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Items: 18

1.

Lysosome and Inflammatory Defects in GBA1-Mutant Astrocytes Are Normalized by LRRK2 Inhibition.

Sanyal A, DeAndrade MP, Novis HS, Lin S, Chang J, Lengacher N, Tomlinson JJ, Tansey MG, LaVoie MJ.

Mov Disord. 2020 Feb 8. doi: 10.1002/mds.27994. [Epub ahead of print]

PMID:
32034799
2.

The role of BTBD9 in the cerebral cortex and the pathogenesis of restless legs syndrome.

Lyu S, Xing H, DeAndrade MP, Perez PD, Zhang K, Liu Y, Yokoi F, Febo M, Li Y.

Exp Neurol. 2020 Jan;323:113111. doi: 10.1016/j.expneurol.2019.113111. Epub 2019 Nov 9.

PMID:
31715135
3.

The Role of BTBD9 in Striatum and Restless Legs Syndrome.

Lyu S, Xing H, DeAndrade MP, Liu Y, Perez PD, Yokoi F, Febo M, Walters AS, Li Y.

eNeuro. 2019 Oct 10;6(5). pii: ENEURO.0277-19.2019. doi: 10.1523/ENEURO.0277-19.2019. Print 2019 Sep/Oct.

4.

Hyperactivity, dopaminergic abnormalities, iron deficiency and anemia in an in vivo opioid receptors knockout mouse: Implications for the restless legs syndrome.

Lyu S, DeAndrade MP, Mueller S, Oksche A, Walters AS, Li Y.

Behav Brain Res. 2019 Nov 18;374:112123. doi: 10.1016/j.bbr.2019.112123. Epub 2019 Jul 31.

PMID:
31376441
5.

Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons.

Schapansky J, Khasnavis S, DeAndrade MP, Nardozzi JD, Falkson SR, Boyd JD, Sanderson JB, Bartels T, Melrose HL, LaVoie MJ.

Neurobiol Dis. 2018 Mar;111:26-35. doi: 10.1016/j.nbd.2017.12.005. Epub 2017 Dec 12.

6.

Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia.

DeAndrade MP, Trongnetrpunya A, Yokoi F, Cheetham CC, Peng N, Wyss JM, Ding M, Li Y.

Mov Disord. 2016 Nov;31(11):1633-1639. doi: 10.1002/mds.26677. Epub 2016 May 31.

7.

Corrigendum: genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.

Lindström S, Thompson DJ, Paterson AD, Li J, Gierach GL, Scott C, Stone J, Douglas JA, Dos-Santos-Silva I, Fernandez-Navarro P, Verghase J, Smith P, Brown J, Luben R, Wareham NJ, Loos RJ, Heit JA, Pankratz VS, Norman A, Goode EL, Cunningham JM, deAndrade M, Vierkant RA, Czene K, Fasching PA, Baglietto L, Southey MC, Giles GG, Shah KP, Chan HP, Helvie MA, Beck AH, Knoblauch NW, Hazra A, Hunter DJ, Kraft P, Pollan M, Figueroa JD, Couch FJ, Hopper JL, Hall P, Easton DF, Boyd NF, Vachon CM, Tamimi RM.

Nat Commun. 2015 Sep 9;6:8358. doi: 10.1038/ncomms9358. No abstract available.

PMID:
26349435
8.

Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.

Lindström S, Thompson DJ, Paterson AD, Li J, Gierach GL, Scott C, Stone J, Douglas JA, dos-Santos-Silva I, Fernandez-Navarro P, Verghase J, Smith P, Brown J, Luben R, Wareham NJ, Loos RJ, Heit JA, Pankratz VS, Norman A, Goode EL, Cunningham JM, deAndrade M, Vierkant RA, Czene K, Fasching PA, Baglietto L, Southey MC, Giles GG, Shah KP, Chan HP, Helvie MA, Beck AH, Knoblauch NW, Hazra A, Hunter DJ, Kraft P, Pollan M, Figueroa JD, Couch FJ, Hopper JL, Hall P, Easton DF, Boyd NF, Vachon CM, Tamimi RM.

Nat Commun. 2014 Oct 24;5:5303. doi: 10.1038/ncomms6303. Erratum in: Nat Commun. 2015;6:8358.

9.

Engineering animal models of dystonia.

Oleas J, Yokoi F, DeAndrade MP, Pisani A, Li Y.

Mov Disord. 2013 Jun 15;28(7):990-1000. doi: 10.1002/mds.25583. Review.

10.

Noninvasive characterization of the histopathologic features of pulmonary nodules of the lung adenocarcinoma spectrum using computer-aided nodule assessment and risk yield (CANARY)--a pilot study.

Maldonado F, Boland JM, Raghunath S, Aubry MC, Bartholmai BJ, Deandrade M, Hartman TE, Karwoski RA, Rajagopalan S, Sykes AM, Yang P, Yi ES, Robb RA, Peikert T.

J Thorac Oncol. 2013 Apr;8(4):452-60. doi: 10.1097/JTO.0b013e3182843721.

11.

Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.

Juran BD, Hirschfield GM, Invernizzi P, Atkinson EJ, Li Y, Xie G, Kosoy R, Ransom M, Sun Y, Bianchi I, Schlicht EM, Lleo A, Coltescu C, Bernuzzi F, Podda M, Lammert C, Shigeta R, Chan LL, Balschun T, Marconi M, Cusi D, Heathcote EJ, Mason AL, Myers RP, Milkiewicz P, Odin JA, Luketic VA, Bacon BR, Bodenheimer HC Jr, Liakina V, Vincent C, Levy C, Franke A, Gregersen PK, Bossa F, Gershwin ME, deAndrade M, Amos CI; Italian PBC Genetics Study Group, Lazaridis KN, Seldin MF, Siminovitch KA.

Hum Mol Genet. 2012 Dec 1;21(23):5209-21. doi: 10.1093/hmg/dds359. Epub 2012 Aug 29.

12.

Motor restlessness, sleep disturbances, thermal sensory alterations and elevated serum iron levels in Btbd9 mutant mice.

DeAndrade MP, Johnson RL Jr, Unger EL, Zhang L, van Groen T, Gamble KL, Li Y.

Hum Mol Genet. 2012 Sep 15;21(18):3984-92. doi: 10.1093/hmg/dds221. Epub 2012 Jun 7.

13.

Enhanced hippocampal long-term potentiation and fear memory in Btbd9 mutant mice.

DeAndrade MP, Zhang L, Doroodchi A, Yokoi F, Cheetham CC, Chen HX, Roper SN, Sweatt JD, Li Y.

PLoS One. 2012;7(4):e35518. doi: 10.1371/journal.pone.0035518. Epub 2012 Apr 19.

14.

Identification of a novel percent mammographic density locus at 12q24.

Stevens KN, Lindstrom S, Scott CG, Thompson D, Sellers TA, Wang X, Wang A, Atkinson E, Rider DN, Eckel-Passow JE, Varghese JS, Audley T, Brown J, Leyland J, Luben RN, Warren RM, Loos RJ, Wareham NJ, Li J, Hall P, Liu J, Eriksson L, Czene K, Olson JE, Pankratz VS, Fredericksen Z, Diasio RB, Lee AM, Heit JA, DeAndrade M, Goode EL, Vierkant RA, Cunningham JM, Armasu SM, Weinshilboum R, Fridley BL, Batzler A, Ingle JN, Boyd NF, Paterson AD, Rommens J, Martin LJ, Hopper JL, Southey MC, Stone J, Apicella C, Kraft P, Hankinson SE, Hazra A, Hunter DJ, Easton DF, Couch FJ, Tamimi RM, Vachon CM.

Hum Mol Genet. 2012 Jul 15;21(14):3299-305. doi: 10.1093/hmg/dds158. Epub 2012 Apr 24.

15.

Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.

Zhang L, Yokoi F, Jin YH, DeAndrade MP, Hashimoto K, Standaert DG, Li Y.

PLoS One. 2011 Mar 29;6(3):e18357. doi: 10.1371/journal.pone.0018357.

16.

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

DeAndrade MP, Yokoi F, van Groen T, Lingrel JB, Li Y.

Behav Brain Res. 2011 Jan 20;216(2):659-65. doi: 10.1016/j.bbr.2010.09.009. Epub 2010 Sep 17.

17.

Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce.

Yokoi F, Yang G, Li J, DeAndrade MP, Zhou T, Li Y.

J Biochem. 2010 Oct;148(4):459-66. doi: 10.1093/jb/mvq078. Epub 2010 Jul 13.

18.

Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome family.

Evans SC, Mims B, McMasters KM, Foster CJ, deAndrade M, Amos CI, Strong LC, Lozano G.

Hum Genet. 1998 Jun;102(6):681-6.

PMID:
9703430

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