The Genome Sequence of the SARS-Associated Coronavirus

By Marco A. Marra, Steven M. Jones, C. Astell, R. Holt, A. Brooks-Wilson, Y. Butterfield, J. Khattra, J. Asano, Sarah A. Barber, Susanna Y. Chan and 48 more. Science, 2003

2,060 citations recorded by the source corpus.

Subfields: Animal Science and Zoology, Infectious Diseases

View Paper: https://www.semanticscholar.org/paper/39a86de17296704ccd074dadb20ba510d4251694

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Citations in the corpus

Assembling millions of short DNA sequences using SSAKE (2006, methodology): “We ran the algorithm on simulated error-free 25mers from the bacteriophage PhiX174 (Sanger et al., 1977), coronavirus SARS TOR2 (Marra et al., 2003), bacteria Haemophilus influenzae (Fleischmann et al., 1995) genomes and on 40 million 25mers from the whole-genome shotgun (WGS) sequence data from…”
What’s new in the renin-angiotensin system? (2004, background): “Initial analyses suggested that SARS-CoV does not belong to any of the three established coronaviral groups [40] [41] [42] [43] .”
The spike protein of SARS-CoV — a target for vaccine and therapeutic development (2009, background): “Its genome RNA encodes a non-structural replicase polyprotein and structural proteins, including spike ( S ), envelope ( E ), membrane ( M ) and nucleocapsid ( N ) protein”
The Molecular Biology of Coronaviruses (2006, background): “It was thus proposed to be the first recognized member of a fourth group of coronaviruses (Marra et al., 2003; Rota et al., 2003).”
Accessory proteins of SARS-CoV and other coronaviruses (2014, background): “Proteins 3a and 3b (p3a and p3b, previously also known as X1 and X2), comprise 274 and 154 amino-acid residues, respectively (Marra et al., 2003; Rota et al., 2003) .”
Multiple organ infection and the pathogenesis of SARS (2005, methodology): “The Vero E6 cells that were used to identify and isolate the SARS coronavirus were derived from the renal epithelial cells of the green monkey (21); this suggests that kidney epithelial cells are inherently vulnerable to SARS infection.”
The Coronavirus Nucleocapsid Is a Multifunctional Protein (2014, background): “N protein [35], of which the short lysine-rich sequence (366–381) near the carboxy-terminus is a putative bipartite NLS that is unique to SARS-CoV N [71,76].”
From SARS to MERS, Thrusting Coronaviruses into the Spotlight (2019, background): “Most of the protein and the amino terminus are situated on the outside of the virus particle or the cell surface [50].”