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Titlebook: Coronaviruses; Michael M. C. Lai,Stephen A. Stohlman Book 1987 The Editor(s) (if applicable) and The Author(s), under exclusive license to

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41#
發(fā)表于 2025-3-28 16:14:10 | 只看該作者
42#
發(fā)表于 2025-3-28 22:22:39 | 只看該作者
43#
發(fā)表于 2025-3-29 01:49:04 | 只看該作者
Nucleotide Sequence of the Porcine Transmissible Gastroenteritis Coronavirus Matrix Protein Genemouse hepatitis coronavirus, 37% with the bovine enteric coronavirus, and 28% with the avian infectious bronchitis virus. Judging from an alignment with MHV and IBV proteins, the amino terminus of the TGEV M protein extends 54 amino acids from the virion envelope which compares with 26 for MHV and 21 for IBV.
44#
發(fā)表于 2025-3-29 06:49:22 | 只看該作者
Coronaviruses: A Historical Perspectiveology and immunology has contributed to new insights into understanding the biology of the viruses and the pathogenesis of the diseases they produce. The number of investigators has also increased over the past several years as evidenced by this Congress which is thus far the largest ever held.
45#
發(fā)表于 2025-3-29 10:59:08 | 只看該作者
46#
發(fā)表于 2025-3-29 12:38:46 | 只看該作者
47#
發(fā)表于 2025-3-29 16:30:10 | 只看該作者
Deduced Amino Acid Sequence and Potential O-Glycosylation Sites for the Bovine Coronavirus Matrix Prr weight of 26,376. The BCV M protein shares extensive sequence homology with the matrix protein of the mouse hepatitis coronavirus (MHV) but differs notably in the amino terminal region external to the virion envelope where BCV apparently uses at least two of its six potential O-glycosylation sites.
48#
發(fā)表于 2025-3-29 20:08:12 | 只看該作者
Temporal Regulation of RNA Synthesis of Bovine Coronavirusates late in infection. However, no clear switching from transcription of subgenomic mRNAs to replication of genomic-sized RNA is seen. Thus, it is not known whether there is a temporal regulation of viral RNA synthesis in coronavirus-infected cells.
49#
發(fā)表于 2025-3-30 03:42:28 | 只看該作者
50#
發(fā)表于 2025-3-30 07:56:27 | 只看該作者
Java Beans and Controller Helpers, from rabbit reticulocytes to identify the proteins coded for by input genomic RNA. We have also confirmed the validity of this approach by identifying the major in vitro translation product in infected L-2 cells.
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