Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Denis A. Akkad"'
Autor:
A. Dessa Sadovnick, Anthony L. Traboulsee, Cecily Q. Bernales, Jay P. Ross, Amanda L. Forwell, Irene M. Yee, Lena Guillot-Noel, Bertrand Fontaine, Isabelle Cournu-Rebeix, Antonio Alcina, Maria Fedetz, Guillermo Izquierdo, Fuencisla Matesanz, Kelly Hilven, Bénédicte Dubois, An Goris, Ianire Astobiza, Iraide Alloza, Alfredo Antigüedad, Koen Vandenbroeck, Denis A. Akkad, Orhan Aktas, Paul Blaschke, Mathias Buttmann, Andrew Chan, Joerg T. Epplen, Lisa-Ann Gerdes, Antje Kroner, Christian Kubisch, Tania Kümpfel, Peter Lohse, Peter Rieckmann, Uwe K. Zettl, Frauke Zipp, Lars Bertram, Christina M Lill, Oscar Fernandez, Patricia Urbaneja, Laura Leyva, Jose Carlos Alvarez-Cermeño, Rafael Arroyo, Aroa M. Garagorri, Angel García-Martínez, Luisa M. Villar, Elena Urcelay, Sunny Malhotra, Xavier Montalban, Manuel Comabella, Thomas Berger, Franz Fazekas, Markus Reindl, Mascha C. Schmied, Alexander Zimprich, Carles Vilariño-Güell
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 7, Pp 2073-2079 (2016)
Multiple sclerosis (MS) is a prevalent neurological disease of complex etiology. Here, we describe the characterization of a multi-incident MS family that nominated a rare missense variant (p.G420D) in plasminogen (PLG) as a putative genetic risk fac
Externí odkaz:
https://doaj.org/article/ad94b930f9574b93ac8b8955b0887d3c
Autor:
Denis A Akkad, Alexandra Olischewsky, Franziska Reiner, Kerstin Hellwig, Sarika Esser, Jörg T Epplen, Tomaz Curk, Ralf Gold, Aiden Haghikia
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0127632 (2015)
Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system that predominantly affects young adults. The genetic contributions to this multifactorial disease were underscored by a genome wide association study (GWAS) conduct
Externí odkaz:
https://doaj.org/article/4eefe1aa1ec54821a0ff63f5b03cb496
Autor:
Wanda M. Gerding, Jörg T. Epplen, Sebastian Ocklenburg, Larissa Arning, Jan G. Hengstler, Christian Beste, Onur Güntürkün, Denis A. Akkad
Publikováno v:
Molecular Neurobiology. 53:6355-6361
Handedness is a multifactorial trait, and genes contributing to the differentiation of the left-right axis during embryogenesis have been identified as a major gene group associated with this trait. The methyltransferase SETDB2 (SET domain, bifurcate
Autor:
Stefanie Jörg, Denis A. Akkad, Anne Waschbisch, Nils Helge Schebb, Caroline May, Alexander Duscha, Stefan Kempa, Aiden Haghikia, Ralf Gold, Diana A. Grohme, Markus Kleinewietfeld, Jan Thöne, Johannes Berg, Annika I. Ostermann, András Balogh, Nicola Wilck, Dominik N. Müller, Anna Hammer, Seray Demir, Ralf A. Linker, Arndt Manzel, De-Hyung Lee
Publikováno v:
Immunity. 43(4):817-829
SummaryGrowing empirical evidence suggests that nutrition and bacterial metabolites might impact the systemic immune response in the context of disease and autoimmunity. We report that long-chain fatty acids (LCFAs) enhanced differentiation and proli
Publikováno v:
International Journal of Immunogenetics. 42:106-110
Summary Variations in two genes of the tumour necrosis factor (TNF) alpha pathway have been implicated in the pathogenesis of autoimmune diseases: polymorphisms in the TNFRSF1A gene, encoding TNF receptor 1, showed significant association with MS in
Autor:
Bartosz Pula, Derek J. Pappas, Xavier Montalban, Larissa Arning, Ralf Gold, Simon Faissner, Andrew T. Chan, Sergio E. Baranzini, Manuel Comabella, Denis A. Akkad, Aiden Haghikia, Sunny Malhotra, Alexander Duscha, Sabrina Ruhrmann
Publikováno v:
Multiple Sclerosis Journal. 21:1262-1270
Background: Whereas cellular immune function depends on energy supply and mitochondrial function, little is known on the impact of immunotherapies on cellular energy metabolism. Objective: The objective of this paper is to assess the effects of inter
Publikováno v:
Journal of Molecular Medicine. 92:177-184
Huntington disease (HD) is caused by the expansion of a CAG repeat within exon 1 of the HTT gene. Although the variation in age at onset (AO) is partly explained by the lengths of the expanded repeats, the unexplained variation is highly heritable, e
Autor:
Thomas Berger, Franz Fazekas, A. Dessa Sadovnick, Lars Bertram, José C. Álvarez-Cermeño, Orhan Aktas, Mathias Buttmann, Cecily Q. Bernales, Irene M. Yee, Antonio Alcina, Kelly Hilven, Bénédicte Dubois, M. Schmied, Joerg T. Epplen, Uwe K. Zettl, Carles Vilariño-Güell, Jay P. Ross, Anthony Traboulsee, Patricia Urbaneja, Alexander Zimprich, Iraide Alloza, Lisa Ann Gerdes, Ianire Astobiza, Peter Lohse, Angel Garcia-Martinez, Fuencisla Matesanz, Guillermo Izquierdo, Aroa M. Garagorri, Tania Kümpfel, Koen Vandenbroeck, Alfredo Antigüedad, Bertrand Fontaine, Manuel Comabella, Oscar Fernandez, Denis A. Akkad, Paul Blaschke, Peter Rieckmann, Xavier Montalban, Christian Kubisch, Markus Reindl, Isabelle Cournu-Rebeix, Elena Urcelay, Lena Guillot-Noel, Frauke Zipp, Andrew T. Chan, Sunny Malhotra, Rafael Arroyo, An Goris, Antje Kroner, Luisa M. Villar, María Fedetz, Amanda L. Forwell, Christina M. Lill, Laura Leyva
Publikováno v:
Sadovnick, A Dessa; Traboulsee, Anthony L; Bernales, Cecily Q; Ross, Jay P; Forwell, Amanda L; Yee, Irene M; Guillot-Noel, Lena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Alcina, Antonio; Fedetz, Maria; Izquierdo, Guillermo; Matesanz, Fuencisla; Hilven, Kelly; Dubois, Bénédicte; Goris, An; Astobiza, Ianire; Alloza, Iraide; Antigüedad, Alfredo; Vandenbroeck, Koen; ... (2016). Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. G3 Genes Genomes Genetics, 6(7), pp. 2073-2079. Genetics Society of America 10.1534/g3.116.030841
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Addi. Archivo Digital para la Docencia y la Investigación
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
G3: Genes, Genomes, Genetics, Vol 6, Iss 7, Pp 2073-2079 (2016)
G3: Genes|Genomes|Genetics
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Addi. Archivo Digital para la Docencia y la Investigación
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
G3: Genes, Genomes, Genetics, Vol 6, Iss 7, Pp 2073-2079 (2016)
G3: Genes|Genomes|Genetics
Multiple sclerosis (MS) is a prevalent neurological disease of complex etiology. Here, we describe the characterization of a multi-incident MS family that nominated a rare missense variant (p.G420D) in plasminogen (PLG) as a putative genetic risk fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f159b6d80fdf536b62121bc5446912ef
Autor:
Christina M Lill, Tian Liu, Brit-Maren M Schjeide, Johannes T Roehr, Denis A Akkad, Vincent Damotte, Antonio Alcina, Miguel A Ortiz, Rafa Arroyo, Aitzkoa Lopez de Lapuente, Paul Blaschke, Alexander Winkelmann, Lisa-Ann Gerdes, Felix Luessi, Oscar Fernadez, Guillermo Izquierdo, Alfredo Antigüedad, Sabine Hoffjan, Isabelle Cournu-Rebeix, Silvana Gromöller, Hans Faber, Maria Liebsch, Esther Meissner, Coralie Chanvillard, Emmanuel Touze, Fernando Pico, Philippe Corcia, Thomas Dörner, Elisabeth Steinhagen-Thiessen, Lars Baeckman, Hauke R Heekeren, Shu-Chen Li, Ulman Lindenberger, Andrew Chan, Hans-Peter Hartung, Orhan Aktas, Peter Lohse, Tania Kümpfel, Christian Kubisch, Joerg T Epplen, Uwe K Zettl, Bertrand Fontaine, Koen Vandenbroeck, Fuencisla Matesanz, Elena Urcelay, Lars Bertram, Frauke Zipp
Publikováno v:
Journal of Medical Genetics. 49:558-562
Background Single nucleotide polymorphisms (SNPs) rs429358 (e4) and rs7412 (e2), both invoking changes in the amino-acid sequence of the apolipoprotein E (APOE) gene, have previously been tested for association with multiple sclerosis (MS) risk. Howe
Autor:
Annegrit Schlichting, Denis A. Akkad, Joerg T. Epplen, Regina Kropatsch, Gabriele Dekomien, Elisabeth Petrasch-Parwez, Dominik Seelow, Wanda M. Gerding
Publikováno v:
Molecular and Cellular Probes. 24:357-363
Generalized progressive retinal atrophy (gPRA) belongs to a group of inherited retinal diseases which are associated with gradual vision loss in various dog breeds, including the Irish Glen of Imaal Terrier (GIT). By genome-wide homozygosity mapping