News

The Y chromosome can disappear over time in human males, which may introduce a number of health problems. While the exact trigger for such degeneration is unknown, environmental factors can play a ...
Now, a stage in this process has been achieved in yeast cells — an entire yeast chromosome has been converted to a synthetic sequence in a stepwise manner. A quote by the theoretical physicist ...
Scientists at the Institute of Cancer Research in London and Linköping University in Sweden have discovered how cells prevent their chromosomes from mistakenly fusing together. Two proteins ...
Many explanations have been put forward: men take more risks or smoke more, oestrogen is protective against health conditions, two X chromosomes are better than one… the list goes on.
Several ORFs with apparently identical functions exist on both chromosomes which were probably acquired by lateral gene transfer. For example, glyA (encoding serine hydroxymethyl transferase ...
A microscopic piece of genetic material known as the Y chromosome made headlines last week. It is nothing new or rare; every man has one in practically every cell, or he would not be a man.
The training of the warriors during the classical periods of Ancient Greece and the Roman Empire have become a point of focus is recent years, with one trainer shedding light on the exact moves ...
It involves a lack of part or all of a second sex chromosome in some or all cells. The symptoms of Turner syndrome (TS) can vary widely from one person to the next. People with Turner syndrome are ...
Chromosome number and meiotic behavior were evaluated in 36 Brazilian accessions of the grass Paspalum (which had never previously been analyzed) to determinate which accessions might be useful in ...
Objectives X chromosome has been considered as a risk factor for SLE, which is a prototype of autoimmune diseases with a significant sex difference (female:male ratio is around 9:1). Our study aimed ...
Mosaic Down syndrome is a variant of Down syndrome. Down syndrome is a congenital (present at birth) genetic condition that occurs when a person has three copies of chromosome 21 instead of two (the ...