Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 204

1.

Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis.

Davisson MT, Cook SA, Akeson EC, Liu D, Heffner C, Gudis P, Fairfield H, Murray SA.

Am J Physiol Renal Physiol. 2015 Jun 15;308(12):F1335-42. doi: 10.1152/ajprenal.00410.2014. Epub 2015 Apr 1.

PMID:
25834070
2.

A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers.

Korstanje R, Caputo CR, Doty RA, Cook SA, Bronson RT, Davisson MT, Miner JH.

Kidney Int. 2014 Jun;85(6):1461-8. doi: 10.1038/ki.2013.493. Epub 2014 Feb 12.

3.

Correlated SEM, FIB-SEM, TEM, and NanoSIMS imaging of microbes from the hindgut of a lower termite: methods for in situ functional and ecological studies of uncultivable microbes.

Carpenter KJ, Weber PK, Davisson ML, Pett-Ridge J, Haverty MI, Keeling PJ.

Microsc Microanal. 2013 Dec;19(6):1490-501. doi: 10.1017/S1431927613013482. Epub 2013 Oct 11.

PMID:
24119340
4.

Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease.

Potter GB, Santos M, Davisson MT, Rowitch DH, Marks DL, Bongarzone ER, Petryniak MA.

Hum Mol Genet. 2013 Sep 1;22(17):3397-414. doi: 10.1093/hmg/ddt190. Epub 2013 Apr 24.

5.

Centralized mouse repositories.

Donahue LR, Hrabe de Angelis M, Hagn M, Franklin C, Lloyd KC, Magnuson T, McKerlie C, Nakagata N, Obata Y, Read S, Wurst W, Hörlein A, Davisson MT.

Mamm Genome. 2012 Oct;23(9-10):559-71. doi: 10.1007/s00335-012-9420-4. Epub 2012 Sep 4.

6.

Discovery Genetics - The History and Future of Spontaneous Mutation Research.

Davisson MT, Bergstrom DE, Reinholdt LG, Donahue LR.

Curr Protoc Mouse Biol. 2012 Jun 1;2:103-118.

7.

A spontaneous mutation in contactin 1 in the mouse.

Davisson MT, Bronson RT, Tadenev AL, Motley WW, Krishnaswamy A, Seburn KL, Burgess RW.

PLoS One. 2011;6(12):e29538. doi: 10.1371/journal.pone.0029538. Epub 2011 Dec 29.

8.

Loss of correlations among proteins in brains of the Ts65Dn mouse model of down syndrome.

Ahmed MM, Sturgeon X, Ellison M, Davisson MT, Gardiner KJ.

J Proteome Res. 2012 Feb 3;11(2):1251-63. doi: 10.1021/pr2011582. Epub 2012 Jan 25.

PMID:
22214338
9.

Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse.

Lindfors C, Nilsson IA, Garcia-Roves PM, Zuberi AR, Karimi M, Donahue LR, Roopenian DC, Mulder J, Uhlén M, Ekström TJ, Davisson MT, Hökfelt TG, Schalling M, Johansen JE.

Proc Natl Acad Sci U S A. 2011 Nov 1;108(44):18108-13. doi: 10.1073/pnas.1114863108. Epub 2011 Oct 24.

10.

Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn.

Reinholdt LG, Ding Y, Gilbert GJ, Czechanski A, Solzak JP, Roper RJ, Johnson MT, Donahue LR, Lutz C, Davisson MT.

Mamm Genome. 2011 Dec;22(11-12):685-91. doi: 10.1007/s00335-011-9357-z. Epub 2011 Sep 28. Erratum in: Mamm Genome. 2011 Dec;22(11-12):692. Gilbert, Griffith T [corrected to Gilbert, Griffith J].

11.

The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentials.

Scott-McKean JJ, Chang B, Hurd RE, Nusinowitz S, Schmidt C, Davisson MT, Costa AC.

Invest Ophthalmol Vis Sci. 2010 Jun;51(6):3300-8. doi: 10.1167/iovs.09-4465. Epub 2010 Feb 3.

12.

ZFP191 is required by oligodendrocytes for CNS myelination.

Howng SY, Avila RL, Emery B, Traka M, Lin W, Watkins T, Cook S, Bronson R, Davisson M, Barres BA, Popko B.

Genes Dev. 2010 Feb 1;24(3):301-11. doi: 10.1101/gad.1864510. Epub 2010 Jan 15.

13.

Otitis media in a mouse model for Down syndrome.

Han F, Yu H, Zhang J, Tian C, Schmidt C, Nava C, Davisson MT, Zheng QY.

Int J Exp Pathol. 2009 Oct;90(5):480-8. doi: 10.1111/j.1365-2613.2009.00677.x.

14.

Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1).

Costa AC, Stasko MR, Schmidt C, Davisson MT.

Behav Brain Res. 2010 Jan 5;206(1):52-62. doi: 10.1016/j.bbr.2009.08.034. Epub 2009 Aug 29.

15.

A mouse model for Meckel syndrome type 3.

Cook SA, Collin GB, Bronson RT, Naggert JK, Liu DP, Akeson EC, Davisson MT.

J Am Soc Nephrol. 2009 Apr;20(4):753-64. doi: 10.1681/ASN.2008040412. Epub 2009 Feb 11.

16.

VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse.

Jin N, Chow CY, Liu L, Zolov SN, Bronson R, Davisson M, Petersen JL, Zhang Y, Park S, Duex JE, Goldowitz D, Meisler MH, Weisman LS.

EMBO J. 2008 Dec 17;27(24):3221-34. doi: 10.1038/emboj.2008.248. Epub 2008 Nov 27.

17.

Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.

Chang B, Mandal MN, Chavali VR, Hawes NL, Khan NW, Hurd RE, Smith RS, Davisson ML, Kopplin L, Klein BE, Klein R, Iyengar SK, Heckenlively JR, Ayyagari R.

Hum Mol Genet. 2008 Dec 15;17(24):3929-41. doi: 10.1093/hmg/ddn295. Epub 2008 Sep 18.

18.

Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome.

Voronov SV, Frere SG, Giovedi S, Pollina EA, Borel C, Zhang H, Schmidt C, Akeson EC, Wenk MR, Cimasoni L, Arancio O, Davisson MT, Antonarakis SE, Gardiner K, De Camilli P, Di Paolo G.

Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9415-20. doi: 10.1073/pnas.0803756105. Epub 2008 Jun 30.

19.

Mitotic chromosome preparations from mouse cells for karyotyping.

Akeson EC, Davisson MT.

Curr Protoc Hum Genet. 2001 May;Chapter 4:Unit4.10. doi: 10.1002/0471142905.hg0410s25.

PMID:
18428279
20.

Editing of the serotonin 2C receptor pre-mRNA: Effects of the Morris Water Maze.

Du Y, Stasko M, Costa AC, Davisson MT, Gardiner KJ.

Gene. 2007 Apr 15;391(1-2):186-97. Epub 2007 Jan 12.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk