Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and NR1H2[original query] |
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| A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia. BMC medical genetics 2011 12 (1): 145. Mouzat Kevin, Mercier Eric, Polge Anne, Evrard Alexandre, Baron Silvère, Balducchi Jean-Pierre, Brouillet Jean-Paul, Lumbroso Serge, Gris Jean-Christop |
| Genetic analysis of genes involved in amyloid-ß degradation and clearance in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2012 28 (3): 553-9. Natunen Teemu, Helisalmi Seppo, Vepsäläinen Saila, Sarajärvi Timo, Antikainen Leila, Mäkinen Petra, Herukka Sanna-Kaisa, Koivisto Anne Maria, Haapasalo Annakaisa, Soininen Hilkka, Hiltunen Mik |
| Polymorphisms in NF-?B, PXR, LXR, PPAR? and risk of inflammatory bowel disease. World journal of gastroenterology 2011 Jan 17 (2): 197-206. Andersen Vibeke, Christensen Jane, Ernst Anja, Jacobsen Bent A, Tjønneland Anne, Krarup Henrik B, Vogel Ul |
| Associations of cerebrovascular metabolism genotypes with neuropsychiatric symptoms and age at onset of Alzheimer's disease dementia. Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999) 2017 Jan 0. Oliveira Fabricio F de, Chen Elizabeth S, Smith Marilia C, Bertolucci Paulo |
| Host Genetic Variants Linked to COVID-19 Neurological Complications and Susceptibility in Young Adults-A Preliminary Analysis. Journal of personalized medicine 2023 1 13 (1): . Kazantseva Anastasiya, Enikeeva Renata, Takhirova Zalina, Davydova Yuliya, Mustafin Rustam, Malykh Sergey, Karunas Alexandra, Kanapin Alexander, Khusnutdinova El |
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