Gene Expression (drug effects) < Gene Expression (genetics) < Gene Expression (physiology)

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List of bibliographic references

Number of relevant bibliographic references: 22.
[0-20] [0 - 20][0 - 22][20-21][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 Burke	Alpha-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. Albanese	Italian 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 Pang	Low-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 Breteler	CYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.
000489 (2001)	J. Hoenicka [Espagne] ; L. Vidal ; M. Godoy ; J J Ochoa ; J. García De Yébenes	New nonsense mutation in the GTP-cyclohydrolase I gene in L-DOPA responsive dystonia-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 Singleton	Ethnic 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 Dallapiccola	Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
000C71 (2003)	Marina A J. Tijssen [Pays-Bas] ; Peter Brown ; David Macmanus ; Mary A. Mclean ; Charles Davie	Magnetic 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 Wüllner	Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease.
000F23 (2004)	Patricia De Carvalho Aguiar [États-Unis] ; Melissa Fazzari ; Joseph Jankovic [États-Unis] ; Laurie J. Ozelius	Examination of the SGCE gene in Tourette syndrome patients with obsessive-compulsive disorder.
000F84 (2004)	Dominic Thyagarajan [Australie] ; Timothy Chataway ; Rong Li ; Wei Ping Gai ; Michael Brenner	Dominantly-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 Gambi	Wide 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 Bayulkem	Association 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. Delong	Rodent 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 Zhao	Alpha-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. Bhat	Interaction between blood lead concentration and delta-amino-levulinic acid dehydratase gene polymorphisms increases the odds of essential tremor.
001A33 (2007)	Laurie J. Ozelius [États-Unis] ; Tatiana Foroud ; Susanne May ; Geetha Senthil ; Paola Sandroni ; Phillip A. Low ; Stephen Reich ; Amy Colcher ; Matthew B. Stern ; William G. Ondo ; Joseph Jankovic [États-Unis] ; Neng Huang ; Caroline M. Tanner ; Peter Novak ; Sid Gilman ; Frederick J. Marshall ; G Frederick Wooten ; Thomas C. Chelimsky ; Clifford W. Shults	G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy.
001A37 (2007)	Anjum Misbahuddin [Royaume-Uni] ; Mark Placzek ; Graham Lennox ; Jan-Willem Taanman ; Thomas T. Warner	Myoclonus-dystonia syndrome with severe depression is caused by an exon-skipping mutation in the epsilon-sarcoglycan gene.
002005 (2008)	Hoon-Chul Kang [Corée du Sud] ; Su Jeong You ; Myung Jae Chey ; Jong Sam Baik ; Jong-Won Kim ; Chang-Seok Ki	Identification of a de novo Lys304Gln mutation in the glycine receptor alpha-1 subunit gene in a Korean infant with hyperekplexia.
002472 (2009)	Akatsuki Kubota [Japon] ; Ayumi Hida ; Yaeko Ichikawa ; Yoshio Momose ; Jun Goto ; Yukifusa Igeta ; Hideji Hashida ; Kunihiro Yoshida ; Syu-Ichi Ikeda ; Ichiro Kanazawa ; Shoji Tsuji	A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations.
002B72 (2010)	Giuseppe De Palma [Italie] ; Finlay D. Dick ; Stefano Calzetti ; Neil W. Scott ; Gordon J. Prescott ; Aileen Osborne ; Neva Haites ; Paola Mozzoni ; Anna Negrotti ; Augusto Scaglioni ; Antonio Mutti	A case-control study of Parkinson's disease and tobacco use: gene-tobacco interactions.

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