Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Disease Susceptibility and FOXP3[original query] |
---|
FoxP3 rs3761548 polymorphism predicts autoimmune disease susceptibility: a meta-analysis. Human immunology 2013 Aug . He Y, Huang N, Li Y, Qiu Z, Li W |
Association of aplastic anemia and FoxP3 gene polymorphisms in Koreans. Hematology (Amsterdam, Netherlands) 2016 Oct 1-6. In Ji Won, Lee Nuri, Roh Eun Youn, Shin Sue, Park Kyoung Un, Song Eun You |
Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis. Human antibodies 2016 Oct . Eftekharian Mohammad Mahdi, Sayad Arezou, Omrani Mir Davood, Ghannad Masoud Sabouri, Noroozi Rezvan, Mazdeh Mehrdokht, Mirfakhraie Reza, Movafagh Abolfazl, Roshanaei Ghodratollah, Azimi Tahereh, Inoko Hidetoshi, Taheri Mohamm |
FOXP3, ICOS and ICOSL gene polymorphisms in systemic sclerosis: FOXP3 rs2294020 is associated with disease progression in a female Italian population. Immunobiology 2017 Oct . D'Amico Fabio, Fiorito Giovanni, Skarmoutsou Evangelia, Granata Mariagrazia, Rossi Giulio A, Trovato Chiara, Bellocchi Chiara, Marchini Maurizio, Beretta Lorenzo, Mazzarino Maria Clorin |
Genetic variations in the TLR3 locus are associated with eosinophilic esophagitis. United European gastroenterology journal 2018 Apr 6 (3): 349-357. Ávila-Castellano Robledo, García-Lozano José-Raúl, Cimbollek Stefan, Lucendo Alfredo J, Bozada Juan-Manuel, Quiralte Joaqu |
Immunorelated gene polymorphisms associated with acute myeloid leukemia. Clinical and experimental immunology 2020 Apr . Liu Q, Hua M, Yan S, Zhang C, Wang R, Yang X, Han F, Hou M, Ma |
FOXP3 Gene Variants in Patients with Systemic Lupus Erythematosus: Association with Disease Susceptibility in Men and Relationship with Abortion in Women. Iranian journal of immunology : IJI 2022 Jun 19 (2): 5. Heydarinejad Paria, Gholijani Nasser, Habibagahi Zahra, Malekmakan Mohammad Reza, Amirghofran Zah |
- Page last reviewed:Feb 1, 2024
- Content source: