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Mutation databases

Polymorphic variations and mRNA expression of the genes encoding interleukins as well as enzymes of oxidative and nitrative stresses as a potential risk of nephrolithiasis development

Paulina Wigner-Jeziorska, Radosław Grębowski, [ ... ], Janusz Szemraj

Phylodynamics of a regional SARS-CoV-2 rapid spreading event in Colorado in late 2020

Kristen J. Wade, Samantha Tisa, [ ... ], Olivia S. Rissland

Prevalence of HIV drug resistance, its correlates and common mutations among people living with HIV failing on ART in northern Uganda: A cross-sectional study

Francis Kayinda, Phyllis Awor, [ ... ], Rhoda Wanyenze

Pan-cancer analysis of PSCA that is associated with immune infiltration and affects patient prognosis

Chenxing Wang, Xingjia Zhu, [ ... ], Yang Yang

An approach for developing a blood-based screening panel for lung cancer based on clonal hematopoietic mutations

Ramu Anandakrishnan, Ryan Shahidi, [ ... ], Ian J. Zyvoloski

In silico analysis of TRPM4 variants of unknown clinical significance

Svetlana I. Tarnovskaya, Anna A. Kostareva, Boris S. Zhorov

Computational investigation of missense somatic mutations in cancer and potential links to pH-dependence and proteostasis

Shalaw Sallah, Jim Warwicker

GTExome: Modeling commonly expressed missense mutations in the human genome

Jill Hoffman, Henry Tan, [ ... ], Scott M. Reed

Backup transcription factor binding sites protect human genes from mutations in the promoter

Jay C. Brown

Characterization of the genomic landscape of canine oral osteosarcoma reveals similarities with appendicular osteosarcoma

Christopher Husted, Sarah Adrianowycz, [ ... ], Heather L. Gardner

Development of a novel and viable knock-in factor V deficiency murine model: Utility for an ultra-rare disease

Juan A. De Pablo-Moreno, Leopoldo González-Brusi, [ ... ], Antonio Liras

Genetic variations and recurrence in stage III Korean colorectal cancer: Insights from tumor-only mutation analysis

Hajin Jeon, Jong Lyul Lee, [ ... ], Jin Ok Yang

Identification of novel compound heterozygous variants in the PEX10 gene in a Han-Chinese family with PEX10-related peroxisome biogenesis disorders

Xiangjun Huang, Xinyue Deng, [ ... ], Lamei Yuan

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