Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
about
The new anthelmintic tribendimidine is an L-type (levamisole and pyrantel) nicotinic acetylcholine receptor agonistA Conserved Nuclear Cyclophilin Is Required for Both RNA Polymerase II Elongation and Co-transcriptional Splicing in Caenorhabditis elegansRegulatory roles of RNA binding proteins in the nervous system of C. elegansMolecular cloning and functional expression of a Caenorhabditis elegans aminopeptidase structurally related to mammalian leukotriene A4 hydrolases.Mutational analysis of the Drosophila snake protease: an essential role for domains within the proenzyme polypeptide chain.Sequenced alleles of the Caenorhabditis elegans sex-determining gene her-1 include a novel class of conditional promoter mutations.Mutations in the unc-52 gene responsible for body wall muscle defects in adult Caenorhabditis elegans are located in alternatively spliced exonssli-1, a negative regulator of let-23-mediated signaling in C. elegansCharacterization of revertants of unc-93(e1500) in Caenorhabditis elegans induced by N-ethyl-N-nitrosourea.Nonsteroidal antiinflammatory drugs cause apoptosis and induce cyclooxygenases in chicken embryo fibroblastsC. elegans twist gene expression in differentiated cell types is controlled by autoregulation through intron elementsMolecular and genetic analyses of the Caenorhabditis elegans dpy-2 and dpy-10 collagen genes: a variety of molecular alterations affect organismal morphology.Systematic analyses of rpm-1 suppressors reveal roles for ESS-2 in mRNA splicing in Caenorhabditis elegans.Analysis of osm-6, a gene that affects sensory cilium structure and sensory neuron function in Caenorhabditis elegansStructural requirements for the tissue-specific and tissue-general functions of the Caenorhabditis elegans epidermal growth factor LIN-3.The allele-specific suppressor sup-39 alters use of cryptic splice sites in Caenorhabditis elegans.The Caenorhabditis elegans spe-39 gene is required for intracellular membrane reorganization during spermatogenesis.Analysis of conserved residues in the betapat-3 cytoplasmic tail reveals important functions of integrin in multiple tissues.Antagonism between G(o)alpha and G(q)alpha in Caenorhabditis elegans: the RGS protein EAT-16 is necessary for G(o)alpha signaling and regulates G(q)alpha activityComponents of the spindle assembly checkpoint regulate the anaphase-promoting complex during meiosis in Caenorhabditis elegans.Mutations in a C. elegans Gqalpha gene disrupt movement, egg laying, and viability.Coordinated tissue-specific regulation of adjacent alternative 3' splice sites in C. elegans.Caenorhabditis elegans UNC-98, a C2H2 Zn finger protein, is a novel partner of UNC-97/PINCH in muscle adhesion complexes.Splicing removes the Caenorhabditis elegans transposon Tc1 from most mutant pre-mRNAs.AU-rich intronic elements affect pre-mRNA 5' splice site selection in Drosophila melanogaster.Suppressors of the cdc-25.1(gf)-associated intestinal hyperplasia reveal important maternal roles for prp-8 and a subset of splicing factors in C. elegans.Exon ligation is proofread by the DExD/H-box ATPase Prp22p.Positive and negative tissue-specific signaling by a nematode epidermal growth factor receptor.Mutations in the alpha 2(IV) basement membrane collagen gene of Caenorhabditis elegans produce phenotypes of differing severities.LET-23-mediated signal transduction during Caenorhabditis elegans development.Molecular cloning and characterization of a novel alpha 1,2-fucosyltransferase (CE2FT-1) from Caenorhabditis elegans.Characterization of a novel G-protein coupled receptor from the parasitic nematode H. contortus with high affinity for serotonin.The Elm1 (ZmHy2) gene of maize encodes a phytochromobilin synthase.
P2860
Q27306806-F1762CC9-8303-4F8C-A338-E1B3A851746EQ27308081-AF2E3437-1A17-4F70-9C21-58F5A6CB938AQ28084486-AB5DD2F3-284C-4DCC-BFD7-27EF0D3EC20FQ29977771-E28E3CAB-B0F1-4CFE-BF86-417FEEB1A2AFQ33962779-84F2EDA7-BBC6-411B-B925-4A30897C627AQ33963641-6B254EF0-8A92-4125-BB6B-873A7D9F1A5FQ33964176-C755EBF6-7184-4491-86D6-38C657E40C4EQ33964849-E4D3101F-575C-48A1-8925-E9D0099770E7Q33970895-BB5D2388-B821-4EA4-BD51-F31886378511Q34020051-EE35003C-D5F0-46D3-8D87-4A018127ECFCQ34154831-E2210144-C72C-4323-8615-00A7E57EDD26Q34439145-6528B336-FC56-4968-B9B0-D5206629A0A7Q34471570-1347EFF7-4CD1-4EED-B17F-D8B3E53B0E44Q34602420-24BD4217-8047-45F6-AEAB-6CE407545CBAQ34608024-B5F9B82A-F03F-44F2-84A5-D2739C2434AFQ34608987-1D1FF739-BD82-43A7-BA1D-56012D955F46Q34618536-BD991639-FCAD-41E9-A90D-ED30CFDFA4F1Q34846048-3475918D-1E64-4537-B656-DCB38EB071CAQ35201877-B3282E8E-5344-4689-A3DA-BBA19CD8F62EQ35598449-388F0E7A-238C-4A39-B97B-1D3633DBB566Q35650374-D6524387-6A16-4396-BCBA-9BEE29B887BFQ35793524-5F0BB893-FD9E-499A-987C-C5A7192A4462Q35941444-CBD8E217-7709-43DE-B285-E9DF157D9397Q36556958-ADD097C4-E1FF-4127-8C1D-07F1034FF0ADQ36827962-2E55D21E-9BA6-4A53-9028-EA13BCBC1AC8Q36990715-BC693E51-00F4-423C-8016-1C689C74ED24Q37059609-6952DA29-F834-4EF4-9686-98D90BF526CFQ37385906-BA77C97F-04EA-49D9-B7E7-C1747AE03217Q37634533-6DFA99C4-D2D4-4E93-9FD3-4D6A6C5901B1Q40974398-5FEEBC1D-6CA2-46B6-B794-F53E1B744994Q42681924-799D1317-8D77-4598-ADCD-7DCEA3E5EC10Q43364096-A87AD853-CCDC-4563-87EC-EB31928BB9CFQ48174547-79C6612F-E8DC-4093-B5ED-1AC500533939
P2860
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
@ast
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
@en
type
label
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
@ast
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
@en
prefLabel
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
@ast
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
@en
P2093
P2860
P356
P1476
Splicing in Caenorhabditis elegans does not require an AG at the 3' splice acceptor site.
@en
P2093
P2860
P304
P356
10.1128/MCB.13.1.626
P407
P577
1993-01-01T00:00:00Z