The theory of massively repeated evolution and full identifications of cancer-driving nucleotides (CDNs) by Lingjie Zhang, Tong Deng, Zhongqi Liufu, Xueyu Liu, Bingjie Chen, Zheng Hu, Chenli Liu, Miles E Tracy, Xuemei Lu, Hai-Jun Wen, Chung-I Wu

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Macrolide resistance in Mycoplasma pneumoniae in adult patients by Panpan Xie, Panpan Xie, Yue Zhang, Yue Zhang, Yanhong Qin, Yanhong Qin, Yun Fang, Yun Fang, Ning Yang, Ning Yang, Yunbiao Bai, Yunbiao Bai, Shimeng Zhi, Shimeng Zhi, Wenkai Niu, Wenkai Niu, Fusheng Wang, Xin Yuan, Xin Yuan, Xin Yuan

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Application of Bioinformatics and Molecular Dynamics Simulation for Designing FGF7 Mutants Stable in Urea Solution by Siavoush Dastmalchi, Ali Akbar Alizadeh

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The role of filaggrin mutations leading to a decrease in the amount of protein in the development of atopic dermatitis and bronchial asthma in children by S. I. Makarova, D. V. Mitrofanov, E. G. Komova, I. V. Kaloshkin, A. B. Shintyapina, L. F. Kaznacheeva, V. V. Zelenskaya, Е. G. Kondyurina, О. A. Batychko, V. A. Vavilin

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Analysis of how antigen mutations disrupt antibody binding interactions toward enabling rapid and reliable antibody repurposing by Sumaiya Islam, Varun M. Chauhan, Robert J. Pantazes

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Genome-wide accumulations of non-random adaptive point mutations drive westward evolution of Helicobacter pylori by R. J. Retnakumar, Prakash Chettri, Sangey Chhophel Lamtha, K. C. Sivakumar, Priya Dutta, Pahil Sen, Sanjit Biswas, Nikita Agarwal, Angitha N. Nath, T. Barani Devi, Namrata Thapa, Jyoti Prakash Tamang, Santanu Chattopadhyay

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Exploring the NANOG-TET2 interaction interface. Effects of a selected mutation and hypothesis on the clinical correlation with anemias by Claudia Testi, Roberta Piacentini, Roberta Piacentini, Alessandro Perrone, Chiara Bartoli, Daniele Leso, Domitilla Pavia, Elisa Pistolesi, Flavio Scipione, Irene Cotronea, Marco Adinolfi Falcone, Marco Ierani, Alberto Boffi, Lorenzo Di Rienzo

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<p><strong>Target-site insensitivity to some acaricides in a field population of <em>Tetranychus urticae</em> Koch (</strong><strong>Acari: Tetranychidae) from Egypt</strong></p> by Haggag Zein, Abdallah M. Afifi, Fatma S. Ali, El-Sayed Shaurub, Mahmoud Ahmed

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A self-powered millifluidic device driven by triboelectric generator for the label-free and real-time detection of DNA hybridization by Tara Ghafouri, Sheida Bagherzadeh‑Nobari, Negin Manavizadeh

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The F204S mutation in adrenodoxin oxidoreductase drives salinomycin resistance in Eimeria tenella by Pei Sun, Chaoyue Wang, Fujie Xie, Linlin Chen, Yuanyuan Zhang, Xinming Tang, Dandan Hu, Yang Gao, Ning Zhang, Zhenkai Hao, Yonglan Yu, Jingxia Suo, Xun Suo, Xianyong Liu

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Elastin genetic point mutation and the risk of pelvic organ prolapse by N. Haya, I. Feferkorn, F. Fares, N. Azzam, R. Auslender, Y. Abramov

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Search for the elusive haplotype of the APOE polymorphism associated with Alzheimer’s disease by Asma Naseer Cheema, Kang-Hsien Fan, Elizabeth Lawrence, Narges Zafari, Ruyu Shi, Muhammad Muaaz Aslam, Vibha Acharya, Alayna Jean Holderman, Annie Bedison, Eleanor Feingold, M. Ilyas Kamboh

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High level non-carbapenemase carbapenem resistance by overlaying mutations of mexR, oprD, and ftsI in Pseudomonas aeruginosa by Yan Yang, Xue Li, Lang Sun, Xiu-Kun Wang, You-Wen Zhang, Jing Pang, Guo-Qing Li, Xin-Xin Hu, Tong-Ying Nie, Xin-Yi Yang, Jian-Hua Liu, Gerrit Brandis, Xue-Fu You, Cong-Ran Li

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Modified pea apyrase has altered nuclear functions and enhances the growth of yeast and Arabidopsis by Manas K. Tripathy, Huan Wang, Robert D. Slocum, Han-Wei Jiang, Ji-Chul Nam, Tanya Sabharwal, Roopadarshini Veerappa, Katherine A. Brown, Katherine A. Brown, Xingbo Cai, Peter Allen Faull, Greg Clark, Stanley J. Roux

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DNMT3A GENE POINT MUTATIONS DETECTION IN ACUTE MYELOID LEUKEMIA PATIENTS USING SEQUENCING TECHNIQUE by A. V. Vinogradov, A. V. Rezaykin, A. G. Sergeev

Subjects: “…point mutation…”
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Proximal spinal muscular atrophy types I-IV: Specific features of molecular genetic diagnosis by V. V. Zabnenkova, E. L. Dadali, A. V. Polyakov

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A case of adrenomyeloneuropathy caused by a novel point mutation in the ABCD1 gene and functional verification by Xiaoxue Shi, Xiaoxue Shi, Xiaoxue Shi, Xuelin Qi, Xuelin Qi, Jinhua Zheng, Jinhua Zheng, Jinhua Zheng, Jianjun Ma, Jianjun Ma, Jianjun Ma, Dongsheng Li, Dongsheng Li, Dongsheng Li

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A Truncating De Novo Point Mutation in a Young Infant with Severe Menkes Disease by Yi-Jie Lin, Che-Sheng Ho, Chyong-Hsin Hsu, Ju-Li Lin, Chih-Kuang Chuang, Jen-Daw Tsai, Nan-Chang Chiu, Hsiang-Yu Lin, Shuan-Pei Lin

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Understanding the structural basis of ALS mutations associated with resistance to sulfonylurea in wheat by Pawan Kumar, Ritika Bishnoi, Pragya Priyadarshini, Parveen Chhuneja, Deepak Singla

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Effects of Somatic Mutations Are Associated with SNP in the Progression of Individual Acute Myeloid Leukemia Patient: The Two-Hit Theory Explains Inherited Predisposition to Pathog... by Soyoung Park, Youngil Koh, Sung-Soo Yoon

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