Movement Disorders (revue) - Corpus (PubMed)

Index « MedMesh.i » - entrée « Gene Expression »
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Gene Duplication < Gene Expression < Gene Expression Profiling  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 46.
[0-20] [0 - 20][0 - 46][20-40]
Ident.Authors (with country if any)Title
000503 (2014) Sarah K. Abbott ; Hongyun Li ; Sonia Sanz Mu Oz ; Bianca Knoch ; Marijka Batterham ; Karen E. Murphy ; Glenda M. Halliday ; Brett GarnerAltered ceramide acyl chain length and ceramide synthase gene expression in Parkinson’s disease.
000751 (2014) Zhan-Fang Sun ; Xiao-Shuang Xiang ; Zhao Chen ; Li Zhang ; Bei-Sha Tang ; Kun Xia ; Hong JiangIncrease of the plasma α-synuclein levels in patients with multiple system atrophy.
000D86 (2012) David A. Elliott ; Woojin S. Kim ; Sarsha Gorissen ; Glenda M. Halliday ; John B J. KwokLeucine-rich repeat kinase 2 and alternative splicing in Parkinson's disease.
001830 (2010) Giuseppe De Palma ; Finlay D. Dick ; Stefano Calzetti ; Neil W. Scott ; Gordon J. Prescott ; Aileen Osborne ; Neva Haites ; Paola Mozzoni ; Anna Negrotti ; Augusto Scaglioni ; Antonio MuttiA case-control study of Parkinson's disease and tobacco use: gene-tobacco interactions.
001B39 (2009) Luca Lovrecic ; Andrej Kastrin ; Jan Kobal ; Zvezdan Pirtosek ; Dimitri Krainc ; Borut PeterlinGene expression changes in blood as a putative biomarker for Huntington's disease.
001E92 (2009) Akatsuki Kubota ; Ayumi Hida ; Yaeko Ichikawa ; Yoshio Momose ; Jun Goto ; Yukifusa Igeta ; Hideji Hashida ; Kunihiro Yoshida ; Syu-Ichi Ikeda ; Ichiro Kanazawa ; Shoji TsujiA novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations.
002152 (2008) Chelsea Stamper ; Andrew Siegel ; Winnie S. Liang ; John V. Pearson ; Dietrich A. Stephan ; Holly Shill ; Don Connor ; John N. Caviness ; Marwan Sabbagh ; Thomas G. Beach ; Charles H. Adler ; Travis DunckleyNeuronal gene expression correlates of Parkinson's disease with dementia.
002354 (2008) Hoon-Chul Kang ; Su Jeong You ; Myung Jae Chey ; Jong Sam Baik ; Jong-Won Kim ; Chang-Seok KiIdentification of a de novo Lys304Gln mutation in the glycine receptor alpha-1 subunit gene in a Korean infant with hyperekplexia.
002564 (2007) Penelope Hogarth ; Luca Lovrecic ; Dimitri KraincSodium phenylbutyrate in Huntington's disease: a dose-finding study.
002786 (2007) Eun Joo Chung ; Won Yong Lee ; Ji-Youn Kim ; Jong-Hun Kim ; Gyeong-Moon Kim ; Chang Seok Ki ; In-Suk KimNovel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease.
002789 (2007) Vanderci Borges ; Patricia De Carvalho Aguiar ; Henrique Ballalai Ferraz ; Laurie J. OzeliusNovel and de novo mutations of the SGCE gene in Brazilian patients with myoclonus-dystonia.
002902 (2007) Anjum Misbahuddin ; Mark Placzek ; Graham Lennox ; Jan-Willem Taanman ; Thomas T. WarnerMyoclonus-dystonia syndrome with severe depression is caused by an exon-skipping mutation in the epsilon-sarcoglycan gene.
002906 (2007) Laurie J. Ozelius ; Tatiana Foroud ; Susanne May ; Geetha Senthil ; Paola Sandroni ; Phillip A. Low ; Stephen Reich ; Amy Colcher ; Matthew B. Stern ; William G. Ondo ; Joseph Jankovic ; Neng Huang ; Caroline M. Tanner ; Peter Novak ; Sid Gilman ; Frederick J. Marshall ; G Frederick Wooten ; Thomas C. Chelimsky ; Clifford W. ShultsG2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy.
002B87 (2006) Ornit Chiba-Falek ; Grisel J. Lopez ; Robert L. NussbaumLevels of alpha-synuclein mRNA in sporadic Parkinson disease patients.
002E43 (2006) Daniela Perani ; Valentina Garibotto ; George M. Hadjigeorgiou ; Dimitra Papadimitriou ; Ferruccio Fazio ; Alexandros PapadimitriouPositron emission tomography changes in PARK1 mutation.
002E91 (2006) Marc Morissette ; Mehdi Dridi ; Frédéric Calon ; Abdallah Hadj Tahar ; Leonard T. Meltzer ; Paul J. Bédard ; Thérèse Di PaoloPrevention of levodopa-induced dyskinesias by a selective NR1A/2B N-methyl-D-aspartate receptor antagonist in parkinsonian monkeys: implication of preproenkephalin.
003017 (2005) Maher A. Noureddine ; Yi-Ju Li ; Joelle M. Van Der Walt ; Robert Walters ; Rita M. Jewett ; Hong Xu ; Tianyuan Wang ; Jeffrey W. Walter ; Burton L. Scott ; Christine Hulette ; Don Schmechel ; Judith E. Stenger ; Fred Dietrich ; Jeffery M. Vance ; Michael A. HauserGenomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.
003032 (2005) Elan D. Louis ; Lakeisha Applegate ; Joseph H. Graziano ; Michael Parides ; Vesna Slavkovich ; Hari K. BhatInteraction between blood lead concentration and delta-amino-levulinic acid dehydratase gene polymorphisms increases the odds of essential tremor.
003146 (2005) Eng-King Tan ; Van R. Chandran ; Stephanie Fook-Chong ; Hui Shen ; Kenneth Yew ; Mei-Lin Teoh ; Yih Yuen ; Yi ZhaoAlpha-synuclein mRNA expression in sporadic Parkinson's disease.
003172 (2005) H A Jinnah ; Ellen J. Hess ; Mark S. Ledoux ; Nutan Sharma ; Mark G. Baxter ; Mahlon R. DelongRodent models for dystonia research: characteristics, evaluation, and utility.
003261 (2004) Ali Sazci ; Emel Ergul ; Kemal BayulkemAssociation of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey.

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