Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and CCR1[original query] |
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Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis. Proceedings of the National Academy of Sciences of the United States of America 2020 6 117 (25): 14405-14411. Manthiram Kalpana, Preite Silvia, Dedeoglu Fatma, Demir Selcan, Ozen Seza, Edwards Kathryn M, Lapidus Sivia, Katz Alexander E, , Feder Henry M, Lawton Maranda, Licameli Greg R, Wright Peter F, Le Julie, Barron Karyl S, Ombrello Amanda K, Barham Beverly, Romeo Tina, Jones Anne, Srinivasalu Hemalatha, Mudd Pamela A, DeBiasi Roberta L, Gül Ahmet, Marshall Gary S, Jones Olcay Y, Chandrasekharappa Settara C, Stepanovskiy Yuriy, Ferguson Polly J, Schwartzberg Pamela L, Remmers Elaine F, Kastner Daniel |
A First Step for the Molecular Characterization of Neurological Involvement of Behçet Syndrome: an Italian Pivotal Study. Journal of molecular neuroscience : MN 2020 11 71 (6): 1284-1289. Padula Maria Carmela, Leccese Pietro, Lascaro Nancy, Padula Angela Anna, Carbone Teresa, Martelli Giuseppe, D'Angelo Salvato |
The rs13075270 and rs13092160 polymorphisms of CCR1 and CCR3 genes on oral aphthous-like lesions in PFAPA syndrome. Cellular and molecular biology (Noisy-le-Grand, France) 2022 Jan 67 (4): 328-333. Li Weiwei, Li Na, Yang Guohai, Li Yanh |
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