about
Two fundamentally distinct PCNA interaction peptides contribute to chromatin assembly factor 1 functionFission yeast Scm3: A CENP-A receptor required for integrity of subkinetochore chromatinInteraction between a geminivirus replication protein and the plant sumoylation systemPlasticity of fission yeast CENP-A chromatin driven by relative levels of histone H3 and H4.Identification of noncoding transcripts from within CENP-A chromatin at fission yeast centromeres.Factors that promote H3 chromatin integrity during transcription prevent promiscuous deposition of CENP-A(Cnp1) in fission yeastTelomeric repeats facilitate CENP-A(Cnp1) incorporation via telomere binding proteins.Tomato yellow leaf curl Sardinia virus rep-derived resistance to homologous and heterologous geminiviruses occurs by different mechanisms and is overcome if virus-mediated transgene silencing is activatedA versatile transreplication-based system to identify cellular proteins involved in geminivirus replicationMpg2 interacts and cooperates with Mpg1 to maintain yeast glycosylation.Geminivirus Rep protein interferes with the plant DNA methylation machinery and suppresses transcriptional gene silencing.Dual interaction of plant PCNA with geminivirus replication accessory protein (Ren) and viral replication protein (Rep)Correction: Telomeric Repeats Facilitate CENP-ACnp1Incorporation via Telomere Binding ProteinsThe Arabidopsis tetratricopeptide thioredoxin-like gene family is required for osmotic stress tolerance and male sporogenesisIdentification of Plant Genes Involved in TYLCV ReplicationThe C4 protein from the geminivirus Tomato yellow leaf curl virus confers drought tolerance in Arabidopsis through an ABA-independent mechanismTTL Proteins Scaffold Brassinosteroid Signaling Components at the Plasma Membrane to Optimize Signal Transduction in Arabidopsis
P50
Q24647319-462E6E08-1885-4B3A-A7BD-B14C4C4A92FBQ28752491-C5E76205-5DCF-4D14-BB06-D600E45F11A2Q30751819-E6876FCB-A902-4800-91AF-7D7E3C85D16FQ33293168-032919B1-D05C-46DA-BCC7-02D8F5563B12Q34181375-2E9FD42E-49A3-4154-930D-5A2FA9F688F1Q34303245-F6C3DBC3-A754-4CC6-B9A4-1E1B3824734EQ34920830-F6748632-CD30-4959-B703-A97C73CCFCB3Q39756743-F4C7A551-71EE-458A-9625-794F09F049FFQ42257190-9BE48060-8F73-446D-95B5-EC1DF86837D6Q43991864-3A8901D9-13DA-4E8A-8E74-74BF8D128E64Q51044706-F54244B3-A84B-4D9F-8BEE-499F434FAE96Q58195832-D62F2442-015E-4FB7-BE2F-EFC3686EAC59Q59418358-FD37BE25-2C85-4C0A-A18A-4A552323E079Q59418370-F290DDA1-3420-496E-AB84-7DBCF8A3CF63Q59418377-9EA687D8-4330-4AEB-89DA-B2821CECC703Q90867060-80428664-BF67-46CB-ACE0-C6BD65451A30Q92689930-0E3C56A1-EF46-4B79-99EB-52B728D651F5
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Araceli G Castillo
@es
Araceli G. Castillo
@en
Araceli G. Castillo
@nl
type
label
Araceli G Castillo
@es
Araceli G. Castillo
@en
Araceli G. Castillo
@nl
prefLabel
Araceli G Castillo
@es
Araceli G. Castillo
@en
Araceli G. Castillo
@nl
P1053
C-5158-2013
P106
P1153
36753133900
P21
P31
P3829
P496
0000-0003-3990-5475
P569
2000-01-01T00:00:00Z