Gametophytic selection in Arabidopsis thaliana supports the selective model of intron length reduction.
about
Origin and evolution of spliceosomal intronsFrequency of intron loss correlates with processed pseudogene abundance: a novel strategy to test the reverse transcriptase model of intron lossEffect of the transposable element environment of human genes on gene length and expressionEvidence against the energetic cost hypothesis for the short introns in highly expressed genesIn plants, expression breadth and expression level distinctly and non-linearly correlate with gene structureEffect of 5'UTR introns on gene expression in Arabidopsis thaliana.Genomic selective constraints in murid noncoding DNARecent proliferation and translocation of pollen group 1 allergen genes in the maize genome.Insights into corn genes derived from large-scale cDNA sequencing.Intergenic and genic sequence lengths have opposite relationships with respect to gene expressionProperties of non-coding DNA and identification of putative cis-regulatory elements in Theileria parvaMutational biases and selective forces shaping the structure of Arabidopsis genes.A universal nonmonotonic relationship between gene compactness and expression levels in multicellular eukaryotes.Selection for the compactness of highly expressed genes in Gallus gallusRates of evolution in stress-related genes are associated with habitat preference in two Cardamine lineages.The small introns of antisense genes are better explained by selection for rapid transcription than by "genomic design"A simple model to explain evolutionary trends of eukaryotic gene architecture and expression: how competition between splicing and cleavage/polyadenylation factors may affect gene expression and splice-site recognition in eukaryotesDeep transcriptome sequencing provides new insights into the structural and functional organization of the wheat genome.On the path to genetic novelties: insights from programmed DNA elimination and RNA splicing.Lineage-specific sequence evolution and exon edge conservation partially explain the relationship between evolutionary rate and expression level in A. thalianaSegmental duplication, microinversion, and gene loss associated with a complex inversion breakpoint region in Drosophila.Evolution of the Exon-Intron Structure in Ciliate Genomes.The relation of codon bias to tissue-specific gene expression in Arabidopsis thaliana.The rise and falls of introns.Intron Length Coevolution across Mammalian GenomesHow many genes are needed to make a pollen tube? Lessons from transcriptomics.High rate of recent intron gain and loss in simultaneously duplicated Arabidopsis genes.Expression quantitative trait locus mapping across water availability environments reveals contrasting associations with genomic features in Arabidopsis.Gene expression: sizing it all up.Pollen-specific, but not sperm-specific, genes show stronger purifying selection and higher rates of positive selection than sporophytic genes in Capsella grandiflora.DNA methylation and small interference RNAs participate in the regulation of MADS-box genes involved in dormancy in sweet cherry (Prunus avium L.).
P2860
Q27498824-9DA2C7BF-F247-4204-A36E-E9F655DF2A7EQ28703895-05D74F3B-7489-4DFA-AA31-539137B52FE4Q28741429-D5121125-3EC8-44F3-AC76-749DFDC0A8F7Q28757923-B038D5FB-BA86-4855-976B-32058B5429D5Q30492350-A42FAD91-45EF-469E-828C-7557375C64A9Q33244118-D331DBCA-3538-4058-BBC1-5786926DE965Q33266436-3ADC62FE-4527-44B3-BAB1-B9F39FFBFCDBQ33269060-B7CB856C-194B-4200-A9BD-DD340CF16E20Q33378109-768B98B0-6654-4082-B35B-816DF2075CC4Q33383196-49900A06-C5C1-4E04-996E-15EBA116A631Q33389555-12D8891C-CA6D-4DF3-8BFF-5320850F9948Q33487174-1F203EEF-F0CE-4BE7-B543-9AE9B0959771Q33545200-DAF3F32C-05DC-466E-81E5-2F13F2BD1582Q33907203-391CBAFB-B185-4BF5-AA5F-2DFF4079740BQ34132422-4A427828-CDCE-43CA-BCEB-8F604A414B7BQ34587115-38F58968-8646-4E62-B653-F474F871956FQ34660002-1FF0E456-83CB-4D67-B3AF-E608DBAE21ACQ35164562-B12A142E-A78C-4D24-9275-CA8A0886CF71Q35682198-9D20BC83-FAA9-4709-9304-75761F74F197Q35781197-D208D327-FB9F-45AF-A276-76AC7E4A4D2BQ36032967-F2396C0C-3F86-4654-BB44-D8047F7A688FQ36125393-36BAD402-EFB6-426C-8E59-FC118DA4EF6BQ36268130-F7A4E2F8-E670-4E52-9135-771397C8993AQ36383352-FAF90EA5-1AA2-4D44-A1C0-8CA21DC69815Q37262015-3C800502-C2EE-4338-AF32-9691F602A0ECQ37380801-966F460C-F337-48A8-828E-D73B80FA4F9CQ38518422-A692B951-EAD1-42F1-85FB-BA89D9843D66Q39191485-3C931C7F-678A-4971-BC44-E10C46790892Q40739708-AD2EC590-8AA2-4AD3-ABF7-75FAE416F556Q45112863-D9508624-4B34-412F-8E86-B2993EF58F74Q53269555-12E83FDB-5126-4B13-9306-39371811FCBC
P2860
Gametophytic selection in Arabidopsis thaliana supports the selective model of intron length reduction.
description
2005 nî lūn-bûn
@nan
2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Gametophytic selection in Arab ...... del of intron length reduction
@nl
Gametophytic selection in Arab ...... el of intron length reduction.
@ast
Gametophytic selection in Arab ...... el of intron length reduction.
@en
type
label
Gametophytic selection in Arab ...... del of intron length reduction
@nl
Gametophytic selection in Arab ...... el of intron length reduction.
@ast
Gametophytic selection in Arab ...... el of intron length reduction.
@en
prefLabel
Gametophytic selection in Arab ...... del of intron length reduction
@nl
Gametophytic selection in Arab ...... el of intron length reduction.
@ast
Gametophytic selection in Arab ...... el of intron length reduction.
@en
P2860
P3181
P1433
P1476
Gametophytic selection in Arab ...... el of intron length reduction.
@en
P2093
Cathal Seoighe
Chris Gehring
P2860
P3181
P356
10.1371/JOURNAL.PGEN.0010013
P407
P577
2005-08-05T00:00:00Z