Stewart GS - Search Results

1

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. Among authors: stewart gs. PLoS Genet. 2012;8(11):e1002945. doi: 10.1371/journal.pgen.1002945. Epub 2012 Nov 8. PLoS Genet. 2012. PMID: 23144622 Free PMC article.

2

Inactivation of ataxia telangiectasia mutated gene in B-cell chronic lymphocytic leukaemia.

Stankovic T, Weber P, Stewart G, Bedenham T, Murray J, Byrd PJ, Moss PA, Taylor AM. Stankovic T, et al. Lancet. 1999 Jan 2;353(9146):26-9. doi: 10.1016/S0140-6736(98)10117-4. Lancet. 1999. PMID: 10023947

3

The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder.

Stewart GS, Maser RS, Stankovic T, Bressan DA, Kaplan MI, Jaspers NG, Raams A, Byrd PJ, Petrini JH, Taylor AM. Stewart GS, et al. Cell. 1999 Dec 10;99(6):577-87. doi: 10.1016/s0092-8674(00)81547-0. Cell. 1999. PMID: 10612394 Free article.

4

hMRE11: genomic structure and a null mutation identified in a transcript protected from nonsense-mediated mRNA decay.

Pitts SA, Kullar HS, Stankovic T, Stewart GS, Last JI, Bedenham T, Armstrong SJ, Piane M, Chessa L, Taylor AM, Byrd PJ. Pitts SA, et al. Among authors: stewart gs. Hum Mol Genet. 2001 May 15;10(11):1155-62. doi: 10.1093/hmg/10.11.1155. Hum Mol Genet. 2001. PMID: 11371508

5

Residual ataxia telangiectasia mutated protein function in cells from ataxia telangiectasia patients, with 5762ins137 and 7271T-->G mutations, showing a less severe phenotype.

Stewart GS, Last JI, Stankovic T, Haites N, Kidd AM, Byrd PJ, Taylor AM. Stewart GS, et al. J Biol Chem. 2001 Aug 10;276(32):30133-41. doi: 10.1074/jbc.M103160200. Epub 2001 May 29. J Biol Chem. 2001. PMID: 11382771 Free article.

6

p53 dysfunction in B-cell chronic lymphocytic leukemia: inactivation of ATM as an alternative to TP53 mutation.

Pettitt AR, Sherrington PD, Stewart G, Cawley JC, Taylor AM, Stankovic T. Pettitt AR, et al. Blood. 2001 Aug 1;98(3):814-22. doi: 10.1182/blood.v98.3.814. Blood. 2001. PMID: 11468183 Free article.

7

Ataxia without telangiectasia revisited: update on genetic findings in two brothers with an ataxia-telangiectasia-like disorder.

Klein C, Stewart GS, Quinn NP, Taylor AM. Klein C, et al. Among authors: stewart gs. Mov Disord. 2001 Jul;16(4):788-9. doi: 10.1002/mds.1136. Mov Disord. 2001. PMID: 11481721 No abstract available.

8

Ataxia telangiectasia mutated-deficient B-cell chronic lymphocytic leukemia occurs in pregerminal center cells and results in defective damage response and unrepaired chromosome damage.

Stankovic T, Stewart GS, Fegan C, Biggs P, Last J, Byrd PJ, Keenan RD, Moss PA, Taylor AM. Stankovic T, et al. Among authors: stewart gs. Blood. 2002 Jan 1;99(1):300-9. doi: 10.1182/blood.v99.1.300. Blood. 2002. PMID: 11756185 Free article.

9

ATM mutations in sporadic lymphoid tumours.

Stankovic T, Stewart GS, Byrd P, Fegan C, Moss PA, Taylor AM. Stankovic T, et al. Among authors: stewart gs. Leuk Lymphoma. 2002 Aug;43(8):1563-71. doi: 10.1080/1042819021000002884. Leuk Lymphoma. 2002. PMID: 12400598 Review.

10

Microarray analysis reveals that TP53- and ATM-mutant B-CLLs share a defect in activating proapoptotic responses after DNA damage but are distinguished by major differences in activating prosurvival responses.

Stankovic T, Hubank M, Cronin D, Stewart GS, Fletcher D, Bignell CR, Alvi AJ, Austen B, Weston VJ, Fegan C, Byrd PJ, Moss PA, Taylor AM. Stankovic T, et al. Among authors: stewart gs. Blood. 2004 Jan 1;103(1):291-300. doi: 10.1182/blood-2003-04-1161. Epub 2003 Sep 4. Blood. 2004. PMID: 12958068 Free article.

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