Movement Disorders (revue) - Checkpoint (Ncbi)

Index « Mesh.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
000042 (1999) M. Neystat [États-Unis] ; T. Lynch ; S. Przedborski ; N. Kholodilov ; M. Rzhetskaya ; R E BurkeAlpha-synuclein expression in substantia nigra and cortex in Parkinson's disease.
000126 (1999) E. Cassetta [Italie] ; N. Del Grosso ; A R Bentivoglio ; E M Valente ; M. Frontali ; A. AlbaneseItalian family with cranial cervical dystonia: clinical and genetic study.
000130 (1999) L. Baum [République populaire de Chine] ; Z Y Dong ; H K Ng ; L K Law ; J. Woo ; C P PangLow-density lipoprotein receptor-related protein (LRP) gene 766T polymorphism and Parkinson's disease.
000473 (2001) B S Harhangi [Pays-Bas] ; B A Oostra ; P. Heutink ; C M Van Duijn ; A. Hofman ; M M BretelerCYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.
000489 (2001) J. Hoenicka [Espagne] ; L. Vidal ; M. Godoy ; J J Ochoa ; J. García De YébenesNew nonsense mutation in the GTP-cyclohydrolase I gene in L-DOPA responsive dystonia-parkinsonism.
000725 (2002) Eric K. Richfield [États-Unis] ; Jean-Paul Vonsattel ; Marcy E. Macdonald ; Zhiqiang Sun ; Yun-Ping P. Deng ; Anton ReinerSelective loss of striatal preprotachykinin neurons in a phenocopy of Huntington's disease.
000842 (2002) Pramod K. Pal [Canada] ; Joanne Leung ; Katya Hedrich ; Ali Samii ; Abraham Lieberman ; Paul A. Nausieda ; Donald B. Calne ; Xandra O. Breakefield ; Christine Klein ; A Jon Stoessl[18F]-Dopa positron emission tomography imaging in early-stage, non-parkin juvenile parkinsonism.
000911 (2002) S H Subramony [États-Unis] ; Dena Hernandez ; Amanda Adam ; Stephanie Smith-Jefferson ; Jennifer Hussey ; Katrina Gwinn-Hardy ; Timothy Lynch ; Olga Mcdaniel ; John Hardy ; Matt Farrer ; Andrew SingletonEthnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians.
000A04 (2003) Giovanni Defazio [Italie] ; Francesco Brancati ; Enza Maria Valente ; Viviana Caputo ; Antonio Pizzuti ; Davide Martino ; Giovanni Abbruzzese ; Paolo Livrea ; Alfredo Berardelli ; Bruno DallapiccolaFamilial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
000B89 (2003) George R. Uhl [États-Unis]Dopamine transporter: basic science and human variation of a key molecule for dopaminergic function, locomotion, and parkinsonism.
000C71 (2003) Marina A J. Tijssen [Pays-Bas] ; Peter Brown ; David Macmanus ; Mary A. Mclean ; Charles DavieMagnetic resonance spectroscopy of cerebral cortex is normal in hereditary hyperekplexia due to mutations in the GLRA1 gene.
000E50 (2004) Sebastian Paus [Allemagne] ; Gert Seeger ; Hans M. Brecht ; Jürgen Köster ; Mahha El-Faddagh ; Markus M. Nöthen ; Thomas Klockgether ; Ullrich WüllnerAssociation study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease.
000E83 (2004) Christoph Kamm [États-Unis] ; Joanne Leung ; Soni Joseph ; William B. Dobyns ; Alison Brashear ; Xandra O. Breakefield ; Laurie J. OzeliusRefined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene.
000F23 (2004) Patricia De Carvalho Aguiar [États-Unis] ; Melissa Fazzari ; Joseph Jankovic [États-Unis] ; Laurie J. OzeliusExamination of the SGCE gene in Tourette syndrome patients with obsessive-compulsive disorder.
000F60 (2004) Sean O'Riordan [Irlande (pays)] ; Laurie J. Ozelius ; Patricia De Carvalho Aguiar ; Michael Hutchinson ; Mary King ; Tim LynchInherited myoclonus-dystonia and epilepsy: further evidence of an association?
000F84 (2004) Dominic Thyagarajan [Australie] ; Timothy Chataway ; Rong Li ; Wei Ping Gai ; Michael BrennerDominantly-inherited adult-onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene.
001004 (2004) Antonino Uncini [Italie] ; Maria Vittoria De Angelis ; Patrizia Di Fulvio ; Michele Ragno ; Grazia Annesi ; Alessandro Filla ; Liborio Stuppia ; Domenico GambiWide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation.
001027 (2004) Ali Sazci [Turquie] ; Emel Ergul ; Kemal BayulkemAssociation of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey.
001129 (2005) H A Jinnah [États-Unis] ; Ellen J. Hess ; Mark S. Ledoux ; Nutan Sharma ; Mark G. Baxter ; Mahlon R. DelongRodent models for dystonia research: characteristics, evaluation, and utility.
001155 (2005) Eng-King Tan [Singapour] ; 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.
001280 (2005) Elan D. Louis [États-Unis] ; 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.

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