Walker SA - Search Results

1

ATR-dependent phosphorylation and activation of ATM in response to UV treatment or replication fork stalling.

Stiff T, Walker SA, Cerosaletti K, Goodarzi AA, Petermann E, Concannon P, O'Driscoll M, Jeggo PA. Stiff T, et al. Among authors: walker sa. EMBO J. 2006 Dec 13;25(24):5775-82. doi: 10.1038/sj.emboj.7601446. Epub 2006 Nov 23. EMBO J. 2006. PMID: 17124492 Free PMC article.

2

DNA-PK autophosphorylation facilitates Artemis endonuclease activity.

Goodarzi AA, Yu Y, Riballo E, Douglas P, Walker SA, Ye R, Härer C, Marchetti C, Morrice N, Jeggo PA, Lees-Miller SP. Goodarzi AA, et al. Among authors: walker sa. EMBO J. 2006 Aug 23;25(16):3880-9. doi: 10.1038/sj.emboj.7601255. Epub 2006 Jul 27. EMBO J. 2006. PMID: 16874298 Free PMC article.

3

Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome.

Ogi T, Walker S, Stiff T, Hobson E, Limsirichaikul S, Carpenter G, Prescott K, Suri M, Byrd PJ, Matsuse M, Mitsutake N, Nakazawa Y, Vasudevan P, Barrow M, Stewart GS, Taylor AM, O'Driscoll M, Jeggo PA. Ogi T, et al. PLoS Genet. 2012;8(11):e1002945. doi: 10.1371/journal.pgen.1002945. Epub 2012 Nov 8. PLoS Genet. 2012. PMID: 23144622 Free PMC article.

4

XLF-Cernunnos promotes DNA ligase IV-XRCC4 re-adenylation following ligation.

Riballo E, Woodbine L, Stiff T, Walker SA, Goodarzi AA, Jeggo PA. Riballo E, et al. Among authors: walker sa. Nucleic Acids Res. 2009 Feb;37(2):482-92. doi: 10.1093/nar/gkn957. Epub 2008 Dec 4. Nucleic Acids Res. 2009. PMID: 19056826 Free PMC article.

5

Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling.

Griffith E, Walker S, Martin CA, Vagnarelli P, Stiff T, Vernay B, Al Sanna N, Saggar A, Hamel B, Earnshaw WC, Jeggo PA, Jackson AP, O'Driscoll M. Griffith E, et al. Nat Genet. 2008 Feb;40(2):232-6. doi: 10.1038/ng.2007.80. Epub 2007 Dec 23. Nat Genet. 2008. PMID: 18157127 Free PMC article.

6

Identification of a novel motif in DNA ligases exemplified by DNA ligase IV.

Marchetti C, Walker SA, Odreman F, Vindigni A, Doherty AJ, Jeggo P. Marchetti C, et al. Among authors: walker sa. DNA Repair (Amst). 2006 Jul 13;5(7):788-98. doi: 10.1016/j.dnarep.2006.03.011. Epub 2006 Jun 2. DNA Repair (Amst). 2006. PMID: 16735143 Free article.

7

Chromosome breakage after G2 checkpoint release.

Deckbar D, Birraux J, Krempler A, Tchouandong L, Beucher A, Walker S, Stiff T, Jeggo P, Löbrich M. Deckbar D, et al. J Cell Biol. 2007 Mar 12;176(6):749-55. doi: 10.1083/jcb.200612047. J Cell Biol. 2007. PMID: 17353355 Free PMC article.

8

Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.

Bicknell LS, Walker S, Klingseisen A, Stiff T, Leitch A, Kerzendorfer C, Martin CA, Yeyati P, Al Sanna N, Bober M, Johnson D, Wise C, Jackson AP, O'Driscoll M, Jeggo PA. Bicknell LS, et al. Nat Genet. 2011 Feb 27;43(4):350-5. doi: 10.1038/ng.776. Nat Genet. 2011. PMID: 21358633

9

Airway macrophage glycolysis controls lung homeostasis and responses to aeroallergen.

Albers GJ, Michalaki C, Ogger PP, Lloyd AF, Causton B, Walker SA, Caldwell A, Halket JM, Sinclair LV, Forde SH, McCarthy C, Hinks TSC, Lloyd CM, Byrne AJ. Albers GJ, et al. Among authors: walker sa. Mucosal Immunol. 2024 Oct 18:S1933-0219(24)00105-3. doi: 10.1016/j.mucimm.2024.10.002. Online ahead of print. Mucosal Immunol. 2024. PMID: 39426627 Free article.

10

Cerebral injury and retinopathy as risk factors for blindness in extremely preterm infants.

Honan BM, McDonald SA, Travers CP, Shukla VV, Ambalavanan N, Cotten CM, Jain VG, Arnold HE, Parikh NA, Tyson JE, Hintz SR, Walker SA, Gantz MG, Das A, Carlo WA. Honan BM, et al. Among authors: walker sa. Arch Dis Child Fetal Neonatal Ed. 2024 Sep 27:fetalneonatal-2024-327707. doi: 10.1136/archdischild-2024-327707. Online ahead of print. Arch Dis Child Fetal Neonatal Ed. 2024. PMID: 39332892

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