about
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplexIdentification of a PRPF4 loss-of-function variant that abrogates U4/U6.U5 tri-snRNP integration and is associated with retinitis pigmentosaAn assembly chaperone collaborates with the SMN complex to generate spliceosomal SnRNPsThe La-related protein LARP7 is a component of the 7SK ribonucleoprotein and affects transcription of cellular and viral polymerase II genesToward an assembly line for U7 snRNPs: interactions of U7-specific Lsm proteins with PRMT5 and SMN complexesThe spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteinsThe SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesisUnique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processingSMNrp is an essential pre-mRNA splicing factor required for the formation of the mature spliceosome.Symmetrical dimethylation of arginine residues in spliceosomal Sm protein B/B' and the Sm-like protein LSm4, and their interaction with the SMN protein.Intronic miR-26b controls neuronal differentiation by repressing its host transcript, ctdsp2Translation and replication of hepatitis C virus genomic RNA depends on ancient cellular proteins that control mRNA fatesStructural basis for dimethylarginine recognition by the Tudor domains of human SMN and SPF30 proteinsThe structure of apo ArnA features an unexpected central binding pocket and provides an explanation for enzymatic cooperativityEvidence that fragile X mental retardation protein is a negative regulator of translationThe HIV-1 Rev activation domain is a nuclear export signal that accesses an export pathway used by specific cellular RNAsCharacterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteinsCo-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophyMethylation of Sm proteins by a complex containing PRMT5 and the putative U snRNP assembly factor pIClnUnrip, a factor implicated in cap-independent translation, associates with the cytosolic SMN complex and influences its intracellular localizationDrug-Encoded Biomarkers for Monitoring Biological TherapiesCharacterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)SMN-mediated assembly of RNPs: a complex storyBinding of the heterogeneous ribonucleoprotein K (hnRNP K) to the Epstein-Barr virus nuclear antigen 2 (EBNA2) enhances viral LMP2A expressionHIV-1 infection of non-dividing cells: evidence that the amino-terminal basic region of the viral matrix protein is important for Gag processing but not for post-entry nuclear import.Arginine methylation in subunits of mammalian pre-mRNA cleavage factor I.Gene targeting of Gemin2 in mice reveals a correlation between defects in the biogenesis of U snRNPs and motoneuron cell death.SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy.Mutant Prpf31 causes pre-mRNA splicing defects and rod photoreceptor cell degeneration in a zebrafish model for Retinitis pigmentosa.A role for the M9 transport signal of hnRNP A1 in mRNA nuclear export.Molding Photonic Boxes into Fluorescent Emitters by Direct Laser Writing.Accumulated common variants in the broader fragile X gene family modulate autistic phenotypesDiversity in the signals required for nuclear accumulation of U snRNPs and variety in the pathways of nuclear transportEvolution of an RNP assembly system: a minimal SMN complex facilitates formation of UsnRNPs in Drosophila melanogasterDeciphering the assembly pathway of Sm-class U snRNPs.The role of RNP biogenesis in spinal muscular atrophy.Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders.Biogenesis of spliceosomal small nuclear ribonucleoproteins.Assisted RNP assembly: SMN and PRMT5 complexes cooperate in the formation of spliceosomal UsnRNPs.Rev-mediated nuclear export of RNA is dominant over nuclear retention and is coupled to the Ran-GTPase cycle.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Utz Fischer
@ast
Utz Fischer
@en
Utz Fischer
@es
Utz Fischer
@nl
Utz Fischer
@sl
type
label
Utz Fischer
@ast
Utz Fischer
@en
Utz Fischer
@es
Utz Fischer
@nl
Utz Fischer
@sl
prefLabel
Utz Fischer
@ast
Utz Fischer
@en
Utz Fischer
@es
Utz Fischer
@nl
Utz Fischer
@sl
P214
P1053
A-4090-2016
P106
P214
P31
P3829
P496
0000-0002-1465-6591
P734
P7859
viaf-20743182