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Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.
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- EMBO Molecular Medicine, 2015, v. 7, n. 12, p. 1565, doi. 10.15252/emmm.201505696
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- Article
Assisted RNP assembly: SMN and PRMT5 complexes cooperate in the formation of spliceosomal UsnRNPs.
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- EMBO Journal, 2002, v. 21, n. 21, p. 5853, doi. 10.1093/emboj/cdf585
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- Article
SMNrp is an essential pre-mRNA splicing factor required for the formation of the mature spliceosome.
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- EMBO Journal, 2001, v. 20, n. 9, p. 2304, doi. 10.1093/emboj/20.9.2304
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- Article
HIV-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.
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- EMBO Journal, 1997, v. 16, n. 15, p. 4531, doi. 10.1093/emboj/16.15.4531
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- Article
Structure and flexibility of the DNA polymerase holoenzyme of vaccinia virus.
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- PLoS Pathogens, 2024, v. 20, n. 5, p. 1, doi. 10.1371/journal.ppat.1011652
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- Article
A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing.
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- PLoS Genetics, 2019, v. 15, n. 10, p. 1, doi. 10.1371/journal.pgen.1008460
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- Article
The La-related protein LARP7 is a component of the 7SK ribonucleoprotein and affects transcription of cellular and viral polymerase II genes.
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- EMBO Reports, 2008, v. 9, n. 6, p. 569, doi. 10.1038/embor.2008.72
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- Article
Phosphorylation regulates the activity of the SMN complex during assembly of spliceosomal U snRNPs.
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- EMBO Reports, 2005, v. 6, n. 1, p. 70, doi. 10.1038/sj.embor.7400301
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- Article
ProteoPlex: stability optimization of macromolecular complexes by sparse-matrix screening of chemical space.
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- Nature Methods, 2015, v. 12, n. 9, p. 859, doi. 10.1038/nmeth.3493
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- Article
Structural basis for dimethylarginine recognition by the Tudor domains of human SMN and SPF30 proteins.
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- Nature Structural & Molecular Biology, 2011, v. 18, n. 12, p. 1414, doi. 10.1038/nsmb.2185
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- Article
The SMN complex drives structural changes in human snRNAs to enable snRNP assembly.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-42324-0
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- Article
Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39787-6
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- Article
Biogenesis of spliceosomal small nuclear ribonucleoproteins.
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- Wiley Interdisciplinary Reviews: RNA, 2011, v. 2, n. 5, p. 718, doi. 10.1002/wrna.87
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- Article
Drug-Encoded Biomarkers for Monitoring Biological Therapies.
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- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0137573
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- Article
Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa.
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- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111754
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- Article
Binding of the Heterogeneous Ribonucleoprotein K (hnRNP K) to the Epstein- Barr Virus Nuclear Antigen 2 (EBNA2) Enhances Viral LMP2A Expression.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0042106
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- Article
Monoclonal antibody specific to a subclass of polyproline-arg motif provides evidence for the presence of an snRNA-free spliceosomal Sm protein complex in vivo: Implications for molecular interactions involving proline-rich sequences of Sm B/B′ proteins
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- Journal of Cellular Biochemistry, 1999, v. 74, n. 2, p. 168, doi. 10.1002/(SICI)1097-4644(19990801)74:2<168::AID-JCB3>3.0.CO;2-J
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- Article
hnRNP R negatively regulates transcription by modulating the association of P‐TEFb with 7SK and BRD4.
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- EMBO Reports, 2022, v. 23, n. 9, p. 1, doi. 10.15252/embr.202255432
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- Article
Crystal Structure of a Variant PAM2 Motif of LARP4B Bound to the MLLE Domain of PABPC1.
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- Biomolecules (2218-273X), 2020, v. 10, n. 6, p. 872, doi. 10.3390/biom10060872
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- Article
Water channels in the plant plasma membrane cloned by immunoselection from a mammalian expression system.
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- Plant Journal, 1994, v. 6, n. 2, p. 187, doi. 10.1046/j.1365-313X.1994.6020187.x
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- Article
Reconstitution of the human U sn RNP assembly machinery reveals stepwise Sm protein organization.
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- EMBO Journal, 2015, v. 34, n. 14, p. 1925, doi. 10.15252/embj.201490350
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- Article
Dirac Cones and Room Temperature Polariton Lasing Evidenced in an Organic Honeycomb Lattice.
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- Advanced Science, 2024, v. 11, n. 21, p. 1, doi. 10.1002/advs.202400672
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- Article
A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs.
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- Nature Cell Biology, 2001, v. 3, n. 11, p. 945, doi. 10.1038/ncb1101-945
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- Article
Rev-mediated nuclear export of RNA is dominant over nuclear retention and is coupled to the Ran–GTPase cycle.
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- Nucleic Acids Research, 1999, v. 27, n. 21, p. 4128, doi. 10.1093/nar/27.21.4128
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- Article
The Vaccinia Virus DNA Helicase Structure from Combined Single-Particle Cryo-Electron Microscopy and AlphaFold2 Prediction.
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- Viruses (1999-4915), 2022, v. 14, n. 10, p. N.PAG, doi. 10.3390/v14102206
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- Article
Dephosphorylation of survival motor neurons (SMN) by PPM1G/PP2Cγ governs Cajal body localization and stability of the SMN complex.
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- Journal of Cell Biology, 2007, v. 179, n. 3, p. 451, doi. 10.1083/jcb.200704163
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- Article
Strong Coupling in Fully Tunable Microcavities Filled with Biologically Produced Fluorescent Proteins.
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- Advanced Optical Materials, 2017, v. 5, n. 1, p. n/a, doi. 10.1002/adom.201600659
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- Article
Fluorescent Proteins: Strong Coupling in Fully Tunable Microcavities Filled with Biologically Produced Fluorescent Proteins (Advanced Optical Materials 1/2017).
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- Advanced Optical Materials, 2017, v. 5, n. 1, p. n/a, doi. 10.1002/adom.201770007
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- Article
The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP.
- Published in:
- eLife, 2023, p. 1, doi. 10.7554/eLife.92409
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- Article
A novel zebrafish model for intermediate type spinal muscular atrophy demonstrates importance of Smn for maintenance of mature motor neurons.
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- Human Molecular Genetics, 2021, v. 30, n. 24, p. 2488, doi. 10.1093/hmg/ddab212
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- Article
A critical examination of the recently reported crystal structures of the human SMN protein.
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- Human Molecular Genetics, 2016, v. 25, n. 21, p. 4717, doi. 10.1093/hmg/ddw298
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- Article
SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy.
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- Human Molecular Genetics, 2014, v. 23, n. 7, p. 1754, doi. 10.1093/hmg/ddt567
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- Article
Molding Photonic Boxes into Fluorescent Emitters by Direct Laser Writing.
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- Advanced Materials, 2017, v. 29, n. 16, p. n/a, doi. 10.1002/adma.201605236
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- Article
Identification and structural analysis of the Schizosaccharomyces pombe SMN complex.
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- Nucleic Acids Research, 2021, v. 49, n. 13, p. 7207, doi. 10.1093/nar/gkab158
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- Article
mRNA metabolism and neuronal disease.
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- FEBS Letters, 2015, v. 589, n. 14, p. 1598, doi. 10.1016/j.febslet.2015.04.052
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- Article
Deciphering the assembly pathway of Sm-class U snRNPs
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- FEBS Letters, 2008, v. 582, n. 14, p. 1997, doi. 10.1016/j.febslet.2008.03.009
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- Article
SMN Tudor domain structure and its interaction with the Sm proteins.
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- Nature Structural Biology, 2001, v. 8, n. 1, p. 27
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- Article
Systemic splicing factor deficiency causes tissue-specific defects: a zebrafish model for retinitis pigmentosa†.
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- Human Molecular Genetics, 2011, v. 20, n. 2, p. 368, doi. 10.1093/hmg/ddq473
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- Article
IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1).
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- Human Molecular Genetics, 2009, v. 18, n. 7, p. 1288, doi. 10.1093/hmg/ddp028
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- Article
Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP.
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- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3236, doi. 10.1093/hmg/ddn219
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- Article
Unrip, a factor implicated in cap-independent translation, associates with the cytosolic SMN complex and influences its intracellular localization.
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- Human Molecular Genetics, 2005, v. 14, n. 20, p. 3099, doi. 10.1093/hmg/ddi343
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- Article
Characterization 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).
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- Human Molecular Genetics, 2004, v. 13, n. 18, p. 2031, doi. 10.1093/hmg/ddh222
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- Article
Evidence that fragile X mental retardation protein is a negative regulator of translation.
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- Human Molecular Genetics, 2001, v. 10, n. 4, p. 329, doi. 10.1093/hmg/10.4.329
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- Article
Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 13, p. 2351, doi. 10.1093/hmg/8.13.2351
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- Article
Interaction of 7SK with the Smn complex modulates snRNP production.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21529-1
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- Article