Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: KCNK18[original query] |
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Functional analysis of missense variants in the TRESK (KCNK18) K channel. Scientific reports 2012 2 237. Andres-Enguix Isabelle, Shang Lijun, Stansfeld Phillip J, Morahan Julia M, Sansom Mark S P, Lafrenière Ronald G, Roy Bishakha, Griffiths Lyn R, Rouleau Guy A, Ebers George C, Cader Zameel M, Tucker Stephen |
Identification of novel genes involved in migraine. Headache 2012 Oct 52 Suppl 2 107-10. Lafrenière Ronald G, Rouleau Guy |
Association analysis of STX1A gene variants in common forms of migraine. Cephalalgia : an international journal of headache 2012 Feb 32 (3): 203-12. Tropeano Maria, Wöber-Bingöl Ciçek, Karwautz Andreas, Wagner Gudrun, Vassos Evangelos, Campos-de-Sousa Sara, Graggaber Andrea, Zesch Heidi E, Kienbacher Christian, Natriashvili Sofia, Kanbur Incifer, Wöber Christian, Collier David |
Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine case-control cohort. Gene 2013 Jul . Maher BH, Taylor M, Stuart S, Okolicsanyi RK, Roy B, Sutherland HG, Haupt LM, Griffiths LR |
KCNK18 (TRESK) genetic variants in Italian patients with migraine. Headache 2014 Oct 54 (9): 1515-22. Rainero Innocenzo, Rubino Elisa, Gallone Salvatore, Zavarise Paola, Carli Daniela, Boschi Silvia, Fenoglio Pierpaola, Savi Lidia, Gentile Salvatore, Benna Paolo, Pinessi Lorenzo, Dalla Volta Giorg |
Molecular factors in migraine. Oncotarget 2016 May . Kowalska Marta, Prendecki MichaÅ, Kozubski Wojciech, Lianeri Margarita, Dorszewska Jolan |
Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes. Human genomics 2016 10 (1): 3. Domitrz Izabela, Kosiorek Michalina, ?ekanowski Cezary, Kami?ska An |
Analysis of Genetic Variants in SCN1A, SCN2A, KCNK18, TRPA1 and STX1A as a Possible Marker of Migraine. Current genomics 2020 Apr 21 (3): 224-236. Kowalska Marta, Prendecki Micha?, Kapelusiak-Pielok Magdalena, Grzelak Teresa, ?agan-J?drzejczyk Urszula, Wiszniewska Ma?gorzata, Kozubski Wojciech, Dorszewska Jolan |
Study of variants in genes implicated in rare familial migraine syndromes and their association with migraine in 200,000 exome-sequenced UK Biobank participants. Annals of human genetics 2022 8 86 (6): 353-360. Markel Katherine Alexis, Curtis Dav |
Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy. International journal of molecular sciences 2022 11 23 (22): . ?l?czkowska Milena, Almomani Rowida, Marchi Margherita, Salvi Erika, de Greef Bianca T A, Sopacua Maurice, Hoeijmakers Janneke G J, Lindsey Patrick, Waxman Stephen G, Lauria Giuseppe, Faber Catharina G, Smeets Hubert J M, Gerrits Monique |
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- Page last updated:Apr 29, 2024
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