M
Mark F. Stinski
Researcher at University of Iowa
Publications - 79
Citations - 6533
Mark F. Stinski is an academic researcher from University of Iowa. The author has contributed to research in topics: Gene & Transcription (biology). The author has an hindex of 39, co-authored 79 publications receiving 6447 citations. Previous affiliations of Mark F. Stinski include University of Iowa Hospitals and Clinics.
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Transfer vectors and microorganisms containing human cytomegalovirus immediate-early promoter-regulatory DNA sequence
TL;DR: The cloning of a eucaryotic promoter-regulatory region that functions preferentially in human cells is described in this paper, which is exemplified by a section of the human cytomegalovirus genome comprising a DNA sequence with regulatory and promoter signals.
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Structural analysis of the major immediate early gene of human cytomegalovirus.
TL;DR: It is hypothesized that this viral gene codes for the major regulatory protein controlling transcription of the viral genome at early times, and its protein product is discussed.
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Temporal Patterns of Human Cytomegalovirus Transcription: Mapping the Viral RNAs Synthesized at Immediate Early, Early, and Late Times After Infection
TL;DR: The transcription of the human cytomegalovirus genome was investigated at immediate early, early, and late times after infection and it is proposed that expression of the immediate early viral genes is required to transcribe theEarly viral genes in the long repeat and adjacent sequences.
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Promoter-regulatory region of the major immediate early gene of human cytomegalovirus
TL;DR: DNA sequence analysis of the upstream regulatory region of IE region 1 detected two distinct repeats of 19 and 18 nucleotides, both being repeated four times, suggesting a putative cruciform structure could form through the surrounding sequences with each 18-nucleotide repeat being located in the unpaired region.
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Organization and expression of the immediate early genes of human cytomegalovirus.
TL;DR: Immunoprecipitation of viral proteins synthesized in vitro as well as in vivo demonstrated that the predominant immediate early protein is synthesized as a protein of 75,000 daltons, but is presumably modified in vivo, resulting in a broad banding pattern ranging from75,000 to 68,000Daltons.