Žygimantė Tarnauskaitė

发表

CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions

Martin A. M. Reijns, Wei Yuan, Michael Aregger, 2018, Nature.

Ribonuclease H2 mutations induce a cGAS/STING‐dependent innate immune response

Martin A. M. Reijns, A. Jackson, G. Grimes, 2016, The EMBO journal.

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

Martin A. M. Reijns, J. Al-Aama, P. Tomançak, 2017, Nature Genetics.

Mutations in DONSON disrupt replication fork stability and cause microcephalic 1 dwarfism . 2 3

Martin A. M. Reijns, Saleem, Abdulrahman, 2017 .

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency

Martin A. M. Reijns, J. Rosenfeld, Sancha Martin, 2018, American journal of human genetics.

RNase H2, mutated in Aicardi‐Goutières syndrome, promotes LINE‐1 retrotransposition

Martin A. M. Reijns, A. Jackson, J. García-Pérez, 2018, The EMBO journal.

Biallelic variants in DNA2 cause microcephalic primordial dwarfism

Martin A. M. Reijns, D. Sillence, J. Marsh, 2019, Human mutation.

Identification of novel pathways linking epithelial-to-mesenchymal transition with resistance to HER2-targeted therapy

T. Le Bihan, V. Brunton, K. Macleod, 2016, Oncotarget.

CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions

Martin A. M. Reijns, D. Durocher, J. Moffat, 2018, Nature.

Structure of the MeCP2–TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders

A. Bird, A. Cook, C. Taylor, 2017, Proceedings of the National Academy of Sciences.

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

Martin A. M. Reijns, P. Tomançak, N. Prescott, 2017, Nature Genetics.