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Mark A. Krasnow

Researcher at Stanford University

Publications -  117
Citations -  21370

Mark A. Krasnow is an academic researcher from Stanford University. The author has contributed to research in topics: Gene & Biology. The author has an hindex of 66, co-authored 103 publications receiving 17906 citations. Previous affiliations of Mark A. Krasnow include University of Basel & University of California, San Francisco.

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SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues.

Carly G. K. Ziegler, +135 more
- 28 May 2020 - 
TL;DR: The data suggest that SARS-CoV-2 could exploit species-specific interferon-driven upregulation of ACE2, a tissue-protective mediator during lung injury, to enhance infection.
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Reconstructing lineage hierarchies of the distal lung epithelium using single cell RNA-seq

TL;DR: The results confirmed the basic outlines of the classical model of epithelial cell-type diversity in the distal lung and led to the discovery of many previously unknown cell- type markers, including transcriptional regulators that discriminate between the different populations.
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Gene expression during the life cycle of Drosophila melanogaster.

TL;DR: These studies define major characteristics of the transcriptional programs that underlie the life cycle, compare development in males and females, and show that large-scale gene expression data collected from whole animals can be used to identify genes expressed in particular tissues and organs or genes involved in specific biological and biochemical processes.
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A molecular cell atlas of the human lung from single-cell RNA sequencing.

TL;DR: Droplet- and plate-based single cell RNA sequencing applied to ~75,000 human cells across all lung tissue compartments and circulating blood, combined with a multi-pronged cell annotation approach, have allowed them to define the gene expression profiles and anatomical locations of 58 cell populations in the human lung.
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Alveolar progenitor and stem cells in lung development, renewal and cancer

TL;DR: There is a switch after birth, when AT2 cells function as stem cells that contribute to alveolar renewal, repair and cancer, and it is proposed that local signals regulate AT2 stem-cell activity.