about
Fus3 controls Ty1 transpositional dormancy through the invasive growth MAPK pathway.Co-translational localization of an LTR-retrotransposon RNA to the endoplasmic reticulum nucleates virus-like particle assembly sitesA nucleosomal surface defines an integration hotspot for the Saccharomyces cerevisiae Ty1 retrotransposonRNA-RNA interactions and pre-mRNA mislocalization as drivers of group II intron loss from nuclear genomes.Inhibition of a yeast LTR retrotransposon by human APOBEC3 cytidine deaminasesNuclear expression of a group II intron is consistent with spliceosomal intron ancestry.5' to 3' mRNA decay factors colocalize with Ty1 gag and human APOBEC3G and promote Ty1 retrotransposition.The Sgs1 helicase of Saccharomyces cerevisiae inhibits retrotransposition of Ty1 multimeric arrays.Meeting report for mobile DNA 2010The intra-S phase checkpoint protein Tof1 collaborates with the helicase Rrm3 and the F-box protein Dia2 to maintain genome stability in Saccharomyces cerevisiae.Hos2 and Set3 promote integration of Ty1 retrotransposons at tRNA genes in Saccharomyces cerevisiaeActivation of a LTR-retrotransposon by telomere erosionThe Ty1 LTR-retrotransposon of budding yeast, Saccharomyces cerevisiaeThe outs and ins of transposition: from mu to kangaroo.Retrotransposition is associated with genome instability during chronological aging.Telomerase and retrotransposons: reverse transcriptases that shaped genomesThe beginning of the end: links between ancient retroelements and modern telomerases.Host factors that control long terminal repeat retrotransposons in Saccharomyces cerevisiae: implications for regulation of mammalian retrovirusesS-phase checkpoint pathways stimulate the mobility of the retrovirus-like transposon Ty1.Fate and structure of DNA microinjected into mouse TK-L cells.Global Epitranscriptomics Profiling of RNA Post-Transcriptional Modifications as an Effective Tool for Investigating the Epitranscriptomics of Stress Response.Incorporation of Y'-Ty1 cDNA destabilizes telomeres in Saccharomyces cerevisiae telomerase-negative mutants.Rrm3 protects the Saccharomyces cerevisiae genome from instability at nascent sites of retrotranspositionTy1 mobilizes subtelomeric Y' elements in telomerase-negative Saccharomyces cerevisiae survivors.Retrohoming: cDNA-mediated mobility of group II introns requires a catalytic RNA.Paralog-Specific Functions of RPL7A and RPL7B Mediated by Ribosomal Protein or snoRNA Dosage in Saccharomyces cerevisiaeHost co-factors of the retrovirus-like transposon Ty1.Saccharomyces cerevisiae ubiquitin-like protein Rub1 conjugates to cullin proteins Rtt101 and Cul3 in vivo.Evidence that Set1, a factor required for methylation of histone H3, regulates rDNA silencing in S. cerevisiae by a Sir2-independent mechanism.The Mediator co-activator complex regulates Ty1 retromobility by controlling the balance between Ty1i and Ty1 promoters.Ty RNA levels determine the spectrum of retrotransposition events that activate gene expression in Saccharomyces cerevisiaeBorder collies of the genome: domestication of an autonomous retrovirus-like transposon
P50
Q27932614-E24B9BA9-DA21-4C62-9F7B-5F10F0E549FEQ28658127-DA43ACD0-C5C2-48E0-A95E-72E9A1C85FBCQ28730814-A9278F50-7E81-4681-906B-CDABD26BDC17Q33606836-9AB89AB0-B284-447C-8300-CED68AEBD722Q33731838-39E56BDB-C9BD-4642-BBB4-54CC9F00197CQ33788514-EA84B95B-A839-4D16-BF79-5536EE54FBF1Q33826821-4674C3D2-D1C5-4645-97D3-72B7EA19BEBFQ33969162-CE76C807-3733-48FA-B902-5ABE8911C165Q34114031-EC6F9E26-E460-414F-8EB5-34238DCAB137Q34509237-74329F4B-7A5A-4B88-9B47-E40433478F90Q34588374-AA83D863-647A-42CA-ABC9-1BD30824E5FBQ34791258-37EE1601-87B0-4958-8F0D-D56FC6F12EE8Q35441519-93931736-50B3-43D9-A871-2D280BFE8C2EQ35610274-26AD6518-5283-4B1E-A880-E8BD78A1C287Q35650977-BD5E0784-31B4-484A-BC8B-69B2578B3B97Q35651418-65DD148B-F852-4490-B70F-3A2C5E04BD68Q35839467-E87C8AF1-0557-4839-BCE5-06C4F1112BEFQ35947037-63B1E03F-413D-45FF-A469-CAE9F9CF4998Q36316468-5861EC47-CC8D-4BFA-8C73-D1C8352A92CEQ36626335-75480C96-2D02-4D9D-9697-5ADB4ECED263Q36745168-38E39BCC-8789-48D6-AB83-FC660F7A5655Q36837155-E72EAC51-357A-4060-899B-B6A1AC6D610FQ37260580-0E6007C5-28F1-4C9A-8EFE-A905C1906FF9Q37598805-65357145-851F-45E0-86AD-1ADB9B5AACF5Q40939387-3E48F740-4678-4448-823E-3D09C311F2C5Q41818615-0C8CCA80-82BC-4CE5-B7F9-E33C33552B90Q42266942-CF88C418-342F-4B5A-BFC7-56EF9CFE0F14Q42609853-64EFA6BC-A9A9-47E6-88EF-6994D901B1F5Q43871051-5B49A1E4-CE1A-4DD8-838F-29B40E0445B8Q52376071-239D31A3-1074-4EF9-B805-30FEB8943A27Q68455726-B13399B5-D928-4B55-B596-05FB5B34A22AQ89183858-C6FF46F3-A562-49D3-874B-8BD740610C3E
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
M. Joan Curcio
@ast
M. Joan Curcio
@en
M. Joan Curcio
@es
M. Joan Curcio
@nl
M. Joan Curcio
@sl
type
label
M. Joan Curcio
@ast
M. Joan Curcio
@en
M. Joan Curcio
@es
M. Joan Curcio
@nl
M. Joan Curcio
@sl
prefLabel
M. Joan Curcio
@ast
M. Joan Curcio
@en
M. Joan Curcio
@es
M. Joan Curcio
@nl
M. Joan Curcio
@sl
P106
P1153
7006918101
P31
P496
0000-0001-5361-3909