1,617 research outputs found

    Crosslingual Retrieval Augmented In-context Learning for Bangla

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    The promise of Large Language Models (LLMs) in Natural Language Processing has often been overshadowed by their limited performance in low-resource languages such as Bangla. To address this, our paper presents a pioneering approach that utilizes cross-lingual retrieval augmented in-context learning. By strategically sourcing semantically similar prompts from high-resource language, we enable multilingual pretrained language models (MPLMs), especially the generative model BLOOMZ, to successfully boost performance on Bangla tasks. Our extensive evaluation highlights that the cross-lingual retrieval augmented prompts bring steady improvements to MPLMs over the zero-shot performance.Comment: In The 1st Bangla Language Processing (BLP) Workshop, held in conjunction with The Conference on Empirical Methods in Natural Language Processing (EMNLP), December 202

    Cross-Lingual Retrieval Augmented Prompt for Low-Resource Languages

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    Multilingual Pretrained Language Models (MPLMs) perform strongly in cross-lingual transfer. We propose Prompts Augmented by Retrieval Crosslingually (PARC) to improve zero-shot performance on low-resource languages (LRLs) by augmenting the context with prompts consisting of semantically similar sentences retrieved from a high-resource language (HRL). PARC improves zero-shot performance on three downstream tasks (sentiment classification, topic categorization, natural language inference) with multilingual parallel test sets across 10 LRLs covering 6 language families in unlabeled (+5.1%) and labeled settings (+16.3%). PARC also outperforms finetuning by 3.7%. We find a significant positive correlation between cross-lingual transfer performance on one side, and the similarity between high- and low-resource languages as well as the amount of low-resource pretraining data on the other side. A robustness analysis suggests that PARC has the potential to achieve even stronger performance with more powerful MPLMs

    Cross-Lingual Retrieval Augmented Prompt for Low-Resource Languages

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    Multilingual Pretrained Language Models (MPLMs) have shown their strong multilinguality in recent empirical cross-lingual transfer studies. In this paper, we propose the Prompts Augmented by Retrieval Crosslingually (PARC) pipeline to improve the zero-shot performance on low-resource languages (LRLs) by augmenting the context with semantically similar sentences retrieved from a high-resource language (HRL) as prompts. PARC improves the zero-shot performance on three downstream tasks (binary sentiment classification, topic categorization and natural language inference) with multilingual parallel test sets across 10 LRLs covering 6 language families in both unlabeled settings (+5.1%) and labeled settings (+16.3%). PARC-labeled also outperforms the finetuning baseline by 3.7%. We find a significant positive correlation between cross-lingual transfer performance on one side, and the similarity between the high- and low-resource languages as well as the amount of low-resource pretraining data on the other side. A robustness analysis suggests that PARC has the potential to achieve even stronger performance with more powerful MPLMs.Comment: Accepted to Findings of ACL 202

    Poly[[diaqua­bis­(μ3-3-carboxyl­ato-4-hy­droxy­benzene­sulfonato)­tri-μ2-pyrazine-tetra­silver(I)] dihydrate]

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    The title coordination polymer, {[Ag4(C7H4O6S)2(C4H4N2)3(H2O)2]·2H2O}n, contains two independent AgI ions. One AgI ion is coordinated by one O atom from a 3-carboxyl­ato-4-hy­droxy­benzene­sulfonate (L) ligand, two N atoms from two pyrazine ligands and a water mol­ecule. The other AgI ion is coordinated by two O atoms from two L ligands and one N atom from a pyrazine ligand. One of the pyrazine ligands lies on an inversion center. The L and pyrazine ligands link the AgI ions into polymeric layers parallel to the ac plane. The layers are connected by inter­molecular O—H⋯O hydrogen bonds. An intra­molecular O—H⋯O hydrogen bond is also present in the L ligand

    Amyloid-like aggregates of neuronal tau induced by formaldehyde promote apoptosis of neuronal cells

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    BACKGROUND: The microtubule associated protein tau is the principle component of neurofibrillar tangles, which are a characteristic marker in the pathology of Alzheimer's disease; similar lesions are also observed after chronic alcohol abuse. Formaldehyde is a common environmental contaminant and also a metabolite of methanol. Although many studies have been done on methanol and formaldehyde intoxication, none of these address the contribution of protein misfolding to the pathological mechanism, in particular the effect of formaldehyde on protein conformation and polymerization. RESULTS: We found that unlike the typical globular protein BSA, the natively-unfolded structure of human neuronal tau was induced to misfold and aggregate in the presence of ~0.01% formaldehyde, leading to formation of amyloid-like deposits that appeared as densely staining granules by electron microscopy and atomic force microscopy, and bound the amyloid-specific dyes thioflavin T and Congo Red. The amyloid-like aggregates of tau were found to induce apoptosis in the neurotypic cell line SH-SY5Y and in rat hippocampal cells, as observed by Hoechst 33258 staining, assay of caspase-3 activity, and flow cytometry using Annexin V and Propidium Iodide staining. Further experiments showed that Congo Red specifically attenuated the caspase-3 activity induced by amyloid-like deposits of tau. CONCLUSION: The results suggest that low concentrations of formaldehyde can induce human tau protein to form neurotoxic aggregates, which could play a role in the induction of tauopathies

    Poly[[tetra­aqua­tetra­kis­[μ3-5-(pyridine-4-carboxamido)­isophthalato]­cobalt(II)­diholmium(III)] tetra­hydrate]

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    In the centrosymmetric polymeric title compound, {[CoHo2(C14H8N2O5)4(H2O)4]·4H2O}n, the HoIII ion is coordinated by one water mol­ecule and four 5-(pyridine-4-carboxamido)­isophthalate (L) ligands in a distorted square-anti­prismatic arrangement. The CoII ion, located on an inversion center, is coordinated by two pyridine N atoms, two carboxyl­ate O atoms and two water mol­ecules in a distorted octa­hedral geometry. One L ligand bridges two Ho ions and one Co ion through two carboxyl­ate groups and one pyridine N atom. The other L ligand bridges two Ho ions and one Co ion through two carboxyl­ate groups, while the uncoordinated pyridine N atom accepts a hydrogen bond from an adjacent coordinated water mol­ecule. Extensive O—H⋯O, N—H⋯O and O—H⋯N hydrogen bonding is present in the crystal
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