| scholarly article | Q13442814 |
| P50 | author | Valerie Reinke | Q57338308 |
| P2093 | author name string | Michael Krause | |
| Peter Okkema | |||
| P2860 | cites work | Protein family expansions and biological complexity | Q21145685 |
| Comparative analysis of function and interaction of transcription factors in nematodes: extensive conservation of orthology coupled to rapid sequence evolution | Q21263171 | ||
| Cloning and properties of the Caenorhabditis elegans TATA-box-binding protein | Q24319316 | ||
| Identification of the differential distribution patterns of mRNAs and consensus binding sequences for mouse DAF-16 homologues | Q24532085 | ||
| Formation, regulation and evolution of Caenorhabditis elegans 3'UTRs | Q24598773 | ||
| Regulation of chromatin by histone modifications | Q24635070 | ||
| A multiparameter network reveals extensive divergence between C. elegans bHLH transcription factors | Q24642967 | ||
| Transcription of the C. elegans let-7 microRNA is temporally regulated by one of its targets, hbl-1 | Q24645262 | ||
| Identification of genes expressed in C. elegans touch receptor neurons | Q59097360 | ||
| Formation of a monomeric DNA binding domain by Skn-1 bZIP and homeodomain elements | Q72752185 | ||
| A conserved transcription motif suggesting functional parallels between Caenorhabditis elegans SKN-1 and Cap'n'Collar-related basic leucine zipper proteins | Q73675896 | ||
| Programmed cell death | Q80152495 | ||
| Regulation of rnt-1 expression mediated by the opposing effects of BRO-1 and DBL-1 in the nematode Caenorhabditis elegans | Q80407878 | ||
| Gfi-1 encodes a nuclear zinc finger protein that binds DNA and functions as a transcriptional repressor | Q24648833 | ||
| DBD--taxonomically broad transcription factor predictions: new content and functionality | Q24650744 | ||
| xol-1, the master sex-switch gene in C. elegans, is a transcriptional target of the terminal sex-determining factor TRA-1 | Q24655177 | ||
| Gene regulatory logic of dopamine neuron differentiation | Q24656218 | ||
| The conserved NAD(H)-dependent corepressor CTBP-1 regulates Caenorhabditis elegans life span | Q24658101 | ||
| A gene expression fingerprint of C. elegans embryonic motor neurons | Q24793234 | ||
| nfi-I affects behavior and life-span in C. elegans but is not essential for DNA replication or survival | Q24813734 | ||
| The EH1 motif in metazoan transcription factors | Q24816494 | ||
| Seeing elegance in gene regulatory networks of the worm | Q27001247 | ||
| The Caenorhabditis elegans HNF4alpha Homolog, NHR-31, mediates excretory tube growth and function through coordinate regulation of the vacuolar ATPase | Q27312136 | ||
| An integrated strategy to study muscle development and myofilament structure in Caenorhabditis elegans | Q27312196 | ||
| Coordinated regulation of intestinal functions in C. elegans by LIN-35/Rb and SLR-2 | Q27313826 | ||
| The Caenorhabditis elegans T-box factor MLS-1 requires Groucho co-repressor interaction for uterine muscle specification | Q27339317 | ||
| A Genome-Wide RNAi Screen for Factors Involved in Neuronal Specification in Caenorhabditis elegans | Q27340115 | ||
| Chromosome-biased binding and gene regulation by the Caenorhabditis elegans DRM complex | Q27340320 | ||
| A role for Set1/MLL-related components in epigenetic regulation of the Caenorhabditis elegans germ line | Q27342739 | ||
| Genome-wide identification of binding sites defines distinct functions for Caenorhabditis elegans PHA-4/FOXA in development and environmental response | Q27348311 | ||
| A widespread distribution of genomic CeMyoD binding sites revealed and cross validated by ChIP-Chip and ChIP-Seq techniques | Q27438090 | ||
| Increased dosage of a sir-2 gene extends lifespan in Caenorhabditis elegans | Q28131824 | ||
| Zinc fingers--folds for many occasions | Q28187358 | ||
| Retinoblastoma protein recruits histone deacetylase to repress transcription | Q28262144 | ||
| Sticky fingers: zinc-fingers as protein-recognition motifs | Q28282409 | ||
| Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
| The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans | Q28345297 | ||
| Different Mi-2 complexes for various developmental functions in Caenorhabditis elegans | Q28475938 | ||
| H3K9me2/3 binding of the MBT domain protein LIN-61 is essential for Caenorhabditis elegans vulva development | Q28477443 | ||
| Phosphatidylinositol 3-kinase signaling inhibits DAF-16 DNA binding and function via 14-3-3-dependent and 14-3-3-independent pathways | Q28588530 | ||
| Temporal and spatial expression patterns of the small heat shock (hsp16) genes in transgenic Caenorhabditis elegans | Q28776675 | ||
| Compact, universal DNA microarrays to comprehensively determine transcription-factor binding site specificities | Q29301030 | ||
| Phosphorylation and functions of the RNA polymerase II CTD | Q29614764 | ||
| Progression through the RNA polymerase II CTD cycle | Q29614782 | ||
| Identification of functional elements and regulatory circuits by Drosophila modENCODE | Q29617551 | ||
| The evolution of gene regulation by transcription factors and microRNAs | Q29617552 | ||
| Possible role of flanking nucleotides in recognition of the AUG initiator codon by eukaryotic ribosomes | Q29618470 | ||
| Transcription regulation and animal diversity | Q29618752 | ||
| Regulation of the Caenorhabditis elegans longevity protein DAF-16 by insulin/IGF-1 and germline signaling | Q29619762 | ||
| Wnt signaling and CEH-22/tinman/Nkx2.5 specify a stem cell niche in C. elegans | Q35132203 | ||
| A CBP/p300 homolog specifies multiple differentiation pathways in Caenorhabditis elegans. | Q35195830 | ||
| pha-4, an HNF-3 homolog, specifies pharyngeal organ identity in Caenorhabditis elegans | Q35204451 | ||
| The forkhead transcription factor UNC-130 is required for the graded spatial expression of the UNC-129 TGF-beta guidance factor in C. elegans | Q35204643 | ||
| Analysis of a Caenorhabditis elegans Twist homolog identifies conserved and divergent aspects of mesodermal patterning | Q35207840 | ||
| UNC-4/UNC-37-dependent repression of motor neuron-specific genes controls synaptic choice in Caenorhabditis elegans | Q35208880 | ||
| Hox and a newly identified E2F co-repress cell death in Caenorhabditis elegans | Q35221460 | ||
| Functional conservation of nematode and vertebrate myogenic regulatory factors | Q35239885 | ||
| The C. elegans vitellogenin genes: short sequence repeats in the promoter regions and homology to the vertebrate genes | Q35557134 | ||
| Enhanced yeast one-hybrid assays for high-throughput gene-centered regulatory network mapping. | Q35607409 | ||
| KIN-29 SIK regulates chemoreceptor gene expression via an MEF2 transcription factor and a class II HDAC. | Q35612504 | ||
| Action of the Caenorhabditis elegans GATA factor END-1 in Xenopus suggests that similar mechanisms initiate endoderm development in ecdysozoa and vertebrates | Q35669861 | ||
| LIN-39/Hox triggers cell division and represses EFF-1/fusogen-dependent vulval cell fusion | Q35805454 | ||
| LIN-61, one of two Caenorhabditis elegans malignant-brain-tumor-repeat-containing proteins, acts with the DRM and NuRD-like protein complexes in vulval development but not in certain other biological processes | Q35844907 | ||
| Gene expression profiling of cells, tissues, and developmental stages of the nematode C. elegans | Q35875150 | ||
| The SynMuv genes of Caenorhabditis elegans in vulval development and beyond | Q35955994 | ||
| Caenorhabditis elegans orthologs of the aryl hydrocarbon receptor and its heterodimerization partner the aryl hydrocarbon receptor nuclear translocator | Q35973611 | ||
| Post-translational modifications influence transcription factor activity: a view from the ETS superfamily | Q36043735 | ||
| A CUL-2 ubiquitin ligase containing three FEM proteins degrades TRA-1 to regulate C. elegans sex determination | Q36119946 | ||
| Control of sex-specific apoptosis in C. elegans by the BarH homeodomain protein CEH-30 and the transcriptional repressor UNC-37/Groucho | Q36151090 | ||
| We gather together: insulators and genome organization | Q36407771 | ||
| Analysis of cell fate from single-cell gene expression profiles in C. elegans | Q36452051 | ||
| Polycomb response elements and targeting of Polycomb group proteins in Drosophila. | Q36567949 | ||
| Cell-specific microarray profiling experiments reveal a comprehensive picture of gene expression in the C. elegans nervous system | Q36570593 | ||
| Analysis of the VPE sequences in the Caenorhabditis elegans vit-2 promoter with extrachromosomal tandem array-containing transgenic strains | Q36643765 | ||
| The Caenorhabditis elegans NK-2 class homeoprotein CEH-22 is involved in combinatorial activation of gene expression in pharyngeal muscle. | Q36723251 | ||
| Mesodermal expression of the C. elegans HMX homolog mls-2 requires the PBC homolog CEH-20 | Q36739362 | ||
| Molecular cloning and sequencing of ama-1, the gene encoding the largest subunit of Caenorhabditis elegans RNA polymerase II. | Q36761409 | ||
| Molecular implementation and physiological roles for histone H3 lysine 4 (H3K4) methylation | Q36824900 | ||
| Automated analysis of embryonic gene expression with cellular resolution in C. elegans. | Q36909568 | ||
| Regulation of vitellogenin gene expression in transgenic Caenorhabditis elegans: short sequences required for activation of the vit-2 promoter | Q36965113 | ||
| Transcriptional regulation | Q37020528 | ||
| Transcription mechanisms | Q37020559 | ||
| The C. elegans intestine | Q37020788 | ||
| An extensive requirement for transcription factor IID-specific TAF-1 in Caenorhabditis elegans embryonic transcription | Q47068840 | ||
| CHR3: a Caenorhabditis elegans orphan nuclear hormone receptor required for proper epidermal development and molting | Q47068843 | ||
| DNA binding and in vivo function of C.elegans PEB-1 require a conserved FLYWCH motif | Q47068846 | ||
| The CSL transcription factor LAG-1 directly represses hlh-6 expression in C. elegans | Q47068931 | ||
| Muscle and nerve-specific regulation of a novel NK-2 class homeodomain factor in Caenorhabditis elegans | Q47068947 | ||
| The heterochronic gene lin-29 encodes a zinc finger protein that controls a terminal differentiation event in Caenorhabditis elegans. | Q47068948 | ||
| EGL-38 Pax regulates the ovo-related gene lin-48 during Caenorhabditis elegans organ development | Q47068965 | ||
| Mab-3 is a direct tra-1 target gene regulating diverse aspects of C. elegans male sexual development and behavior | Q47068980 | ||
| Alteration of the DNA binding domain disrupts distinct functions of the C. elegans Pax protein EGL-38. | Q47069010 | ||
| The UNC-3 Olf/EBF protein represses alternate neuronal programs to specify chemosensory neuron identity | Q47069018 | ||
| Control of type-D GABAergic neuron differentiation by C. elegans UNC-30 homeodomain protein | Q47069020 | ||
| Two C. elegans histone methyltransferases repress lin-3 EGF transcription to inhibit vulval development | Q47069021 | ||
| Transcription factor NFY globally represses the expression of the C. elegans Hox gene Abdominal-B homolog egl-5. | Q47069062 | ||
| The C. elegans Mi-2 chromatin-remodelling proteins function in vulval cell fate determination. | Q47069081 | ||
| The T-box factor TBX-2 and the SUMO conjugating enzyme UBC-9 are required for ABa-derived pharyngeal muscle in C. elegans | Q47069121 | ||
| The MADS-Box factor CeMEF2 is not essential for Caenorhabditis elegans myogenesis and development | Q47069122 | ||
| RLE-1, an E3 ubiquitin ligase, regulates C. elegans aging by catalyzing DAF-16 polyubiquitination | Q47069128 | ||
| TBP-like factor is required for embryonic RNA polymerase II transcription in C. elegans | Q47069152 | ||
| Regulation of touch receptor differentiation by the Caenorhabditis elegans mec-3 and unc-86 genes. | Q47069187 | ||
| Environmentally induced foregut remodeling by PHA-4/FoxA and DAF-12/NHR. | Q47069222 | ||
| C. elegans STAT: evolution of a regulatory switch | Q47069274 | ||
| Overlapping roles of two Hox genes and the exd ortholog ceh-20 in diversification of the C. elegans postembryonic mesoderm. | Q47069324 | ||
| MEP-1 and a homolog of the NURD complex component Mi-2 act together to maintain germline-soma distinctions in C. elegans | Q47069337 | ||
| Structure, expression, and evolution of a heat shock gene locus in Caenorhabditis elegans that is flanked by repetitive elements | Q47069348 | ||
| An early pharyngeal muscle enhancer from the Caenorhabditis elegans ceh-22 gene is targeted by the Forkhead factor PHA-4. | Q47069384 | ||
| Identification of direct DAF-16 targets controlling longevity, metabolism and diapause by chromatin immunoprecipitation | Q47069404 | ||
| The Snail-like CES-1 protein of C. elegans can block the expression of the BH3-only cell-death activator gene egl-1 by antagonizing the function of bHLH proteins | Q47069456 | ||
| The C. elegans sex-determining GLI protein TRA-1A is regulated by sex-specific proteolysis | Q47069490 | ||
| Identification of cis-regulatory elements from the C. elegans Hox gene lin-39 required for embryonic expression and for regulation by the transcription factors LIN-1, LIN-31 and LIN-39. | Q47069526 | ||
| lag-1, a gene required for lin-12 and glp-1 signaling in Caenorhabditis elegans, is homologous to human CBF1 and Drosophila Su(H). | Q47069543 | ||
| Regulation of postembryonic G(1) cell cycle progression in Caenorhabditis elegans by a cyclin D/CDK-like complex | Q47069561 | ||
| The T-box transcription factors TBX-37 and TBX-38 link GLP-1/Notch signaling to mesoderm induction in C. elegans embryos | Q47069575 | ||
| The C. elegans CBFbeta homolog, BRO-1, regulates the proliferation, differentiation and specification of the stem cell-like seam cell lineages | Q47069599 | ||
| Genomic cis-regulatory architecture and trans-acting regulators of a single interneuron-specific gene battery in C. elegans | Q47397388 | ||
| A gene-centered C. elegans protein-DNA interaction network | Q47594680 | ||
| The TBP-like factor CeTLF is required to activate RNA polymerase II transcription during C. elegans embryogenesis. | Q47822426 | ||
| Caenorhabditis elegans twist plays an essential role in non-striated muscle development. | Q47900059 | ||
| Transcriptionally repressed germ cells lack a subpopulation of phosphorylated RNA polymerase II in early embryos of Caenorhabditis elegans and Drosophila melanogaster. | Q47912453 | ||
| A trans-spliced leader sequence on actin mRNA in C. elegans. | Q48343028 | ||
| Identification of SUMO-dependent chromatin-associated transcriptional repression components by a genome-wide RNAi screen. | Q50336137 | ||
| Notch-GATA synergy promotes endoderm-specific expression of ref-1 in C. elegans. | Q50657632 | ||
| A Lin-9 complex is recruited by B-Myb to activate transcription of G2/M genes in undifferentiated embryonal carcinoma cells. | Q51791801 | ||
| In vitro and in vivo characterization of Caenorhabditis elegans PHA-4/FoxA response elements. | Q51904383 | ||
| Somatic misexpression of germline P granules and enhanced RNA interference in retinoblastoma pathway mutants. | Q52043143 | ||
| The REF-1 family of bHLH transcription factors pattern C. elegans embryos through Notch-dependent and Notch-independent pathways. | Q52047995 | ||
| Transcriptional outputs of the Caenorhabditis elegans forkhead protein DAF-16. | Q52102444 | ||
| Polycomb group regulation of Hox gene expression in C. elegans. | Q52104494 | ||
| elt-1, a gene encoding a Caenorhabditis elegans GATA transcription factor, is highly expressed in the germ lines with msp genes as the potential targets. | Q52172509 | ||
| A gut-to-pharynx/tail switch in embryonic expression of the Caenorhabditis elegans ges-1 gene centers on two GATA sequences. | Q52206867 | ||
| DAF-16 target genes that control C. elegans life-span and metabolism. | Q52604952 | ||
| Maternal deployment of the embryonic SKN-1-->MED-1,2 cell specification pathway in C. elegans | Q42598422 | ||
| The nuclear receptor superfamily has undergone extensive proliferation and diversification in nematodes | Q42692444 | ||
| The polycomb complex protein mes-2/E(z) promotes the transition from developmental plasticity to differentiation in C. elegans embryos. | Q43115568 | ||
| Methylation and demethylation activities of a C. elegans MLL-like complex attenuate RAS signalling. | Q43147808 | ||
| A compendium of Caenorhabditis elegans regulatory transcription factors: a resource for mapping transcription regulatory networks | Q43251350 | ||
| Diversity in DNA recognition by heat shock transcription factors (HSFs) from model organisms | Q43475183 | ||
| Characterization of CeHDA-7, a class II histone deacetylase interacting with MEF-2 in Caenorhabditis elegans | Q44020755 | ||
| Cell fates and fusion in the C. elegans vulval primordium are regulated by the EGL-18 and ELT-6 GATA factors -- apparent direct targets of the LIN-39 Hox protein. | Q44193732 | ||
| Cis regulatory requirements for vulval cell-specific expression of the caenorhabditis elegans fibroblast growth factor gene egl-17 | Q44413789 | ||
| A cell-specific enhancer that specifies lin-3 expression in the C. elegans anchor cell for vulval development | Q44683376 | ||
| A new class of C. elegans synMuv genes implicates a Tip60/NuA4-like HAT complex as a negative regulator of Ras signaling | Q44833513 | ||
| Transcriptional control and patterning of the pho-1 gene, an essential acid phosphatase expressed in the C. elegans intestine | Q45284298 | ||
| The unc-86 gene product couples cell lineage and cell identity in C. elegans | Q45300411 | ||
| Potential regulatory elements of nematode vitellogenin genes revealed by interspecies sequence comparison. | Q45928004 | ||
| Restriction of mesendoderm to a single blastomere by the combined action of SKN-1 and a GSK-3beta homolog is mediated by MED-1 and -2 in C. elegans | Q46047227 | ||
| The bZip proteins CES-2 and ATF-2 alter the timing of transcription for a cell-specific target gene in C. elegans | Q46822751 | ||
| Antagonistic functions of SET-2/SET1 and HPL/HP1 proteins in C. elegans development | Q46925893 | ||
| Cyclin E expression during development in Caenorhabditis elegans | Q47068705 | ||
| pha-4 is Ce-fkh-1, a fork head/HNF-3alpha,beta,gamma homolog that functions in organogenesis of the C. elegans pharynx | Q47068744 | ||
| Multiple enhancers contribute to expression of the NK-2 homeobox gene ceh-22 in C. elegans pharyngeal muscle | Q47068752 | ||
| The noncanonical binding site of the MED-1 GATA factor defines differentially regulated target genes in the C. elegans mesendoderm | Q47068778 | ||
| Wnt signaling and a Hox protein cooperatively regulate psa-3/Meis to determine daughter cell fate after asymmetric cell division in C. elegans. | Q47068833 | ||
| Neurogenesis in the nematode Caenorhabditis elegans | Q34624030 | ||
| Diverse transcription factor binding features revealed by genome-wide ChIP-seq in C. elegans | Q34625961 | ||
| An MLL/COMPASS subunit functions in the C. elegans dosage compensation complex to target X chromosomes for transcriptional regulation of gene expression | Q34626783 | ||
| Post-transcriptional regulation of the E/Daughterless ortholog HLH-2, negative feedback, and birth order bias during the AC/VU decision in C. elegans | Q34642010 | ||
| Identification of residues of the Caenorhabditis elegans LIN-1 ETS domain that are necessary for DNA binding and regulation of vulval cell fates | Q34645825 | ||
| The C. elegans homologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception | Q34651267 | ||
| Chromatin remodelling during development | Q34698385 | ||
| The LIN-15A and LIN-56 transcriptional regulators interact to negatively regulate EGF/Ras signaling in Caenorhabditis elegans vulval cell-fate determination | Q34714971 | ||
| Trans-splicing and operons | Q34720214 | ||
| Members of the H3K4 trimethylation complex regulate lifespan in a germline-dependent manner in C. elegans | Q34784199 | ||
| The FLYWCH transcription factors FLH-1, FLH-2, and FLH-3 repress embryonic expression of microRNA genes in C. elegans | Q34828352 | ||
| Core promoter T-blocks correlate with gene expression levels in C. elegans | Q34867860 | ||
| Control of neuronal subtype identity by the C. elegans ARID protein CFI-1. | Q34874075 | ||
| Zinc fingers in sex determination: only one of the two C. elegans Tra-1 proteins binds DNA in vitro | Q34994640 | ||
| OrthoList: a compendium of C. elegans genes with human orthologs | Q35007364 | ||
| Using a structural and logics systems approach to infer bHLH-DNA binding specificity determinants | Q35040989 | ||
| Readers of histone modifications | Q35092783 | ||
| Some C. elegans class B synthetic multivulva proteins encode a conserved LIN-35 Rb-containing complex distinct from a NuRD-like complex | Q35130721 | ||
| The C. elegans pharynx: a model for organogenesis | Q37020818 | ||
| A condensin-like dosage compensation complex acts at a distance to control expression throughout the genome | Q37135166 | ||
| Cis-regulatory mutations in the Caenorhabditis elegans homeobox gene locus cog-1 affect neuronal development | Q37152773 | ||
| Transcriptome profiling of the C. elegans Rb ortholog reveals diverse developmental roles | Q37188176 | ||
| Linking asymmetric cell division to the terminal differentiation program of postmitotic neurons in C. elegans | Q37215105 | ||
| The C. elegans Snail homolog CES-1 can activate gene expression in vivo and share targets with bHLH transcription factors | Q37235372 | ||
| DNA-binding specificity and in vivo targets of Caenorhabditis elegans nuclear factor I. | Q37274531 | ||
| X chromosome repression by localization of the C. elegans dosage compensation machinery to sites of transcription initiation | Q37367035 | ||
| SKN-1 domain folding and basic region monomer stabilization upon DNA binding | Q37367381 | ||
| Condition-adapted stress and longevity gene regulation by Caenorhabditis elegans SKN-1/Nrf. | Q37419745 | ||
| Recent advances in understanding the molecular mechanisms regulating C. elegans transcription | Q37696431 | ||
| Epigenomics of centromere assembly and function | Q37776921 | ||
| Decoding the histone H4 lysine 20 methylation mark | Q37782080 | ||
| Cell signaling and transcriptional regulation via histone phosphorylation | Q37861959 | ||
| Regulation of organogenesis by the Caenorhabditis elegans FoxA protein PHA-4. | Q38292410 | ||
| Transcriptional regulation of AQP-8, a Caenorhabditis elegans aquaporin exclusively expressed in the excretory system, by the POU homeobox transcription factor CEH-6. | Q38299638 | ||
| Regulation of metallothionein gene transcription. Identification of upstream regulatory elements and transcription factors responsible for cell-specific expression of the metallothionein genes from Caenorhabditis elegans | Q38319731 | ||
| The TRA-1A sex determination protein of C. elegans regulates sexually dimorphic cell deaths by repressing the egl-1 cell death activator gene | Q38321297 | ||
| The DAF-3 Smad binds DNA and represses gene expression in the Caenorhabditis elegans pharynx. | Q38330879 | ||
| Identification of C. elegans DAF-12-binding sites, response elements, and target genes | Q38335332 | ||
| Regulation of sperm gene expression by the GATA factor ELT-1. | Q38352378 | ||
| RNA Pol II accumulates at promoters of growth genes during developmental arrest. | Q38435681 | ||
| Co-regulation by Notch and Fos is required for cell fate specification of intermediate precursors during C. elegans uterine development | Q39752379 | ||
| Cis-regulatory mechanisms of left/right asymmetric neuron-subtype specification in C. elegans | Q39752816 | ||
| Activity of a C. elegans GATA transcription factor, ELT-1, expressed in yeast | Q39757513 | ||
| A C. elegans E/Daughterless bHLH protein marks neuronal but not striated muscle development | Q39758198 | ||
| A model of repression: CTD analogs and PIE-1 inhibit transcriptional elongation by P-TEFb | Q39895224 | ||
| SKN-1 links C. elegans mesendodermal specification to a conserved oxidative stress response | Q39896060 | ||
| A transcriptional regulatory cascade that controls left/right asymmetry in chemosensory neurons of C. elegans | Q39896857 | ||
| The FoxF/FoxC factor LET-381 directly regulates both cell fate specification and cell differentiation in C. elegans mesoderm development | Q40002173 | ||
| The spatial dynamics of tissue-specific promoters during C. elegans development | Q40014678 | ||
| Sumoylation of LIN-1 promotes transcriptional repression and inhibition of vulval cell fates. | Q40462309 | ||
| Locus encoding a family of small heat shock genes in Caenorhabditis elegans: two genes duplicated to form a 3.8-kilobase inverted repeat | Q40666309 | ||
| Transcription and translation. | Q40929088 | ||
| Coordinated transcriptional regulation of the unc-25 glutamic acid decarboxylase and the unc-47 GABA vesicular transporter by the Caenorhabditis elegans UNC-30 homeodomain protein | Q41680627 | ||
| CeMyoD accumulation defines the body wall muscle cell fate during C. elegans embryogenesis | Q41714153 | ||
| Identification and analysis of internal promoters in Caenorhabditis elegans operons | Q41735826 | ||
| The C. elegans NeuroD homolog cnd-1 functions in multiple aspects of motor neuron fate specification. | Q41759994 | ||
| Massively parallel sequencing of the polyadenylated transcriptome of C. elegans | Q41941343 | ||
| The C. elegans Twist target gene, arg-1, is regulated by distinct E box promoter elements | Q42123738 | ||
| MIG-32 and SPAT-3A are PRC1 homologs that control neuronal migration in Caenorhabditis elegans | Q42156705 | ||
| C. elegans sequences that control trans-splicing and operon pre-mRNA processing | Q42413466 | ||
| High nucleosome occupancy is encoded at X-linked gene promoters in C. elegans | Q42588662 | ||
| A spatial and temporal map of C. elegans gene expression | Q42588671 | ||
| A census of human transcription factors: function, expression and evolution | Q29622841 | ||
| XBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans | Q30478329 | ||
| SUMO regulates the assembly and function of a cytoplasmic intermediate filament protein in C. elegans | Q30492693 | ||
| Functional conservation between members of an ancient duplicated transcription factor family, LSF/Grainyhead | Q30815054 | ||
| The Caenorhabditis elegans peb-1 gene encodes a novel DNA-binding protein involved in morphogenesis of the pharynx, vulva, and hindgut | Q30980715 | ||
| The ELT-2 GATA-factor and the global regulation of transcription in the C. elegans intestine | Q33264001 | ||
| EDGEdb: a transcription factor-DNA interaction database for the analysis of C. elegans differential gene expression. | Q33269614 | ||
| Specificity of DNA-binding by the FAX-1 and NHR-67 nuclear receptors of Caenorhabditis elegans is partially mediated via a subclass-specific P-box residue | Q33313520 | ||
| The genomic distribution and function of histone variant HTZ-1 during C. elegans embryogenesis | Q33369072 | ||
| Dynamic expression of small non-coding RNAs, including novel microRNAs and piRNAs/21U-RNAs, during Caenorhabditis elegans development | Q33449910 | ||
| The landscape of C. elegans 3'UTRs | Q33593704 | ||
| Alternative trans-splicing of Caenorhabditis elegans sma-9/schnurri generates a short transcript that provides tissue-specific function in BMP signaling | Q33611000 | ||
| The C. elegans cell death specification gene ces-1 encodes a snail family zinc finger protein | Q33876675 | ||
| Identification of grandchildless loci whose products are required for normal germ-line development in the nematode Caenorhabditis elegans | Q33958810 | ||
| Sequence requirements for myosin gene expression and regulation in Caenorhabditis elegans | Q33961648 | ||
| A simple method for gene expression and chromatin profiling of individual cell types within a tissue | Q34000729 | ||
| Targeting X chromosomes for repression | Q34003258 | ||
| cdk-7 Is required for mRNA transcription and cell cycle progression in Caenorhabditis elegans embryos | Q34025380 | ||
| RNA polymerase II C-terminal domain phosphorylation patterns in Caenorhabditis elegans operons, polycistronic gene clusters with only one promoter | Q34045680 | ||
| Operons in C. elegans: polycistronic mRNA precursors are processed by trans-splicing of SL2 to downstream coding regions | Q34060309 | ||
| A POP-1 repressor complex restricts inappropriate cell type-specific gene transcription during Caenorhabditis elegans embryogenesis | Q34078126 | ||
| A functional NR4A nuclear receptor DNA-binding domain is required for organ development in Caenorhabditis elegans | Q34082563 | ||
| Six and Eya promote apoptosis through direct transcriptional activation of the proapoptotic BH3-only gene egl-1 in Caenorhabditis elegans | Q34100473 | ||
| Chromosomal clustering of muscle-expressed genes in Caenorhabditis elegans | Q34148035 | ||
| The Caenorhabditis elegans heterochronic regulator LIN-14 is a novel transcription factor that controls the developmental timing of transcription from the insulin/insulin-like growth factor gene ins-33 by direct DNA binding | Q34230931 | ||
| A regulatory network of T-box genes and the even-skipped homologue vab-7 controls patterning and morphogenesis in C. elegans | Q34315560 | ||
| Native E2F/RBF complexes contain Myb-interacting proteins and repress transcription of developmentally controlled E2F target genes | Q34358237 | ||
| Expression pattern, regulation, and biological role of runt domain transcription factor, run, in Caenorhabditis elegans | Q34440372 | ||
| Similarity of DNA binding and transcriptional regulation by Caenorhabditis elegans MAB-3 and Drosophila melanogaster DSX suggests conservation of sex determining mechanisms. | Q34490364 | ||
| Identification of transcription start sites of trans-spliced genes: uncovering unusual operon arrangements | Q34497400 | ||
| Broad chromosomal domains of histone modification patterns in C. elegans | Q34548272 | ||
| A global analysis of C. elegans trans-splicing | Q34548280 | ||
| mec-3, a homeobox-containing gene that specifies differentiation of the touch receptor neurons in C. elegans | Q34560342 | ||
| synMuv B proteins antagonize germline fate in the intestine and ensure C. elegans survival | Q34592502 | ||
| Caenorhabditis elegans chromosome arms are anchored to the nuclear membrane via discontinuous association with LEM-2 | Q34613778 | ||
| P921 | main subject | Caenorhabditis elegans | Q91703 |
| P304 | page(s) | 1-34 | |
| P577 | publication date | 2013-06-04 | |
| P1433 | published in | WormBook | Q8036839 |
| P1476 | title | Transcriptional regulation of gene expression in C. elegans |
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