Chromosomes, Artificial, P1 Bacteriophage
"Chromosomes, Artificial, P1 Bacteriophage" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
DNA constructs that are derived from the DNA of BACTERIOPHAGE P1. They can carry large amounts (about 100-300 kilobases) of other sequence for a variety of bioengineering purposes.
| Descriptor ID |
D027042
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| MeSH Number(s) |
A11.284.187.178.195 G05.360.162.178.195 G05.360.337.249.195
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| Concept/Terms |
Chromosomes, Artificial, P1 Bacteriophage- Chromosomes, Artificial, P1 Bacteriophage
- P1-Derived Artificial Chromosomes
- Artificial Chromosome, P1-Derived
- Artificial Chromosomes, P1-Derived
- Chromosome, P1-Derived Artificial
- Chromosomes, P1-Derived Artificial
- P1 Derived Artificial Chromosomes
- P1-Derived Artificial Chromosome
- Artificial Chromosomes, P1 Bacteriophage
- Bacteriophage P1 Artificial Chromosomes
- PAC (Chromosome)
- PACs (Chromosomes)
- Chromosomes, P1 Bacteriophage Artificial
- P1 Bacteriophage Artificial Chromosomes
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Below are MeSH descriptors whose meaning is more general than "Chromosomes, Artificial, P1 Bacteriophage".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Artificial, P1 Bacteriophage".
This graph shows the total number of publications written about "Chromosomes, Artificial, P1 Bacteriophage" by people in this website by year, and whether "Chromosomes, Artificial, P1 Bacteriophage" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosomes, Artificial, P1 Bacteriophage" by people in Profiles.
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Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders. J Med Genet. 2004 Feb; 41(2):113-9.
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Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6. Nat Genet. 2003 Feb; 33(2):145-53.
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Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse. Genome Res. 2002 May; 12(5):713-28.