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Publications by C. L. Clark

Mutation of Glutamine to Arginine at Position 548 of IE2 86 in Human Cytomegalovirus Leads to Decreased Expression of IE2 40, IE2 60, UL83, and UL84 and Increased Transcription of US8-9 and US29-32

Journal of Virology

English

Small Bowel Transplantation.

BMJ

1992

English

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Cell Cycle Arrest by Human Cytomegalovirus 86-kDa IE2 Protein Resembles Premature Senescence

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Corrigendum: Human Cytomegalovirus IE2 86 kDa Protein Induces STING Degradation and Inhibits cGAMP-Mediated IFN-β Induction

Frontiers in Microbiology

Microbiology

2018

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Human Cytomegalovirus IE2 86-Kilodalton Protein Binds P53 but Does Not Abrogate G1 Checkpoint Function.

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IE2 Protein Is Insufficient for Transcriptional Repression of the Human Cytomegalovirus US3 Promoter.

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The Yo-Yo IE2 Test

Medicine and Science in Sports and Exercise

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Human Cytomegalovirus IE1-72 Protein Interacts With P53 and Inhibits P53-Dependent Transactivation by a Mechanism Different From That of IE2-86 Protein

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Interaction Network of Proteins Associated With Human Cytomegalovirus IE2-p86 Protein During Infection: A Proteomic Analysis

PLoS ONE

Multidisciplinary

2013

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Human Cytomegalovirus IE2 Protein Disturbs Brain Development by the Dysregulation of Neural Stem Cell Maintenance and the Polarization of Migrating Neurons

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Binding of Cellular Repressor Protein or the IE2 Protein to a Cis-Acting Negative Regulatory Element Upstream of a Human Cytomegalovirus Early Promoter.

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by C. L. Clark

Mutation of Glutamine to Arginine at Position 548 of IE2 86 in Human Cytomegalovirus Leads to Decreased Expression of IE2 40, IE2 60, UL83, and UL84 and Increased Transcription of US8-9 and US29-32

Small Bowel Transplantation.

Related publications

Cell Cycle Arrest by Human Cytomegalovirus 86-kDa IE2 Protein Resembles Premature Senescence

Corrigendum: Human Cytomegalovirus IE2 86 kDa Protein Induces STING Degradation and Inhibits cGAMP-Mediated IFN-β Induction

Human Cytomegalovirus IE2 86-Kilodalton Protein Binds P53 but Does Not Abrogate G1 Checkpoint Function.

IE2 Protein Is Insufficient for Transcriptional Repression of the Human Cytomegalovirus US3 Promoter.

The Yo-Yo IE2 Test

Human Cytomegalovirus IE1-72 Protein Interacts With P53 and Inhibits P53-Dependent Transactivation by a Mechanism Different From That of IE2-86 Protein

Interaction Network of Proteins Associated With Human Cytomegalovirus IE2-p86 Protein During Infection: A Proteomic Analysis

Human Cytomegalovirus IE2 Protein Disturbs Brain Development by the Dysregulation of Neural Stem Cell Maintenance and the Polarization of Migrating Neurons

Binding of Cellular Repressor Protein or the IE2 Protein to a Cis-Acting Negative Regulatory Element Upstream of a Human Cytomegalovirus Early Promoter.