Actualités
[Les actualités sur ce site / à l'UNIL]
DGM papers
- PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa
- Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa
- A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance
- SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system
- Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A
Genetics news (medwor...
- FDA Approves A New, Monoclonal Antibody For Lymphoma
- Gene-Z: Ipod-Based Tablet Performs Genetic Analysis on microRNAs
- The Challenge of Obesity.
- U.K. Researchers Launch Clinical Trial of Mercaptopurine (6-MP) In Women with Hereditary Breast and Ovarian Cancer
- Dual Color STED Microscopy Resolves Living Cell Interactions at 80nm
