Direct Download Links

The top reason people use Pinterest is to find information about products and brands.1 Direct links help you convert more of the people shopping on Pinterest into active customers on your site or store.

Brands who started using direct links for consideration campaigns have seen an average of 96% more clicks to site with the links enabled, compared to their previous campaigns on Pinterest.2 That even includes cost savings, with a whopping 38% decrease in cost per outbound click.2

Download File 🔥 https://ssurll.com/2y4J42 🔥

You can track links by using server side coding such as PHP to add, in the case of CJ an SID which can be unique as the case as a username, product code/name on your website. So the resulting link will now appear as :

Direct links in Pinterest ads take users directly to your site, rather than to a closeup, after clicking on the ad. Ads with direct links also contain a call-to-action (CTA) below the ad creative that drives users to click and take action on your website. This feature can lead to more traffic and conversions on your website.

when we hover over a page in graph view it highlights all linked pages. if we could differentiate direct links which were created right inside the same page it would be really beneficial. (may be using different colours or arrows or something)

Point users to the right database resource within the Web of Science platform using our list of direct links. Link to a database, or even an individual index within the Core Collection. Descriptions are included to help you quickly communicate the resource.

With the end of Flash fast approaching, I was wondering if our community here might be able to compile some links that would perhaps allow us to complete our Flash dailies while waiting for them to be converted.

I'm hopeful that there are other links like this that might allow us to keep playing games like this one, Test Your Strength, Kiko Pop, Qasalan Expellibox, and whatever other Flash dailies you all can think of.

I have a weird setup where my library is not local so I am used to stream direct urls and this setup is working with vlc on apple tv. If i want to stream a direct link on infuse without using same apple id on infuse iphone, whats the option. I love the underlying infuse player and was wondering if

infuse://x-callback-url/play?url=

would work as this works in ios and stream starts playing. How to achieve this in apple tv.

Pinterest first announced deeplinking back in July, and enhanced direct links in September, providing more ways for brands to direct users to a specific page in their own mobile app, or to a URL, facilitating direct connection.

In addition to this, Pinterest also says that brands that have been using direct links for consideration campaigns have seen an average of 96% more clicks to site with the links enabled, compared to their previous campaigns on Pinterest.

It can be useful to launch directly into a trace waterfall display from a Trace ID from third-party services.For example, you might wire an error reporting tool to launch directly into a trace in Honeycomb.

We recommend using Open Source players (e.g. Dash.js and HLS.js) for video playback. You will see these, as well as a list of progressive mp4 links as well as an HTTP Live Streaming (HLS) and a Dynamic Adaptive Streaming over HTTP (DASH) link.

DASH, otherwise known as Dynamic Adaptive Streaming over HTTP, links are for serving Vimeo-hosted files in another player, typically non-Apple devices or environments. Known for being highly customizable, DASH supports the most features out of any other streaming protocol.

The direct links under both the Play the Video and Download the Video dropdown menus contain the same files. For downloads, we return a special header to tell the browser to download it to the local disk instead of playing it back, but nothing prevents downloading the Play URL (or prevents playing back download URLs, if used in a player).

Vimeo's privacy settings and custom embed settings do not apply to third-party player links. The third-party player you're using might support its own set of customizations, but you will need to check out their support documentation for more info.

If you downgrade to Free or Starter or to Basic or Plus, any direct links you've shared or embedded will no longer work (for example, your embedded video will no longer load). If you decide to re-upgrade to Standard or Pro or higher, your links will automatically reactivate.

Transcription of the VERNALIZATION1 gene (VRN1) is induced by prolonged cold (vernalization) to trigger flowering of cereal crops, such as wheat and barley. VRN1 encodes a MADS box transcription factor that promotes flowering by regulating the expression of other genes. Here we use transcriptome sequencing (RNA-seq) and chromatin immunoprecipitation sequencing (ChIP-seq) to identify direct targets of VRN1. Over 500 genomic regions were identified as potential VRN1-binding targets by ChIP-seq. VRN1 binds the promoter of FLOWERING LOCUS T-like 1, a promoter of flowering in vernalized plants. VRN1 also targets VERNALIZATION2 and ODDSOC2, repressors of flowering that are downregulated in vernalized plants. RNA-seq identified additional VRN1 targets that might play roles in triggering flowering. Other targets of VRN1 include genes that play central roles in low-temperature-induced freezing tolerance, spike architecture and hormone metabolism. This provides evidence for direct regulatory links between the vernalization response pathway and other important traits in cereal crops.

Molecular analyses have identified potential downstream regulatory targets of the VRN1 gene. These include VRN2 and VRN3, which, like VRN1, influence vernalization requirement20. VRN2 is a repressor of flowering that is expressed in long days before vernalization, but is downregulated in vernalized plants or in plants that carry active alleles of VRN1 (refs 9, 10, 23, 24, 25). VRN3 encodes the cereal orthologue of FLOWERING LOCUS T (hereafter referred to as FT1) (ref. 26). In Arabidopsis, the FLOWERING LOCUS T protein is expressed in leaves in long days and then transported to the shoot apex to accelerate inflorescence development27. It seems likely that FT1 has a similar function in cereals28. FT1 is expressed at low levels before vernalization, irrespective of day length, but is induced by long days in vernalized plants, or in plants that have active alleles of VRN1 (refs 10, 26). Thus, the expression of VRN1 is a prerequisite for long-day induction of FT1 in cereals. Another regulatory target of VRN1 is a second MADS box transcription factor, ODDSOC2, which represses flowering but is downregulated by vernalization or in plants that have active alleles of VRN1 (refs 29, 30). In addition, a series of C-REPEAT BINDING FACTOR (CBF) genes, which are induced by low temperatures to increase freezing tolerance31, show reduced expression in lines that carry active alleles of VRN1 (refs 32, 33). Whether VRN1 directly regulates any of these potential targets is unclear.

Optimal seasonal timing of flowering and grain production is critical to adapt cereals to temperate climates. The timing and duration of inflorescence development also influences key components of yield in cereal crops. For these reasons, VRN1 is a major target for selection in cereal breeding. Understanding how VRN1 functions can provide important insights into crop biology and inform future cereal breeding strategies. In this study, we used chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) to identify sequences bound by the VRN1 protein in barley, a model for temperate cereals and related grasses. This identified genes that act downstream of VRN1 in the vernalization response and also revealed direct connections between VRN1 and pathways that control other key traits.

Between 146 and 514 direct targets of VRN1 were identified by ChIP-seq, depending on the fold enrichment used as a cutoff value (50 versus 20-fold). Even at the least stringent enrichment limit (20-fold), all the target regions identified contain a potential CArG box motif identified by MEME (Multiple EM for Motif Elicitation36; Supplementary Data 2). The false discovery rate values for peaks with more than 20-fold enrichment were generally below 5% (Supplementary Data 2). Thus, 20-fold enrichment was selected as an arbitrary cutoff point for subsequent discussion, although potentially some genuine targets have been omitted. It is important to note that the current genome sequence reference data sets do not represent the entire barley genome37, so some targets present in the ChIP-seq data sets will not be identified by the subsequent bioinformatic analysis. The ChIP-seq data set can be realigned to future genomic reference sequences of barley to address this limitation. Binding of VRN1 to putative targets was retested with a second antibody-epitope tag combination using a VRN1::GFP fusion construct12, showing that the enrichment of VRN1-binding sites by ChIP is not dependent on the HA-tag/antibody (Supplementary Figs 3 and 5).

A key question for this study is which genes are targeted by VRN1 to promote rapid flowering after vernalization? Putative targets of VRN1 identified by ChIP-seq and ChIP-PCR include known regulators of flowering, such as FT1, VRN2 and ODDSOC2. These genes are regulated by vernalization and by active alleles of VRN1, consistent with the idea that these genes are downstream targets of the VRN1 gene (see Introduction). SOC1-like and CONSTANS-like genes, which regulate the reproductive development of rice38,39, were also identified as direct targets of VRN1. FT1 was identified as a direct binding target of VRN1 and also shows altered expression during early development in the early flowering VRN1-HA transgenic plants (Figs 2 and 4). Genetic activation of FT1 is sufficient to accelerate the flowering of barley26, consistent with the idea that the activation of FT1 (resulting from elevated VRN1 expression) plays a major role in eliciting the early flowering phenotype of VRN1-HA transgenic plants. e24fc04721