67-BDE4-4465-9A9E-63BBB495E982Q40351078-E874EE01-ED5F-42A7-BC21-1907538D678BQ41201433-3937A588-0F09-4B30-9803-5B16A5E18253Q42578063-C8854B6C-638E-4CAC-B2BA-53BEFAA092ACQ47682737-021C391F-DE60-450A-AA40-F2DCCFD84BAEQ47978384-E37EFBFB-E1C7-4B8F-A846-D933B790A8D9Q50315563-6D547DE4-59BD-4212-A346-E5CCAAEABF58Q55068112-A67C8827-3F91-4588-85BB-C319F56C3948Q57185100-0A96A46A-C02A-49A8-B9D9-88FF941B0664Q59483278-E5B95F8D-6F72-4D36-9BF0-7B320B0611ADQ59483285-B7669850-21A0-495A-9F85-760A2B7C3C4DQ59483333-7F5F3916-7E8A-4931-B526-1D7EDFF2D9EBQ59483490-2BA741B8-1D36-438A-AA15-6B355878B7E8Q59483671-4B22FB14-4B3B-461E-806F-970F4E01502AQ59483680-C27B0896-90B6-4BB0-BBAB-E08230E52744
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Beth Sullivan
@ast
Beth Sullivan
@en
Beth Sullivan
@es
Beth Sullivan
@nl
Beth Sullivan
@sl
Бет О’Салливаны
@ru
type
label
Beth Sullivan
@ast
Beth Sullivan
@en
Beth Sullivan
@es
Beth Sullivan
@nl
Beth Sullivan
@sl
Бет О’Салливаны
@ru
prefLabel
Beth Sullivan
@ast
Beth Sullivan
@en
Beth Sullivan
@es
Beth Sullivan
@nl
Beth Sullivan
@sl
Бет О’Салливаны
@ru
P1053
Q-3456-2017
P106
P108
P1153
7201481607
P21
P31
P3829
P496
0000-0001-5216-4603