Reply to testing for herpesvirus infection is essential in children with chromosomal-instability syndromes

Journal of Virology

Volumn 87, Issue 6, 2013, Pages 3618-3618

  Kulinski, Joseph M ^a   Tarakanova, Vera L ^a,b  

^a Human and Molecular Genetics Center   (United States)

^b MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATM PROTEIN;

ATAXIA TELANGIECTASIA; CHILD; CHROMOSOMAL INSTABILITY SYNDROME; DISEASE EXACERBATION; ENVIRONMENTAL FACTOR; ENZYME DEFICIENCY; FANCONI ANEMIA; GAMMAHERPESVIRINAE; GENETIC DISORDER; HERPES VIRUS INFECTION; HUMAN; IMMUNE RESPONSE; LETTER; NIJMEGEN BREAKAGE SYNDROME; NONHUMAN; PATHOGENESIS; PATHOPHYSIOLOGY; PRIORITY JOURNAL;

ANIMALS; ATAXIA TELANGIECTASIA; CELL CYCLE PROTEINS; DNA DAMAGE; DNA-BINDING PROTEINS; GAMMAHERPESVIRINAE; HERPESVIRIDAE INFECTIONS; LYMPHOCYTE ACTIVATION; PROTEIN-SERINE-THREONINE KINASES; TUMOR SUPPRESSOR PROTEINS;

EID: 84874698238     PISSN: 0022538X     EISSN: 10985514     Source Type: Journal    
DOI: 10.1128/JVI.03401-12     Document Type: Letter

References (4)

1. Lankisch P, Adler H, Borkhardt A. 2013. Testing for herpesvirus infection is essential in children with chromosomal-instability syndromes. J. Virol. 87:3616-3617.
2. Theunissen JW, Kaplan MI, Hunt PA, Williams BR, Ferguson DO, Alt FW, Petrini JH. 2003. Checkpoint failure and chromosomal instability without lymphomagenesis in Mre11(ATLD1/ATLD1) mice. Mol. Cell 12: 1511-1523.
3. Williams BR, Mirzoeva OK, Morgan WF, Lin J, Dunnick W, Petrini JH. 2002. A murine model of Nijmegen breakage syndrome. Curr. Biol. 12: 648-653.
4. Cheng NC, van de Vrugt HJ, van der Valk MA, Oostra AB, Krimpenfort P, de Vries Y, Joenje H, Berns A, Arwert F. 2000. Mice with a targeted disruption of the Fanconi anemia homolog Fanca. Hum. Mol. Genet. 9:1805-1811.