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intragenic suppressor

См. также в других словарях:

  • suppressor mutation — a mutation that partially or completely masks phenotypic expression of another (primary) mutation but occurs at a different site from it (i.e., causes suppression); it may be intragenic or intergenic. The term is used particularly to describe a… …   Medical dictionary

  • MT-ND1 — NADH dehydrogenase, subunit 1 (complex I) Identifiers Symbols ND1; MTND1 External IDs …   Wikipedia

  • Epistasis — See Epistaxis for the condition known colloquially as a nosebleed. See Epitasis for the main action of a classical drama. See Epitaxy for the method of depositing a monocrystalline film on a monocrystalline substrate. See also: Quantitative Trait …   Wikipedia

  • Cyclin-dependent kinase inhibitor 1C — (p57, Kip2) Identifiers Symbols CDKN1C; BWCR; BWS; KIP2; WBS; p57 External IDs …   Wikipedia

  • Mutation — A permanent change, a structural alteration, in the DNA or RNA. In humans and many other organisms, mutations occur in DNA. However, in retroviruses like HIV, mutations occur in RNA which is the genetic material of retroviruses. In most cases,… …   Medical dictionary

  • suppression — 1. Deliberately excluding from conscious thought. Cf.:repression. 2. Arrest of the secretion of a fluid, such as urine or bile. Cf.:retention (2). 3. Checking of an abnormal flow or discharge, as in s. of a hemorrhage …   Medical dictionary

  • Homologous recombination — Figure 1. During meiosis, homologous recombination can produce new combinations of genes as shown here between similar but not identical copies of human chromosome 1. Homologous recombination is a type of genetic recombination in which nucleotide …   Wikipedia

  • SEL1L — Sel 1 suppressor of lin 12 like (C. elegans), also known as SEL1L, is a human gene.cite web | title = Entrez Gene: SEL1L sel 1 suppressor of lin 12 like (C. elegans)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • miR-203 — microRNA secondary structure and sequence conservation Identifiers Symbol mir 203 Rfam …   Wikipedia

  • Oncogenomics — is relatively new sub field of genomics, which applies high throughput technologies to characterize genes associated with cancer. Oncogenomics is synonymous with cancer genomics . Cancer is a genetic disease caused by accumulation of mutations to …   Wikipedia

  • NBPF16 — Neuroblastoma Breakpoint Family, Member 16 Identifiers Symbols NBPF16; AG3 External IDs …   Wikipedia

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