Found: 11
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Metagenomics Analysis of Breast Microbiome Highlights the Abundance of Rothia Genus in Tumor Tissues.
- Published in:
- Journal of Personalized Medicine, 2023, v. 13, n. 3, p. 450, doi. 10.3390/jpm13030450
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- Article
Targeted Gene Panel Sequencing Unveiled New Pathogenic Mutations in Patients With Breast Cancer.
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- Bioinformatics & Biology Insights, 2023, v. 17, p. 1, doi. 10.1177/11779322231182054
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- Article
Large scale genomic analysis of 3067 SARS-CoV-2 genomes reveals a clonal geo-distribution and a rich genetic variations of hotspots mutations.
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- PLoS ONE, 2020, v. 15, n. 11, p. 1, doi. 10.1371/journal.pone.0240345
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- Article
Genomic analysis of two Bacillus safensis isolated from Merzouga desert reveals desert adaptive and potential plant growth-promoting traits.
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- Functional & Integrative Genomics, 2022, v. 22, n. 6, p. 1173, doi. 10.1007/s10142-022-00905-0
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- Article
Genomic Diversity and Hotspot Mutations in 30,983 SARS-CoV-2 Genomes: Moving Toward a Universal Vaccine for the "Confined Virus"?
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- Pathogens, 2020, v. 9, n. 10, p. 829, doi. 10.3390/pathogens9100829
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- Article
Targeted Gene Panel Sequencing Unveiled New Pathogenic Mutations in Patients With Breast Cancer.
- Published in:
- Bioinformatics & Biology Insights, 2023, p. 1, doi. 10.1177/11779322231182054
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- Publication type:
- Article
A Comprehensive Analysis of 3 Moroccan Genomes Revealed Contributions From Both African and European Ancestries.
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- Evolutionary Bioinformatics, 2024, p. 1, doi. 10.1177/11769343241229278
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- Article
In Silico Analyses of All STAT3 Missense Variants Leading to Explore Divergent AD-HIES Clinical Phenotypes.
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- Evolutionary Bioinformatics, 2023, p. 1, doi. 10.1177/11769343231169374
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- Article
In Silico Analyses of All STAT3 Missense Variants Leading to Explore Divergent AD-HIES Clinical Phenotypes.
- Published in:
- Evolutionary Bioinformatics, 2023, v. 19, p. 1, doi. 10.1177/11769343231169374
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- Article
Genomic analysis of Paenibacillus sp. MDMC362 from the Merzouga desert leads to the identification of a potentially thermostable catalase.
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- Antonie van Leeuwenhoek, 2023, v. 116, n. 1, p. 21, doi. 10.1007/s10482-022-01793-x
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- Article
Variants of human CLDN9 cause mild to profound hearing loss.
- Published in:
- Human Mutation, 2021, v. 42, n. 10, p. 1321, doi. 10.1002/humu.24260
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- Article