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Our Science – Swing Website

Deborah A. Swing, BS, AA, RLATG

Selected Publications

1)  Smith S, Tripathi R, Goodings C, Cleveland S, Mathias E, Hardaway JA, Elliott N, Yi Y, Chen X, Downing J, Mullighan C, Swing DA, Tessarollo L, Li L, Love P, Jenkins NA, Copeland NG, Thompson MA, Du Y, Davé UP.
LIM Domain Only-2 (LMO2) Induces T-Cell Leukemia by Two Distinct Pathways.
PLoS ONE. 9: e85883, 2014.
[Journal]
2)  Arnold ES, Ling SC, Huelga SC, Lagier-Tourenne C, Polymenidou M, Ditsworth D, Kordasiewicz HB, McAlonis-Downes M, Platoshyn O, Parone PA, Da Cruz S, Clutario KM, Swing D, Tessarollo L, Marsala M, Shaw CE, Yeo GW, Cleveland DW.
ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43.
Proc. Natl. Acad. Sci. U.S.A. 110: E736-45, 2013.
[Journal]
3)  Anderson MJ, Naiche LA, Wilson CP, Elder C, Swing DA, Lewandoski M.
TCreERT2, a Transgenic Mouse Line for Temporal Control of Cre-Mediated Recombination in Lineages Emerging from the Primitive Streak or Tail Bud.
PLoS ONE. 8: e62479, 2013.
[Journal]
4)  Berquam-Vrieze KE, Swing DA, Tessarollo L, Dupuy AJ.
Characterization of transgenic mice expressing cancer-associated variants of human NOTCH1.
Genesis. 50: 112-8, 2012.
[Journal]
5)  Li J, Akagi K, Hu Y, Trivett AL, Hlynialuk CJ, Swing DA, Volfovsky N, Morgan TC, Golubeva Y, Stephens RM, Smith DE, Symer DE.
Mouse endogenous retroviruses can trigger premature transcriptional termination at a distance.
Genome Res. 22: 870-84, 2012.
[Journal]
6)  Waldron-Roby E, Ratovitski T, Wang X, Jiang M, Watkin E, Arbez N, Graham RK, Hayden MR, Hou Z, Mori S, Swing D, Pletnikov M, Duan W, Tessarollo L, Ross CA.
Transgenic mouse model expressing the caspase 6 fragment of mutant huntingtin.
J. Neurosci. 32: 183-93, 2012.
[Journal]
7)  Ramonet D, Daher JP, Lin BM, Stafa K, Kim J, Banerjee R, Westerlund M, Pletnikova O, Glauser L, Yang L, Liu Y, Swing DA, Beal MF, Troncoso JC, McCaffery JM, Jenkins NA, Copeland NG, Galter D, Thomas B, Lee MK, Dawson TM, Dawson VL, Moore DJ.
Dopaminergic Neuronal Loss, Reduced Neurite Complexity and Autophagic Abnormalities in Transgenic Mice Expressing G2019S Mutant LRRK2.
PLoS ONE. 6: e18568, 2011.
[Journal]
8)  Tebbenkamp AT, Swing D, Tessarollo L, Borchelt DR.
Premature death and neurologic abnormalities in transgenic mice expressing a mutant huntingtin exon-2 fragment.
Hum. Mol. Genet. 20: 1633-42, 2011.
[Journal]
9)  Tebbenkamp AT, Green C, Xu G, Denovan-Wright EM, Rising AC, Fromholt SE, Brown HH, Swing D, Mandel RJ, Tessarollo L, Borchelt DR.
Transgenic mice expressing caspase-6-derived N-terminal fragments of mutant huntingtin develop neurologic abnormalities with predominant cytoplasmic inclusion pathology composed largely of a smaller proteolytic derivative.
Hum Mol Genet. 20: 2770-82, 2011.
[Journal]
10)  Smith WW, Liu Z, Liang Y, Masuda N, Swing DA, Jenkins NA, Copeland NG, Troncoso JC, Pletnikov M, Dawson TM, Martin LJ, Moran TH, Lee MK, Borchelt DR, Ross CA.
Synphilin-1 attenuates neuronal degeneration in the A53T alpha-synuclein transgenic mouse model.
Hum. Mol. Genet. 19: 2087-98, 2010.
[Journal]
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This page was last updated on 4/15/2014.