about
The iPlant Collaborative: Cyberinfrastructure for Plant BiologyComparative functional genomics of the fission yeastsThe B73 Maize Genome: Complexity, Diversity, and DynamicsArgonaute slicing is required for heterochromatic silencing and spreadingLeveraging the national cyberinfrastructure for biomedical researchRole of transposable elements in heterochromatin and epigenetic controlThe iPlant Collaborative: Cyberinfrastructure for Enabling Data to Discovery for the Life SciencesThaleMine: A Warehouse for Arabidopsis Data Integration and Discovery.The fission yeast Jmj2 reverses histone H3 Lysine 4 trimethylation.Epigenetic natural variation in Arabidopsis thalianaEpigenomic consequences of immortalized plant cell suspension culture.Mapping epigenetic mutations in fission yeast using whole-genome next-generation sequencing.Arabidopsis thaliana chromosome 4 replicates in two phases that correlate with chromatin state.Efficient parallel and out of core algorithms for constructing large bi-directed de Bruijn graphs.Sucrose-mediated transcriptional regulation of sucrose symporter activity in the phloemHeritable epigenetic variation among maize inbredsSpreading of heterochromatin is limited to specific families of maize retrotransposonsCENP-B preserves genome integrity at replication forks paused by retrotransposon LTR.Genomic distribution of H3K9me2 and DNA methylation in a maize genomeAraport: the Arabidopsis information portalFinding the right template: RNA Pol IV, a plant-specific RNA polymerase.The development of an Arabidopsis model system for genome-wide analysis of polyploidy effects.Replication, repair, and reactivation.RNA-directed DNA methylation enforces boundaries between heterochromatin and euchromatin in the maize genome.Epigenetic reprogramming and small RNA silencing of transposable elements in pollenComprehensive analysis of imprinted genes in maize reveals allelic variation for imprinting and limited conservation with other species.In vivo mapping of arabidopsis scaffold/matrix attachment regions reveals link to nucleosome-disfavoring poly(dA:dT) tracts.Repliscan: a tool for classifying replication timing regionsLid2 is required for coordinating H3K4 and H3K9 methylation of heterochromatin and euchromatin.Protein phosphorylation plays a key role in sucrose-mediated transcriptional regulation of a phloem-specific proton-sucrose symporter.Genomic Analysis of the DNA Replication Timing Program during Mitotic S Phase in Maize (Zea mays) Root Tips.Examining the Causes and Consequences of Context-Specific Differential DNA Methylation in Maize.The Next Generation of Training for Arabidopsis Researchers: Bioinformatics and Quantitative Biology.Genome-Wide Analysis of the Arabidopsis thaliana Replication Timing Program.Genetic perturbation of the maize methylome.Genome-wide transposon tagging reveals location-dependent effects on transcription and chromatin organization in Arabidopsis.It's a small RNA world, after all.MicroRNA-targeted and small interfering RNA-mediated mRNA degradation is regulated by argonaute, dicer, and RNA-dependent RNA polymerase in Arabidopsis.Parent-of-origin effects on gene expression and DNA methylation in the maize endospermVariation in DNA Methylation Patterns is More Common among Maize Inbreds than among Tissues
P50
Q21129222-94A6BA62-22A4-437C-87DB-32424D72F40DQ22065619-3B89C2AD-5E3B-4BDC-B3D9-CC6EB90D4885Q22065899-725A9947-DB45-475F-90FD-F7A9E84A8925Q28260028-4C915E75-0F2A-4E4E-9755-CB4DE2DED0C7Q28658731-B2B0EA38-0F66-4328-8CEC-13A66FCAE932Q29616253-8C8C3F39-5EA6-44A3-9690-9420F1F0EE7DQ31036204-32B23B9C-CA60-4019-8C1E-59207907E5CAQ31151193-255CF50B-38FF-42A2-9686-E9797F243E86Q33286778-CF608089-CA78-47BD-8C7C-487DCD95C03AQ33288249-1BF7B5A6-1635-4485-A947-71C4564BA030Q33391940-B762A8E6-A641-4EE3-9ED3-A33359E995A5Q33441157-939BA72C-8625-4ADE-BA5E-1C2D9A704253Q33604860-B68841EE-63C3-451D-870E-20F33E9025C3Q33747026-9D6EC870-5C56-4520-9B61-35F8857B7D0AQ34076261-213088B3-BE90-4A7F-A4E2-B8C98E6FABB7Q34085631-31887909-CE85-4C46-8FD1-8B9EC65F1FC9Q34524725-CB5B6DEE-5CBA-4CBF-8A4C-F9AD1F5CAEE4Q34674382-BF38D004-21CC-4D3E-9A08-6ED05034393FQ35224770-22FC3C2E-3BDD-4B99-8549-296FB2E61C82Q35254350-68DF05AD-C86E-438B-9055-E4E96CCF53B7Q36076278-77989450-D25D-4F3C-B5BE-8C010EF203DBQ36262557-53641BD9-C5F2-414F-8B78-CB11BCCE4B80Q36330813-8CFCDBE6-3892-4131-BF18-26A9A69AD83EQ36331974-EC702EF1-67EA-4AB5-A633-91E1A25F65E9Q37142129-D55AA6D8-9243-48B9-AD2F-3B06B909BFFBQ37353105-179390E8-0054-49B8-ABEA-EE866FDAC652Q38450777-6CCEB960-6E4F-4AC3-A115-F56FF8C02BC3Q38636606-D86718BA-12D4-4D67-A290-B371B2965B8CQ42145705-EA4A59C2-700A-4353-A942-F068C76BE4C2Q44603596-9402A964-4B5B-4212-8B87-48CF5D587658Q44874982-E212BF2A-ED53-41E5-B65D-611015047D9AQ46744224-F57C66F1-9E10-45A8-9D78-3C2B0F58A225Q46889477-3B4D9160-A27A-49C6-838C-9EE09E794739Q47208099-D673B868-92A2-47D2-A085-78F3C1732E40Q48242919-4582CE69-D00B-43E6-AB9C-25222F896F7EQ48882970-78C2FC54-1DC3-43A9-9B7A-9A3D03DF2054Q50756189-C52E9D57-7C18-4481-8F26-48823271826EQ52014040-BC03ABA8-E394-40CA-B26A-46D08D223EEFQ53486761-BA58376F-C258-413B-BCAD-FD7C6EB56AC5Q53486775-3D2C570E-EE50-45F7-8D27-54D2E6B6E505
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Matthew Vaughn
@ast
Matthew Vaughn
@en
Matthew Vaughn
@es
Matthew Vaughn
@fr
Matthew Vaughn
@nl
Matthew Vaughn
@sl
type
label
Matthew Vaughn
@ast
Matthew Vaughn
@en
Matthew Vaughn
@es
Matthew Vaughn
@fr
Matthew Vaughn
@nl
Matthew Vaughn
@sl
altLabel
Matt Vaughn
@en
prefLabel
Matthew Vaughn
@ast
Matthew Vaughn
@en
Matthew Vaughn
@es
Matthew Vaughn
@fr
Matthew Vaughn
@nl
Matthew Vaughn
@sl
P106
P1153
9737168200
P21
P2456
P31
P496
0000-0002-1384-4283