about
Selective Methylation of Histone H3 Variant H3.1 Regulates Heterochromatin ReplicationMolecular basis for the methylation specificity of ATXR5 for histone H3.Arabidopsis homologs of retinoblastoma-associated protein 46/48 associate with a histone deacetylase to act redundantly in chromatin silencing.Regulation of heterochromatic DNA replication by histone H3 lysine 27 methyltransferases.Contributions of flowering time genes to sunflower domestication and improvementConnecting the sun to flowering in sunflower adaptation.Histone methyltransferases regulating rRNA gene dose and dosage control in Arabidopsis.MORC family ATPases required for heterochromatin condensation and gene silencing.Identification of Multiple Proteins Coupling Transcriptional Gene Silencing to Genome Stability in Arabidopsis thaliana.Complete Transcriptome RNA-Seq.FRIGIDA-related genes are required for the winter-annual habit in ArabidopsisTranscriptional activities of the Pax6 gene eyeless regulate tissue specificity of ectopic eye formation in Drosophila.ATXR5 and ATXR6 are H3K27 monomethyltransferases required for chromatin structure and gene silencing.Large-scale heterochromatin remodeling linked to overreplication-associated DNA damage.Open and closed: the roles of linker histones in plants and animals.Accessing the Inaccessible: The Organization, Transcription, Replication, and Repair of Heterochromatin in Plants.Peering through the pore: The role of AtTPR in nuclear transport and development.FLOWERING LOCUS C EXPRESSOR family proteins regulate FLOWERING LOCUS C expression in both winter-annual and rapid-cycling Arabidopsis.Isolation of LUMINIDEPENDENS: a gene involved in the control of flowering time in Arabidopsis.SUPPRESSOR OF FRI 4 encodes a nuclear-localized protein that is required for delayed flowering in winter-annual Arabidopsis.Pleiotropy of FRIGIDA enhances the potential for multivariate adaptation.Hypomorphic alleles reveal FCA-independent roles for FY in the regulation of FLOWERING LOCUS C.The nuclear pore protein AtTPR is required for RNA homeostasis, flowering time, and auxin signaling.HUA2 is required for the expression of floral repressors in Arabidopsis thaliana.Genetic interactions between FLM and other flowering-time genes in Arabidopsis thaliana.Does CONSTANS act as a transcription factor or as a co-activator? The answer may be - yesNatural allelic variation identifies new genes in the Arabidopsis circadian systemAGL24acts as a promoter of flowering inArabidopsisand is positively regulated by vernalizationRemoval of polysaccharides from plant DNA by ethanol precipitationThe gibberellic acid biosynthesis mutant ga1-3 of Arabidopsis thaliana is responsive to vernalizationLoss of FLOWERING LOCUS C activity eliminates the late-flowering phenotype of FRIGIDA and autonomous pathway mutations but not responsiveness to vernalizationA robust method for detecting single-nucleotide changes as polymorphic markers by PCRRegulation of flowering time by histone acetylation in ArabidopsisFunctional redundancy and new roles for genes of the autonomous floral-promotion pathwayThe timing of floweringBORDER proteins protect expression of neighboring genes by promoting 3' Pol II pausing in plants
P50
Q27682182-533E7A8F-BE30-4366-8F99-D9DB914C84C8Q33879023-99677C3B-DA83-483B-A95D-6D7980F9F171Q34079184-F3C3D7F6-AED2-4683-AA19-B5DA8587EF4CQ34242051-1CA9FADA-138A-49AF-BE2C-4630E01962C4Q34477609-9ED361C3-316B-46E9-A62E-F4CB195E2C02Q35194703-397DD226-639C-4265-851F-82E6ED1A4125Q35945072-8FBB4DF7-29C3-4A91-86B3-72F79D2F8875Q36035505-BA02A1CF-1048-4614-BDA8-FFDC9DB0AE71Q36038151-AC9F8F7B-F960-4713-8189-0F64201323B7Q36180848-72343C22-274B-4A5E-92EB-19EF14365429Q36855269-05423B97-80DE-4205-9178-22D2548C2047Q37366553-4022BAD4-BCBE-40F0-A69F-2D19A7B1A81DQ37368327-50BADB67-DD6D-4146-8DED-510C7343141CQ37589864-97E6EBAE-35CB-4A8A-B411-78EC67B87DC5Q37615684-5CDBB314-61CF-41A0-BDCB-3E2941FD3CA8Q38657331-DDC10EAA-C23E-4101-96BF-8DEB9E68ACB6Q42124622-6FFA7843-5636-4B53-A62B-A76AB4D873CFQ47899270-9C081A63-D2BB-404A-80AF-0B4F956859C0Q48086662-86418A2D-D279-43AD-ADA2-71BB0101A4F6Q50791931-6152EC4F-DB33-4BB3-8D55-D096E06AFC8BQ50970427-60916582-9049-4163-9D07-65626E02D5CFQ51156963-CA0BBDF9-8B5F-4441-91A9-09C2ED71E421Q51984637-981F99A5-F49E-4B86-88A4-86B09EDEA485Q52059857-55F7E4EB-85E9-431E-8350-11E0AF0A8A67Q52099118-275F5B66-823F-41E0-9350-F44A2486A383Q55016979-79AB7D77-081A-468F-82E2-711885B81597Q59303599-80521A74-BFAE-4105-ABA2-CE53583368BEQ59654021-54AAC837-303D-4385-A8B9-8044CC960937Q72857870-3314D53C-53F5-4823-A88E-8DB32E7D1053Q73098949-BB9DAD15-2791-46B6-AA01-E542EDE0CA3EQ73703464-E6DBA1EA-B82E-4A7A-8A20-3761B0F1276CQ74652659-7D160DDB-F2CF-4830-81B4-9F15F437FA33Q79237658-89EEC112-B2B8-4430-AB8E-970A4F93662CQ81070404-5904C105-282F-4F25-BAFB-370BDC9EC1BCQ85156243-2B95BC5E-EB13-4ED2-9AE7-59BBF0242A53Q90287698-4ADD84EC-6FEC-4667-9C53-6C40C0094E91
P50
description
researcher
@en
wetenschapper
@nl
name
Michaels SD
@nl
Scott D. Michaels
@en
type
label
Michaels SD
@nl
Scott D. Michaels
@en
altLabel
Michaels SD
@en
prefLabel
Michaels SD
@nl
Scott D. Michaels
@en
P106
P31
P496
0000-0001-5248-3487