Results 301 to 310 of about 664,651 (329)
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2013
Genome-wide association screens (GWASs) for a large number of human genetic diseases generate novel hypotheses about familial and sporadic mutations. Gene targeting in embryonic stem cell (ESC), along with the new repertoire of zinc-finger nucleases (ZFNs), TAL effector nucleases (TALENs) and recombinase-mediated cassette exchange (RMCE) techniques ...
Floss, T., Guimera, J.
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Genome-wide association screens (GWASs) for a large number of human genetic diseases generate novel hypotheses about familial and sporadic mutations. Gene targeting in embryonic stem cell (ESC), along with the new repertoire of zinc-finger nucleases (ZFNs), TAL effector nucleases (TALENs) and recombinase-mediated cassette exchange (RMCE) techniques ...
Floss, T., Guimera, J.
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2003
Herpes genomes are large and complex, with many interactions among herpes encoded proteins, herpes DNA and RNA, and the host cell. These interactions begin as the virus enters the cell, and continue as the decision for latency or lytic replication is made.
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Herpes genomes are large and complex, with many interactions among herpes encoded proteins, herpes DNA and RNA, and the host cell. These interactions begin as the virus enters the cell, and continue as the decision for latency or lytic replication is made.
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2007
Localized mutagenesis can be used to obtain mutants in genes of interest based on linkage to selectable markers. Mutagens diethylsulfate and hydroxylamine are used to obtain predominantly transition mutations in the DNA either by whole chromosomal mutagenesis or mutagenesis of DNA isolated as purified plasmid or packaged in transducing phage particles.
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Localized mutagenesis can be used to obtain mutants in genes of interest based on linkage to selectable markers. Mutagens diethylsulfate and hydroxylamine are used to obtain predominantly transition mutations in the DNA either by whole chromosomal mutagenesis or mutagenesis of DNA isolated as purified plasmid or packaged in transducing phage particles.
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Annual Review of Genetics, 1985
TOTAL SYNTHESIS OF MUTANTS . . . . . . . . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 424 Solid Phase Chemical Synthesis of Oligodeoxyribonucleotides .. . ..... 424 Assembly of Oligodeoxyribonucleotides into Double-Strand DNA 427 Mutation by Partial Gene Synthesis (Cassette Mutagenesis)
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TOTAL SYNTHESIS OF MUTANTS . . . . . . . . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 424 Solid Phase Chemical Synthesis of Oligodeoxyribonucleotides .. . ..... 424 Assembly of Oligodeoxyribonucleotides into Double-Strand DNA 427 Mutation by Partial Gene Synthesis (Cassette Mutagenesis)
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Methods in molecular biology (Clifton, N.J.), 2012
Mutants are a valuable tool for solving many problems in physiology, genetics, and molecular biology. Soon after cell suspension and protoplast culture emerged as techniques in plant biology, they were applied to the isolation of selectable markers that were unavailable through classical methods using whole plant systems.
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Mutants are a valuable tool for solving many problems in physiology, genetics, and molecular biology. Soon after cell suspension and protoplast culture emerged as techniques in plant biology, they were applied to the isolation of selectable markers that were unavailable through classical methods using whole plant systems.
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