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Platelet genomics and proteomics in human health and disease
Iain C. Macaulay, Philippa Carr, Arief Gusnanto, Willem H. Ouwehand, Des Fitzgerald, Nicholas A. Watkins
Iain C. Macaulay, Philippa Carr, Arief Gusnanto, Willem H. Ouwehand, Des Fitzgerald, Nicholas A. Watkins
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Platelet genomics and proteomics in human health and disease

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Abstract

Proteomic and genomic technologies provide powerful tools for characterizing the multitude of events that occur in the anucleate platelet. These technologies are beginning to define the complete platelet transcriptome and proteome as well as the protein-protein interactions critical for platelet function. The integration of these results provides the opportunity to identify those proteins involved in discrete facets of platelet function. Here we summarize the findings of platelet proteome and transcriptome studies and their application to diseases of platelet function.

Authors

Iain C. Macaulay, Philippa Carr, Arief Gusnanto, Willem H. Ouwehand, Des Fitzgerald, Nicholas A. Watkins

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Figure 1

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Platelet transcript profiling by microarray. Generally, 1 of 2 approache...
Platelet transcript profiling by microarray. Generally, 1 of 2 approaches can be used to identify expressed transcripts in platelets. (A) With single-channel oligonucleotide arrays, mRNA is isolated from platelets, labeled, and hybridized to the microarray. The array is then processed and scanned, and genes are identified as “present,” “marginal,” or “absent.” Comparisons between samples can then be made in silico to identify differentially expressed genes. (B) In a 2-channel experiment, RNA from 2 individuals is isolated, each sample is labeled with a different fluorescent dye, and the 2 are compared directly on a microarray. In this case, the individuals have a different dose-response curve for a platelet agonist. Differentially expressed genes can then be directly identified.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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