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Kim M. Summers

Researcher at University of Queensland

Publications -  192
Citations -  8405

Kim M. Summers is an academic researcher from University of Queensland. The author has contributed to research in topics: Gene & Population. The author has an hindex of 37, co-authored 184 publications receiving 6896 citations. Previous affiliations of Kim M. Summers include The Roslin Institute & QIMR Berghofer Medical Research Institute.

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A promoter-level mammalian expression atlas

Alistair R. R. Forrest, +280 more
- 27 Mar 2014 - 
TL;DR: For example, the authors mapped transcription start sites (TSSs) and their usage in human and mouse primary cells, cell lines and tissues to produce a comprehensive overview of mammalian gene expression across the human body.
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Microglial brain region−dependent diversity and selective regional sensitivities to aging

TL;DR: It is found that microglia have distinct region-dependent transcriptional identities and age in a regionally variable manner, and in the young adult brain, differences in bioenergetic and immunoregulatory pathways were the major sources of heterogeneity and suggested that cerebellar and hippocampalmicroglia exist in a more immune-vigilant state.
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Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells

Erik Arner, +108 more
- 27 Feb 2015 - 
TL;DR: The data support a highly generalizable model in which enhancer transcription is the earliest event in successive waves of transcriptional change during cellular differentiation or activation.
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An integrated expression atlas of miRNAs and their promoters in human and mouse.

Derek De Rie, +74 more
- 21 Aug 2017 - 
TL;DR: An integrated expression atlas of miRNAs and their promoters by deep-sequencing 492 short RNA libraries, with matching Cap Analysis Gene Expression (CAGE) data, is created, establishing a foundation for detailed analysis of miRNA expression patterns and transcriptional control regions.
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Abnormal Extracellular Matrix Protein Transport Associated With Increased Apoptosis of Vascular Smooth Muscle Cells in Marfan Syndrome and Bicuspid Aortic Valve Thoracic Aortic Aneurysm

TL;DR: The findings suggest the presence of a fundamental cellular abnormality in BAV thoracic aorta, possibly of genetic origin, and alteration in both the amount and quality of secreted proteins and an increased degree of VSMC apoptosis in MS and BAV.