Found: 12
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Key point generation as an instrument for generating core statements of a political debate on Twitter.
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- Frontiers in Artificial Intelligence, 2024, p. 1, doi. 10.3389/frai.2024.1200949
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- Article
From Keyness to Distinctiveness – Triangulation and Evaluation in Computational Literary Studies.
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- Journal of Literary Theory (18625290), 2021, v. 15, n. 1/2, p. 81, doi. 10.1515/jlt-2021-2011
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- Article
Gattungsgeschichte und ihr Gattungsbegriff am Beispiel der Novellen.
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- Journal of Literary Theory (18625290), 2019, v. 13, n. 2, p. 227, doi. 10.1515/jlt-2019-0009
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- Article
Refining Genotypes and Phenotypes in KCNA2 -Related Neurological Disorders.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 6, p. 2824, doi. 10.3390/ijms22062824
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- Article
Succinic Semialdehyde Dehydrogenase Deficiency: In Vitro and In Silico Characterization of a Novel Pathogenic Missense Variant and Analysis of the Mutational Spectrum of ALDH5A1.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 22, p. 8578, doi. 10.3390/ijms21228578
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- Article
A large and diverse brain organoid dataset of 1,400 cross-laboratory images of 64 trackable brain organoids.
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- Scientific Data, 2024, v. 11, n. 1, p. 1, doi. 10.1038/s41597-024-03330-z
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- Article
Can Firm Performance and Corporate Reputation Be Improved by Communicating CSR in Social Media?: A Pilot Study Analysis.
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- International Journal of Applied Management Sciences & Engineering, 2021, v. 8, n. 2, p. 1, doi. 10.4018/IJAMSE.2021070101
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- Article
Isovaleric aciduria identified by newborn screening: Strategies to predict disease severity and stratify treatment.
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- Journal of Inherited Metabolic Disease, 2023, v. 46, n. 6, p. 1063, doi. 10.1002/jimd.12653
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- Article
Exploring genotype–phenotype correlations in glutaric aciduria type 1.
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- Journal of Inherited Metabolic Disease, 2023, v. 46, n. 3, p. 371, doi. 10.1002/jimd.12608
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- Article
Phenotypic diversity, disease progression, and pathogenicity of MVK missense variants in mevalonic aciduria.
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- Journal of Inherited Metabolic Disease, 2021, v. 44, n. 5, p. 1272, doi. 10.1002/jimd.12412
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- Article
Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder.
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- Human Mutation, 2021, v. 42, n. 9, p. 1094, doi. 10.1002/humu.24245
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- Article
Altered HCN4 channel C-linker interaction is associated with familial tachycardia–bradycardia syndrome and atrial fibrillation.
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- European Heart Journal, 2013, v. 34, n. 35, p. 2768, doi. 10.1093/eurheartj/ehs391
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- Article