User profiles for S. J. Boulton
Simon BoultonPrincipal Group Leader, The Francis Crick Institute Verified email at crick.ac.uk Cited by 23383 |
[PDF][PDF] Playing the end game: DNA double-strand break repair pathway choice
DNA double-strand breaks (DSBs) are highly toxic lesions that can drive genetic instability.
To preserve genome integrity, organisms have evolved several DSB repair mechanisms, of …
To preserve genome integrity, organisms have evolved several DSB repair mechanisms, of …
Double-strand break repair: 53BP1 comes into focus
S Panier, SJ Boulton - Nature reviews Molecular cell biology, 2014 - nature.com
DNA double-strand break (DSB) signalling and repair is crucial to preserve genomic integrity
and maintain cellular homeostasis. p53-binding protein 1 (53BP1) is an important regulator …
and maintain cellular homeostasis. p53-binding protein 1 (53BP1) is an important regulator …
Cellular functions of the BRCA tumour-suppressor proteins
SJ Boulton - Biochemical Society Transactions, 2006 - portlandpress.com
Inherited germline mutations in either BRCA1 or BRCA2 confer a significant lifetime risk of
developing breast or ovarian cancer. Defining how these two genes function at the cellular …
developing breast or ovarian cancer. Defining how these two genes function at the cellular …
Homologous-recombination-deficient tumours are dependent on Polθ-mediated repair
Large-scale genomic studies have shown that half of epithelial ovarian cancers (EOCs)
have alterations in genes regulating homologous recombination (HR) repair 1 . Loss of HR …
have alterations in genes regulating homologous recombination (HR) repair 1 . Loss of HR …
[HTML][HTML] Components of the Ku-dependent non-homologous end-joining pathway are involved in telomeric length maintenance and telomeric silencing
SJ Boulton, SP Jackson - The EMBO journal, 1998 - embopress.org
… Boulton 1 and … All strains were checked by PCR screening as described previously (Boulton
and … (CRC; grants SP2143/0103), and SJBoulton is supported by a CRC studentship. …
and … (CRC; grants SP2143/0103), and SJBoulton is supported by a CRC studentship. …
[PDF][PDF] RIF1 is essential for 53BP1-dependent nonhomologous end joining and suppression of DNA double-strand break resection
The appropriate execution of DNA double-strand break (DSB) repair is critical for genome
stability and tumor avoidance. 53BP1 and BRCA1 directly influence DSB repair pathway …
stability and tumor avoidance. 53BP1 and BRCA1 directly influence DSB repair pathway …
Saccharomyces cerevisiae Ku70 potentiates illegitimate DNA double‐strand break repair and serves as a barrier to error‐prone DNA repair pathways.
SJ Boulton, SP Jackson - The EMBO journal, 1996 - embopress.org
… SJBoulton and SPJackson … Although no DNA-PKCS homologue appears to exist in S.cerei'isiae
by strict sequence criteria (SJBoulton and SPJackson, unpublished data), S.cerex'isiae …
by strict sequence criteria (SJBoulton and SPJackson, unpublished data), S.cerex'isiae …
Poly (ADP-ribose)–dependent regulation of DNA repair by the chromatin remodeling enzyme ALC1
Posttranslational modifications play key roles in regulating chromatin plasticity. Although
various chromatin-remodeling enzymes have been described that respond to specific histone …
various chromatin-remodeling enzymes have been described that respond to specific histone …
Identification of a Saccharomyces Cerevisiae Ku80 Homologue: Roles in DNA Double Strand Break Rejoining and in Telomeric Maintenance
SJ Boulton, SP Jackson - Nucleic acids research, 1996 - academic.oup.com
Ku is a heterodimer of polypeptides of approximately 70 and 80 kDa (Ku70 and Ku80,
respectively) that binds to DNA ends. Mammalian cells lacking Ku are defective in DNA double-…
respectively) that binds to DNA ends. Mammalian cells lacking Ku are defective in DNA double-…
[HTML][HTML] Polθ inhibitors elicit BRCA-gene synthetic lethality and target PARP inhibitor resistance
To identify approaches to target DNA repair vulnerabilities in cancer, we discovered
nanomolar potent, selective, low molecular weight (MW), allosteric inhibitors of the polymerase …
nanomolar potent, selective, low molecular weight (MW), allosteric inhibitors of the polymerase …