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Grant Details

Grant Number: 3U01CA076513-04S1 Interpret this number
Primary Investigator: Haile, Robert
Organization: University Of Southern California
Project Title: Risk of Cancer in a-T Families
Fiscal Year: 2003
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Abstract

An abstract does not currently exist for this grant

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Publications

Functional significance of a deep intronic mutation in the ATM gene and evidence for an alternative exon 28a.
Authors: Coutinho G, Xie J, Du L, Brusco A, Krainer AR, Gatti RA
Source: Hum Mutat, 2005 Feb;25(2), p. 118-24.
PMID: 15643608
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Ataxia-telangiectasia, an evolving phenotype.
Authors: Chun HH, Gatti RA
Source: DNA Repair (Amst), 2004 Aug-Sep;3(8-9), p. 1187-96.
PMID: 15279807
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Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations.
Authors: Coutinho G, Mitui M, Campbell C, Costa Carvalho BT, Nahas S, Sun X, Huo Y, Lai CH, Thorstenson Y, Tanouye R, Raskin S, Kim CA, Llerena J Jr, Gatti RA
Source: Am J Med Genet A, 2004 Apr 1;126A(1), p. 33-40.
PMID: 15039971
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Nonclassical splicing mutations in the coding and noncoding regions of the ATM Gene: maximum entropy estimates of splice junction strengths.
Authors: Eng L, Coutinho G, Nahas S, Yeo G, Tanouye R, Babaei M, Dörk T, Burge C, Gatti RA
Source: Hum Mutat, 2004 Jan;23(1), p. 67-76.
PMID: 14695534
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Early diagnosis of ataxia-telangiectasia using radiosensitivity testing.
Authors: Sun X, Becker-Catania SG, Chun HH, Hwang MJ, Huo Y, Wang Z, Mitui M, Sanal O, Chessa L, Crandall B, Gatti RA
Source: J Pediatr, 2002 Jun;140(6), p. 724-31.
PMID: 12072877
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Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families.
Authors: Resnick IB, Kondratenko I, Togoev O, Vasserman N, Shagina I, Evgrafov O, Tverskaya S, Cerosaletti KM, Gatti RA, Concannon P
Source: J Pediatr, 2002 Mar;140(3), p. 355-61.
PMID: 11953735
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