细菌染色体分离是一种细菌染色体分离.

Same author

Polar explorers: membrane proteins that determine division site placement.

Cell·2001

Same author

The MinE ring required for proper placement of the division site is a mobile structure that changes its cellular location during the Escherichia coli division cycle.

Proceedings of the National Academy of Sciences of the United States of America·2001

Same author

Structural basis for the topological specificity function of MinE.

Nature structural biology·2000

Same author

Cell division inhibitors SulA and MinC/MinD block septum formation at different steps in the assembly of the Escherichia coli division machinery.

Molecular microbiology·2000

Same author

Membrane redistribution of the Escherichia coli MinD protein induced by MinE.

Journal of bacteriology·2000

Same author

Backbone and side-chain 1H, 15N, and 13C assignments for the topological specificity domain of the MinE cell division protein.

Journal of biomolecular NMR·1999

Same journal

A viral ORFeome library for systems-level genetic dissection of host-pathogen interactions.

Cell·2026

Same journal

Co-option of lysosomal machinery shapes the evolution of the intracellular photosymbiosis supporting coral reefs.

Cell·2026

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LEF1 and niche factors determine T cell stemness across chronic diseases.

Cell·2026

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Recurrent patterns of TOP1-mediated neuronal genomic damage shared by major neurodegenerative disorders.

Cell·2026

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Four-dimensional molecular mapping from a spatial snapshot reveals the dynamics of hair follicle organogenesis.

Cell·2026

Same journal

Whole-cell particle-based digital twin simulations from 4D lattice light-sheet microscopy data.

Cell·2026

相关实验视频

细菌染色体分离是一种细菌染色体分离.

相关概念视频

Polar explorers: membrane proteins that determine division site placement.

The MinE ring required for proper placement of the division site is a mobile structure that changes its cellular location during the Escherichia coli division cycle.

Structural basis for the topological specificity function of MinE.

Cell division inhibitors SulA and MinC/MinD block septum formation at different steps in the assembly of the Escherichia coli division machinery.

Membrane redistribution of the Escherichia coli MinD protein induced by MinE.

Backbone and side-chain 1H, 15N, and 13C assignments for the topological specificity domain of the MinE cell division protein.

A viral ORFeome library for systems-level genetic dissection of host-pathogen interactions.

Co-option of lysosomal machinery shapes the evolution of the intracellular photosymbiosis supporting coral reefs.

LEF1 and niche factors determine T cell stemness across chronic diseases.

Recurrent patterns of TOP1-mediated neuronal genomic damage shared by major neurodegenerative disorders.

Four-dimensional molecular mapping from a spatial snapshot reveals the dynamics of hair follicle organogenesis.

Whole-cell particle-based digital twin simulations from 4D lattice light-sheet microscopy data.

相关实验视频

细菌染色体分离是一种细菌染色体分离.

相关概念视频

相关文章

Polar explorers: membrane proteins that determine division site placement.

The MinE ring required for proper placement of the division site is a mobile structure that changes its cellular location during the Escherichia coli division cycle.

Structural basis for the topological specificity function of MinE.

Cell division inhibitors SulA and MinC/MinD block septum formation at different steps in the assembly of the Escherichia coli division machinery.

Membrane redistribution of the Escherichia coli MinD protein induced by MinE.

Backbone and side-chain 1H, 15N, and 13C assignments for the topological specificity domain of the MinE cell division protein.

A viral ORFeome library for systems-level genetic dissection of host-pathogen interactions.

Co-option of lysosomal machinery shapes the evolution of the intracellular photosymbiosis supporting coral reefs.

LEF1 and niche factors determine T cell stemness across chronic diseases.

Recurrent patterns of TOP1-mediated neuronal genomic damage shared by major neurodegenerative disorders.

Four-dimensional molecular mapping from a spatial snapshot reveals the dynamics of hair follicle organogenesis.

Whole-cell particle-based digital twin simulations from 4D lattice light-sheet microscopy data.