Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and STX1A[original query] |
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| Search for genetic variants of the SYNTAXIN 1A (STX1A) gene: the -352 A>T variant in the STX1A promoter associates with impaired glucose metabolism in an Italian obese population. International journal of obesity (2005) 2008 Mar 32 (3): 413-20. Romeo S, Sentinelli F, Cavallo M G, Leonetti F, Fallarino M, Mariotti S, Baroni M |
| Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A. European journal of human genetics : EJHG 2013 Dec 21 (12): 1462-6. von Kanel Thomas, Stanke Frauke, Weber Melanie, Schaller Andre, Racine Julien, Kraemer Richard, Chanson Marc, Tümmler Burkhard, Gallati Sabi |
| Molecular factors in migraine. Oncotarget 2016 May . Kowalska Marta, Prendecki MichaÅ, Kozubski Wojciech, Lianeri Margarita, Dorszewska Jolan |
| SNARE Complex Polymorphisms Associate with Alterations of Visual Selective Attention in Alzheimer's Disease. Journal of Alzheimer's disease : JAD 2019 Apr . Costa Andrea Saul, Guerini Franca Rosa, Arosio Beatrice, Galimberti Daniela, Zanzottera Milena, Bianchi Anna, Nemni Raffaello, Clerici Mar |
| 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 |
| Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility. The journal of headache and pain 2023 6 24 (1): 78. Daniela Felício, Andreia Dias, Sandra Martins, Estefânia Carvalho, Alexandra M Lopes, Nádia Pinto, Carolina Lemos, Mariana Santos, Miguel Alves-Ferrei |
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