about
Minor spliceosome components are predominantly localized in the nucleusIdentification of an evolutionarily divergent U11 small nuclear ribonucleoprotein particle in DrosophilaThe significant other: splicing by the minor spliceosomeMissing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epitheliaAn Ancient Mechanism for Splicing Control: U11 snRNP as an Activator of Alternative SplicingGene expression profiling of U12-type spliceosome mutant Drosophila reveals widespread changes in metabolic pathwaysGlobal analysis of the nuclear processing of transcripts with unspliced U12-type introns by the exosome.Transcriptome analysis reveals signature of adaptation to landscape fragmentationThe Glanville fritillary genome retains an ancient karyotype and reveals selective chromosomal fusions in LepidopteraBranchpoint selection in the splicing of U12-dependent introns in vitroSNP design from 454 sequencing of Podosphaera plantaginis transcriptome reveals a genetically diverse pathogen metapopulation with high levels of mixed-genotype infection.Identification and validation of human papillomavirus encoded microRNAsThe abundance of the spliceosomal snRNPs is not limiting the splicing of U12-type introns.Transcriptional co-activator protein p100 interacts with snRNP proteins and facilitates the assembly of the spliceosomeRegulation of gene expression through inefficient splicing of U12-type intronsAlternative exon definition events control the choice between nuclear retention and cytoplasmic export of U11/U12-65K mRNA.Daphnia magna transcriptome by RNA-Seq across 12 environmental stressors.Bacteriophage Mu integration in yeast and mammalian genomes.Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency.The U11-48K protein contacts the 5' splice site of U12-type introns and the U11-59K protein.Temperature treatments during larval development reveal extensive heritable and plastic variation in gene expression and life history traits.Evolutionarily conserved exon definition interactions with U11 snRNP mediate alternative splicing regulation on U11-48K and U11/U12-65K genes.Virus-encapsulated DNA origami nanostructures for cellular delivery.Flight-induced changes in gene expression in the Glanville fritillary butterfly.Genetics. Minor splicing, disrupted.Temperature- and sex-related effects of serine protease alleles on larval development in the Glanville fritillary butterfly.Functional genomics of life history variation in a butterfly metapopulation.Weight and nutrition affect pre-mRNA splicing of a muscle gene associated with performance, energetics and life history.Rapid transcriptome characterization for a nonmodel organism using 454 pyrosequencing.HnRNPH1/H2, U1 snRNP, and U11 snRNP cooperate to regulate the stability of the U11-48K pre-mRNA.Requirement of TFIIH kinase subunit Mat1 for RNA Pol II C-terminal domain Ser5 phosphorylation, transcription and mRNA turnoverTudor staphylococcal nuclease is an evolutionarily conserved component of the programmed cell death degradome.RNA structural requirements for stability and minus-strand synthesis in the dsRNA bacteriophage phi 6.Mutations in the U11/U12-65K protein associated with isolated growth hormone deficiency lead to structural destabilization and impaired binding of U12 snRNA.IntEREst: intron-exon retention estimator.Identification of the packaging regions within the genomic RNA segments of bacteriophage phi 6Dynamic exchanges of RNA interactions leading to catalytic core formation in the U12-dependent spliceosome
P50
Q24322622-3C954714-7252-426C-B69C-0A6AE2FE4E29Q28268106-EC1CAA98-2999-4892-AE73-EB4B2D0241CDQ28277280-C9633C6C-D3F7-42C5-833D-11A2663C5BE6Q28586598-702F9E9B-2463-4AC3-B0CF-214B81A77A55Q29031490-D23890EA-1E81-446C-A343-C976563B92FAQ33719236-4EFA22C8-5023-4F05-8A59-178D8ED7ECA0Q33791281-02DDC814-6970-4D4D-B41C-FBA84EA217ADQ33838013-4301B171-8585-4E70-AB18-246364463AE4Q34184923-F004F742-FB09-4402-B3E6-C49CCB30CD0FQ34364420-4BB2BC4A-E369-4178-871B-328987F48396Q34540774-B4BAE62C-97E0-45B9-9BB1-5C65D31365BDQ34922162-AC0AF346-40E7-40B1-96A5-98A3C9E6E968Q35057511-2C92FAAB-01CD-4292-96AA-06E39DA916F1Q35917031-3162D9F2-7EDD-42CB-8287-EAE5CFA755FDQ36191883-3F500450-FF52-4B1C-8409-C76345928EFAQ36382872-86E6C36B-74E8-40C6-9B2A-3B66A991455DQ36887343-9E4C72F7-0ED0-4FA5-A0F3-3872C31D5F02Q37014688-DA996D55-394C-41E4-A65A-5C29FE1C6813Q37644374-36AAD161-2140-4DAD-A9B3-804B1868E869Q38292661-A5EDF82F-5F0E-460E-93CF-8AB95CEF43FAQ38326768-CDCD4FA5-7661-4B57-B842-25294556B70EQ38826832-C0455639-ADCC-44BE-A704-505A92CE40A4Q39015663-CB182DB1-BBC2-44F0-BECE-6988C9F8B76FQ40582600-226B7E67-6087-4E0F-B16B-C6BCC3DA164FQ41935516-14B1012D-710C-4632-9BB1-8068A2579E73Q41996227-6C9F2EC1-BBD4-4B8E-81CE-EBBD787505DDQ42017903-CCA5BA47-1D51-4145-9512-BC990F757618Q42027284-6795B416-D161-4970-AF4B-AAD2484BF890Q42030448-AEDA417C-8322-4611-B110-69852260D775Q42146699-55FEFCD9-9AD9-4AC4-A330-4A1AB545F038Q42787982-AA3E20D1-51AF-47CB-9F1D-C3F7D9974F0FQ43263626-1F24B106-89FC-43B6-BB7C-153AE8DCC426Q44500300-32DFE6AB-9F4A-4E52-8A61-833223F4F923Q47279190-01826283-71B2-4940-883B-F43AC1650C7EQ55100251-665028A5-D09E-465F-AC8E-1CA3128CA65BQ72293986-34401FE7-C172-4D46-938C-51E7C0DF4757Q73427970-9FDDFAB6-F8FD-44C2-B6F9-FFF34EA28673
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mikko J Frilander
@ast
Mikko J Frilander
@en
Mikko J Frilander
@es
Mikko J Frilander
@nl
Mikko J Frilander
@sl
type
label
Mikko J Frilander
@ast
Mikko J Frilander
@en
Mikko J Frilander
@es
Mikko J Frilander
@nl
Mikko J Frilander
@sl
prefLabel
Mikko J Frilander
@ast
Mikko J Frilander
@en
Mikko J Frilander
@es
Mikko J Frilander
@nl
Mikko J Frilander
@sl
P1053
B-6660-2009
P106
P21
P31
P3829
P496
0000-0002-1732-4808
P569
2000-01-01T00:00:00Z