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2. Analysis of novel missense ATR mutations reveals new splicing defects underlying Seckel syndrome. Issue 12 (24th September 2018)

3. Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome. Issue 3 (29th November 2019)

4. Ribonuclease H2 mutations induce a cGAS/STING‐dependent innate immune response. (22nd February 2016)

5. RNA:DNA hybrids are a novel molecular pattern sensed by TLR9. (21st February 2014)

6. RNase H2, mutated in Aicardi‐Goutières syndrome, promotes LINE‐1 retrotransposition. (29th June 2018)

7. The Structure of a Conserved Telomeric Region Associated with Variant Antigen Loci in the Blood Parasite Trypanosoma congolense. (25th August 2018)