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Results for
""Mutation""[mesh_terms]

10228 Results

Searching titles within these results

Microbial cross-feeding stabilized by segregation of a dependent mutant from its independent ancestor.

Sima Setayeshgar, Anthony J Zmuda, Olivia F Schakel, James B McKinlay, Ryan K Fritts

The ISME journal 2025;19(1):

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Abstract

Insertions and deletions in protein evolution and engineering.

Jorick Franceus, Tom Desmet, Simone Savino

Biotechnology advances 2022;60():108010

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Abstract

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants.

Tommaso Mazza, Douglas C Wallace, Angelo Luigi Vescovi, Shiping Zhang, Marie T Lott, Vincent Procaccio, Massimo Carella, Alessandro Napoli, Niccolò Liorni, Agnese Giovannetti, Tommaso Biagini, Francesco Petrizzelli, Luca Parca, Salvatore Daniele Bianco, Viviana Caputo

Nature communications 2023;14(1):5058

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Effects of Synonymous Mutations beyond Codon Bias: The Evidence for Adaptive Synonymous Substitutions from Microbial Evolution Experiments.

Luz Angela Alonso Morales, Rees Kassen, Susan F Bailey

Genome biology and evolution 2022;13(9):evab141

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MFDSMC: Accurate Identification of Cancer-Driver Synonymous Mutations Using Multiperspective Feature Representation Learning.

Lihua Wang, Junfeng Xia, Chen Ye, Na Cheng

Journal of chemical information and modeling 2025;65(12):6382-6396

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Abstract

Sodium azide mutagenesis induces a unique pattern of mutations.

Gary J Muehlbauer, Justin C Fay, Li Lei, Peter L Morrell, Monika Spiller, Erik Legg, Skylar R Wyant, Shane Heinen, Adrian O Stec, Giulia Frascarelli, Chaochih Liu, Kevin P Smith

PLoS genetics 2025;21(6):e1011634

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Spontaneous epimutations in plants.

Robert J Schmitz, Frank Johannes

The New phytologist 2020;221(3):1253-1259

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Genetic analysis and literature review of a Poirier-Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2B.

Bingbo Zhou, Ling Hui, Chuan Zhang, Shengju Hao, Yupei Wang, Xue Chen, Xinyuan Tian, Danyang Li

Molecular genetics & genomic medicine 2024;12(1):e2327

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Integrating evidence from protein domains to identify cancer driver mutations.

Daria Ostroverkhova, Yiru Sheng, Igor Rogozin, Anna R Panchenko

Protein science : a publication of the Protein Society 2026;35(2):e70422

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Unveiling the role of iPLAβ in neurodegeneration: From molecular mechanisms to advanced therapies.

Jiabin Liu, Jifeng Guo, Jieqiong Tan, Beisha Tang

Pharmacological research 2024;202():107114

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Elucidating the Structural Impacts of Protein InDels.

Filip Jagodzinski, Nurit Haspel, Muneeba Jilani, Alistair Turcan

Biomolecules 2022;12(10):1435

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Fitness difference between two synonymous mutations of Phytophthora infestans ATP6 gene.

Xiaoxian Yuan, Lixia Chen, Abdul Waheed, Yan-Ping Wang, Jiasui Zhan, Hanmei Fang, Oswald Nkurikiyimfura, Lina Yang, Guodong Lu

BMC ecology and evolution 2024;24(1):36

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Hyperparathyroid genes: sequences reveal answers and questions.

Stephen J Marx

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2012;17 Suppl 3(Suppl 3):18-27

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A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma.

James MacFarlane, Ruth T Casey, Eamonn R Maher, Benjamin G Challis, Olivier Giger, Soo-Mi Park, Anne Warren, Alison Marker, Kieren Allinson, Basetti Madhu, Chad Bisambar, Keat Cheah Seong

Clinical endocrinology 2021;93(5):528-538

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Personalized Management of Pheochromocytoma and Paraganglioma.

Karel Pacak, Ashley Grossman, Graeme Eisenhofer, Matthias Kroiss, Martin Fassnacht, Felix Beuschlein, David Taieb, Nicole Bechmann, Svenja Nölting

Endocrine reviews 2022;43(2):199-239

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Abstract

Results: 1 – 15 / 10228

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Results for ""Mutation""[mesh_terms]

Microbial cross-feeding stabilized by segregation of a dependent mutant from its independent ancestor.

Insertions and deletions in protein evolution and engineering.

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants.

Effects of Synonymous Mutations beyond Codon Bias: The Evidence for Adaptive Synonymous Substitutions from Microbial Evolution Experiments.

MFDSMC: Accurate Identification of Cancer-Driver Synonymous Mutations Using Multiperspective Feature Representation Learning.

Sodium azide mutagenesis induces a unique pattern of mutations.

Spontaneous epimutations in plants.

Genetic analysis and literature review of a Poirier-Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2B.

Integrating evidence from protein domains to identify cancer driver mutations.

Unveiling the role of iPLAβ in neurodegeneration: From molecular mechanisms to advanced therapies.

Elucidating the Structural Impacts of Protein InDels.

Fitness difference between two synonymous mutations of Phytophthora infestans ATP6 gene.

Hyperparathyroid genes: sequences reveal answers and questions.

A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma.

Personalized Management of Pheochromocytoma and Paraganglioma.

Results for
""Mutation""[mesh_terms]