Concannon P - Search Results

1

Expression pattern of the Nijmegen breakage syndrome gene, Nbs1, during murine development.

Wilda M, Demuth I, Concannon P, Sperling K, Hameister H. Wilda M, et al. Among authors: concannon p. Hum Mol Genet. 2000 Jul 22;9(12):1739-44. doi: 10.1093/hmg/9.12.1739. Hum Mol Genet. 2000. PMID: 10915761

2

V(D)J rearrangement in Nijmegen breakage syndrome.

Yeo TC, Xia D, Hassouneh S, Yang XO, Sabath DE, Sperling K, Gatti RA, Concannon P, Willerford DM. Yeo TC, et al. Among authors: concannon p. Mol Immunol. 2000 Dec;37(18):1131-9. doi: 10.1016/s0161-5890(01)00026-8. Mol Immunol. 2000. PMID: 11451418

3

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome.

Varon R, Vissinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanová E, Cooper PR, Nowak NJ, Stumm M, Weemaes CM, Gatti RA, Wilson RK, Digweed M, Rosenthal A, Sperling K, Concannon P, Reis A. Varon R, et al. Among authors: concannon p. Cell. 1998 May 1;93(3):467-76. doi: 10.1016/s0092-8674(00)81174-5. Cell. 1998. PMID: 9590180 Free article.

4

Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation.

Demuth I, Bradshaw PS, Lindner A, Anders M, Heinrich S, Kallenbach J, Schmelz K, Digweed M, Meyn MS, Concannon P. Demuth I, et al. Among authors: concannon p. DNA Repair (Amst). 2008 Aug 2;7(8):1192-201. doi: 10.1016/j.dnarep.2008.03.020. Epub 2008 May 12. DNA Repair (Amst). 2008. PMID: 18468965 Free PMC article.

5

Human SNM1B is required for normal cellular response to both DNA interstrand crosslink-inducing agents and ionizing radiation.

Demuth I, Digweed M, Concannon P. Demuth I, et al. Among authors: concannon p. Oncogene. 2004 Nov 11;23(53):8611-8. doi: 10.1038/sj.onc.1207895. Oncogene. 2004. PMID: 15467758

6

Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome.

Vissinga CS, Yeo TC, Woessner J, Massa HF, Wilson RK, Trask BJ, Concannon P. Vissinga CS, et al. Among authors: concannon p. Cytogenet Cell Genet. 1999;87(1-2):80-4. doi: 10.1159/000015396. Cytogenet Cell Genet. 1999. PMID: 10640816

7

Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

Cerosaletti KM, Lange E, Stringham HM, Weemaes CM, Smeets D, Sölder B, Belohradsky BH, Taylor AM, Karnes P, Elliott A, Komatsu K, Gatti RA, Boehnke M, Concannon P. Cerosaletti KM, et al. Among authors: concannon p. Am J Hum Genet. 1998 Jul;63(1):125-34. doi: 10.1086/301927. Am J Hum Genet. 1998. PMID: 9634525 Free PMC article.

8

Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation.

Cerosaletti KM, Desai-Mehta A, Yeo TC, Kraakman-Van Der Zwet M, Zdzienicka MZ, Concannon P. Cerosaletti KM, et al. Among authors: concannon p. Mutagenesis. 2000 May;15(3):281-6. doi: 10.1093/mutage/15.3.281. Mutagenesis. 2000. PMID: 10792024

9

Dual functions of Nbs1 in the repair of DNA breaks and proliferation ensure proper V(D)J recombination and T-cell development.

Saidi A, Li T, Weih F, Concannon P, Wang ZQ. Saidi A, et al. Among authors: concannon p. Mol Cell Biol. 2010 Dec;30(23):5572-81. doi: 10.1128/MCB.00917-10. Epub 2010 Oct 4. Mol Cell Biol. 2010. PMID: 20921278 Free PMC article.

10

Nijmegen breakage syndrome in a Dutch patient not resulting from a defect in NBS1.

Hiel JA, Weemaes CM, van Engelen BG, Smeets D, Ligtenberg M, van Der Burgt I, van Den Heuvel LP, Cerosaletti KM, Gabreëls FJ, Concannon P. Hiel JA, et al. Among authors: concannon p. J Med Genet. 2001 Jun;38(6):E19. doi: 10.1136/jmg.38.6.e19. J Med Genet. 2001. PMID: 11389166 Free PMC article. No abstract available.

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