- frame deletion
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удаление кадра
Англо-русский словарь технических терминов. 2005.
frame deletion
Смотреть что такое "frame deletion" в других словарях:
Deletion (genetics) — Deletion on a chromosome In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) (sign: Δ) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is missing. Deletion is the loss of … Wikipedia
frame|shift — «FRAYM SHIHFT», adjective. Genetics. having to do with or causing an insertion or deletion in a codon that results in an incorrect genetic message: »a frameshift mutation, a frameshift mutagen … Useful english dictionary
Deletion — Loss of a segment of DNA from a chromosome (and hence from the genome). The first human chromosome deletion was detected in 1963 by Jerome Lejeune and his colleagues in Paris. They discovered loss of part of 5p, the short (p) arm of chromosome 5 … Medical dictionary
Frame shift — Ein Frameshift oder Rasterschub beziehungsweise Leserasterverschiebung ist eine besondere Art der Mutation. Es handelt sich um eine Verschiebung des Leserasters von Genen auf der DNA. Die genetische Information auf der DNA ist in Form von… … Deutsch Wikipedia
frame-shift mutation — Insertion or deletion of a number of bases not divisible by three in an open reading frame in a DNA sequence. Such mutations usually result in the generation, downstream, of nonsense, chain termination codons … Dictionary of molecular biology
deletion mutation — A mutation in which one or more (sequential) nucleotides is lost from the genome. If the number lost is not divisible by 3 and is in a coding region, the result is a frame shift mutation … Dictionary of molecular biology
SNRPN upstream reading frame protein — SNRPN upstream reading frame, also known as SNURF, is a human gene.cite web | title = Entrez Gene: SNURF SNRPN upstream reading frame| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=8926| accessdate = ] PBB … Wikipedia
Genmutationen — Eine Genmutation ist eine erbliche Veränderung (Chromosomenaberration oder Mutation) eines Gens, die nur das jeweilige Gen selbst betrifft. Sind von der Veränderung mehrere Gene betroffen, handelt es sich um eine strukturelle… … Deutsch Wikipedia
Genmutation — Eine Genmutation ist eine erbliche Veränderung (Chromosomenaberration oder Mutation) eines Gens, die nur das jeweilige Gen selbst betrifft. Sind von der Veränderung mehrere Gene betroffen, handelt es sich um eine strukturelle… … Deutsch Wikipedia
CYB5R3 — Cytochrome b5 reductase 3, also known as CYB5R3, is a human gene. PBB Summary section title = summary text = Two forms of NADH cytochrome b5 reductase are known, a membrane bound form in somatic cells (anchored in the endoplasmic reticulum,… … Wikipedia
Notch 3 — Identifiers Symbols NOTCH3; CADASIL; CASIL External IDs OMIM: … Wikipedia
