X-chromosome inactivation is a fascinating cellular process that plays a crucial role in managing genetic balance between genders, particularly in females who carry two copies of the X chromosome.This unique form of chromosomal silencing is vital for preventing the overexpression of genes linked to the X chromosome, thereby influencing various genetic disorders.
X chromosome inactivation is a fascinating and crucial biological process whereby one of a female’s two X chromosomes is rendered inactive to ensure that gene dosage remains balanced between the sexes.This intricate mechanism plays a significant role in the development of genetic diseases, including conditions such as Fragile X Syndrome and Rett Syndrome, which are linked to mutations on the X chromosome.