Movement Disorders (revue) - Checkpoint (Ncbi)

Index « Mesh.i » - entrée « DNA Primers »
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List of bibliographic references

Number of relevant bibliographic references: 24.
[0-20] [0 - 20][0 - 24][20-23][20-40]
Ident.Authors (with country if any)Title
000330 (2000) S. Buervenich [Suède] ; O. Sydow ; A. Carmine ; Z. Zhang ; M. Anvret ; L. OlsonAlcohol dehydrogenase alleles in Parkinson's disease.
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.
000A67 (2003) Eng-King Tan [Singapour] ; Yanni Tan ; Anthea Chai ; Christopher Tan ; Hui Shen ; Sau-Ying Lum ; Stephanie M C. Fook-Cheong ; Mei-Ling Teoh ; Yuan Yih ; Meng-Cheong Wong ; Yi ZhaoDopamine D2 receptor TaqIA and TaqIB polymorphisms in Parkinson's disease.
000E57 (2004) Laura Cif [France] ; Enza Maria Valente ; Simone Hemm ; Christine Coubes ; Nathalie Vayssiere ; Stéphanie Serrat ; Annalisa Di Giorgio ; Philippe CoubesDeep brain stimulation in myoclonus-dystonia syndrome.
000E69 (2004) Lorraine N. Clark [États-Unis] ; Shehla Afridi ; Helen Mejia-Santana ; Juliette Harris ; Elan D. Louis ; Lucien J. Cote ; Howard Andrews ; Andrew Singleton ; Fabienne Wavrant De-Vrieze ; John Hardy ; Richard Mayeux ; Stanley Fahn ; Cheryl Waters ; Blair Ford ; Steven Frucht ; Ruth Ottman ; Karen MarderAnalysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.
000E72 (2004) Okan Dogu [Turquie] ; Janel Johnson ; Dena Hernandez ; Melissa Hanson ; John Hardy ; Hulya Apaydin ; Sibel Ozekmekçi ; Serhan Sevim ; Katrina Gwinn-Hardy ; Andrew SingletonA consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion.
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.
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.
001034 (2004) Eng-King Tan [Singapour] ; Henry Chung ; Vandana R. Chandran ; Chris Tan ; Hui Shen ; Kenneth Yew ; Ratnagopal Pavanni ; Kathi-Avelu Puvan ; Meng-Cheong Wong ; Mei-Lin Teoh ; Yuan Yih ; Yi ZhaoNurr1 mutational screen in Parkinson's disease.
001081 (2005) Christine Sato [Canada] ; Angharad Morgan ; Anthony E. Lang ; Shabnam Salehi-Rad ; Toshitaka Kawarai ; Yan Meng ; Peter N. Ray ; Lindsay A. Farrer ; Peter St George-Hyslop ; Ekaterina RogaevaAnalysis of the glucocerebrosidase gene in Parkinson's disease.
001140 (2005) Anna H Kansson [Suède] ; Lars Westberg ; Staffan Nilsson ; Silvia Buervenich ; Andrea Carmine ; Björn Holmberg ; Olof Sydow ; Lars Olson ; Bo Johnels ; Elias Eriksson ; Hans NissbrandtInvestigation of genes coding for inflammatory components in Parkinson's disease.
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.
001265 (2005) Daniela Berg [Allemagne] ; Marc Niwar ; Sylvia Maass ; Alexander Zimprich ; J Carsten Möller ; Ullrich Wuellner ; Tanja Schmitz-Hübsch ; Christine Klein ; Eng-King Tan ; Ludger Schöls ; Laura Marsh ; Ted M. Dawson ; Bernd Janetzky ; Thomas Müller ; Dirk Woitalla ; Vladimir Kostic ; Peter P. Pramstaller ; Wolfgang H. Oertel ; Peter Bauer ; Rejko Krueger ; Thomas Gasser ; Olaf RiessAlpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patients.
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.
001308 (2005) Jason D. Dapper [États-Unis] ; Monica J. JusticeDefining the breakpoints of the quaking(viable) mouse mutation reveals a duplication from a Parkin intron.
001486 (2006) Joseph J. Higgins [États-Unis] ; Roni Q. Lombardi ; Joanna Pucilowska ; Joseph Jankovic [États-Unis] ; Lawrence I. Golbe ; Leo VerhagenHS1-BP3 gene variant is common in familial essential tremor.
001576 (2006) Eng-King Tan [Singapour] ; Kenneth Yew ; Eva Chua ; K. Puvan ; Hui Shen ; Esther Lee ; Kim-Yoong Puong ; Yi Zhao ; Ratnagopal Pavanni ; Meng-Cheong Wong ; Dominic Jamora ; Deidre De Silva ; Kyaw-Thu Moe ; Fung-Peng Woon ; Yih Yuen ; Louis TanPINK1 mutations in sporadic early-onset Parkinson's disease.
001967 (2007) Jordi Clarimon [États-Unis] ; Francesco Brancati ; Elizabeth Peckham ; Enza Maria Valente ; Bruno Dallapiccola ; Giovanni Abruzzese ; Paolo Girlanda ; Giovanni Defazio ; Alfredo Berardelli ; Mark Hallett ; Andrew B. SingletonAssessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasm.
001E34 (2008) Nardo Nardocci [Italie] ; Giovanna Zorzi ; Chiara Barzaghi ; Federica Zibordi ; Claudia Ciano ; Daniele Ghezzi ; Barbara GaravagliaMyoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families.
002005 (2008) Hoon-Chul Kang [Corée du Sud] ; 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.
002435 (2009) Donald L. Gilbert [États-Unis] ; Elizabeth J. Leslie ; Mehdi Keddache ; Nancy D. LeslieA novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.

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