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Year | Number of Results |
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2003 | 1 |
2004 | 1 |
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ATM haplotypes and associated mutations in Iranian patients with ataxia-telangiectasia: recurring homozygosity without a founder haplotype.
Hum Genet. 2005 Jul;117(2-3):101-6. doi: 10.1007/s00439-005-1254-7. Epub 2005 Apr 21.
Hum Genet. 2005.
PMID: 15843990
Transcriptional response to ionizing radiation in human radiation sensitive cell lines.
Landmark H, Nahas SA, Aarøe J, Gatti R, Børresen-Dale AL, Rødningen OK.
Landmark H, et al.
Radiother Oncol. 2007 Jun;83(3):256-60. doi: 10.1016/j.radonc.2007.04.017. Epub 2007 May 23.
Radiother Oncol. 2007.
PMID: 17512073
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Correction of prototypic ATM splicing mutations and aberrant ATM function with antisense morpholino oligonucleotides.
Du L, Pollard JM, Gatti RA.
Du L, et al.
Proc Natl Acad Sci U S A. 2007 Apr 3;104(14):6007-12. doi: 10.1073/pnas.0608616104. Epub 2007 Mar 26.
Proc Natl Acad Sci U S A. 2007.
PMID: 17389389
Free PMC article.
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Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons.
Lai CH, Chun HH, Nahas SA, Mitui M, Gamo KM, Du L, Gatti RA.
Lai CH, et al.
Proc Natl Acad Sci U S A. 2004 Nov 2;101(44):15676-81. doi: 10.1073/pnas.0405155101. Epub 2004 Oct 21.
Proc Natl Acad Sci U S A. 2004.
PMID: 15498871
Free PMC article.
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ATM mutations on distinct SNP and STR haplotypes in ataxia-telangiectasia patients of differing ethnicities reveal ancestral founder effects.
Campbell C, Mitui M, Eng L, Coutinho G, Thorstenson Y, Gatti RA.
Campbell C, et al.
Hum Mutat. 2003 Jan;21(1):80-5. doi: 10.1002/humu.10156.
Hum Mutat. 2003.
PMID: 12497634
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