Emond MJ - Search Results

1

The human WRN and BLM RecQ helicases differentially regulate cell proliferation and survival after chemotherapeutic DNA damage.

Mao FJ, Sidorova JM, Lauper JM, Emond MJ, Monnat RJ. Mao FJ, et al. Among authors: emond mj. Cancer Res. 2010 Aug 15;70(16):6548-55. doi: 10.1158/0008-5472.CAN-10-0475. Epub 2010 Jul 27. Cancer Res. 2010. PMID: 20663905 Free PMC article.

2

The Werner syndrome protein has separable recombination and survival functions.

Swanson C, Saintigny Y, Emond MJ, Monnat RJ Jr. Swanson C, et al. Among authors: emond mj. DNA Repair (Amst). 2004 May 4;3(5):475-82. doi: 10.1016/j.dnarep.2004.01.002. DNA Repair (Amst). 2004. PMID: 15084309 Free article.

3

Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype.

Kamath-Loeb AS, Zavala-van Rankin DG, Flores-Morales J, Emond MJ, Sidorova JM, Carnevale A, Cárdenas-Cortés MD, Norwood TH, Monnat RJ, Loeb LA, Mercado-Celis GE. Kamath-Loeb AS, et al. Among authors: emond mj. Sci Rep. 2017 Mar 9;7:44081. doi: 10.1038/srep44081. Sci Rep. 2017. PMID: 28276523 Free PMC article. Clinical Trial.

4

Unexpectedly low loss of heterozygosity in genetically unstable Werner syndrome cell lines.

Brooks-Wilson AR, Emond MJ, Monnat RJ Jr. Brooks-Wilson AR, et al. Among authors: emond mj. Genes Chromosomes Cancer. 1997 Feb;18(2):133-42. Genes Chromosomes Cancer. 1997. PMID: 9115963

5

Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes.

Moser MJ, Bigbee WL, Grant SG, Emond MJ, Langlois RG, Jensen RH, Oshima J, Monnat RJ Jr. Moser MJ, et al. Among authors: emond mj. Cancer Res. 2000 May 1;60(9):2492-6. Cancer Res. 2000. PMID: 10811130

6

Loss of Werner syndrome protein function promotes aberrant mitotic recombination.

Prince PR, Emond MJ, Monnat RJ Jr. Prince PR, et al. Among authors: emond mj. Genes Dev. 2001 Apr 15;15(8):933-8. doi: 10.1101/gad.877001. Genes Dev. 2001. PMID: 11316787 Free PMC article.

7

The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage.

Colgin LM, Hackmann AF, Emond MJ, Monnat RJ Jr. Colgin LM, et al. Among authors: emond mj. Proc Natl Acad Sci U S A. 2002 Feb 5;99(3):1437-42. doi: 10.1073/pnas.032655699. Epub 2002 Jan 29. Proc Natl Acad Sci U S A. 2002. PMID: 11818556 Free PMC article.

8

Homologous recombination resolution defect in werner syndrome.

Saintigny Y, Makienko K, Swanson C, Emond MJ, Monnat RJ Jr. Saintigny Y, et al. Among authors: emond mj. Mol Cell Biol. 2002 Oct;22(20):6971-8. doi: 10.1128/MCB.22.20.6971-6978.2002. Mol Cell Biol. 2002. PMID: 12242278 Free PMC article.

9

Microwell arrays reveal cellular heterogeneity during the clonal expansion of transformed human cells.

Chang TC, Tang W, Koh WJ, Rettie AJ, Emond MJ, Monnat RJ Jr, Folch A. Chang TC, et al. Among authors: emond mj. Technology (Singap World Sci). 2015 Dec;3(4):163-171. doi: 10.1142/S2339547815200046. Technology (Singap World Sci). 2015. PMID: 27158641 Free PMC article.

10

Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines.

Prince PR, Ogburn CE, Moser MJ, Emond MJ, Martin GM, Monnat RJ Jr. Prince PR, et al. Among authors: emond mj. Hum Genet. 1999 Jul-Aug;105(1-2):132-8. doi: 10.1007/s004399900078. Hum Genet. 1999. PMID: 10480367

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