Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia (English)
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- New search for: Fuchs, Tania
- New search for: Gavarini, Sophie
- New search for: Saunders-Pullman, Rachel
- New search for: Raymond, Deborah
- New search for: Ehrlich, Michelle E
- New search for: Bressman, Susan B
- New search for: Ozelius, Laurie J
- New search for: Fuchs, Tania
- New search for: Gavarini, Sophie
- New search for: Saunders-Pullman, Rachel
- New search for: Raymond, Deborah
- New search for: Ehrlich, Michelle E
- New search for: Bressman, Susan B
- New search for: Ozelius, Laurie J
In:
Nature Genetics
;
41
, 3
;
286-288
;
2009
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ISSN:
- Article (Journal) / Electronic Resource
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Title:Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia
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Contributors:Fuchs, Tania ( author ) / Gavarini, Sophie ( author ) / Saunders-Pullman, Rachel ( author ) / Raymond, Deborah ( author ) / Ehrlich, Michelle E ( author ) / Bressman, Susan B ( author ) / Ozelius, Laurie J ( author )
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Published in:Nature Genetics ; 41, 3 ; 286-288
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Publisher:
- New search for: Nature Publishing Group
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Publication date:2009-03-01
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Size:3 pages
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ISSN:
-
DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 41, Issue 3
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 265
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Modern lights| 2009
- 267
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In the aftermath of warAronson, Jay D. et al. | 2009
- 269
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The neurokinin B pathway in human reproductionLatronico, Ana Claudia et al. | 2009
- 270
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Processing the H3K36me3 signatureSims III, Robert J / Reinberg, Danny et al. | 2009
- 272
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FGF9 on the moveSpicer, Douglas et al. | 2009
- 275
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Research Highlights| 2009
- 277
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Variant in the sequence of the LINGO1 gene confers risk of essential tremorStefansson, Hreinn / Steinberg, Stacy / Petursson, Hjorvar / Gustafsson, Omar / Gudjonsdottir, Iris H / Jonsdottir, Gudrun A / Palsson, Stefan T / Jonsson, Thorlakur / Saemundsdottir, Jona / Bjornsdottir, Gyda et al. | 2009
- 280
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New susceptibility locus for coronary artery disease on chromosome 3q22.3Erdmann, Jeanette / Großhennig, Anika / Braund, Peter S / König, Inke R / Hengstenberg, Christian / Hall, Alistair S / Linsel-Nitschke, Patrick / Kathiresan, Sekar / Wright, Ben / Trégouët, David-Alexandre et al. | 2009
- 283
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Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery diseaseTrégouët, David-Alexandre / König, Inke R / Erdmann, Jeanette / Munteanu, Alexandru / Braund, Peter S / Hall, Alistair S / Großhennig, Anika / Linsel-Nitschke, Patrick / Perret, Claire / DeSuremain, Maylis et al. | 2009
- 286
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Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystoniaFuchs, Tania / Gavarini, Sophie / Saunders-Pullman, Rachel / Raymond, Deborah / Ehrlich, Michelle E / Bressman, Susan B / Ozelius, Laurie J et al. | 2009
- 289
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FGF9 monomer–dimer equilibrium regulates extracellular matrix affinity and tissue diffusionHarada, Masayo / Murakami, Hirotaka / Okawa, Akihiko / Okimoto, Noriaki / Hiraoka, Shuichi / Nakahara, Taka / Akasaka, Ryogo / Shiraishi, Yo-ichi / Futatsugi, Noriyuki / Mizutani-Koseki, Yoko et al. | 2009
- 299
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Systems genetics of complex traits in Drosophila melanogasterAyroles, Julien F / Carbone, Mary Anna / Stone, Eric A / Jordan, Katherine W / Lyman, Richard F / Magwire, Michael M / Rollmann, Stephanie M / Duncan, Laura H / Lawrence, Faye / Anholt, Robert R H et al. | 2009
- 308
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α-Synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicityGitler, Aaron D / Chesi, Alessandra / Geddie, Melissa L / Strathearn, Katherine E / Hamamichi, Shusei / Hill, Kathryn J / Caldwell, Kim A / Caldwell, Guy A / Cooper, Antony A / Rochet, Jean-Christophe et al. | 2009
- 316
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Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicityYeger-Lotem, Esti / Riva, Laura / Su, Linhui Julie / Gitler, Aaron D / Cashikar, Anil G / King, Oliver D / Auluck, Pavan K / Geddie, Melissa L / Valastyan, Julie S / Karger, David R et al. | 2009
- 324
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Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1Zheng, Wei / Long, Jirong / Gao, Yu-Tang / Li, Chun / Zheng, Ying / Xiang, Yong-Bin / Wen, Wanqing / Levy, Shawn / Deming, Sandra L / Haines, Jonathan L et al. | 2009
- 329
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SNPs in BRAP associated with risk of myocardial infarction in Asian populationsOzaki, Kouichi / Sato, Hiroshi / Inoue, Katsumi / Tsunoda, Tatsuhiko / Sakata, Yasuhiko / Mizuno, Hiroya / Lin, Tsung-Hsien / Miyamoto, Yoshinari / Aoki, Asako / Onouchi, Yoshihiro et al. | 2009
- 334
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variantsKathiresan, Sekar / Voight, Benjamin F / Purcell, Shaun / Musunuru, Kiran / Ardissino, Diego / Mannucci, Pier M / Anand, Sonia / Engert, James C / Samani, Nilesh J / Schunkert, Heribert et al. | 2009
- 342
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Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGudbjartsson, Daniel F / Bjornsdottir, Unnur S / Halapi, Eva / Helgadottir, Anna / Sulem, Patrick / Jonsdottir, Gudrun M / Thorleifsson, Gudmar / Helgadottir, Hafdis / Steinthorsdottir, Valgerdur / Stefansson, Hreinn et al. | 2009
- 348
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Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressureNewton-Cheh, Christopher / Larson, Martin G / Vasan, Ramachandran S / Levy, Daniel / Bloch, Kenneth D / Surti, Aarti / Guiducci, Candace / Kathiresan, Sekar / Benjamin, Emelia J / Struck, Joachim et al. | 2009
- 354
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TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproductionTopaloglu, A Kemal / Reimann, Frank / Guclu, Metin / Yalin, Ayse Serap / Kotan, L Damla / Porter, Keith M / Serin, Ayse / Mungan, Neslihan O / Cook, Joshua R / Ozbek, Mehmet N et al. | 2009
- 359
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Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequenceBenko, Sabina / Fantes, Judy A / Amiel, Jeanne / Kleinjan, Dirk-Jan / Thomas, Sophie / Ramsay, Jacqueline / Jamshidi, Negar / Essafi, Abdelkader / Heaney, Simon / Gordon, Christopher T et al. | 2009
- 365
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A TARBP2 mutation in human cancer impairs microRNA processing and DICER1 functionMelo, Sonia A / Ropero, Santiago / Moutinho, Catia / Aaltonen, Lauri A / Yamamoto, Hiroyuki / Calin, George A / Rossi, Simona / Fernandez, Agustin F / Carneiro, Fatima / Oliveira, Carla et al. | 2009
- 371
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Co-regulated transcriptional networks contribute to natural genetic variation in Drosophila sleepHarbison, Susan T / Carbone, Mary Anna / Ayroles, Julien F / Stone, Eric A / Lyman, Richard F / Mackay, Trudy F C et al. | 2009
- 376
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Differential chromatin marking of introns and expressed exons by H3K36me3Kolasinska-Zwierz, Paulina / Down, Thomas / Latorre, Isabel / Liu, Tao / Liu, X Shirley / Ahringer, Julie et al. | 2009