GSE55988 |
mRNA profile in DR-related mutants |
GSE56270 |
Differential spatial and structural organization of the X chromosome underlies dosage compensation in C. elegans. |
GSE59716 |
Condensin-Driven Remodeling of X-Chromosome Topology during Dosage Compensation |
GSE60672 |
RNA-seq of C.elegans treated with bcat-1 RNAi and controls |
GSE62856 |
Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RIP-Seq) |
GSE62858 |
Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq) |
GSE62859 |
Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (ribosome) |
GSE62861 |
Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes |
GSE63717 |
Condensin-Driven Remodeling of X-Chromosome Topology during Dosage Compensation [Hi-C] |
GSE63803 |
To identify ATFS-1 target genes during mitochondrial stress |
GSE66504 |
Identification of N6-adenine methylation in C. elegans DNA |
GSE67954 |
CSR-1 and P granules suppress sperm-specific transcription in the C. elegans germline |
GSE68988 |
Maternal piRNAs are essential for germline development following de-novo establishment of endo-siRNAs in Caenorhabditis elegans |
GSE70117 |
RNA sequencing analysis of DAF-16 target gene expression when math-33 function is genetically inactivated |
GSE71720 |
Defining the Roles and Regulation of the GATA-factor ELT-2 in the C. elegans Endoderm |
GSE72232 |
Deep sequencing of poly(A)-selected RNAs from whole nematode C. elegans during aging |
GSE72233 |
Deep sequencing of small RNAs from whole nematode C. elegans during aging |
GSE72234 |
RNA-seq and small RNA-seq analysis of N2 wildtype and mir-71(n4115) C. elegans during aging |
GSE73589 |
Osmosensory neurons modulate hypertonic stress resistance in C. elegans by controlling protein damage in non-neuronal cells |
GSE74133 |
LEM-2 ChIP-seq to study chromatin anchoring |
GSE74134 |
Perinuclear anchoring of H3K9-methylated chromatin stabilizes induced cell fate |
GSE75128 |
A Small RNA-Catalytic Argonaute Pathway Tunes Germline Transcript Levels to Ensure Embryonic Divisions |
GSE75160 |
Whole RNA sequencing to identify targets of ets-4 that are responsible for rege-1 (C30F12.1) phenotype |
GSE75162 |
Whole RNA sequencing to identify targets of the RNase domain protein encoded by rege-1 (C30F12.1) |
GSE75163 |
Whole RNA sequencing to identify targets of ETS-4 and REGE-1 |
GSE76455 |
Long-range signaling at the neural-intestinal axis promotes organismal heme homeostasis |
GSE77654 |
A Tunable Mechanism Determines the Transgenerational Duration of Small RNA Inheritance in C.elegans |
GSE77944 |
Single-cell transcriptomes of each cell of the C. elegans embryo until the 16-cell stage |
GSE78252 |
Mitochondrial stress induces chromatin reorganization to promote longevity and UPRmt |
GSE78779 |
CEL-Seq2: sensitive highly-multiplexed single-cell RNA-Seq |
GSE78990 |
Two Conserved Histone Demethylases Regulate Mitochondrial Stress-Induced Longevity |
GSE79567 |
Nucleosome fragility is associated with future transcriptional response to developmental cues and stress in C. elegans |
GSE79994 |
XRN2 Autoregulation and Control of Polycistronic Gene Expression in Caenorhabditis elegans |
GSE80807 |
mRNA expression profile of dop-1 mutants to wild- type animals during adulthood (L4+48 hours) using RNA-seq |
GSE83133 |
A-to-I RNA editing promotes developmental-stage specific gene and lncRNA expression |
GSE83216 |
Developmental transcriptomes of the two sexes in Caenorhabditis elegans during sexual maturation |
GSE83523 |
Transcriptome characterization of embryogenesis at a single cell resolution [C. elegans] |
GSE84307 |
An H4K16 histone acetyltransferase mediates decondensation of the X chromosome in C. elegans males |
GSE85835 |
Transgenerational inheritance of mitochondrial stress adaptation in C. elegans |
GSE87078 |
mRNA Next Generation Sequencing of long-lived C. elegans mutants lacking the replication-independent histone variant H3.3 |
GSE87528 |
Developmental constraints shape the evolution of the nematode mid-developmental transition |
GSE89295 |
Gene expression changes in dauer defective strains |
GSE89890 |
Gene regulation by small RNAs and ADAR RNA editing |
GSE92690 |
Transcriptome profiling of P-granule-depleted or P-granule mutant gonads versus control gonads over time |
GSE92850 |
LSM2-8 and XRN-2 contribute to the silencing of H3K27me3 marked genes through targeted RNA decay I |
GSE92851 |
LSM2-8 and XRN-2 contribute to the silencing of H3K27me3 marked genes through targeted RNA decay |
GSE93826 |
Gene changes over aging in the C.elegans rrf-3(pk1426) mutant |
GSE94077 |
Analysis of nonsense-mediated mRNA decay in daf-2 mutants |
GSE94455 |
The Conserved Intron Binding Protein EMB-4 Plays Differential Roles in Germline Small RNA Pathways of C. elegans |
GSE94463 |
A Highly Conserved GAD-1 Is Required for Pre-mRNA Splicing and Transcription Elongation by Forming Spliceosome with NineTeen Complex |
GSE94798 |
Untangling the Role of H3K9 Methylations in Transgenerational Small RNA Inheritance |
GSE94879 |
Analysis of C. elegans muscle transcriptome using trans-splicing-based RNA tagging (SRT) |
GSE96824 |
QsRNA-seq: a method for high-throughput profiling and quantifying small RNAs |
GSE97355 |
Genetic Analysis of a Metazoan Pathway using Transcriptomic Phenotypes |
GSE97425 |
Genome-wide discovery of active regulatory elements and transcription factor footprints in Caenorhabditis elegans using DNase-seq |
GSE97592 |
RNA sequencing of drh-3(rrr2) mutants |
GSE97775 |
Two distinct transcription termination modes dictated by promoters |
GSE98130 |
LIN-41 and OMA ribonucleoprotein complexes mediate a translational repression-to-activation switch controlling oocyte meiotic maturation and the oocyte-to-embryo transition in Caenorhabditis elegans |
GSE98195 |
A Chinese herbal formula, Gengnianchun, ameliorates β-amyloid peptide toxicity in a Caenorhabditis elegans model of Alzheimer’s disease |
GSE98758 |
Genome-wide DNA accessibility maps and differential gene expression using ChIP-seq, ATAC-seq and RNA-seq for the human secondary fibroblast cell line hiF-T and whole worms with and without knockdown of FACT complex |
GSE98935 |
ALG-5 is a miRNA-associated Argonaute required for proper developmental timing in the Caenorhabditis elegans germline |
GSE100623 |
SET-9 and SET-26, the C. elegans homologs of human MLL5, are critical for germline development and longevity |
GSE100651 |
Genome-wide maps of chromatin structure in wild-type and nanos mutant primordial germ cells in C. elegans |
GSE100652 |
Chromatin reprogramming in primordial germ cells requires Nanos-dependent down-regulation of the synMuvB transcription factor LIN-15B |
GSE100723 |
H3K9me2 and BRCA1 cooperate to prevent satellite repeat transcription, R-loop formation and germline sterility [RNA-seq] |
GSE100724 |
H3K9me2 and BRCA1 cooperate to prevent satellite repeat transcription, R-loop formation and germline sterility [ChIP-seq] |
GSE100726 |
H3K9me2 and BRCA1 cooperate to prevent satellite repeat transcription, R-loop formation and germline sterility |
GSE100829 |
The C. elegans ortholog of TDP-43 regulates the chromatin localization of the heterochromatin protein 1 homolog, HPL-2 |
GSE101524 |
Variations in diet type and temperature significantly affect the transcriptional profile of C. elegans |
GSE101645 |
Transcriptomic analysis of wild-type and lin-22 mutants in C.elegans |
GSE101647 |
Transcriptomic analysis of control and Myzocytiopsis humicola-infected C. elegans |
GSE101964 |
Adult-specific trimethylation of histone H3 lysine 4 is prone to dynamic changes with aging in C. elegans somatic cells |
GSE102679 |
Two evolutionary developmental strategies for miRNA gene regulation in animal embryogenesis [CE_miRNA-seq] |
GSE102680 |
Two evolutionary developmental strategies for miRNA gene regulation in animal embryogenesis [CE_RNA-seq] |
GSE102682 |
Two evolutionary developmental strategies for miRNA gene regulation in animal embryogenesis |
GSE103775 |
Genetic Adaptation of C. elegans to Environment Changes II: Multigenerational Analysis of Genome-wide Chromatin Remodeling |
GSE103776 |
Effect of liquid cultivations on N2 and AB1 strains of C. elegans |
GSE104378 |
Cell-type specific sequencing of microRNAs from complex animal tissues I |
GSE104470 |
Cell-type specific sequencing of microRNAs from complex animal tissues |
GSE104500 |
RNA-Seq of L4 C. elegans |
GSE104502 |
Short Poly(A) Tails are a Conserved Feature of Highly Expressed Genes |
GSE105036 |
The effects of mitochondrial- and histone stress on the C. elegans transcriptome |
GSE106647 |
Transcriptome analysis of C. elegans embryos lacking ADARs and the 26G pathway |
GSE106814 |
LIN-41 RIP-Seq |
GSE106889 |
Differential expression of H3.3 genes and their role in modulating temperature stress response in Caenorhabditis elegans |
GSE107229 |
Cell-type specific sequencing of microRNAs from complex animal tissues V |
GSE109692 |
Sequencing of Caenorhabditis elegans wildtype strain (N2) treated with T25B9.1 RNAi for 5 days after L4 larvae stage. |
GSE110582 |
Whole genome mapping of DNA G-quadruplexes in multiple species by G4-seq |
GSE110701 |
Disruption in A-to-I editing levels affects C. elegans development more than a complete lack of editing |
GSE110833 |
Sequencing of C.elegans at different time points treated with bcat-1 RNAi and controls |
GSE110834 |
Sequencing of Caenorhabditis elegans at 5 different time point after Rotenone and DMSO treatment (mRNA) |
GSE110835 |
Sequencing of Caenorhabditis elegans treated with L4440, M05B5.3 and T14F9.5 at two different time points |
GSE110836 |
Sequencing of Caenorhabditis elegans at 4 time points treated with RNAi |
GSE110837 |
Sequencing of Caenorhabditis elegans treated with 3 different RNAi. |
GSE110838 |
Sequencing of Caenorhabditis elegans after 9 different RNAi treatments |
GSE110839 |
Sequencing of Caenorhabditis elegans treated with L4440 and 6B3B.9 |
GSE110840 |
Sequencing of Caenorhabditis elegans deletion mutants treated with RNAi |
GSE110841 |
Sequencing of Caenorhabditis elegans wildtype strain (N2) treated with T25B9.1 RNAi for 2 and 5 days after L4 larvae stage. |
GSE110842 |
Sequencing of Caenorhabditis elegans overexpression mutants. |
GSE110843 |
Sequencing of Caenorhabditis elegans at two different time points after Rotenone and DMSO treatment (mRNA) |
GSE110846 |
Sequencing of Caenorhabditis elegans at 5 different time point after Rotenone and DMSO treatment (smallRNA) |
GSE110849 |
Sequencing of Caenorhabditis elegans at two different time points after Rotenone and DMSO treatment (smallRNA) |
GSE111338 |
Identification of DAF-16/FoxO targets associated with longevity |
GSE111800 |
Small RNA-mediated genomic silencing promotes telomere stability in the absence of telomerase |
GSE111995 |
RppH can faithfully replace TAP to allow cloning of 5’-triphosphate carrying small RNAs |
GSE112753 |
RNA-seq on D5 C. elegans in WT(N2), alg-1(gk214), alg-2(ok304) |
GSE112775 |
ALG-1 and ALG-2 |
GSE112978 |
Next Generation Sequencing and Quantitative Analysis of mRNAs in Wild Type and ceh-60 Mutant Caenorhabditis elegans |
GSE112979 |
Genome-wide occupancy of the CEH-60 and UNC-62 Transcription Factors in Caenorhabditis elegans |
GSE112981 |
Analysis of the transcription factor CEH-60 in Caenorhabditis elegans development |
GSE113841 |
Genomic distribution of H3K9me2 in wild-type vs. arle-14 mutant C. elegans embryos |
GSE115161 |
Regulation of Translation Elongation Revealed by Ribosome Profiling [Dataset_4] |
GSE115162 |
Regulation of Translation Elongation Revealed by Ribosome Profiling |
GSE115281 |
C. elegans DLC-1 is a component of diverse ribonucleoprotein complexes |
GSE115320 |
Systematic evaluation of C. elegans lincRNAs with CRISPR knockout mutants [lncRNA-seq] |
GSE115321 |
Systematic evaluation of C. elegans lincRNAs with CRISPR knockout mutants [miRNA-seq] |
GSE115324 |
Systematic evaluation of C. elegans lincRNAs with CRISPR knockout mutants |
GSE115695 |
RBM-5 modulates U2AF large subunit-dependent alternative splicing in C. elegans |
GSE115884 |
Spatio-temporal m(i)RNA architecture and 3' UTR regulation in the C. elegans germline |
GSE115998 |
Gene expression changes in mrg-1 mutant L1 larvae compared to wild type. |
GSE115999 |
Gene expression changes upon depletion of H3K36 methylation by mutating met-1 and RNAi depleting mes-4 in worm L1 larvae |
GSE116037 |
Active chromatin marks, H3K36me and MRG-1, drive spatial sequestration of heterochromatin |
GSE116367 |
Transcriptional analysis of early and late generation nuclear RNAi deficient animals |
GSE117169 |
An extracellular Argonaute protein mediates export of repeat-associated small RNAs into vesicles in parasitic nematodes |
GSE117222 |
WDR-23 and SKN-1 Nrf2 coordinate with the BLI-3 dual oxidase in response to iodide-triggered oxidative stress |
GSE117471 |
Local inhibition of PRC2 activity by histone H3.3K27M drives replication defects through misregulation of the JNK pathway [RNA-seq] |
GSE117531 |
Local inhibition of PRC2 activity by histone H3.3K27M drives replication defects through misregulation of the JNK pathway [ChIP-seq] |
GSE117533 |
Local inhibition of PRC2 activity by histone H3.3K27M drives replication defects through misregulation of the JNK pathway |
GSE117658 |
Caenorhabditis elegans heterochromatin factor SET-32 plays an essential role in transgenerational initiation of nuclear RNAi-mediated epigenetic silencing (ChIP-Seq) |
GSE117659 |
Caenorhabditis elegans heterochromatin factor SET-32 plays an essential role in transgenerational initiation of nuclear RNAi-mediated epigenetic silencing (RNA-Seq) |
GSE117660 |
Caenorhabditis elegans heterochromatin factor SET-32 plays an essential role in transgenerational initiation of nuclear RNAi-mediated epigenetic silencing (sRNA-Seq) |
GSE117662 |
Caenorhabditis elegans heterochromatin factor SET-32 plays an essential role in transgenerational initiation of nuclear RNAi-mediated epigenetic silencing |
GSE118379 |
The spatial and temporal dynamics of the nuclear RNAi-targeted retrotransposon transcripts in Caenorhabditis elegans [RNA-seq] |
GSE118428 |
The spatial and temporal dynamics of the nuclear RNAi-targeted retrotransposon transcripts in Caenorhabditis elegans [ncRNA-seq] |
GSE118429 |
The spatial and temporal dynamics of the nuclear RNAi-targeted retrotransposon transcripts in Caenorhabditis elegans |
GSE118433 |
Identification of LIN-29 target genes |
GSE119696 |
Pre-clinical evaluation of cysteamine bitartrate as a therapeutic agent for mitochondrial respiratory chain disease (worm) |
GSE119723 |
Pre-clinical evaluation of cysteamine bitartrate as a therapeutic agent for mitochondrial respiratory chain disease |
GSE119993 |
Comparison of gene expression in the long-lived hsb-1 mutant and hsf-1 overexpression C. elegans strains |
GSE120405 |
RNA co-immunoprecipitation coupled to RNA sequencing (RIP-seq) to identify somatic target mRNAs of the TRIM-NHL protein LIN41 |
GSE121129 |
RNA sequencing of cell-specific profile of AVK |
GSE122015 |
A-to-I RNA editing affects lncRNAs expression after heat shock |
GSE122125 |
Comparative Transcriptomic Signature of the Simulated Microgravity Response in C. elegans |
GSE122335 |
An unstructured MET-2/SETDB1 cofactor ensures H3K9me2, focus formation and perinuclear anchoring [ChIP-seq] |
GSE122339 |
An unstructured MET-2/SETDB1 cofactor ensures H3K9me2, focus formation and perinuclear anchoring [RNA-seq] |
GSE122341 |
An unstructured MET-2/SETDB1 cofactor ensures H3K9me2, focus formation and perinuclear anchoring |
GSE122544 |
RNA sequencing to identify NPR-8-regulated genes in C. elegans defense against pathogen infection |
GSE122639 |
Binding of an X-specific condensin correlates with a reduction in active histone modifications at gene regulatory elements |
GSE122728 |
RNASeq of C. elegans exposed to silver (Ag) or silicon dioxide (SiO2) nanoparticles |
GSE122996 |
High-throughput transcriptome sequencing reveals extremely high doses of ionizing radiation-response genes in Caenorhabditis elegans |
GSE123862 |
Loss of miR-83 extends lifespan and affects target gene expression in an age-dependent manner in Caenorhabditis elegans |
GSE124049 |
Neuronal Small RNAs Control Behavior Transgenerationally |
GSE124994 |
Multi-omics and genome-scale modeling reveal a metabolic shift during C. elegans ageing |
GSE125051 |
C. elegans cnd-1/NeuroD1 functions with the Hox gene ceh-13/labial to control multiple genes required for nervous system development and function |
GSE125716 |
Expression analysis of C. elegans eat-2, eat-2; acs-22 and eat-2; pmk-1; acs-22 mutants |
GSE125718 |
Expression analysis of C. elegans wild-type N2, eat-2, acs-20 and eat-2; acs-20 mutants |
GSE126585 |
RNA-seq using the Cel-Seq2 method, of wild type and 35-polyglutamine (polyQ35) expressing C. elegans worms treated with RNAi toward anc-1, or left untreated (EV) gene expression profiles. |
GSE126632 |
HLH-30/TFEB is a master regulator of reproductive quiescence |
GSE126656 |
The transcription factors TFEB and TFE3 link the FLCN-AMPK signaling axis to innate immune response and pathogen resistance |
GSE127917 |
NFYB-1 regulates mitochondrial function and longevity via lysosomal prosaposin |
GSE128030 |
The transcription factors TFEB and TFE3 link the FLCN-AMPK signaling axis to innate immune response and pathogen resistance [RNA-seq] |
GSE128746 |
The C. elegans SET-2 histone methyltransferase maintains germline fate by preventing progressive transcriptomic deregulation across generations |
GSE128935 |
Endogenous siRNAs promote proteostasis and longevity in germline-less Caenorhabditis elegans |
GSE129928 |
H3K9me2 protects lifespan against the transgenerational burden of germline transcription in C. elegans |
GSE130782 |
mRNA sequencing time course of C. elegans samples at time point 0 hours until time point 15 hours at 25 degree. |
GSE130811 |
mRNA-seq time course of C. elegans sampled from 5h until 48h at 25 degrees |
GSE130927 |
Bulk RNA sequencing of cell specific profile of RIS |
GSE131870 |
Ferritin regulation upon ETS-4/SPDEF depletion promotes cold survival in C. elegans |
GSE131997 |
N2, daf-1(m40), and daf-1(m40);daf-3(mgDf90) adult, gravid hermaphrodites |
GSE132594 |
The transcriptional response of C. elegans to statins: general and p38 dependent responses |
GSE132794 |
Neuronal TORC1 modulates longevity via AMPK and cell nonautonomous regulation of mitochondrial dynamics in C. elegans |
GSE132838 |
RNA Sequencing of CTRL and Heat Stressed C. elegans [RNA-seq] |
GSE132876 |
RNA Sequencing of CTRL and Heat Stressed C. elegans |
GSE133356 |
LSM2-8 and XRN-2 contribute to the silencing of H3K27me3 marked genes through targeted RNA decay II |
GSE133421 |
mRNA sequencing time course of C. elegans samples at time point 1 hours until time point 16 hours at room temperature |
GSE133576 |
State transitions of a developmental oscillator |
GSE134196 |
The C. elegans ortholog of human selenium binding protein 1 is a pro-aging factor protecting against selenite toxicity |
GSE134535 |
Expression data from the complex I mutant gas-1 (fc21) C. elegans worms in comparison to wildtype N2 Bristol worm and under the inluence combination drug therapy |
GSE134627 |
meg-3 meg-4 mutants are defective in exogenous RNAi signal amplification |
GSE134628 |
meg-3 meg-4 upregulate endogenous sRNAs targeting RNAi genes and downregulate their mRNAs |
GSE134629 |
The hrde-1 mutation suppresses the rde-11 and sid-1 sRNA upregulation phenotype of meg-3 meg-4 mutants |
GSE134638 |
P granules protect RNA interference genes from silencing by piRNAs |
GSE134687 |
Oligosaccharyl transferase that maintains ER homeostasis enhances immunity via up-regulating p38 MAP kinase signaling in C. elegans |
GSE134989 |
RNA-seq analysis in syp-2::AID and N2 controls with and without auxin treatment (4 hours at 4 mM concentration) |
GSE136576 |
RNA-seq: Loss of a heterochromatin anchor rescues altered genome organization and EDMD muscle defects triggered by a laminopathy mutation |
GSE136577 |
Loss of a heterochromatin anchor rescues altered genome organization and EDMD muscle defects triggered by a laminopathy mutation |
GSE136612 |
The time course of microRNA transcriptomes during C. elegans ageing |
GSE137267 |
Repression of an activity-dependent autocrine insulin signal is required for sensory neuron development in C. elegans |
GSE137734 |
henn-1/HEN1 promotes germline immortality in Caenorhabditis elegans |
GSE137861 |
FOXO and HSF1 rejuvenate immunity via positive feedback regulation of insulin/IGF-1 signaling |
GSE138035 |
C. elegans LPIN-1 moderates lifespan-shortening effects of dietary glucose via maintaining ω-6 polyunsaturated fatty acids |
GSE138129 |
VRK-1 Extends Lifespan by Activation of AMPK via Phosphorylation |
GSE138199 |
Organism Dual RNA-Seq Reveals the Control on both Pathogen and Host through BarA/UvrY of Vibrio parahaemolyticus for Successful Infection |
GSE139530 |
CDE-1 suppresses the production of risiRNA by coupling polyuridylation and degradation of 26S rRNA |
GSE139878 |
Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (iCLIP results) |
GSE139879 |
Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq datasets) |
GSE139880 |
Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling) |
GSE139881 |
Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins |
GSE140804 |
Loss of histone H3.3 results in DNA replication defects and altered origin dynamics in C. elegans. |
GSE140863 |
C. elegans development (ChIP-Seq) |
GSE140865 |
C. elegans development |
GSE140866 |
mRNA-seq of wild-type(N2), hlh-11 knock-out(KO) and hlh-11 over-expression(OE) worms |
GSE141041 |
mRNA-seq of worms and the mitochondrial unfolded protein response (UPRmt) |
GSE141514 |
mRNA sequencing time course of C. elegans samples at time point 1 hours until time point 24 hours at 25 degrees [N2 control] |
GSE143794 |
RNAseq of C. elegans grown with different bacteria isolates |
GSE143837 |
C. elegans establishes germline versus soma by balancing inherited histone methylation [RNA-seq] |
GSE143838 |
C. elegans establishes germline versus soma by balancing inherited histone methylation [ChIP-seq] |
GSE143839 |
C. elegans establishes germline versus soma by balancing inherited histone methylation |
GSE144118 |
Genome-wide expression analysis of C. elegans nematodes after feeding RNAi impairment of the transcription factors lin-32 and hlh-2 |
GSE144289 |
microRNA form extracellular vesicles-enriched preparations of the free-livingnematode Caenorhabditis elegans (strain N2, Bristol) cultured in vitro |
GSE145123 |
Neuronal HSF-1 activity coordinates fat desaturation across tissues in C. elegans via TGF-b/BMP signalling |
GSE145255 |
Gene expression profile of C. elegans biogenic amine synthesis mutants |
GSE146443 |
Genome-wide profiling of age-dependent changes in gene expression between L4 larvae and Day 6 adult Caenorhabditis elegans |
GSE147388 |
mRNA sequencing time course of C. elegans samples at time point 1 hours until time point 24 hours at 25 degree [blmp-1(tm548) mutant] |
GSE147401 |
The zinc-finger protein OEF-1 stabilizes patterns of activating and silencing modifications in the C. elegans germ line |
GSE147894 |
mRNA-seq time course of C. elegans sampled at and after release from dauer starvation at 25 degrees |
GSE148337 |
Regulation of the transcriptional response to mechanical trauma by vhp-1 |
GSE149071 |
The RNA Polymerase II subunit RPB-9 directs transcriptional elongation at piRNA loci in C. elegans |
GSE149300 |
Transcriptome analyses revealed differentially expressed genes in DAF-16 WT and KR mutants. |
GSE149422 |
Three Rules Explain Transgenerational Small RNA Inheritance in C. elegans |
GSE150135 |
Transcriptomic analysis of C. elegans infected with Myzocytiopsis humicola or treated with its extract |
GSE151164 |
Caenorhabditis elegans AF4/FMR2 family homolog affl-2 regulates heat shock induced gene expression |
GSE151216 |
Differential gene expression analysis to identify canonical Wnt signaling target genes in QR neuroblast descendants in C. elegans |
GSE151715 |
Protease-mediated processing of Argonaute proteins controls small RNA association [smallRNA-Seq] |
GSE151716 |
Protease-mediated processing of Argonaute proteins controls small RNA association [RIP-Seq] |
GSE151717 |
Protease-mediated processing of Argonaute proteins controls small RNA association |
GSE152257 |
Defining the transcriptomic fingerprints of benzo[a]pyrene exposure in Caenorhabditis elegans |
GSE153233 |
Two miRNAs are sufficient for C. elegans embryogenesis |
GSE154324 |
RNA-Seq to identify NMUR-1-regulated genes in C. elegans defense against pathogen infection |
GSE154338 |
A PTEN variant uncouples longevity from impaired fitness in C. elegans via tuning the activity of FOXO and NRF |
GSE154678 |
Two isoforms of the essential C. elegans Argonaute CSR-1 differentially regulate sperm and oocyte fertility through distinct small RNA classes |
GSE155392 |
Combinatorial action of temporally-segregated transcription factors |
GSE156507 |
Comparing the transcriptomic responses of Caenorhabditis elegans exposed to cadmium from L1 to L3 versus L1 to L4 stage |
GSE156540 |
Protease-mediated processing of Argonaute proteins controls small RNA association [small RNA RIP-seq] |
GSE156548 |
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (ChIP-seq) |
GSE156549 |
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (RNA-seq) |
GSE156550 |
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (smallRNA-seq) |
GSE156551 |
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 |
GSE158729 |
RNA-Sequencing used to identify the targets of NHR-49, a transcription factor that acts in distinct tissues to promote longevity versus immunity |
GSE160304 |
The ZSWIM8 ubiquitin ligase mediates target-directed microRNA degradation |
GSE161984 |
ChIP-seq of wild type and ets-5-gfp worms |
GSE161985 |
mRNAseq of wild type and ets-5 mutant C. elegans BAG neurons |
GSE162002 |
Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity |
GSE163389 |
The ZSWIM8 ubiquitin ligase mediates target-directed microRNA degradation [dataset 4] |
GSE165078 |
Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription in C. elegans |
GSE165793 |
An optimized ribodepletion approach for C. elegans RNA-sequencing libraries |
GSE166512 |
Gene Regulatory Network inference in long-lived C. elegans reveals modular properties that are predictive of novel ageing genes |
GSE166788 |
NHR-49 controls a HIF-1 independent hypoxia adaptation pathway in Caenorhabditis elegans |
GSE167165 |
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity [ATAC-seq] |
GSE167166 |
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity [CUT&RUN; ChICseq] |
GSE167167 |
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity [RNA-seq] |
GSE167168 |
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity |
GSE168322 |
Anti-aging effects of Vicatia thibetica de Boiss root extract on Caenorhabditis elegans and doxorubicin-induced mice via promoting collagen and stress resistance |
GSE168803 |
Condensin DC spreads linearly and bidirectionally from recruitment sites to create loop-anchored TADs in C. elegans |
GSE168923 |
A structural role for histone methyltransferase MET-2 represses transcription independent of H3K9me catalysis [ChIP-seq] |
GSE168924 |
A structural role for histone methyltransferase MET-2 represses transcription independent of H3K9me catalysis [RNA-seq] |
GSE168925 |
A structural role for histone methyltransferase MET-2 represses transcription independent of H3K9me catalysis |
GSE169137 |
Bulk RNA seq of sorted C. elegans neurons |
GSE169250 |
Condensin DC spreads linearly and bidirectionally from recruitment sites to create loop-anchored TADs in C. elegans (ChIP-seq) |
GSE169458 |
Mobility of condensin DC is key to its function in repressing transcription |
GSE169524 |
Mobility of condensin DC is key to its function in repressing transcription [ChIP-seq] |
GSE169640 |
Rhythmic transcription drives mRNA level oscillations during C. elegans development [RNA-Seq] |
GSE169641 |
Rhythmic transcription drives mRNA level oscillations during C. elegans development [ChIP-Seq] |
GSE169642 |
Rhythmic transcription drives mRNA level oscillations during C. elegans development |
GSE171089 |
Transcriptional Response to Dauer-Inducing Ascarosides in Late L1 in C. elegans |
GSE172070 |
C. elegans small RNA-seq profiling of three different lotr-1 mutant alleles |
GSE173287 |
RNA sequencing of cell-specific profile of wild type and unc-4 VAs |
GSE173580 |
RNA-seq Files : The Hypoxia Response Pathway Promotes PEP Carboxykinase And Gluconeogenesis In C. elegans |
GSE173581 |
The Hypoxia Response Pathway Promotes PEP Carboxykinase And Gluconeogenesis In C. elegans |
GSE174368 |
Phosphorylation of the Argonaute ALG-1 regulates microRNA binding during C. elegans development |
GSE175950 |
RNA sequencing of wild type C.elegans exposed to Haptoglossa zoospora for 6 or 12 hours |
GSE179166 |
daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71 |
GSE184076 |
Crotamiton derivative JM03 extends lifespan and improves 1 oxidative and hypertonic stress resistance in Caenorhabditis 2 elegans via inhibiting OSM-9 |
GSE184149 |
RNAs regulated by MEC-8 in C. elegnas touch receptor neurons |
GSE184415 |
Transcriptome of insulin signalling associated transcription factor targets |
GSE185304 |
MSTR-1::FLAG and N2 |
GSE186202 |
RNA sequencing to study the molecular relationships between temperature, aging, and NPR-8 |
GSE191294 |
mRNA-seq of worms who raised on control RNAi or prp-19 RNAi were untreated or treated with atp-2 RNAi |
GSE192794 |
LOTR-1 interacts with ZNFX-1 to balance epigenetic signals in the C. elegans germline |
GSE196043 |
mRNA aging shapes the Cap2 methylome in mammalian mRNA |
GSE197410 |
Transcellular chaperone signaling is an intercellular stress-response that is distinct from the HSF-1 mediated HSR [RNA-seq] |
GSE197411 |
Transcellular chaperone signaling is an intercellular stress-response that is distinct from the HSF-1 mediated HSR [WGS] |
GSE197412 |
Transcellular chaperone signaling is an intercellular stress-response that is distinct from the HSF-1 mediated HSR |
GSE197834 |
Using single-worm RNA sequencing to study C. elegans responses to pathogen infection |
GSE198552 |
Maternal H3K36 and H3K27 HMTs protect germline development via regulation of the transcription factor LIN-15B |
GSE199192 |
The CHARGE syndrome ortholog CHD-7 regulates TGF-b pathways in C. elegans |
GSE200459 |
Crotamiton derivative JM03 extends lifespan and improves oxidative and hypertonic stress resistance in Caenorhabditis elegans via inhibiting OSM-9 |
GSE202877 |
Mechanistic study of Lcr35 probiotic properties using C. elegans model |
GSE203297 |
Comparative analysis of piRNA sequences, targets and functions in Caenorhabditis nematodes |
GSE205061 |
Afadin and Zyxin contribute to coupling between cell junctions and contracting actomyosin networks during apical constriction |
GSE205337 |
Within-species control reveals novel immune response genes in Caenorhabditis elegans |
GSE206756 |
Transcriptomic analysis of pals-25(icb98gf) mutants in C. elegans |
GSE208558 |
Effect of mstr-1 knockout on global mRNA expression in C. elegans |
GSE208700 |
A Comprehensive Survey of C. elegans Argonaute Proteins Reveals Organism-wide Gene Regulatory Networks and Functions [Argonaute IP] |
GSE208701 |
A Comprehensive Survey of C. elegans Argonaute Proteins Reveals Organism-wide Gene Regulatory Networks and Functions [mutants] |
GSE208702 |
A Comprehensive Survey of C. elegans Argonaute Proteins Reveals Organism-wide Gene Regulatory Networks and Functions |
GSE211555 |
Specialized germline P-bodies are required to specify germ cell fate in C. elegans embryos |
GSE211846 |
Chromatin epimutations in transgenerational epigenetic inheritance |
GSE213508 |
Whole-organism C. elegans L2 GRH-1 ChIP-seq (experiment 1 of 2) |
GSE213509 |
Whole-organism C. elegans L2 GRH-1 ChIP-seq (experiment 2 of 2) |
GSE213510 |
Whole-organism C. elegans L2 GRH-1 ChIP-seq |
GSE215256 |
Ketamine induces apical extracellular matrix modifications in C. elegans |
GSE220744 |
Homeodomain-interacting protein kinase maintains neuronal homeostasis during normal Caenorhabditis elegans aging and systemically regulates longevity from serotonergic and GABAergic neurons |
GSE228099 |
High-fidelity encoding of mechanostimuli by tactile food-sensing neurons requires an ensemble of ion channels |
GSE229078 |
Bulk RNA seq of sorted C. elegans neurons |
GSE230883 |
ADBP-1 regulates ADR-2 nuclear localization to control editing substrate selection |
GSE239800 |
The differential microRNA profile between male and hermaphrodite gonads |
GSE240821 |
The C. elegans Myc-family of transcription factors coordinate a dynamic adaptive response to dietary restriction |
GSE243842 |
High power of 0.26 Terahertz radiation induced genes involved in immune system and nervous system changes in the nematode Caenorhabditis Elegans |
GSE244073 |
Pre-piRNA trimming safeguards piRNAs against erroneous targeting by RNA-Dependent RNA Polymerase |
GSE244493 |
RNA helicase HEL-1 promotes longevity by specifically activating DAF-16/FOXO transcription factor signaling in Caenorhabditis elegans |
GSE244494 |
Reduced insulin/IGF1 signaling prevents immune aging via ZIP-10/bZIP–mediated feedforward loop |
GSE244495 |
Prefoldin 6 mediates longevity response from heat shock factor 1 to FOXO in C. elegans |
GSE245900 |
Dynamic regulation of miRNA accumulation during C. elegans larval development [smallRNA-Seq 3] |
GSE245902 |
Dynamic regulation of miRNA accumulation during C. elegans larval development [smallRNA-Seq 5] |
GSE245904 |
Dynamic regulation of miRNA accumulation during C. elegans larval development |
GSE256553 |
Control ChIP-seq from whole organism (ENCSR101VVI) |
GSE256565 |
Control ChIP-seq from whole organism (ENCSR187HHD) |
GSE256593 |
Control ChIP-seq from whole organism (ENCSR007JPR) |
GSE256594 |
TF ChIP-seq from whole organism (ENCSR107BQR) |
GSE256595 |
Control ChIP-seq from whole organism (ENCSR107LHB) |
GSE256608 |
TF ChIP-seq from whole organism (ENCSR110CKX) |
GSE256617 |
TF ChIP-seq from whole organism (ENCSR111LGE) |
GSE256618 |
Control ChIP-seq from whole organism (ENCSR111NKF) |
GSE256639 |
Control ChIP-seq from whole organism (ENCSR194OUP) |
GSE256734 |
TF ChIP-seq from whole organism (ENCSR292NVQ) |
GSE256812 |
Control ChIP-seq from whole organism (ENCSR030PDY) |
GSE256845 |
TF ChIP-seq from whole organism (ENCSR032FII) |
GSE256848 |
TF ChIP-seq from whole organism (ENCSR133PLZ) |
GSE256849 |
TF ChIP-seq from whole organism (ENCSR213XFQ) |
GSE256852 |
TF ChIP-seq from whole organism (ENCSR133RTP) |
GSE256895 |
Control ChIP-seq from whole organism (ENCSR139CXE) |
GSE256907 |
TF ChIP-seq from whole organism (ENCSR311NAQ) |
GSE256977 |
Control ChIP-seq from whole organism (ENCSR225ALY) |
GSE257000 |
TF ChIP-seq from whole organism (ENCSR321VWM) |
GSE257005 |
Control ChIP-seq from whole organism (ENCSR040FYF) |
GSE257007 |
Control ChIP-seq from whole organism (ENCSR041BTW) |
GSE257026 |
Control ChIP-seq from whole organism (ENCSR324PNK) |
GSE257041 |
TF ChIP-seq from whole organism (ENCSR233MSN) |
GSE257078 |
TF ChIP-seq from whole organism (ENCSR162MNX) |
GSE257106 |
TF ChIP-seq from whole organism (ENCSR327NRA) |
GSE257122 |
TF ChIP-seq from whole organism (ENCSR238YNR) |
GSE257132 |
Control ChIP-seq from whole organism (ENCSR332LQE) |
GSE257155 |
Control ChIP-seq from whole organism (ENCSR055WPE) |
GSE257158 |
Control ChIP-seq from whole organism (ENCSR169GCJ) |
GSE257204 |
Control ChIP-seq from whole organism (ENCSR178IVN) |
GSE257230 |
Control ChIP-seq from whole organism (ENCSR064VSR) |
GSE257239 |
TF ChIP-seq from whole organism (ENCSR182IGG) |
GSE257256 |
Control ChIP-seq from whole organism (ENCSR246FAX) |
GSE257268 |
TF ChIP-seq from whole organism (ENCSR185SVY) |
GSE257313 |
TF ChIP-seq from whole organism (ENCSR081BBL) |
GSE257348 |
TF ChIP-seq from whole organism (ENCSR345JIR) |
GSE257365 |
Control ChIP-seq from whole organism (ENCSR347AVI) |
GSE257374 |
Control ChIP-seq from whole organism (ENCSR091ZYU) |
GSE257381 |
Control ChIP-seq from whole organism (ENCSR251RZP) |
GSE257386 |
Control ChIP-seq from whole organism (ENCSR095MXI) |
GSE257427 |
TF ChIP-seq from whole organism (ENCSR359GJP) |
GSE257439 |
TF ChIP-seq from whole organism (ENCSR260GEE) |
GSE257460 |
TF ChIP-seq from whole organism (ENCSR264JKE) |
GSE257470 |
TF ChIP-seq from whole organism (ENCSR266NAT) |
GSE257475 |
TF ChIP-seq from whole organism (ENCSR371DPT) |
GSE257502 |
TF ChIP-seq from whole organism (ENCSR274WQG) |
GSE257504 |
Control ChIP-seq from whole organism (ENCSR276KDH) |
GSE257556 |
TF ChIP-seq from whole organism (ENCSR376OYD) |
GSE257631 |
Control ChIP-seq from whole organism (ENCSR545DXH) |
GSE257636 |
TF ChIP-seq from whole organism (ENCSR686FKU) |
GSE257664 |
TF ChIP-seq from whole organism (ENCSR379UPR) |
GSE257731 |
TF ChIP-seq from whole organism (ENCSR557ZYT) |
GSE257734 |
Control ChIP-seq from whole organism (ENCSR559HIP) |
GSE257745 |
Control ChIP-seq from whole organism (ENCSR561ULE) |
GSE257747 |
TF ChIP-seq from whole organism (ENCSR693VPE) |
GSE257756 |
Control ChIP-seq from whole organism (ENCSR866EST) |
GSE257780 |
Control ChIP-seq from whole organism (ENCSR568HWW) |
GSE257850 |
TF ChIP-seq from whole organism (ENCSR698RXJ) |
GSE257954 |
Control ChIP-seq from whole organism (ENCSR884LDO) |
GSE257970 |
TF ChIP-seq from whole organism (ENCSR891WMQ) |
GSE257994 |
Control ChIP-seq from whole organism (ENCSR896VBS) |
GSE258000 |
Control ChIP-seq from whole organism (ENCSR709XYX) |
GSE258018 |
Control ChIP-seq from whole organism (ENCSR713MAY) |
GSE258046 |
TF ChIP-seq from whole organism (ENCSR406IHG) |
GSE258063 |
TF ChIP-seq from whole organism (ENCSR905YIL) |
GSE258079 |
Control ChIP-seq from whole organism (ENCSR908SMR) |
GSE258120 |
TF ChIP-seq from whole organism (ENCSR604KUU) |
GSE258131 |
TF ChIP-seq from whole organism (ENCSR607BSL) |
GSE258199 |
TF ChIP-seq from whole organism (ENCSR420ATF) |
GSE258204 |
TF ChIP-seq from whole organism (ENCSR917KLO) |
GSE258205 |
Control ChIP-seq from whole organism (ENCSR917QWA) |
GSE258223 |
TF ChIP-seq from whole organism (ENCSR735XWN) |
GSE258246 |
Control ChIP-seq from whole organism (ENCSR420LNH) |
GSE258257 |
Control ChIP-seq from whole organism (ENCSR745OUC) |
GSE258262 |
Control ChIP-seq from whole organism (ENCSR620OAL) |
GSE258270 |
TF ChIP-seq from whole organism (ENCSR623HHL) |
GSE258318 |
TF ChIP-seq from whole organism (ENCSR422GZR) |
GSE258322 |
TF ChIP-seq from whole organism (ENCSR422XRE) |
GSE258328 |
Control ChIP-seq from whole organism (ENCSR749OUM) |
GSE258329 |
TF ChIP-seq from whole organism (ENCSR632XME) |
GSE258347 |
TF ChIP-seq from whole organism (ENCSR753PGF) |
GSE258356 |
Control ChIP-seq from whole organism (ENCSR934KWG) |
GSE258378 |
TF ChIP-seq from whole organism (ENCSR427JJZ) |
GSE258411 |
Control ChIP-seq from whole organism (ENCSR760TJW) |
GSE258413 |
TF ChIP-seq from whole organism (ENCSR938NRX) |
GSE258414 |
TF ChIP-seq from whole organism (ENCSR639CLM) |
GSE258415 |
Control ChIP-seq from whole organism (ENCSR639KBJ) |
GSE258422 |
Control ChIP-seq from whole organism (ENCSR939PJG) |
GSE258440 |
TF ChIP-seq from whole organism (ENCSR435FDM) |
GSE258454 |
TF ChIP-seq from whole organism (ENCSR438PSB) |
GSE258498 |
Control ChIP-seq from whole organism (ENCSR767ZKR) |
GSE258500 |
TF ChIP-seq from whole organism (ENCSR943FFC) |
GSE258544 |
Control ChIP-seq from whole organism (ENCSR446MQH) |
GSE258553 |
Control ChIP-seq from whole organism (ENCSR449ROG) |
GSE258569 |
TF ChIP-seq from whole organism (ENCSR450GPA) |
GSE258574 |
Control ChIP-seq from whole organism (ENCSR948SUV) |
GSE258617 |
Control ChIP-seq from whole organism (ENCSR654ODD) |
GSE258618 |
TF ChIP-seq from whole organism (ENCSR955ZJN) |
GSE258623 |
TF ChIP-seq from whole organism (ENCSR955ZWH) |
GSE258627 |
Control ChIP-seq from whole organism (ENCSR782TWP) |
GSE258667 |
Control ChIP-seq from whole organism (ENCSR961THO) |
GSE258689 |
Control ChIP-seq from whole organism (ENCSR792LGD) |
GSE258735 |
TF ChIP-seq from whole organism (ENCSR968HCJ) |
GSE258759 |
TF ChIP-seq from whole organism (ENCSR470XFF) |
GSE258852 |
Control ChIP-seq from whole organism (ENCSR975BES) |
GSE258857 |
Control ChIP-seq from whole organism (ENCSR671YDD) |
GSE258859 |
TF ChIP-seq from whole organism (ENCSR475ZYS) |
GSE258861 |
TF ChIP-seq from whole organism (ENCSR806QUX) |
GSE258868 |
TF ChIP-seq from whole organism (ENCSR807UTG) |
GSE258877 |
TF ChIP-seq from whole organism (ENCSR977VOU) |
GSE258878 |
TF ChIP-seq from whole organism (ENCSR673WIC) |
GSE258882 |
TF ChIP-seq from whole organism (ENCSR674PDL) |
GSE258891 |
TF ChIP-seq from whole organism (ENCSR980XNE) |
GSE258914 |
Control ChIP-seq from whole organism (ENCSR481GBB) |
GSE258926 |
Control ChIP-seq from whole organism (ENCSR484UJP) |
GSE258945 |
Control ChIP-seq from whole organism (ENCSR981QSV) |
GSE258970 |
Control ChIP-seq from whole organism (ENCSR490CWU) |
GSE258976 |
Control ChIP-seq from whole organism (ENCSR814NFI) |
GSE259011 |
TF ChIP-seq from whole organism (ENCSR498FBJ) |
GSE259041 |
TF ChIP-seq from whole organism (ENCSR992FVB) |
GSE259049 |
Control ChIP-seq from whole organism (ENCSR821PFS) |
GSE259054 |
TF ChIP-seq from whole organism (ENCSR505TSF) |
GSE259093 |
Control ChIP-seq from whole organism (ENCSR507IIG) |
GSE259114 |
Control ChIP-seq from whole organism (ENCSR830PLY) |
GSE259134 |
TF ChIP-seq from whole organism (ENCSR517OZM) |
GSE259141 |
TF ChIP-seq from whole organism (ENCSR836LVI) |
GSE259165 |
Control ChIP-seq from whole organism (ENCSR523RCF) |
GSE259208 |
TF ChIP-seq from whole organism (ENCSR534TFA) |
GSE260938 |
An Intricate Network Involving the Argonaute ALG-1 Modulates Organismal Resistance to Oxidative Stress miRNAs in a longevity model and an alg-1 overexpression model. |
GSE261784 |
Transcriptomic Analysis of the Spatiotemporal Axis of Oogenesis and Fertilization in C. elegans |
GSE268926 |
Effect of fasting on transcription in intestinal cells dissected from adult C. elegans |
GSE268974 |
Effect of RNA Polymerase I (RPOA-2) degradation on transcription in intestinal cells dissected from adult C. elegans |