Bromovirus
Alfamovirus
Chenopodium quinoa
Plant Viral Movement Proteins
Fabaceae
The large family of plants characterized by pods. Some are edible and some cause LATHYRISM or FAVISM and other forms of poisoning. Other species yield useful materials like gums from ACACIA and various LECTINS like PHYTOHEMAGGLUTININS from PHASEOLUS. Many of them harbor NITROGEN FIXATION bacteria on their roots. Many but not all species of "beans" belong to this family.
Plants, Medicinal
Protoplasts
Base Sequence
Molecular Sequence Data
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
A brome mosaic virus intergenic RNA3 replication signal functions with viral replication protein 1a to dramatically stabilize RNA in vivo. (1/238)
Brome mosaic virus (BMV), a positive-strand RNA virus in the alphavirus-like superfamily, encodes two RNA replication proteins. The 1a protein has putative helicase and RNA-capping domains, whereas 2a contains a polymerase-like domain. Saccharomyces cerevisiae expressing 1a and 2a is capable of replicating a BMV RNA3 template produced by in vivo transcription of a DNA copy of RNA3. Although insufficient for RNA3 replication, the expression of 1a protein alone results in a dramatic and specific stabilization of the RNA3 template in yeast. As one step toward understanding 1a-induced stabilization of RNA3, the interactions involved, and its possible relation to RNA replication, we have identified the cis-acting sequences required for this effect. We find that 1a-induced stabilization is mediated by a 150- to 190-base segment of the RNA3 intergenic region corresponding to a previously identified enhancer of RNA3 replication. Moreover, this segment is sufficient to confer 1a-induced stability on a heterologous beta-globin RNA. Within this intergenic segment, partial deletions that inhibited 1a-induced stabilization in yeast expressing 1a alone resulted in parallel decreases in the levels of negative- and positive-strand RNA3 replication products in yeast expressing 1a and 2a. In particular, a small deletion encompassing a motif corresponding to the box B element of RNA polymerase III promoters dramatically reduced the ability of RNAs to respond to 1a or 1a and 2a. These and other findings suggest that 1a-induced stabilization likely reflects an early template selection step in BMV RNA replication. (+info)The N-terminal half of the brome mosaic virus 1a protein has RNA capping-associated activities: specificity for GTP and S-adenosylmethionine. (2/238)
The N-terminal half of the brome mosaic virus (BMV) 1a replication-associated protein contains sequence motifs found in RNA methyltransferases. We demonstrate that recombinant BMV methyltransferase-like (MT) domain expressed in Escherichia coli forms an adduct with a guanine nucleotide in a reaction that requires S-adenosylmethionine (AdoMet) and divalent cations. Moieties in GTP and AdoMet required for adduct formation were determined using a competition assay and chemical analogues. In the guanine nucleotide the ribose 2' hydroxyl, the triphosphates, the base C6 keto group, and possibly the N1 imine are required. In AdoMet, the methyl group and the ability to transfer a methyl group to guanine nucleotide were demonstrated to be required for adduct formation. The effects of methyltransferase inhibitors on viral RNA synthesis was determined using an in vitro RNA synthesis assay. These results are consistent with the previously reported activities of alphaviral nsP1 methyltransferase protein and identify the chemical moieties required for the BMV methyltransferase activity. (+info)Effect of C-terminal deletions in the movement protein of cowpea chlorotic mottle virus on cell-to-cell and long-distance movement. (3/238)
In order to elucidate the function of the C-terminal region of cowpea chlorotic mottle bromovirus (CCMV) movement protein (MP) in cell-to-cell movement, a set of deletions ranging from 10 to 80 amino acids (deltaMP10, deltaMP20, deltaMP33, deltaMP43, deltaMP60 and deltaMP80) was engineered into the MP gene encoded by the biologically active clone C3/deltaCP-EGFP, a variant of CCMV RNA3 that contained wild-type (wt) MP and the enhanced green fluorescent protein (EGFP) gene in place of the coat protein (CP). The effect of each MP deletion on cell-to-cell movement was examined in three susceptible host plants: Chenopodium quinoa, Nicotiana benthamiana and cowpea (Vigno sinensis cv. Black Eye). The results indicate that, except for mutant deltaMP43, infections resulting from the deletion mutants remained subliminal. Interestingly, infections resulting from inoculating mutant deltaMP43, which lacked the 43 most C-terminal amino acids, spread rapidly between cells and the number of infected cells expressing EGFP approached that of control inoculations made with C3/deltaCP-EGFP. To verify whether the presence of wt CP altered the movement behaviour of these mutants, each MP deletion was also incorporated into the genetic background of wt CCMV RNA3 (pCC3) and inoculated independently to all three hosts. The results suggest that the overall movement process exhibited by each MP mutant is influenced profoundly by the presence of CP and the particular host plant tested. (+info)RNA recombination in brome mosaic virus, a model plus strand RNA virus. (4/238)
Studies on the molecular mechanism of genetic recombination in RNA viruses have progressed at the time when experimental systems of efficient recombination crossovers were established. The system of brome mosaic virus (BMV) represents one of the most useful and most advanced tools for investigation of the molecular aspects of the mechanism of RNA-RNA recombination events. By using engineered BMV RNA components, the occurrence of both homologous and nonhomologous crosses were demonstrated among the segments of the BMV RNA genome. Studies show that the two types of crossovers require different RNA signal sequences and that both types depend upon the participation of BMV replicase proteins. Mutations in the two BMV-encoded replicase polypeptides (proteins 1a and 2a) reveal that their different regions participate in homologous and in nonhomologous crossovers. Based on all these data, it is most likely that homologous and nonhomologous recombinant crosses do occur via two different types of template switching events (copy-choice mechanism) where viral replicase complex changes RNA templates during viral RNA replication at distinct signal sequences. In this review we discuss various aspects of the mechanism of RNA recombination in BMV and we emphasize future projections of this research. (+info)Initiation of genomic plus-strand RNA synthesis from DNA and RNA templates by a viral RNA-dependent RNA polymerase. (5/238)
In contrast to the synthesis of minus-strand genomic and plus-strand subgenomic RNAs, the requirements for brome mosaic virus (BMV) genomic plus-strand RNA synthesis in vitro have not been previously reported. Therefore, little is known about the biochemical requirements for directing genomic plus-strand synthesis. Using DNA templates to characterize the requirements for RNA-dependent RNA polymerase template recognition, we found that initiation from the 3' end of a template requires one nucleotide 3' of the initiation nucleotide. The addition of a nontemplated nucleotide at the 3' end of minus-strand BMV RNAs led to initiation of genomic plus-strand RNA in vitro. Genomic plus-strand initiation was specific since cucumber mosaic virus minus-strand RNA templates were unable to direct efficient synthesis under the same conditions. In addition, mutational analysis of the minus-strand template revealed that the -1 nontemplated nucleotide, along with the +1 cytidylate and +2 adenylate, is important for RNA-dependent RNA polymerase interaction. Furthermore, genomic plus-strand RNA synthesis is affected by sequences 5' of the initiation site. (+info)Use of DNA, RNA, and chimeric templates by a viral RNA-dependent RNA polymerase: evolutionary implications for the transition from the RNA to the DNA world. (6/238)
All polynucleotide polymerases have a similar structure and mechanism of catalysis, consistent with their evolution from one progenitor polymerase. Viral RNA-dependent RNA polymerases (RdRp) are expected to have properties comparable to those from this progenitor and therefore may offer insight into the commonalities of all classes of polymerases. We examined RNA synthesis by the brome mosaic virus RdRp on DNA, RNA, and hybrid templates and found that precise initiation of RNA synthesis can take place from all of these templates. Furthermore, initiation can take place from either internal or penultimate initiation sites. Using a template competition assay, we found that the BMV RdRp interacts with DNA only three- to fourfold less well than it interacts with RNA. Moreover, a DNA molecule with a ribonucleotide at position -11 relative to the initiation nucleotide was able to interact with RdRp at levels comparable to that observed with RNA. These results suggest that relatively few conditions were needed for an ancestral RdRp to replicate DNA genomes. (+info)Mapping the molecular determinant of pathogenicity in a hammerhead viroid: a tetraloop within the in vivo branched RNA conformation. (7/238)
Chrysanthemum chlorotic mottle viroid (CChMVd) is an RNA of 398-399 nt that can adopt hammerhead structures in both polarity strands. We have identified by Northern-blot hybridization a nonsymptomatic strain (CChMVd-NS) that protects against challenge inoculation with the symptomatic strain (CChMVd-S). Analysis of CChMVd-NS cDNA clones has revealed a size and sequence very similar to those of the CChMVd-S strain. Some of the mutations observed in CChMVd-NS molecular variants were previously identified in CChMVd-S RNA, but others were never found in this RNA. When bioassayed in chrysanthemum, cDNA clones containing the CChMVd-NS specific mutations were infectious but nonsymptomatic. Site-directed mutagenesis showed that one of the CChMVd-NS-specific mutations, a UUUC --> GAAA substitution, was sufficient to change the symptomatic phenotype into the nonsymptomatic one without altering the final accumulation level of the viroid RNA. The pathogenicity determinant-to our knowledge, a determinant of this class has not been described previously in hammerhead viroids-is located in a tetraloop of the computer-predicted branched conformation for CChMVd RNA. Analysis of the sequence heterogeneity found in CChMVd-S and -NS variants strongly supports the existence of such a conformation in vivo, showing that the rod-like or quasi-rod-like secondary structure is not a universal paradigm for viroids. (+info)Brome mosaic virus defective RNAs generated during infection of barley plants. (8/238)
Brome mosaic virus (BMV) purified from systemically infected barley leaves 8 weeks post-inoculation (p.i.) contained defective RNAs (D-RNAs). The D-RNAs were detected in total and virion RNAs extracted from infected plants at 8 weeks p.i. or later, but not before, when barley plants had been inoculated with virions either containing or lacking D-RNA. The D-RNAs were derived from genomic RNA3 by double or mainly single deletions in the 3a protein ORF, and formed a heterogeneous population. By using in vitro transcripts of D-RNA synthesized from full-length cDNA clones, the D-RNAs were shown to replicate in a helper virus-dependent manner and to be packaged into virions in barley protoplasts. Subgenomic RNA4 was produced from the D-RNA and the coat protein was also expressed. Existence of the D-RNAs together with BMV genomic RNAs in inoculated protoplasts decreased the accumulation of 3a protein but it had no apparent effect on the accumulation of BMV genomic RNA3 or the coat protein. This is the first report of naturally occurring D-RNAs generated during prolonged infection with BMV. (+info)
Chemical virology: decorating the interior of the cowpea chlorotic mottle virus</em>...
Kushner DB~Ahlquist P, 2003 / Papers / YeastPhenome.org
RNA replication protein elisa and antibody
Remarkable variability of apple mosaic virus capsid protein gene after nucleotide position 141, Archives of Virology | 10.1007...
Multishell structures of virus coat proteins | Gelbart Lab
Browse by Person - InterNano Nanomanufacturing Library
Difference between revisions of Bromovirus - microbewiki
Difference between revisions of Bromovirus - microbewiki
OCA4 (YCR095C) Result Summary | BioGRID
Harrison Brome | Nettwerk
KAKEN - Research Projects | Cellular and molecular studies on the transmembrane mechanism of neuroimmuno-interaction (KAKENHI...
Brome mosaic virus - Wikipedia
Browse by Person - InterNano Nanomanufacturing Library
doxorubicin-conjugated tobacco mosaic virus capsid protein mutant assemblies
Biology - The College of New Rochelle
RCSB PDB
- 1I4B: The solution structure of the major family of the mutant stem loop C 5UUA3 triloop of brome mosaic...
View By Volumne
Visualitza per matèria Virus de lhepatitis C
Postdoctoral positions available
plant viruses
11 Indiana BMV branches temporarily close due to staff shortages
Mutational Analysis of Cucumber Mosaic Virus Movement Protein Gene<...
Machlomovirus - Wikipedia
ScholarSpace at University of Hawaii at Manoa: Infectious clones development and transmission biology of maize chlorotic mottle...
FMV - Feathery Mottle Virus (plant disease) | AcronymFinder
Cowpea mottle virus ATCC ® PVAS-518™
ChemIDplus - 83062-04-8 - RNA (velvet tobacco mottle virus 2) - Searchable synonyms, formulas, resource links, and other...
Custom Spherical Mirrors | BMV Optical Technologies Inc. | Mirrors | Optics | ProdSpec | Photonics Buyers Guide
IJMS | Free Full-Text | Molecular Biology of Prune Dwarf Virus-A Lesser Known Member of the Bromoviridae but a Vital Component...
CLN-infected plant in the middle of health corn plants
Hybrid inoculated at the 3-leaf stage of growth with MCMV and MDMV
Frontiers | In silico MCMV Silencing Concludes Potential Host-Derived miRNAs in Maize | Plant Science
Watermelon silver mottle virus ATCC ® PVMC-55™
Spatial Variation in Germination of Two Annual Brome Species in the No by Erin K. Espeland, Jane M. Mangold et al.
Phylogenetic Analysis of PDV Movement Protein Compared to Bromoviridae Members as Justification of Possible Intercellular...
Detailed view of viral replication machinery lends new insights into infection
Coopers Hawk | Brome®
CCMV Classic Commercial Motor Vehicles | Commer QX C Series Mk III, Interim Mk III & Mk IV | Commer Mk III Interim 36619H
Analysis of RNA stability and (-) strand content in viral infections using biotinylated RNA probes. - Science Exchange
International coalition keeps devastating maize disease at bay, but risks still linger - CIMMYT
EP 0832191 A4 20001115 - RECOMBINANT VIRAL NUCLEIC ACIDS
Mottle - definition of mottle by The Free Dictionary
Optimization of an Elastic Network Augmented Coarse Grained Model to Study CCMV Capsid Deformation - pdf descargar
CADASIL: molecular studies on the most common hereditary vascular dementing disorder
Bromus inermis Smooth Brome, Pumpellys brome PFAF Plant Database
Using planting date to manage bean pod mottle virus in soybean
Cactus mild mottle virus is a new cactus-infecting tobamovirus, Archives of Virology | 10.1007/s00705-005-0617-7 | DeepDyve
Ocular Microbiology - Bascom Palmer Eye Institute
Lindenbach Lab
Installing the Pole Adapter on the Plus (video) | Brome®
People - Bornberglab - Bioinformatics at the IEB
CCMV Classic Commercial Motor Vehicles | Albion CX22S & CS24S | Albion CX22S UPJ92F
Bromovirus
... is a genus of viruses, in the family Bromoviridae. Plants serve as natural hosts. There are six species in this ... PMID 11309487; PMCID: PMC33148 ICTV Report: Bromoviridae Viralzone: Bromovirus (Articles with short description, Short ... virus Cowpea chlorotic mottle virus Melandrium yellow fleck virus Spring beauty latent virus Viruses in the genus Bromovirus ...
Brome mosaic virus
Ahlquist, P. (1992). "Bromovirus RNA replication and transcription". Current Opinion in Genetics & Development. 2 (1): 71-76. ... icosahedral RNA plant virus belonging to the genus Bromovirus, family Bromoviridae, in the Alphavirus-like superfamily. BMV was ...
Cowpea chlorotic mottle virus
Horst RK (2008). "Bean Yellow Stipple = Cowpea Chlorotic Mottle Bromovirus Yellow Stipple=Cowpea Chlorotic Mottle Bromovirus". ... Belonging to the bromovirus genus, cowpea chlorotic mottle virus (CCMV) is a small spherical plant virus. Other members of this ... The following viruses are closely related to CCMV and are members of the Bromovirus genus: Broad bean mottle virus Brome mosaic ... Sibert BS, Navine AK, Pennington J, Wang X, Ahlquist P (2018-12-26). "Cowpea chlorotic mottle bromovirus replication proteins ...
Positive-strand RNA virus
Other +ssRNA viruses of plants have also been reported to be capable of recombination, such as Brom mosaic bromovirus and ... "Co-infection with two strains of Brome mosaic bromovirus reveals common RNA recombination sites in different hosts". Virus ...
Cassia (genus)
The plant pathogenic viruses cassia yellow blotch bromovirus and cassia yellow spot potyvirus were first described from Cassia ...
Paul Ahlquist
Diaz, A., Gallei, A., and Ahlquist, P. Bromovirus RNA Replication Compartment Formation Requires Concerted Action of 1a's Self- ... Essential Host Genes Affecting Bromovirus RNA Replication. PLoS One, 6(8):e23988, 2011. Scholthof, K.-B. G., Adkins, S., ...
Bromoviridae
The following genera are assigned to the family: Alfamovirus Anulavirus Bromovirus Cucumovirus Ilarvirus Oleavirus Viruses in ...
List of virus genera
Bowservirus Bracovirus Brambyvirus Brevihamaparvovirus Bridgettevirus Brigitvirus Britbratvirus Brizovirus Bromovirus Bronvirus ...
List of MeSH codes (B04)
... bromovirus MeSH B04.715.081.180 - cucumovirus MeSH B04.715.081.400 - ilarvirus MeSH B04.715.081.700 - oleavirus MeSH B04.715. ... bromovirus MeSH B04.820.081.180 - cucumovirus MeSH B04.820.081.400 - ilarvirus MeSH B04.820.081.700 - oleavirus MeSH B04.820. ... bromovirus MeSH B04.820.464.150 - comovirus MeSH B04.820.464.180 - cucumovirus MeSH B04.820.464.600 - potyvirus MeSH B04.820. ... bromovirus MeSH B04.715.464.100 - caulimovirus MeSH B04.715.464.150 - comovirus MeSH B04.715.464.180 - cucumovirus MeSH B04.715 ...
View source for Taxonomy Index - microbewiki
Details of DPV Cowpea chlorotic mottle virus and References
MESH TREE NUMBER CHANGES - 2015 MeSH
Bromoviridae | ICTV
Genus Bromovirus. Type species Brome mosaic virus. Distinguishing features. Beetle vectors are recorded for most bromoviruses ... Virion Mr is constant among members of the genera Bromovirus, Cucumovirus and some Ilarvirus members, but varies among the ... List of other related viruses which may be members of the genus Bromovirus but have not been approved as species. None reported ... They are either tRNA-like and can be aminoacylated (genera Bromovirus and Cucumovirus) or form other structures that are not ...
DeCS
Code System Concept
Space warping order parameters and symmetry: application to multiscale simulation of macromolecular assemblies. | J Phys Chem...
Bromovirus/química; Capsídeo/química; Substâncias Macromoleculares/química; Simulação de Dinâmica Molecular; RNA Viral/química ... Bromovirus / Vírus Satélite do Mosaico do Tabaco / Substâncias Macromoleculares / Simulação de Dinâmica Molecular Idioma: ... Bromovirus / Vírus Satélite do Mosaico do Tabaco / Substâncias Macromoleculares / Simulação de Dinâmica Molecular Idioma: ...
Select Publications - Morgridge Institute for Research
Biologie Digitale de l'ARN - IBMC
Résumé , Liens , BibTeX , Étiquettes: ase Sequence Bromovirus/*genetics/metabolism Genetic Complementation Test Genome, ... Brome mosaic virus (BMV), a bromovirus, has a tripartite RNA genome with a subgenomic RNA4 for coat protein expression. All ... Brome mosaic virus (BMV), a bromovirus, has a tripartite RNA genome with a subgenomic RNA4 for coat protein expression. All ... keywords = {ase Sequence Bromovirus/*genetics/metabolism Genetic Complementation Test Genome, FLORENTZ, FRUGIER, Genetic ...
Publikace: Katedra buněčné biologie a genetiky
MESH TREE NUMBER CHANGES - 2015 MeSH
MESH TREE NUMBER CHANGES - 2015 MeSH
MESH TREE NUMBER CHANGES - 2015 MeSH
MESH TREE NUMBER CHANGES - 2015 MeSH
MESH TREE NUMBER CHANGES - 2015 MeSH
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Vol 8, Issue 1, 1996
| Emirates Journal of Food and Agriculture
Plant Disease (2021) 105 (9 - 1420) - Pestinfo-Wiki
Virus-Based Nanoreactors with GALT Activity for Classic Galactosemia Therapy - PubMed
TREE NUMBER DESCRIPTOR
Bromovirus B04.715.081.180 Cucumovirus B04.715.081.400 Ilarvirus B04.715.081.700 Oleavirus B04.715.102 Caulimoviridae B04.715. ... Bromovirus B04.715.464.100 Caulimovirus B04.715.464.150 Comovirus B04.715.464.180 Cucumovirus B04.715.464.600 Potyvirus B04.715 ... Bromovirus B04.820.081.180 Cucumovirus B04.820.081.400 Ilarvirus B04.820.081.700 Oleavirus B04.820.087 Bunyaviridae B04.820. ...
Cell Type-Dependent RNA Recombination Frequency in the Japanese Encephalitis Virus
MeSH Browser
use BROMOVIRUS to search BROME MOSAIC VIRUSES 1994-96. History Note. 94; BROME MOSAIC VIRUSES was see BROMOVIRUS 1994-96. Date ... Bromovirus Preferred Term Term UI T053218. Date01/01/1999. LexicalTag ABX. ThesaurusID NLM (1994). ... Bromovirus. Tree Number(s). B04.715.081.080. B04.715.464.080. B04.820.578.282.080. Unique ID. D017795. RDF Unique Identifier. ... Bromovirus Preferred Concept UI. M0026886. Registry Number. txid12300. Related Numbers. txid12302. txid12303. Scope Note. A ...
MeSH Browser
use BROMOVIRUS to search BROME MOSAIC VIRUSES 1994-96. History Note. 94; BROME MOSAIC VIRUSES was see BROMOVIRUS 1994-96. Date ... Bromovirus Preferred Term Term UI T053218. Date01/01/1999. LexicalTag ABX. ThesaurusID NLM (1994). ... Bromovirus. Tree Number(s). B04.715.081.080. B04.715.464.080. B04.820.578.282.080. Unique ID. D017795. RDF Unique Identifier. ... Bromovirus Preferred Concept UI. M0026886. Registry Number. txid12300. Related Numbers. txid12302. txid12303. Scope Note. A ...
Scegli la categoria - lookformedical.com
Scegli la categoria - lookformedical.com
BIOSIS Previews 說明
3J7N | Genus
chains in the Genus database with same CATH superfamily 4OQ8 A; 1ZA7 A; 1STM A; 3J7L A; 1JS9 A; 1YC6 1; 3J7N A; 4NIA A; 1A34 A; 4OQ9 A; 3J7M A; 1CWP A; #chains in the Genus database with same CATH topology 3C7G A; 2K0G A; 4OHY A; 2OA2 A; 3MPB A; 3T1M A; 3FFQ A; 2XHN A; 4XCB A; 5J96 B; 1YQ2 A; 2MHF A; 2ZX3 A; 2DCT A; 2WO7 A; 4NO4 A; 5F5A A; 3J7L A; 5EFU A; 1F9K A; 1KGY A; 3KCX A; 2XLF A; 1VB4 A; 4XJZ A; 5DG2 A; 3VBO A; 1VRH 2; 3TEX A; 4TLG A; 1R08 1; 4QWN A; 4JC1 A; 1RHI 2; 2V72 A; 5FY7 A; 3Q9O A; 1LHN A; 1PVC 1; 4LHN A; 3M3C A; 1VBD 1; 4BU2 A; 5JPM B; 1AYN 2; 4WM7 B; 1QNW A; 1DZT A; 5I8Y A; 4AHW A; 1GOF A; 5JZG C; 1HV1 A; 1Q8O A; 1SLC A; 3LA3 A; 2YPJ A; 2EIC A; 4HON A; 4XHX A; 5LK7 B; 1JYW A; 1T6G C; 1RUJ 3; 1FV3 A; 2WJS A; 4MGQ A; 3NJX A; 1OA4 A; 1VBA 3; 1O91 A; 4Y33 A; 3I49 A; 3IDE A; 5CKM A; 3VD7 A; 3KZ4 C; 1QHD A; 3K51 A; 4IV3 A; 1HXS 3; 4DS0 A; 4HVR A; 5JI9 A; 4FXG B; 4H14 A; 5FP4 A; 2BNO A; 5CZK A; 1QJU 1; 4Y1U A; 3FFZ A; 1ENX A; 4V2W A; 5EZW A; 3WW1 A; 1IGO A; 1CR7 A; 1POQ A; 2KXL A; 1G9F ...
c33c
Difference between revisions of "Taxonomy Index" - microbewiki
Bromwich integral | Article about Bromwich integral by The Free Dictionary
Cilevirus<...
MESH TREE NUMBER CHANGES - 2015 MeSH
MESH TREE NUMBER CHANGES - 2015 MeSH
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µ
MESH TREE NUMBER CHANGES - 2015 MeSH
MESH TREE NUMBER CHANGES - 2015 MeSH
Cowpea1
- Of all viruses detected, only two viruses, cucumber mosaic virus and a novel bromovirus related to cowpea chlorotic mottle virus and brome mosaic virus, were mechanically transmitted from wild plants to common bean plants. (pestinfo.org)
Assembly2
- Role of surface charge density in nanoparticle-templated assembly of bromovirus protein cages. (umassmed.edu)
- Host ESCRT proteins are required for bromovirus RNA replication compartment assembly and function. (morgridge.org)