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Results for
""Point Mutation""[mesh_terms]

551 Results

Searching titles within these results

The analysis of protein folding kinetic data produced in protein engineering experiments.

Alan R Davidson, Arash Zarrine-Afsar

Methods (San Diego, Calif.) 2005;34(1):41-50

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Mechanism of cancer: Oncohistones in action.

Kui-Ming Chan, Junhong Han, Xinyi Zeng, Qian Jing, Xiaoyan Hu, Lei Qiu

Journal of genetics and genomics = Yi chuan xue bao 2019;45(5):227-236

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Abstract

On the effect of a point mutation on the reactivity of CuZn superoxide dismutase: a theoretical study.

Andrea Amadei, Maira D'Alessandro, Maurizio Paci, Alfredo Di Nola, Massimiliano Aschi

The journal of physical chemistry. B 2007;110(14):7538-44

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Abstract

Gating and ion selectivity of Channelrhodopsins are critical for photo-activated orientation of Chlamydomonas as shown by in vivo point mutation.

Johannes Oppermann, Olga Baidukova, Simon Kelterborn, Rodrigo G Fernandez Lahore, Dimitri Schumacher, Heide Evers, Yousef Yari Kamrani, Peter Hegemann

Nature communications 2022;13(1):7253

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Commentary: mutations of transferrin receptor 2 (Trf-2) and iron storage disease.

E Beutler

Blood cells, molecules & diseases 2001;27(1):294-5

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Influence of Model Structures on Predictors of Protein Stability Changes from Single-Point Mutations.

Cesare Rollo, Corrado Pancotti, Giovanni Birolo, Ivan Rossi, Tiziana Sanavia, Piero Fariselli

Genes 2023;14(12):2228

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Myalgic Becker Muscular Dystrophy Due to an Exon 15 Point Mutation: Case Series and Literature Review.

Zachary Tavallaee, Tyler Hamby, Warren Marks

Journal of clinical neuromuscular disease 2022;24(2):106-110

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Effect of dehydration on photoinduced transformation in gelatin films made with 14-fluoro bacteriorhodopsin derivatives.

Anna B Druzhko, Sergey K Pirutin, Angel R de Lera, Rosana Alvarez, Howard H Weetall

Applied biochemistry and biotechnology 2005;120(2):121-32

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The biochemical basis of hereditary fructose intolerance.

David J Timson, Nadia Bouteldja

Journal of inherited metabolic disease 2010;33(2):105-12

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Molecular Determinants and Bottlenecks in the Dissociation Dynamics of Biotin-Streptavidin.

Pratyush Tiwary

The journal of physical chemistry. B 2018;121(48):10841-10849

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Familial Growth Hormone Deficiency and Mutations in the GHRH Receptor Gene.

Maria Alba, Roberto Salvatori

Vitamins and hormones 2004;69():209-20

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Fingerprints of Calcium-Binding Protein Conformational Dynamics Monitored by Surface Plasmon Resonance.

Daniele Dell'Orco, Karl-Wilhelm Koch

ACS chemical biology 2017;11(9):2390-7

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Discovery of an Unnatural DNA Modification Derived from a Natural Secondary Metabolite.

Tong Wang, Rahul M Kohli

Cell chemical biology 2021;28(1):97-104.e4

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A review on point mutations via proton transfer in DNA base pairs in the absence and presence of electric fields.

Anju Choorakottayil Pushkaran, Alya A Arabi

International journal of biological macromolecules 2024;277(Pt 2):134051

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From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes.

N Gattermann

Leukemia research 2000;24(2):141-51

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Results for ""Point Mutation""[mesh_terms]

The analysis of protein folding kinetic data produced in protein engineering experiments.

Mechanism of cancer: Oncohistones in action.

On the effect of a point mutation on the reactivity of CuZn superoxide dismutase: a theoretical study.

Gating and ion selectivity of Channelrhodopsins are critical for photo-activated orientation of Chlamydomonas as shown by in vivo point mutation.

Commentary: mutations of transferrin receptor 2 (Trf-2) and iron storage disease.

Influence of Model Structures on Predictors of Protein Stability Changes from Single-Point Mutations.

Myalgic Becker Muscular Dystrophy Due to an Exon 15 Point Mutation: Case Series and Literature Review.

Effect of dehydration on photoinduced transformation in gelatin films made with 14-fluoro bacteriorhodopsin derivatives.

The biochemical basis of hereditary fructose intolerance.

Molecular Determinants and Bottlenecks in the Dissociation Dynamics of Biotin-Streptavidin.

Familial Growth Hormone Deficiency and Mutations in the GHRH Receptor Gene.

Fingerprints of Calcium-Binding Protein Conformational Dynamics Monitored by Surface Plasmon Resonance.

Discovery of an Unnatural DNA Modification Derived from a Natural Secondary Metabolite.

A review on point mutations via proton transfer in DNA base pairs in the absence and presence of electric fields.

From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes.

Results for
""Point Mutation""[mesh_terms]