1,129 research outputs found
Multi-lingual neural title generation for e-Commerce browse pages
To provide better access of the inventory to buyers and better search engine
optimization, e-Commerce websites are automatically generating millions of
easily searchable browse pages. A browse page consists of a set of slot
name/value pairs within a given category, grouping multiple items which share
some characteristics. These browse pages require a title describing the content
of the page. Since the number of browse pages are huge, manual creation of
these titles is infeasible. Previous statistical and neural approaches depend
heavily on the availability of large amounts of data in a language. In this
research, we apply sequence-to-sequence models to generate titles for high- &
low-resourced languages by leveraging transfer learning. We train these models
on multi-lingual data, thereby creating one joint model which can generate
titles in various different languages. Performance of the title generation
system is evaluated on three different languages; English, German, and French,
with a particular focus on low-resourced French language.Comment: To appear in NAACL 2018 (Industry track), 8 page
Использование слабо формализуемых зависимостей в модели функциональных отношений
Рассматриваются вопросы формирования слабо формализуемых, так называемых, оценочных зависимостей в составе модели функциональных отношений и их использования для оценки состояния объекта и определения влияния отдельных атрибутов на обобщенную оценку объекта. Приводятся результаты использования предлагаемого подхода для анализа уровня энергосбережения региона и определения приоритетных мероприятий по развитию энергосберегающего бизнеса
Plasmodium yoelii infection of BALB/c mice results in expansion rather than induction of CD4+ Foxp3+ regulatory T cells
Recently, we demonstrated elevated numbers of CD4(+) Foxp3(+) regulatory T (Treg) cells in Plasmodium yoelii‐infected mice contributing to the regulation of anti‐malarial immune response. However, it remains unclear whether this increase in Treg cells is due to thymus‐derived Treg cell expansion or induction of Treg cells in the periphery. Here, we show that the frequency of Foxp3(+) Treg cells expressing neuropilin‐1 (Nrp‐1) decreased at early time‐points during P. yoelii infection, whereas percentages of Helios(+) Foxp3(+) Treg cells remained unchanged. Both Foxp3(+) Nrp‐1(+) and Foxp3(+) Nrp‐1(−) Treg cells from P. yoelii‐infected mice exhibited a similar T‐cell receptor Vβ chain usage and methylation pattern in the Treg‐specific demethylation region within the foxp3 locus. Strikingly, we did not observe induction of Foxp3 expression in Foxp3(−) T cells adoptively transferred to P. yoelii‐infected mice. Hence, our results suggest that P. yoelii infection triggered expansion of naturally occurring Treg cells rather than de novo induction of Foxp3(+) Treg cells
Equine recurrent uveitis - A spontaneous horse model of uveitis
Equine recurrent uveitis (ERU) is an autoimmune disease that occurs with a high prevalence (10%) in horses. ERU represents the only reliable spontaneous model for human autoimmune uveitis. We already identified and characterized novel autoantigens (malate dehydrogenase, recoverin, CRALBP) by analyzing the autoantibody-binding pattern of horses affected by spontaneous recurrent uveitis (ERU) to the retinal proteome. CRALBP also seems to be relevant to human autoimmune uveitis. Proteomic screening of vitreous and retinal samples from ERU diseased cases in comparison to healthy controls has led to the identification of a series of differentially regulated proteins, which are functionally linked to the immune system and the maintenance of the blood-retinal barrier. Copyright (c) 2008 S. Karger AG, Basel
Comparing internal migration across the countries of Latin America: A multidimensional approach.
While considerable progress has been made in understanding the way particular aspects of internal migration, such as its intensity, age profile and spatial impact, vary between countries around the world, little attention to date has been given to establishing how these dimensions of migration interact in different national settings. We use recently developed measures of internal migration that are scale-independent to compare the overall intensity, age composition, spatial impact, and distance profile of internal migration in 19 Latin American countries. Comparisons reveal substantial cross-national variation but cluster analysis suggests the different dimensions of migration evolve systematically to form a broad sequence characterised by low intensities, young ages at migration, unbalanced flows and high friction of distance at lower levels of development, trending to high intensities, an older age profile of migration, more closely balanced flows and lower friction of distance at later stages of development. However, the transition is not linear and local contingencies, such as international migration and political control, often distort the migration-development nexus, leading to unique migration patterns in individual national contexts
Identification of hydroxyapatite spherules provides new insight into subretinal pigment epithelial deposit formation in the aging eye.
Accumulation of protein- and lipid-containing deposits external to the retinal pigment epithelium (RPE) is common in the aging eye, and has long been viewed as the hallmark of age-related macular degeneration (AMD). The cause for the accumulation and retention of molecules in the sub-RPE space, however, remains an enigma. Here, we present fluorescence microscopy and X-ray diffraction evidence for the formation of small (0.5-20 μm in diameter), hollow, hydroxyapatite (HAP) spherules in Bruch's membrane in human eyes. These spherules are distinct in form, placement, and staining from the well-known calcification of the elastin layer of the aging Bruch's membrane. Secondary ion mass spectrometry (SIMS) imaging confirmed the presence of calcium phosphate in the spherules and identified cholesterol enrichment in their core. Using HAP-selective fluorescent dyes, we show that all types of sub-RPE deposits in the macula, as well as in the periphery, contain numerous HAP spherules. Immunohistochemical labeling for proteins characteristic of sub-RPE deposits, such as complement factor H, vitronectin, and amyloid beta, revealed that HAP spherules were coated with these proteins. HAP spherules were also found outside the sub-RPE deposits, ready to bind proteins at the RPE/choroid interface. Based on these results, we propose a novel mechanism for the growth, and possibly even the formation, of sub-RPE deposits, namely, that the deposit growth and formation begin with the deposition of insoluble HAP shells around naturally occurring, cholesterol-containing extracellular lipid droplets at the RPE/choroid interface; proteins and lipids then attach to these shells, initiating or supporting the growth of sub-RPE deposits
Assessing equity in systematic reviews: realising the recommendations of the Commission on Social Determinants of Health.
LST1 promotes the assembly of a molecular machinery responsible for tunneling nanotube formation
Carefully orchestrated intercellular communication is an essential prerequisite for the development
of multicellular organisms. In recent years, tunneling nanotubes (TNT) have emerged as a novel
and widespread mechanism of cell-cell communication. However, the molecular basis of their
formation is still poorly understood. In the present study we report that the transmembrane MHC
class III protein LST1 induces the formation of functional nanotubes and is required for endogenous
nanotube generation. Mechanistically, we found LST1 to induce nanotube formation by recruiting
the small GTPase RalA to the plasma membrane and promoting its interaction with the exocyst
complex. Furthermore, we determined LST1 to recruit the actin-crosslinking protein filamin to the
plasma membrane and to interact with M-Sec, myosin and myoferlin. These results allow us to
suggest a molecular model for nanotube generation. In this proposal LST1 functions as a membrane
scaffold mediating the assembly of a multimolecular complex, which controls the formation of
functional nanotubes
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