Single-Cell Proteomics Reveal Hidden Layers of Gene Expression
Single cell gene expression studies often rely on single-cell RNA sequencing (scRNA-seq) alone. While scRNA-seq reveals which genes…
Common Food Additive Solves Decades-Long Neuroscience Problem
Stanford scientists have found an unexpectedly simple way to mass-produce tiny brain-like structures in the lab. This breakthrough…
Stem Cell Transplants Without Toxic Chemo or Radiation
A Stanford Medicine team has developed a novel antibody-based approach that prepares patients for stem cell transplants without…
Genetic Study Suggests Ways to Catch Blood Cancer Earlier
Newswise — As we age, our cells replicate, and the DNA in these cells can acquire mistakes —…
Precise modulation of BRG1 levels reveals features of mSWI/SNF dosage sensitivity
BRG1 binding exhibits a linear response to its dosage In mES cells, Brg1 encodes the major catalytic subunit…
Integrative machine learning models predict prostate cancer diagnosis and biochemical recurrence risk: Advancing precision oncology
Identification of BCR related genes based on Weighted gene co-expression network analysis (WGCNA) WGCNA is a systems biology…
Double trouble: gene-regulating duo shapes cell fate and disease
Newswise — CLEVELAND—Shedding light on what determines how cells become what they are meant to be—nerves, bone, muscles,…
Brain cells beat AI in learning speed and efficiency
Researchers have demonstrated that brain cells learn faster and carry out complex networking more effectively than machine learning…
Stem cell transplant without toxic preparation successfully treats genetic disease
“Bone marrow or stem cell transplants are most commonly used in blood cancers, in which the bone marrow…
Ancient viral DNA found to regulate human gene expression
A new international study suggests that ancient viral DNA embedded in our genome, which were long dismissed as…
Therapeutic strategies for fragile X syndrome and implications for other gene-silencing disorders
Ng, S. B. et al. Exome sequencing identifies the cause of a Mendelian disorder. Nat. Genet. 42, 30–35…