An international team led by Monash University researchers has uncovered the genetic code governing the way genetic mutations affect mRNA and result in disease.
Alternative splicing exhibits lineage-specific variability, with mammals and birds reaching the highest levels despite conserved intron-rich architectures, while unicellular eukaryotes and prokaryotes ...
1don MSN
Study unveils mechanisms driving axonal accumulation of TDP-43 and associated nerve damage in ALS
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscle wasting and limb ...
A team led by Neil King, a biochemistry professor at the University of Washington School of Medicine, is now exploring a new ...
Long interspersed nuclear element-1 (LINE-1 or L1) is the only active, self-copying genetic element in the human ...
IFLScience on MSN
Hormone Therapy For Trans Women Shifts Dozens Of Proteins To Align With Their Gender Identity
The protein changes observed in a group of trans women after gender-affirming hormone treatment were similar to what is seen ...
It was previously shown 4 that the protein GREM1 fosters cellular heterogeneity in pancreatic cancer, by promoting the original epithelial state of cells. By combining analyses of mouse models of ...
Texas A&M researchers found that in an aggressive kidney cancer, RNA builds “droplet hubs” that activate tumor genes. By creating a molecular switch to dissolve these hubs, they stopped cancer growth ...
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