Gabriella Forte
Wellcome Centre for Cell-Matrix Research(GB)University of Manchester(GB)
Publications by Year
Research Areas
RNA Research and Splicing, interferon and immune responses, Glioma Diagnosis and Treatment, RNA regulation and disease, Lysosomal Storage Disorders Research
Most-Cited Works
- → Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature(2012)928 cited
- → Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1(2015)601 cited
- → Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling(2014)586 cited
- → Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study(2013)433 cited
- → N-Terminal Acetylation Inhibits Protein Targeting to the Endoplasmic Reticulum(2011)194 cited
- → mTORC1 directly inhibits AMPK to promote cell proliferation under nutrient stress(2020)159 cited
- → A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1(2013)152 cited
- → Nitrogen Regulates AMPK to Control TORC1 Signaling(2015)95 cited
- → Brain‐targeted stem cell gene therapy corrects mucopolysaccharidosis type II via multiple mechanisms(2018)87 cited
- → Sec61p Is Required for ERAD-L(2008)85 cited