Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Multiple Sclerosis and L3MBTL3[original query] |
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Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.
![]() Science advances 2016 Jun 2 (6): e1501678. Andlauer Till F M, Buck Dorothea, Antony Gisela, Bayas Antonios, Bechmann Lukas, Berthele Achim, Chan Andrew, Gasperi Christiane, Gold Ralf, Graetz Christiane, Haas Jürgen, Hecker Michael, Infante-Duarte Carmen, Knop Matthias, Kümpfel Tania, Limmroth Volker, Linker Ralf A, Loleit Verena, Luessi Felix, Meuth Sven G, Mühlau Mark, Nischwitz Sandra, Paul Friedemann, Pütz Michael, Ruck Tobias, Salmen Anke, Stangel Martin, Stellmann Jan-Patrick, Stürner Klarissa H, Tackenberg Björn, Then Bergh Florian, Tumani Hayrettin, Warnke Clemens, Weber Frank, Wiendl Heinz, Wildemann Brigitte, Zettl Uwe K, Ziemann Ulf, Zipp Frauke, Arloth Janine, Weber Peter, Radivojkov-Blagojevic Milena, Scheinhardt Markus O, Dankowski Theresa, Bettecken Thomas, Lichtner Peter, Czamara Darina, Carrillo-Roa Tania, Binder Elisabeth B, Berger Klaus, Bertram Lars, Franke Andre, Gieger Christian, Herms Stefan, Homuth Georg, Ising Marcus, Jöckel Karl-Heinz, Kacprowski Tim, Kloiber Stefan, Laudes Matthias, Lieb Wolfgang, Lill Christina M, Lucae Susanne, Meitinger Thomas, Moebus Susanne, Müller-Nurasyid Martina, Nöthen Markus M, Petersmann Astrid, Rawal Rajesh, Schminke Ulf, Strauch Konstantin, Völzke Henry, Waldenberger Melanie, Wellmann Jürgen, Porcu Eleonora, Mulas Antonella, Pitzalis Maristella, Sidore Carlo, Zara Ilenia, Cucca Francesco, Zoledziewska Magdalena, Ziegler Andreas, Hemmer Bernhard, Müller-Myhsok Bertr |
Association of SHMT1, MAZ, ERG, and L3MBTL3 Gene Polymorphisms with Susceptibility to Multiple Sclerosis. Biochemical genetics 2019 Jun 57 (3): 355-370. Nazari Mehrabani Seyede Zahra, Shushizadeh Mohammad Hossein, Abazari Mohammad Foad, Nouri Aleagha Maryam, Ardalan Abbas, Abdollahzadeh Rasoul, Azarnezhad Asa |
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis. Human molecular genetics 2022 1 31 (13): 2155-2163. Alcina Antonio, Fedetz Maria, Vidal-Cobo Isabel, Andrés-León Eduardo, García-Sánchez Maria-Isabel, Barroso-Del-Jesus Alicia, Eichau Sara, Gil-Varea Elia, Luisa-Maria Villar , Saiz Albert, Leyva Laura, Vandenbroeck Koen, Otaegui David, Izquierdo Guillermo, Comabella Manuel, Urcelay Elena, Matesanz Fuencis |
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