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Point mutation

Resistance mechanisms and fitness of pyraclostrobin-resistant isolates of Lasiodiplodia theobromae from mango orchards

Rui He, Ye Yang, [ ... ], Yajuan Hu

Sperm parameters and mitochondrial DNA sequence variants among patients at a fertility clinic in Ghana

Bartholomew Dzudzor, Bismarck Bimah, Vincent Amarh, Augustine Ocloo

In silico analysis of deleterious SNPs of human MTUS1 gene and their impacts on subsequent protein structure and function

Liza Teresa Rozario, Tanima Sharker, Tasnin Akter Nila

Rapid detection of multidrug-resistant tuberculosis based on allele-specific recombinase polymerase amplification and colorimetric detection

Nuntita Singpanomchai, Yukihiro Akeda, [ ... ], Panan Ratthawongjirakul

Selective transport of fluorescent proteins into the phage nucleus

Katrina T. Nguyen, Joseph Sugie, [ ... ], Joe Pogliano

Decreased glucocerebrosidase activity and substrate accumulation of glycosphingolipids in a novel GBA1 D409V knock-in mouse model

Nicole K. Polinski, Terina N. Martinez, [ ... ], Kuldip D. Dave

Increased elastase sensitivity and decreased intramolecular interactions in the more transmissible 501Y.V1 and 501Y.V2 SARS-CoV-2 variants’ spike protein–an in silico analysis

Suman Pokhrel, Benjamin R. Kraemer, [ ... ], Daria Mochly-Rosen

Structure-activity mapping of ARHGAP36 reveals regulatory roles for its GAP homology and C-terminal domains

Patricia R. Nano, Taylor K. Johnson, [ ... ], James K. Chen

Prevalence of colorectal cancer biomarkers and their impact on clinical outcomes in Riyadh, Saudi Arabia

Amjad Alharbi, Haifa Bin Dokhi, [ ... ], Nouf Alomran

Improved transformation efficiency of group A Streptococcus by inactivation of a type I restriction modification system

Meredith B. Finn, Kathryn M. Ramsey, [ ... ], Michael R. Wessels

Risk of rapid evolutionary escape from biomedical interventions targeting SARS-CoV-2 spike protein

Debra Van Egeren, Alexander Novokhodko, [ ... ], Arijit Chakravarty

Lack of collagen α6(IV) chain in mice does not cause severe-to-profound hearing loss or cochlear malformation, a distinct phenotype from nonsyndromic hearing loss with COL4A6 missense mutation

Shaoying Tang, Tomoko Yonezawa, [ ... ], Toshitaka Oohashi

Identifying treatment options for BRAF^V600 wild-type metastatic melanoma: A SU2C/MRA genomics-enabled clinical trial

Patricia M. LoRusso, Aleksandar Sekulic, [ ... ], Jeffrey M. Trent

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