A collaboration between Monash Health, the Australian Genomics Health Alliance (AGHA) and researchers at the Monash Biomedicine Discovery Institute has led to the discovery of a rare single gene mutation in a patient that ...
Jul 24, 2020
0
156
The biology underpinning a rare genetic mutation that allows its carrier to live virtually pain-free, heal more rapidly and experience reduced anxiety and fear, has been uncovered by new research from UCL.
May 23, 2023
1
474
A team of researchers affiliated with multiple institutions in the U.S. and the U.K. has found that a single error during cell division can trigger a cascade of mutational events, generating many of the features found in ...
About 1 in 750 babies born in the United States has some kind of craniofacial malformation, accounting for about one-third of all birth defects.
Jan 25, 2018
0
123
Autism spectrum disorders (ASDs) affect about one percent of the world's population. In the United States alone, about 1 in 68 children are on the spectrum, and between 40 and 60 percent of them are also diagnosed with some ...
Apr 13, 2016
1
232
UBC researchers are the first in the world to conduct a molecular-level structural analysis of the omicron variant spike protein.
Dec 23, 2021
0
230
Cancer cells demand enormous amounts of molecular "food" to survive and grow, and a study published March 27 online in Nature by researchers at The University of Texas MD Anderson Cancer Center may have identified a new approach ...
Mar 27, 2019
0
923
Scientists at Rutgers University-Newark have discovered that when a key protein needed to generate new brain cells during prenatal and early childhood development is missing, part of the brain goes haywire—causing an imbalance ...
Jan 9, 2020
0
507
Women with ovarian cancer who have undergone four or more rounds of chemotherapy typically haven't had much hope that another treatment option will lengthen their lives in a meaningful way. However, a new research study shows ...
Jul 3, 2019
0
4
The most common mutation in the human genome is the C>T mutation, which causes half of all genetic diseases resulting from point mutations. For example, the one causing Hutchinson-Gilford progeria syndrome, a genetic disease ...
Jun 2, 2022
0
695
