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Items: 11

1.

Response to "Unexpected mutations after CRISPR-Cas9 editing in vivo".

Wilson CJ, Fennell T, Bothmer A, Maeder ML, Reyon D, Cotta-Ramusino C, Fernandez CA, Marco E, Barrera LA, Jayaram H, Albright CF, Cox GF, Church GM, Myer VE.

Nat Methods. 2018 Apr;15(4):236-237. doi: 10.1038/nmeth.4552. Epub 2018 Mar 30. No abstract available.

PMID:
29600989
2.

Characterization of the interplay between DNA repair and CRISPR/Cas9-induced DNA lesions at an endogenous locus.

Bothmer A, Phadke T, Barrera LA, Margulies CM, Lee CS, Buquicchio F, Moss S, Abdulkerim HS, Selleck W, Jayaram H, Myer VE, Cotta-Ramusino C.

Nat Commun. 2017 Jan 9;8:13905. doi: 10.1038/ncomms13905.

3.

A DNA damage response screen identifies RHINO, a 9-1-1 and TopBP1 interacting protein required for ATR signaling.

Cotta-Ramusino C, McDonald ER 3rd, Hurov K, Sowa ME, Harper JW, Elledge SJ.

Science. 2011 Jun 10;332(6035):1313-7. doi: 10.1126/science.1203430.

4.

A genetic screen identifies the Triple T complex required for DNA damage signaling and ATM and ATR stability.

Hurov KE, Cotta-Ramusino C, Elledge SJ.

Genes Dev. 2010 Sep 1;24(17):1939-50. doi: 10.1101/gad.1934210.

5.

Cell biology forum: Genome-wide view of mitosis.

Swedlow JR, Cotta-Ramusino C, Elledge SJ.

Nature. 2010 Apr 1;464(7289):684-5. doi: 10.1038/464684a. No abstract available.

PMID:
20360724
6.

Methods to study replication fork collapse in budding yeast.

Liberi G, Cotta-Ramusino C, Lopes M, Sogo J, Conti C, Bensimon A, Foiani M.

Methods Enzymol. 2006;409:442-62.

PMID:
16793417
7.

Rad51-dependent DNA structures accumulate at damaged replication forks in sgs1 mutants defective in the yeast ortholog of BLM RecQ helicase.

Liberi G, Maffioletti G, Lucca C, Chiolo I, Baryshnikova A, Cotta-Ramusino C, Lopes M, Pellicioli A, Haber JE, Foiani M.

Genes Dev. 2005 Feb 1;19(3):339-50.

8.

Exo1 processes stalled replication forks and counteracts fork reversal in checkpoint-defective cells.

Cotta-Ramusino C, Fachinetti D, Lucca C, Doksani Y, Lopes M, Sogo J, Foiani M.

Mol Cell. 2005 Jan 7;17(1):153-9.

9.

Branch migrating sister chromatid junctions form at replication origins through Rad51/Rad52-independent mechanisms.

Lopes M, Cotta-Ramusino C, Liberi G, Foiani M.

Mol Cell. 2003 Dec;12(6):1499-510.

10.

Checkpoint-mediated control of replisome-fork association and signalling in response to replication pausing.

Lucca C, Vanoli F, Cotta-Ramusino C, Pellicioli A, Liberi G, Haber J, Foiani M.

Oncogene. 2004 Feb 12;23(6):1206-13.

PMID:
14647447
11.

The DNA replication checkpoint response stabilizes stalled replication forks.

Lopes M, Cotta-Ramusino C, Pellicioli A, Liberi G, Plevani P, Muzi-Falconi M, Newlon CS, Foiani M.

Nature. 2001 Aug 2;412(6846):557-61.

PMID:
11484058

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