- replacement mutation
- трансверсия (заместительная мутация)* * *трансверсия
English-russian biological dictionary. 2013.
English-russian biological dictionary. 2013.
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
mutation — n. [L. mutare, to change] A structural change in a gene, consisting of a replacement, duplication, or deletion of one or several pairs in the DNA … Dictionary of invertebrate zoology
mutation — Sudden heritable change in genetic material, often resulting from an alteration of a single gene by the duplication, replacement, or deletion of a number of DNA base pairs … Expanded glossary of Cycad terms
Point mutation — Illustration of three types of point mutations. A point mutation, or single base substitution, is a type of mutation that causes the replacement of a single base nucleotide with another nucleotide of the genetic material, DNA or RNA. Often the… … Wikipedia
Hormone replacement therapy (male-to-female) — Hormone replacement therapy (HRT) for transgender and transsexual people replaces the hormones naturally occurring in their bodies with those of the other sex. However, not all cases of hormone replacement therapy are used by transgendered people … Wikipedia
Opaline budgerigar mutation — The Opaline budgerigar mutation is one of approximately 30 mutations affecting the colour or appearance of budgerigars. It is the underlying mutation of the Opaline variety. When combined with the Yellowface II and Clearwing mutations the Rainbow … Wikipedia
point mutation — noun A mutation that involves the replacement, addition or deletion of a small number of bases (especially just one) at a specific site within a gene … Wiktionary
point mutation — Mutationthat causes the replacement of a single base pair with another pair … Dictionary of molecular biology
Morbus Fabry — Klassifikation nach ICD 10 E75.2 Sonstige Sphingolipidosen (inkl. Fabry (Anderson )Krankheit) … Deutsch Wikipedia
genetic disease, human — Introduction any of the diseases and disorders that are caused by mutations in one or more genes (gene). With the increasing ability to control infectious and nutritional diseases in developed countries, there has come the realization … Universalium
Health and Disease — ▪ 2009 Introduction Food and Drug Safety. In 2008 the contamination of infant formula and related dairy products with melamine in China led to widespread health problems in children, including urinary problems and possible renal tube… … Universalium