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Point mutation

Evaluating the effect of mutations and ligand binding on transthyretin homotetramer dynamics

Tadeo. E. Saldaño, Giuseppe Zanotti, Gustavo Parisi, Sebastian Fernandez-Alberti

Multiple quay cranes scheduling for double cycling in container terminals

Yanling Chu, Xiaoju Zhang, Zhongzhen Yang

Molecular characterization of occult hepatitis B virus infection in patients with end-stage liver disease in Colombia

Julio Cesar Rendon, Fabian Cortes-Mancera, [ ... ], Maria-Cristina Navas

Reverse epithelial-mesenchymal transition contributes to the regain of drug sensitivity in tyrosine kinase inhibitor-resistant non-small cell lung cancer cells

An-Fu Lee, Man-Chin Chen, [ ... ], Yu-Peng Liu

Activation of Dun1 in response to nuclear DNA instability accounts for the increase in mitochondrial point mutations in Rad27/FEN1 deficient S. cerevisiae

Aneta Kaniak-Golik, Renata Kuberska, Piotr Dzierzbicki, Ewa Sledziewska-Gojska

Highly mutable tandem DNA repeats generate a cell wall protein variant more frequent in disease-causing Candida albicans isolates than in commensal isolates

Zhuo Zhou, Zoe Jordens, [ ... ], Jan Schmid

Genetic basis of calcifying cystic odontogenic tumors

Akane Yukimori, Yu Oikawa, [ ... ], Kei Sakamoto

Baculoviral delivery of CRISPR/Cas9 facilitates efficient genome editing in human cells

Sanne Hindriksen, Arne J. Bramer, [ ... ], Michael A. Hadders

Development of a range of fluorescent reagentless biosensors for ATP, based on malonyl-coenzyme A synthetase

Renée Vancraenenbroeck, Simone Kunzelmann, Martin R. Webb

SensiScreen^® KRAS exon 2-sensitive simplex and multiplex real-time PCR-based assays for detection of KRAS exon 2 mutations

Alice Riva, Michael BØrgesen, [ ... ], Milo Frattini

Identification of key amino acid residues in the hTGR5–nomilin interaction and construction of its binding model

Takashi Sasaki, Moeko Mita, [ ... ], Ryuichiro Sato

Detection of genome-edited mutant clones by a simple competition-based PCR method

Takeshi Harayama, Howard Riezman

Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling

Swati Tomar, Raman Sethi, [ ... ], Poh San Lai

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