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Items: 8


Lack of pairing during meiosis triggers multigenerational transgene silencing in Caenorhabditis elegans.

Leopold LE, Heestand BN, Seong S, Shtessel L, Ahmed S.

Proc Natl Acad Sci U S A. 2015 May 19;112(20):E2667-76. doi: 10.1073/pnas.1501979112. Epub 2015 May 4.


Collaboration between mitochondria and the nucleus is key to long life in Caenorhabditis elegans.

Chang HW, Shtessel L, Lee SS.

Free Radic Biol Med. 2015 Jan;78:168-78. doi: 10.1016/j.freeradbiomed.2014.10.576. Epub 2014 Nov 4. Review.


CEP-1, the Caenorhabditis elegans p53 homolog, mediates opposing longevity outcomes in mitochondrial electron transport chain mutants.

Baruah A, Chang H, Hall M, Yuan J, Gordon S, Johnson E, Shtessel LL, Yee C, Hekimi S, Derry WB, Lee SS.

PLoS Genet. 2014 Feb 27;10(2):e1004097. doi: 10.1371/journal.pgen.1004097. eCollection 2014 Feb.


Caenorhabditis elegans POT-1 and POT-2 repress telomere maintenance pathways.

Shtessel L, Lowden MR, Cheng C, Simon M, Wang K, Ahmed S.

G3 (Bethesda). 2013 Feb;3(2):305-13. doi: 10.1534/g3.112.004440. Epub 2013 Feb 1.


Caenorhabditis elegans POT-2 telomere protein represses a mode of alternative lengthening of telomeres with normal telomere lengths.

Cheng C, Shtessel L, Brady MM, Ahmed S.

Proc Natl Acad Sci U S A. 2012 May 15;109(20):7805-10. doi: 10.1073/pnas.1119191109. Epub 2012 Apr 30.


In vivo analysis of conserved C. elegans tomosyn domains.

Burdina AO, Klosterman SM, Shtessel L, Ahmed S, Richmond JE.

PLoS One. 2011;6(10):e26185. doi: 10.1371/journal.pone.0026185. Epub 2011 Oct 14.


Telomere dysfunction in human bone marrow failure syndromes.

Shtessel L, Ahmed S.

Nucleus. 2011 Jan-Feb;2(1):24-9. doi: 10.4161/nucl.2.1.13993. Review.


The MRT-1 nuclease is required for DNA crosslink repair and telomerase activity in vivo in Caenorhabditis elegans.

Meier B, Barber LJ, Liu Y, Shtessel L, Boulton SJ, Gartner A, Ahmed S.

EMBO J. 2009 Nov 18;28(22):3549-63. doi: 10.1038/emboj.2009.278. Epub 2009 Sep 24.

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