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Genetic human enhancement emerges as a potential frontier in disease prevention by precisely targeting genetic predispositions to various illnesses. Through techniques like CRISPR, specific genes associated with diseases can be edited or modified, offering the prospect of reducing the hereditary risk of conditions such as cancer, cardiovascular ...
Human Enhancement (2009) is a non-fiction book edited by philosopher Nick Bostrom and philosopher and bioethicist Julian Savulescu. Savulescu and Bostrom write about the ethical implications of human enhancement and to what extent it is worth striving towards.
Genetic and epigenetic alterations: Human genetic enhancement for pro-longevity and protective genes – see genetics of aging [147] [108] Cellular reprogramming : in vivo reprogramming to complement or augment human regenerative capacity and rejuvenate or replace cells [ 148 ] [ 149 ] [ 108 ]
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. There are over 6,000 known genetic disorders in humans.
Common causes of secondary hypogonadism include: Kallmann syndrome. This genetic condition refers to an abnormally developed hypothalamus, which can affect the secretion of pituitary hormones.
Human genetics is the study of inheritance as it occurs in human beings.Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.
Genetic engineering could potentially fix severe genetic disorders in humans by replacing the defective gene with a functioning one. [5] It is an important tool in research that allows the function of specific genes to be studied. [6] Drugs, vaccines and other products have been harvested from organisms engineered to produce them. [7]
In humans, the main cause is genetic drift. [18] Serial founder effects and past small population size (increasing the likelihood of genetic drift) may have had an important influence in neutral differences between populations. [citation needed] The second main cause of genetic variation is due to the high degree of neutrality of most mutations ...