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7,327 results for “Pathway”

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dryad32/100

Data from: Evolutionary routes to biochemical innovation revealed by integrative analysis of a plant-defense related specialized metabolic pathway

Open the record for dataset details and reuse information.

publicSep 2017View details →
dryad32/100

Data from: High-resolution chemical dissection of a model eukaryote reveals targets, pathways and gene functions

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publicNov 2014View details →
dryad32/100

Alternative pathways to diversity across ecologically distinct lizard radiations

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publicDec 2020View details →
dryad32/100

Cortical astrocytes independently regulate sleep depth and duration via separate GPCR pathways

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publicDec 2020View details →
dryad32/100

Pathways to care and preferences for improving tuberculosis services among tuberculosis patients in Zambia

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publicApr 2021View details →
zenodo28/100

How to open up my journal - Pathways into open access

<p>This decision tree&nbsp;helps you to choose the right path for the open access transformation of your society journal. Together with your publishing partners you can&nbsp;discuss the&nbsp;optimal business model. A selection can be found at the end.</p>

opencc-by-4.0Feb 2020View details →
dryad28/100

Data from: Live, dead, and fossil mollusks in Florida freshwater springs and spring-fed rivers: taphonomic pathways and the formation of multi-sourced, time-averaged death assemblages

Taphonomic processes are informative about the magnitude and timing of paleoecological changes but remain poorly understood with respect to freshwater invertebrates in spring-fed rivers and streams. We compared taphonomic alteration among freshwater gastropods in live, dead (surficial shell accumulations), and fossil (late Pleistocene-early Holocene in situ sediments) assemblages from two Florida spring-fed systems, the Wakulla and Silver/Ocklawaha Rivers. We assessed taphonomy of two gastropod species: the native <i>Elimia floridensis</i> (n=2504) and introduced <i>Melanoides tuberculata</i> (n=168). We quantified seven taphonomic attributes (aperture condition, color, fragmentation, abrasion, juvenile spire condition, dissolution, and exterior luster) and combined those attributes into a total taphonomic score (TT). Fossil <i>E. floridensis</i> specimens exhibited the greatest degradation (highest TT scores), whereas live specimens of both species were least degraded. Specimens of <i>E. floridensis</i> from death assemblages were less altered than fossil specimens of the same species. Within death assemblages, specimens of <i>M. tuberculata</i> were significantly less altered than specimens of <i>E. floridensis</i>, but highly degraded specimens dominated in both species. Radiocarbon dates on fossils clustered between 9792 and 7087 cal. BP, whereas death assemblage ages ranged from 10,692 to 1173 cal. BP. Possible explanations for the observed taphonomic patterns include: (1) rapid taphonomic shell alteration, (2) prolonged near-surface exposure to moderate alteration rates, and/or (3) introduction of reworked fossil shells into surficial assemblages. Combined radiocarbon dates and taphonomic analyses suggest that all these processes may have played a role in death assemblage formation. In these fluvial settings, shell accumulations develop as a complex mixture of specimens derived from multiple sources and characterized by multi-millennial time averaging. These findings suggest that, when available, fossil assemblages may be more appropriate than death assemblages for assessing pre-industrial faunal associations and recent anthropogenic changes in freshwater ecosystems.

opencc-zeroMay 2020View details →
zenodo28/100

Data for "Cold surge pathways in East Asia and their tropical impacts"

<p>This repository archives codes for analysis and plot presented in a manuscript submitted to Journal of Climate:&nbsp;&quot;Cold surge pathways in East Asia and their tropical impacts&quot;. The codes are written in GrADS and&nbsp;Octave&nbsp;format.&nbsp;</p> <p>The repository also includes&nbsp;a Fortran package for isentropic polar cold air mass diagnosis as in Iwasaki et al. (2014). The package was specifically created by Dr. Y. Kanno.</p>

opencc-by-4.0Jul 2020View details →
dryad28/100

Data from: Impact of a novel community testing pathway for people with suspected COVID-19 in Wales: a cost-minimisation analysis

<p><b>Objective: </b>To compare NHS organisations testing pathways for patients with suspected COVID-19 in the community versus standard hospital testing practices</p> <p><b>Perspective</b>: NHS commissioners and services</p> <p><b>Methods</b>: During the containment phase of the Covid-19 pandemic we developed a community model pathway for Covid-19 testing in Wales with testing teams undertaking swabbing for Covid-19 in individuals usual place of residence. We undertook a cost-minimisation analysis comparing the costs to the NHS in Wales of community testing for COVID-19 versus standard hospital testing practices and ambulance conveyancing. We analysed data from patients with suspected COVID-19 between January and February 2020 and applied assumptions of costs from national contractual and reference costs for ambulances, staffing and transportation with market costs at the time of publication.</p> <p><b>Results</b>: 177 patients with suspected COVID-19 underwent community testing via local NHS organisations between January and February 2020 with a mean age of 46.1 (IQR 27.5-56.3). This was 92% of total patients who were tested for Covid-19 during this period. We estimate, compared to standard hospital testing practices cash savings in improved productivity for the NHS of £152,190 during this time period, in addition to further non-monetised benefits for hospital and ambulance flow.</p> <p><b>Conclusions</b>: Community testing for COVID-19 in Wales is now an established pathway and continues to bring benefits for patients, local healthcare organisations and the NHS. Further application of this model in other settings and to other infectious diseases may herald promising returns.</p>

opencc-zeroAug 2020View details →
dryad28/100

Phylogenomic analysis sheds light on the evolutionary pathways towards acoustic communication in Orthoptera

<p>Acoustic communication is enabled by the evolution of specialised hearing and sound producing organs. In this study, we performed a large-scale macroevolutionary study to understand how both hearing and sound production evolved and affected diversification in the insect order Orthoptera, which includes many familiar singing insects, such as crickets, katydids, and grasshoppers. Using phylogenomic data, we firmly establish phylogenetic relationships among the major lineages and divergence time estimates within Orthoptera, as well as the lineage-specific and dynamic patterns of evolution for hearing and sound producing organs. In the suborder Ensifera, we infer that forewing-based stridulation and tibial tympanal ears co-evolved, but in the suborder Caelifera, abdominal tympanal ears first evolved in a non-sexual context, and later co-opted for sexual signalling when sound producing organs evolved. However, we find little evidence that the evolution of hearing and sound producing organs increased diversification rates in those lineages with known acoustic communication.</p>

opencc-zeroDec 2019View details →
zenodo28/100

Supplementary Materials for Digenic Variants in the FGF21 Signaling Pathway Associated with Severe Insulin Resistance and Pseudoacromegaly

<p>Supplementary Materials for&nbsp;Digenic Variants in the FGF21 Signaling Pathway Associated with Severe Insulin Resistance and Pseudoacromegaly. This includes additional photographs of the proband and family, bone age x-ray, smell identification testing, ERK phosphorylation in HeLa Cells, Candidate genes from research exome, and full plasmid sequences used in the study.</p>

opencc-by-4.0Sep 2020View details →
dryad28/100

Pathways linking female personality with reproductive success are trait and year-specific

<p>Personality  (i.e.  among-individual  variation  in  average  behavior)  often  covaries  with  fitness,  but  how  such  personality-fitness  relationships  come  about  is  poorly  understood.  Here,  we  explore  potential  mechanisms  by  which  two  female  personality  traits  (female-female  aggression  and  female  nest  defense  as  manifested  by  hissing  behavior)  were  linked  with  annual  reproductive  success  in  a  population  of  great  tits  (<i>Parus  major</i>),  a  socially  monogamous  species  with  biparental  care.  We  hypothesized  that  personality-related  differences  in  reproductive  success  result  from  variation  in  reproductive  decision  (lay  date,  brood  size)  and/or  parental  provisioning  rates.  Relative  support  for  these  mechanisms  was  evaluated  using  path-analysis  on  data  collected  in  two  successive  years.  We  reveal  that  larger  broods  were  provisioned  at  a  higher  rate  by  both  parents  and  that  female,  but  not  male,  provisioning  rate  was  involved  in  the  trade-off  between  offspring  number  (brood  size)  and  fledgling  mass.  Among-individual  variation  in  female  aggression,  via  its  association  with  female  provisioning  rate,  was  negatively  linked  to  fledgling  mass  (i.e.  indirect  effect),  yet  only  in  one  of  the  study  years.  Male  provisioning  rate  did  not  influence  these  relationships.  In  contrast,  among-individual  variation  in  hissing  behavior  was  directly  and  negatively  linked  with  fledgling  mass  in  both  years,  via  an  underlying  mechanism  that  remains  to  be  identified  (i.e.  direct  effect).  Together,  our  findings  emphasize  that  personality-fitness  relationships  may  come  about  via  different  mechanisms  across  personality  traits  and/or  years,  thereby  illustrating  additional  complexity  in  how  selection  might  act  on  and  maintain  among-individual  variation  in  behavioral  phenotypes  in  the  wild.</p>

opencc-zeroDec 2019View details →
zenodo28/100

Supplementary material 1 from: Pergl J, Brundu G, Harrower CA, Cardoso AC, Genovesi P, Katsanevakis S, Lozano V, Perglová I, Rabitsch W, Richards G, Roques A, Rorke SL, Scalera R, Schönrogge K, Stewart A, Tricarico E, Tsiamis K, Vannini A, Vilà M, Zenetos A, Roy HE (2020) Applying the Convention on Biological Diversity Pathway Classification to alien species in Europe. In: Wilson JR, Bacher S, Daehler CC, Groom QJ, Kumschick S, Lockwood JL, Robinson TB, Zengeya TA, Richardson DM. NeoBiota 62: 333-363. https://doi.org/10.3897/neobiota.62.53796

Table S1

opencc-zeroOct 2020View details →
zenodo28/100

Supplementary material 1 from: Faulkner KT, Hulme PE, Pagad S, Wilson JRU, Robertson MP (2020) Classifying the introduction pathways of alien species: are we moving in the right direction? In: Wilson JR, Bacher S, Daehler CC, Groom QJ, Kumschick S, Lockwood JL, Robinson TB, Zengeya TA, Richardson DM. NeoBiota 62: 143-159. https://doi.org/10.3897/neobiota.62.53543

Evidence used to assess the introduction pathway classification frameworks

opencc-zeroOct 2020View details →
zenodo28/100

Pathway simulation runs for manuscript "To and beyond the 2030 Agenda: systems change for accelerating sustainability progress"

<p>Files contains&nbsp;the simulation runs generated by the source code from &#39;https://github.com/enayatmoallemi/Moallemi_et_al_SDG_SSP_Assessment&#39;.</p> <p>Files &#39;<a href="https://zenodo.org/api/files/340806c1-e040-4036-bcbf-09d44c7f6f29/SDG_experiments_sc1000.tar.gz">SDG_experiments_sc250.tar.gz</a>&#39; to &#39;<a href="https://zenodo.org/api/files/340806c1-e040-4036-bcbf-09d44c7f6f29/SDG_experiments_sc1000.tar.gz">SDG_experiments_sc5000.tar.gz</a> include&nbsp;sensitivity analysis experiments (for different sample sizes from 250 to 5000) .</p> <p><br> Files &#39;<a href="https://zenodo.org/api/files/340806c1-e040-4036-bcbf-09d44c7f6f29/SDG_SSP5-85_exploration_sc10000.tar.gz">SDG_SSP1-26_exploration_sc10000.tar.gz</a>&#39; to &#39;<a href="https://zenodo.org/api/files/340806c1-e040-4036-bcbf-09d44c7f6f29/SDG_SSP5-85_exploration_sc10000.tar.gz">SDG_SSP5-85_exploration_sc10000.tar.gz</a>&#39; include&nbsp;exploratory analysis experiments of the five SSP-RCP combinations over time.</p>

opencc-by-4.0Dec 2020View details →
zenodo28/100

Raw data and Figures for the article "Strain Wave Pathway to Semiconductor-to-Metal Transition Revealed by Time Resolved X-ray Powder Diffraction"

<p>- Raw data from Jungfrau Integrating pixel detector (together with azimuthally averaged curves)</p> <p>- Script to create time resolved data from raw data</p> <p>- Scripts to generates main figures of the article.</p>

opencc-by-4.0Dec 2020View details →
dryad28/100

RNA-seq data from TAS4464, a NEDD8-activating enzyme inhibitor, activates both intrinsic and extrinsic apoptotic pathways via c-Myc-mediated regulation in acute myeloid leukemia

<p class="BDAbstract"><span><span><span><span><span><span><span><span><span><span><span>TAS4464, a potent, selective small molecule NEDD8-activating enzyme (NAE) inhibitor, leads to inactivation of cullin-RING E3 ubiquitin ligases (CRLs) and consequent accumulations of its substrate proteins. Here, we investigated the antitumor properties and action mechanism of TAS4464 in acute myeloid leukemia (AML). TAS4464 induced apoptotic cell death in various AML cell lines. TAS4464 treatments resulted in the activation of both the caspase-9-mediated in intrinsic apoptotic pathway and caspase-8-mediated extrinsic apoptotic pathway in AML cells; combined treatment with inhibitors of these caspases markedly diminished TAS4464 induced apoptosis. In each apoptotic pathway, TAS4464 induced the mRNA transcription of the intrinsic proapoptotic factor NOXA and decreased that of the extrinsic antiapoptotic factor c-FLIP. RNA-sequencing analysis showed that the signaling pathway of the CRL substrate c-Myc was enriched after TAS4464 treatment. Chromatin immunoprecipitation (ChIP) assay revealed that TAS4464 induced c-Myc bound to the <i>PMAIP1</i> (encoding NOXA) and <i>CFLAR</i> (encoding c-FLIP) promoter regions, and siRNA-mediated c-Myc knockdown neutralized both TAS4464-mediated NOXA induction and c-FLIP downregulation. TAS4464 activated both caspase-8 and caspase-9 along with an increase in NOXA and a decrease in c-FLIP, resulting in complete tumor remission in a human AML xenograft model. These findings suggest that NAE inhibition leads to anti-AML activity via a novel c-Myc-dependent apoptosis induction mechanism.</span></span></span></span></span></span></span></span></span></span></span></p>

opencc-zeroJan 2021View details →
dryad28/100

Perceptual correlates of homosynaptic long term potentiation in human nociceptive pathways: a replication study

<p>Animal studies have shown that high-frequency stimulation (HFS) of peripheral C-fibers induces long-term potentiation (LTP) within spinal nociceptive pathways. The aim of this replication study was to assess if a perceptual correlate of LTP can be observed in humans. In 20 healthy volunteers we applied HFS to the left or right volar forearm. Before and after applying HFS we delivered single electrical test stimuli through the HFS electrode while a second electrode at the contralateral arm served as control condition. Moreover, to test the efficacy of the HFS protocol we quantified changes in mechanical pinprick sensitivity before and after HFS of the skin surrounding both electrodes. The perceived intensity was collected for both electrical and mechanical stimuli. After HFS, the perceived pain intensity elicited by the mechanical pinprick stimuli applied on the skin surrounding the HFS-treated site was significantly higher compared to control site (heterotopic effect). Furthermore, we found a higher perceived pain intensity for single electrical stimuli delivered to the HFS-treated site compared to the control site (homotopic effect). Whether the homotopic effect reflects a perceptual correlate of homosynaptic LTP remains to be elucidated.</p>

opencc-zeroJan 2021View details →
zenodo28/100

Supplementary material 3 from: McGrannachan CM, Pagad S, McGeoch MA (2021) A multiregional assessment of transnational pathways of introduction. NeoBiota 64: 43-67. https://doi.org/10.3897/neobiota.64.60642

Table S1. List of 101 countries used in the analysis of introduction pathway trends

opencc-zeroJan 2021View details →
dryad28/100

Data from: Exogenous restoration of TUSC2 expression induces responsiveness to erlotinib in wildtype epidermal growth factor receptor (EGFR) lung cancer cells through context specific pathways resulting in enhanced therapeutic efficacy

Expression of the tumor suppressor gene TUSC2 is reduced or absent in most lung cancers and is associated with worse overall survival. In this study, we restored TUSC2 gene expression in several wild type EGFR non-small cell lung cancer (NSCLC) cell lines resistant to the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor erlotinib and analyzed their sensitivity to erlotinib in vitro and in vivo. A significant inhibition of cell growth and colony formation was observed with TUSC2 transient and stable expression. TUSC2-erlotinib cooperativity in vitro could be reproduced in vivo in subcutaneous tumor growth and lung metastasis formation lung cancer xenograft mouse models. Combination treatment with intravenous TUSC2 nanovesicles and erlotinib synergistically inhibited tumor growth and metastasis, and increased apoptotic activity. High-throughput qRT-PCR array analysis enabling multi-parallel expression profile analysis of eighty six receptor and non-receptor tyrosine kinase genes revealed a significant decrease of FGFR2 expression level, suggesting a potential role of FGFR2 in TUSC2-enhanced sensitivity to erlotinib. Western blots showed inhibition of FGFR2 by TUSC2 transient transfection, and marked increase of PARP, an apoptotic marker, cleavage level after TUSC2-erlotinb combined treatment. Suppression of FGFR2 by AZD4547 or gene knockdown enhanced sensitivity to erlotinib in some but not all tested cell lines. TUSC2 inhibits mTOR activation and the latter cell lines were responsive to the mTOR inhibitor rapamycin combined with erlotinib. These results suggest that TUSC2 restoration in wild type EGFR NSCLC may overcome erlotinib resistance, and identify FGFR2 and mTOR as critical regulators of this activity in varying cellular contexts. The therapeutic activity of TUSC2 could extend the use of erlotinib to lung cancer patients with wildtype EGFR.

opencc-zeroDec 2014View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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