Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Majid Belouchi"'
Autor:
Cynthia V Bourassa, Jean-Baptiste Rivière, Patrick A Dion, Geneviève Bernard, Sabrina Diab, Michel Panisset, Sylvain Chouinard, Nicolas Dupré, Hélène Fournier, John Raelson, Majid Belouchi, Guy A Rouleau
Publikováno v:
PLoS ONE, Vol 6, Iss 1, p e16254 (2011)
Essential tremor (ET) is a complex genetic disorder for which no causative gene has been found. Recently, a genome-wide association study reported that two variants in the LINGO1 locus were associated to this disease. The aim of the present study was
Externí odkaz:
https://doaj.org/article/4bc29343cc0b4aab9350dd534097d709
Autor:
Dafna D. Gladman, David Ellinghaus, Proton Rahman, H.-Erich Wichmann, Sophie Debrus, Michael Weichenthal, John Verner Raelson, Andre Franke, Yanming Li, Lam C. Tsoi, Christian Gieger, Sulev Kõks, Philip E. Stuart, Stephan Weidinger, Stefan Schreiber, Külli Kingo, Majid Belouchi, Tõnu Esko, Ulrich Mrowietz, Gerald G. Krueger, Cynthia Helms, Gonçalo R. Abecasis, Anne M. Bowcock, Rajan P. Nair, Anna T Onken, Eva Ellinghaus, James T. Elder, Andres Metspalu, Trilokraj Tejasvi
Publikováno v:
Journal of Investigative Dermatology
Journal of Investigative Dermatology; Vol 132
The Journal of investigative dermatology
J. Invest. Dermatol. 132, 1133-1140 (2012)
Journal of Investigative Dermatology; Vol 132
The Journal of investigative dermatology
J. Invest. Dermatol. 132, 1133-1140 (2012)
Psoriatic arthritis (PsA) is a chronic inflammatory musculoskeletal disease affecting up to 30% of psoriasis vulgaris (PsV) cases and approximately 0.25 to 1% of the general population. To identify common susceptibility loci, we performed a meta-anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2af15b76b99560da32c934fa1a5fe8b
Autor:
Sophie Debrus, Susanna Nikolaus, James T. Elder, Eva Ellinghaus, H.-Erich Wichmann, Tobias Balschun, Sarah L. West, Christian Gieger, Trilokraj Tejasvi, Richard C. Trembath, Stephan Weidinger, Philip E. Stuart, Gonçalo R. Abecasis, Sulev Kõks, Michael Kabesch, Christopher G. Mathew, Rajan P. Nair, Majid Belouchi, Jonathan Barker, Michael Weichenthal, John Verner Raelson, Michael Nothnagel, Külli Kingo, David Ellinghaus, Tõnu Esko, Stefan Schreiber, Andre Franke, Orazio Palmieri, Vito Annese, Andres Metspalu
Publikováno v:
The American Journal of Human Genetics
Am. J. Hum. Genet. 90, 636-647 (2012)
Am. J. Hum. Genet. 90, 636-647 (2012)
Psoriasis (PS) and Crohn disease (CD) have been shown to be epidemiologically, pathologically, and therapeutically connected, but little is known about their shared genetic causes. We performed meta-analyses of five published genome-wide association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4289f8bf8236ec116fc85c8c19b5183a
Autor:
Manfred Kunz, James T. Elder, Yun Li, Christian Gieger, Stephan Weidinger, Ulrich Mrowietz, Dafna D. Gladman, Tom H. Karlsen, Eva Ellinghaus, Gonçalo R. Abecasis, Bernadette Eberlein, Claudia Reinhard, Trilokraj Tejasvi, Sophie Debrus, John J. Voorhees, Philip E. Stuart, Stefan Schreiber, Sylviane Lambert, Gabriele Mayr, Johann E. Gudjonsson, Mario Albrecht, Majid Belouchi, Rajan P. Nair, Michael Weichenthal, Dieter Kabelitz, Andre Franke, H.-Erich Wichmann, Jun Ding, Stefan W. Stoll, Proton Rahman, John Verner Raelson, David Ellinghaus, Helene Fournier
Publikováno v:
Nature Genetics. 42:991-995
Andre Franke and colleagues report a genome-wide association study for psoriasis vulgaris in a German cohort with replication in German and North American psoriasis cohorts. They identify variants in TRAF3IP2, encoding a protein involved in IL-17 med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e56c7505beda741be8f2d5499e2003ac
https://doi.org/10.1038/ng.689
https://doi.org/10.1038/ng.689
Autor:
Seung-Hwan Lee, Majid Belouchi, Ken Dimock, Nicole Beauchemin, Kathryn V. Holmes, Silvia M. Vidal, Douglas A. Gray, John Realson
Publikováno v:
Trends in Genetics
Genetic studies of host susceptibility to infection contribute to our understanding of an organism's response to pathogens at the immunological, cellular, and molecular levels. In this review we describe how the study of host genetics in mouse models
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c568a78be46253f9eb6741a5e5fd22c5
https://doi.org/10.1016/s0168-9525(03)00172-0
https://doi.org/10.1016/s0168-9525(03)00172-0
Publikováno v:
American Journal of Medical Genetics. 85:20-30
The activity of cytochrome oxidase (CO), the terminal enzyme of the mitochondrial electron transport chain, has been reported to be lower in the brains of Alzheimer disease (AD) patients. This suggests that a modification of mitochondrial DNA (mtDNA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f6f2be1cabbd96e74aa0a1d3bbe0547
https://doi.org/10.1002/(sici)1096-8628(19990702)85:1<20::aid-ajmg6>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19990702)85:1<20::aid-ajmg6>3.0.co
Autor:
Michel Panisset, Patrick A. Dion, Nancy D. Merner, John Verner Raelson, Annie Levert, Geneviève Bernard, Sabrina Diab, Simon Girard, Helene Fournier, Nicolas Dupré, Dan Spiegelman, Anne Noreau, Cynthia V. Bourassa, Hélène Catoire, Guy A. Rouleau, Patrick Cossette, Jean-Baptiste Rivière, Anna Szuto, Veronique V. Belzil, Sylvain Chouinard, Majid Belouchi, Alexandre Dionne-Laporte, Pascale Hince
Publikováno v:
American journal of human genetics. 91(2)
Essential tremor (ET) is a common neurodegenerative disorder that is characterized by a postural or motion tremor. Despite a strong genetic basis, a gene with rare pathogenic mutations that cause ET has not yet been reported. We used exome sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3d2f954dbff8f830d9ba7a8c93e15ed
https://pubmed.ncbi.nlm.nih.gov/23526429
https://pubmed.ncbi.nlm.nih.gov/23526429
Publikováno v:
Analytical biochemistry. 339(2)
[1,2], is widelyused in forensic analyses but also extends its applica-tion to pathology, molecular diagnostics, and environ-mental microbiology. Recently, two new methods forWGA have been introduced. The Wrst is based onstrand displacement synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99df2c5895d9059bf042e9d30c0078d0
https://pubmed.ncbi.nlm.nih.gov/15797576
https://pubmed.ncbi.nlm.nih.gov/15797576
Autor:
Geneviève Bernard, Patrick A. Dion, Cynthia V. Bourassa, Guy A. Rouleau, Majid Belouchi, Sabrina Diab, John Verner Raelson, Michel Panisset, Sylvain Chouinard, Nicolas Dupré, Jean-Baptiste Rivière, Helene Fournier
Publikováno v:
PLoS ONE, Vol 6, Iss 1, p e16254 (2011)
PLoS ONE
PLoS ONE
Essential tremor (ET) is a complex genetic disorder for which no causative gene has been found. Recently, a genome-wide association study reported that two variants in the LINGO1 locus were associated to this disease. The aim of the present study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6286074e42b32db99b2c6aa6b24b313d
https://doi.org/10.1371/journal.pone.0016254
https://doi.org/10.1371/journal.pone.0016254