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Inbreeding is also used to reveal deleterious recessive alleles, which can then be eliminated through assortative breeding or through culling. In plant breeding, inbred lines are used as stocks for the creation of hybrid lines to make use of the effects of heterosis. Inbreeding in plants also occurs naturally in the form of self-pollination.
Darwin's wife, Emma, was his first cousin, and he was concerned about the impact of inbreeding on his ten children, three of whom died at age ten or younger; three others had childless long-term marriages. [16] [17] [18] Humans do not seek to completely minimize inbreeding, but rather to maintain an optimal amount of inbreeding vs. outbreeding.
Genetic purging is the increased pressure of natural selection against deleterious alleles prompted by inbreeding. [1]Purging occurs because deleterious alleles tend to be recessive, which means that they only express all their harmful effects when they are present in the two copies of the individual (i.e., in homozygosis).
Inbreeding in a population reduces fitness by causing deleterious recessive alleles to become more common in the population, and also by reducing adaptive potential. The so-called "50/500 rule", where a population needs 50 individuals to prevent inbreeding depression, and 500 individuals to guard against genetic drift at-large, is an oft-used ...
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.
Women can avoid many of these problems with one treatment: hormone replacement therapy, or HRT. Alternatively called MHT, for menopausal hormone therapy, HRT refers to the combination of estrogen ...
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In both humans and animals, it can be the result of inbreeding. [10] Unlike alveolar or maxillary prognathism, which are common traits in some populations, mandibular prognathism is typically pathological. However, it is more common among East Asian populations but overall, the condition is polygenic. [11]