Molecular engineering of the herpes simplex virus genome: insertion of a second L-S junction into the genome causes additional genome inversions.
about
A human cytomegalovirus mutant resistant to the nucleoside analog 9-([2-hydroxy-1-(hydroxymethyl)ethoxy]methyl)guanine (BW B759U) induces reduced levels of BW B759U triphosphateCRISPR-Cas9 as a Powerful Tool for Efficient Creation of Oncolytic VirusesFunctional profiling of a human cytomegalovirus genomeEarly events associated with infection of Epstein-Barr virus infection of primary B-cellsViral strategies for studying the brain, including a replication-restricted self-amplifying delta-G vesicular stomatis virus that rapidly expresses transgenes in brain and can generate a multicolor golgi-like expressionMechanism and application of genetic recombination in herpesviruses.Construction and characterization of murine cytomegaloviruses that contain transposon insertions at open reading frames m09 and M83.In vitro and in vivo characterization of a murine cytomegalovirus with a transposon insertional mutation at open reading frame M43.Murine cytomegalovirus open reading frame M27 plays an important role in growth and virulence in mice.Construction and properties of a viable herpes simplex virus 1 recombinant lacking coding sequences of the alpha 47 geneThe cDNA of UL15, a highly conserved herpes simplex virus 1 gene, effectively replaces the two exons of the wild-type virus.Herpes simplex viruses: is a vaccine tenable?Insertion and deletion mutagenesis of the human cytomegalovirus genomeMurine cytomegalovirus with a transposon insertional mutation at open reading frame m155 is deficient in growth and virulence in mice.Identification of a herpes simplex virus 1 glycoprotein gene within a gene cluster dispensable for growth in cell culture.In vitro and in vivo characterization of a murine cytomegalovirus with a mutation at open reading frame m166.Infection of human cytomegalovirus in cultured human gingival tissue.Murine cytomegalovirus with a transposon insertional mutation at open reading frame M35 is defective in growth in vivo.Replication of the herpes simplex virus genome: does it really go around in circles?High-efficiency targeted editing of large viral genomes by RNA-guided nucleases.Herpes simplex virus type 1 DNA replication is specifically required for high-frequency homologous recombination between repeated sequences.A novel herpes simplex virus 1 gene, UL43.5, maps antisense to the UL43 gene and encodes a protein which colocalizes in nuclear structures with capsid proteinsThe a sequence is dispensable for isomerization of the herpes simplex virus type 1 genome.Circularization and cleavage of guinea pig cytomegalovirus genomesPropagation and recovery of intact, infectious Epstein-Barr virus from prokaryotic to human cells.Herpesvirus-dependent amplification and inversion of cell-associated viral thymidine kinase gene flanked by viral a sequences and linked to an origin of viral DNA replication.Expression of herpes simplex virus glycoprotein C from a DNA fragment inserted into the thymidine kinase gene of this virus.Site-specific inversion sequence of the herpes simplex virus genome: domain and structural features.Requirement for double-strand breaks but not for specific DNA sequences in herpes simplex virus type 1 genome isomerization events.Herpes simplex virus type 1 recombination: the Uc-DR1 region is required for high-level a-sequence-mediated recombination.Herpes simplex virus type 1 recombination: role of DNA replication and viral a sequencesThe open reading frames UL3, UL4, UL10, and UL16 are dispensable for the replication of herpes simplex virus 1 in cell culture.The herpes simplex virus type 1 (HSV-1) a sequence serves as a cleavage/packaging signal but does not drive recombinational genome isomerization when it is inserted into the HSV-2 genome.Characterization of DNA sequence-common and sequence-specific proteins binding to cis-acting sites for cleavage of the terminal a sequence of the herpes simplex virus 1 genome.Structural organization of the termini of the L and S components of the genome of pseudorabies virus.Sequence requirements for DNA rearrangements induced by the terminal repeat of herpes simplex virus type 1 KOS DNARecombinogenic properties of herpes simplex virus type 1 DNA sequences resident in simian virus 40 minichromosomes.Physical mapping and nucleotide sequence of a herpes simplex virus type 1 gene required for capsid assembly.The UL20 gene of herpes simplex virus 1 encodes a function necessary for viral egressIdentification of the thymidine kinase gene of feline herpesvirus: use of degenerate oligonucleotides in the polymerase chain reaction to isolate herpesvirus gene homologs.
P2860
Q24628878-856A4458-A8B4-4C61-9BBD-77A6BAF2EB73Q26766798-7BF3EF49-7EB5-4302-A153-974E427B2E7BQ28185252-01633F26-6853-4AB6-A23F-D0A6B50D3E4AQ28476230-8434140A-03F0-4772-83CB-CE399BF2A2E4Q30495981-B7A67BC8-1655-485A-956B-A43D321766FDQ33729830-BD8C7DEC-9915-4419-A069-A848F6C3CAF1Q33809617-11548205-0B46-47AC-9CD3-251F45A48677Q33811459-B79F3C45-AD91-4F32-A03B-87378F931386Q33837391-258A9C40-36C3-46F0-9DED-044906E297E8Q33929730-A5253C22-6ED8-4049-9BCF-4591D9EEAC8FQ33937122-D9E78268-579B-4E03-8C58-848DA6556E3EQ34139375-AC587317-A123-4739-BB65-FD6FED993292Q34354191-1BED2402-FF29-4C98-94A2-EBECA40DB1D0Q34437908-A7B91C49-E105-4B6E-9E67-B455BFE2F83BQ34633054-18479A44-797C-49EC-A282-DA0EF249B424Q34756883-AFBB85B3-DF67-477E-A8BB-F3DBAE612081Q35100976-C983C275-D6C8-4472-8D28-016232F836D8Q35105296-FB62ABFE-ECF5-48BD-8BC3-2FC1AF8F320BQ35145669-1C1A7236-09B1-40C1-A56A-2FB93D924EC2Q35161635-0EBDD8DA-C860-4EE8-AC91-CFC12ADAA24BQ35839093-4DF2FA3C-EC03-469C-94DA-F8433CC01AAFQ35859663-9167473B-5422-4267-B0FB-6DAECAEB4EBEQ35873937-AD40C62A-33F0-4FCC-B3AA-68EE54FD39F4Q35885882-6755A7E4-CD7D-4B36-86BC-CF352C71D2CAQ36173276-D8D94A91-307C-4025-AB34-78BB6660E028Q36312310-053CD48C-BDA5-4454-8276-61FE1EF92C1DQ36318979-FF15C268-0640-41A8-90CD-BBC803D54677Q36379766-A6AE53FB-5692-4020-814A-5E4C5DBFDDFDQ36618719-3D603D93-105E-46B4-96D3-F73C5A7A8325Q36634197-EDB34F91-F673-462A-B878-420B4500DCFEQ36656071-0C7E4E03-6F05-49F4-8D6D-79773D125A41Q36680507-67FD7A8A-5381-42F8-860B-A225CA20FBFBQ36687506-788B45DC-D35B-4EB0-B0E6-0B4A33A563C4Q36781380-22603709-7A04-419E-98DE-44500ADB0CC9Q36784133-611E2D25-9985-4FC0-9688-ED216D1A6E17Q36784220-194EF05C-AB7E-432B-AABA-D28CD5627066Q36799354-1C593E46-ABD1-42AF-B580-2CCD20F34941Q36827458-F998E79C-E373-4D67-8DD0-871E51EB8216Q36827799-172FB315-B122-4196-907C-DAF207E7F777Q36829677-42406022-7C74-4913-B8D2-36B2D965A962
P2860
Molecular engineering of the herpes simplex virus genome: insertion of a second L-S junction into the genome causes additional genome inversions.
description
1980 nî lūn-bûn
@nan
1980 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1980 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
name
Molecular engineering of the h ...... additional genome inversions.
@ast
Molecular engineering of the h ...... additional genome inversions.
@en
Molecular engineering of the h ...... additional genome inversions.
@nl
type
label
Molecular engineering of the h ...... additional genome inversions.
@ast
Molecular engineering of the h ...... additional genome inversions.
@en
Molecular engineering of the h ...... additional genome inversions.
@nl
prefLabel
Molecular engineering of the h ...... additional genome inversions.
@ast
Molecular engineering of the h ...... additional genome inversions.
@en
Molecular engineering of the h ...... additional genome inversions.
@nl
P1433
P1476
Molecular engineering of the h ...... additional genome inversions.
@en
P2093
P304
P356
10.1016/0092-8674(80)90172-5
P407
P433
P577
1980-11-01T00:00:00Z