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Results: 14

1.

Genetic deletion of transglutaminase 2 does not rescue the phenotypic deficits observed in R6/2 and zQ175 mouse models of Huntington's disease.

Menalled LB, Kudwa AE, Oakeshott S, Farrar A, Paterson N, Filippov I, Miller S, Kwan M, Olsen M, Beltran J, Torello J, Fitzpatrick J, Mushlin R, Cox K, McConnell K, Mazzella M, He D, Osborne GF, Al-Nackkash R, Bates GP, Tuunanen P, Lehtimaki K, Brunner D, Ghavami A, Ramboz S, Park L, Macdonald D, Munoz-Sanjuan I, Howland D.

PLoS One. 2014 Jun 23;9(6):e99520. doi: 10.1371/journal.pone.0099520. eCollection 2014.

2.

Increased Body Weight of the BAC HD Transgenic Mouse Model of Huntington's Disease Accounts for Some but Not All of the Observed HD-like Motor Deficits.

Kudwa AE, Menalled LB, Oakeshott S, Murphy C, Mushlin R, Fitzpatrick J, Miller SF, McConnell K, Port R, Torello J, Howland D, Ramboz S, Brunner D.

PLoS Curr. 2013 Jul 30;5. pii: ecurrents.hd.0ab4f3645aff523c56ecc8ccbe41a198. doi: 10.1371/currents.hd.0ab4f3645aff523c56ecc8ccbe41a198.

3.

High-Throughput Automated Phenotyping of Two Genetic Mouse Models of Huntington's Disease.

Balci F, Oakeshott S, Shamy JL, El-Khodor BF, Filippov I, Mushlin R, Port R, Connor D, Paintdakhi A, Menalled L, Ramboz S, Howland D, Kwak S, Brunner D.

PLoS Curr. 2013 Jul 11;5. pii: ecurrents.hd.124aa0d16753f88215776fba102ceb29. doi: 10.1371/currents.hd.124aa0d16753f88215776fba102ceb29.

4.

Comprehensive behavioral and molecular characterization of a new knock-in mouse model of Huntington's disease: zQ175.

Menalled LB, Kudwa AE, Miller S, Fitzpatrick J, Watson-Johnson J, Keating N, Ruiz M, Mushlin R, Alosio W, McConnell K, Connor D, Murphy C, Oakeshott S, Kwan M, Beltran J, Ghavami A, Brunner D, Park LC, Ramboz S, Howland D.

PLoS One. 2012;7(12):e49838. doi: 10.1371/journal.pone.0049838. Epub 2012 Dec 20.

5.

Prediction of death in the SMNĪ”7 mouse model of spinal muscular atrophy: insight into disease stage and progression.

El-Khodor BF, Cirillo K, Beltran JA, Mushlin R, Winberg ML, Charney R, Chomicova O, Marino T, Ramboz S.

J Neurosci Methods. 2012 Aug 15;209(2):259-68. doi: 10.1016/j.jneumeth.2012.06.020. Epub 2012 Jun 29.

PMID:
22750651
6.

Clique-finding for heterogeneity and multidimensionality in biomarker epidemiology research: the CHAMBER algorithm.

Mushlin RA, Gallagher S, Kershenbaum A, Rebbeck TR.

PLoS One. 2009;4(3):e4862. doi: 10.1371/journal.pone.0004862. Epub 2009 Mar 16.

7.

Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.

Van Ness B, Ramos C, Haznadar M, Hoering A, Haessler J, Crowley J, Jacobus S, Oken M, Rajkumar V, Greipp P, Barlogie B, Durie B, Katz M, Atluri G, Fang G, Gupta R, Steinbach M, Kumar V, Mushlin R, Johnson D, Morgan G.

BMC Med. 2008 Sep 8;6:26. doi: 10.1186/1741-7015-6-26.

8.

Genomic messaging system language including command extensions for clinical data categories.

Robson B, Mushlin R.

J Proteome Res. 2005 Mar-Apr;4(2):275-99.

PMID:
15822903
11.

LifeLines: using visualization to enhance navigation and analysis of patient records.

Plaisant C, Mushlin R, Snyder A, Li J, Heller D, Shneiderman B.

Proc AMIA Symp. 1998:76-80.

12.

Progress notes model.

Aghili H, Mushlin RA, Williams RM, Rose JS.

Proc AMIA Annu Fall Symp. 1997:12-6.

13.

PUPA: a pulse programming assistant for NMR imaging.

Foxvog D, Li XF, Vargas JE, Bourne JR, Sztipanovits J, Mushlin R, Harrison CG.

IEEE Trans Biomed Eng. 1987 Dec;34(12):938-43. No abstract available.

PMID:
3692515
14.

Triplet state properties of polycyclic aromatic hydrocarbon-DNA and porphyrin-DNA complexes determined by optically detected zero field magnetic resonance.

Clarke RH, Harris G, Lasser N, Mushlin RA.

Photochem Photobiol. 1983 Jan;37(1):9-15. No abstract available.

PMID:
6836032
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