Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: TRPM3[original query] |
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Association of TRPM Channel Gene Polymorphisms with Systemic Sclerosis. In vivo (Athens, Greece) 0 29 (6): 763-770. Oztuzcu Serdar, Onat Ahmet M, Pehlivan Yavuz, Alibaz-Oner Fatma, Donmez Salim, Cetin Gozde Y, Yolbas Servet, Bozgeyik Ibrahim, Yilmaz Neslihan, Ozgen Metin, Cagatay Yonca, Kisacik Bunyamin, Koca Suleyman S, Pamuk Omer Nuri, Sayarlioglu Mehmet, Direskeneli Haner, Demiryurek Abdullah |
Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/chronic fatigue syndrome. The application of clinical genetics 2016 9 39-47. Marshall-Gradisnik Sonya, Huth Teilah, Chacko Anu, Johnston Samantha, Smith Pete, Staines Dona |
Association of TRPM3 Polymorphism (rs10780946) and Aspirin-Exacerbated Respiratory Disease (AERD). Lung 2016 Feb . Narayanankutty Arun, Palma-Lara Icela, Pavón-Romero Gandhi, Pérez-Rubio Gloria, Camarena Ángel, Teran Luis M, Falfán-Valencia Ramc |
Single nucleotide polymorphisms and genotypes of transient receptor potential ion channel and acetylcholine receptor genes from isolated B lymphocytes in myalgic encephalomyelitis/chronic fatigue syndrome patients. The Journal of international medical research 2016 Nov . Marshall-Gradisnik Sonya, Johnston Samantha, Chacko Anu, Nguyen Thao, Smith Peter, Staines Dona |
Differences in somatic mutation landscape of hepatocellular carcinoma in Asian American and European American populations. Oncotarget 2016 May . Yao Song, Johnson Christopher, Hu Qiang, Yan Li, Liu Biao, Ambrosone Christine B, Wang Jianmin, Liu So |
Genome-Wide Association Study Reveals Distinct Genetic Susceptibility of Thyroid Nodules From Thyroid Cancer.
The Journal of clinical endocrinology and metabolism 2018 Aug . Hwangbo Yul, Lee Eun Kyung, Son Ho-Young, Im Sun-Wha, Kwak Soo-Jung, Yoon Ji Won, Kim Min Joo, Kim Jeongseon, Choi Hoon Sung, Ryu Chang Hwan, Lee You Jin, Kim Jong-Il, Cho Nam H, Park Young J |
Genetic variation of the gene coding for microRNA-204 (miR-204) is a risk factor in acute myeloid leukaemia. BMC cancer 2018 01 18 (1): 107. Butrym Aleksandra, ?acina Piotr, Kuliczkowski Kazimierz, Bogunia-Kubik Katarzyna, Mazur Grzego |
A novel candidate gene in autosomal dominant facial pruritus. Clinical and experimental dermatology 2021 8 47 (1): 184-186. Thompson B A, Dear K, Donaldson E, Nixon R, Winship I |
Association of protein function-altering variants with cardiometabolic traits: the strong heart study. Scientific reports 2022 Jun 12 (1): 9317. Shan Yue, Cole Shelley A, Haack Karin, Melton Phillip E, Best Lyle G, Bizon Christopher, Kobes Sayuko, Köro?lu Çi?dem, Baier Leslie J, Hanson Robert L, Sanna Serena, Li Yun, Franceschini No |
De novo TRPM3 missense variant associated with neurodevelopmental delay and manifestations of cerebral palsy. Cold Spring Harbor molecular case studies 2023 9 . Jagadish Chandrabose Sundaramurthi, Anita M Bagley, Hannah Blau, Leigh Carmody, Amy Crandall, Daniel Danis, Michael Gargano, Anxhela Gjyshi Gustafson, Ellen M Raney, Mallory Shingle, Jon R Davids, Peter N Robins |
Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Frontiers in nutrition 2023 4 10 1040993. Buckner Teresa, Johnson Randi K, Vanderlinden Lauren A, Carry Patrick M, Romero Alex, Onengut-Gumuscu Suna, Chen Wei-Min, Kim Soojeong, Fiehn Oliver, Frohnert Brigitte I, Crume Tessa, Perng Wei, Kechris Katerina, Rewers Marian, Norris Jill |
Prognostic and immunological significance of calcium-related gene signatures in renal clear cell carcinoma. Frontiers in pharmacology 2023 1 13 1055841. Liu An, Li Fei, Wang Bao, Yang Le, Xing Hai, Su Chang, Gao Li, Zhao Minggao, Luo Lanx |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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