HuGE Literature Finder
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| Association of JAK/STAT genetic variants with cutaneous melanoma. Frontiers in oncology 2022 12 943483. Gomez Gabriela Vilas Bôas, Lourenço Gustavo Jacob, Monteiro Lummy Maria Oliveira, Rocha Rafael Silva, Fernández Kimberly Anne McGrail, Recio Juan Angel, Torricelli Caroline, Coser Lilian Oliveira, Oliveira Alexandre Leite Rodrigues, Carron Juliana, Moraes Aparecida Machado, Lima Carmen Silvia Pass |
| Immunorelated gene polymorphisms associated with acute myeloid leukemia. Clinical and experimental immunology 2020 Apr . Liu Qinqin, Hua Mingqiang, Yan Shuxin, Zhang Chen, Wang Ruiqing, Yang Xinyu, Han Fengjiao, Hou Ming, Ma Daox |
| Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes. Blood 2019 Apr . Hadjadj Jérôme, Aladjidi Nathalie, Fernandes Helder, Leverger Guy, Magérus-Chatinet Aude, Mazerolles Fabienne, Stolzenberg Marie-Claude, Jacques Sidonie, Picard Capucine, Rosain Jérémie, Fourrage Cécile, Hanein Sylvain, Zarhrate Mohammed, Pasquet Marléne, Abou Chahla Wadih, Barlogis Vincent, Bertrand Yves, Pellier Isabelle, Bottolier Lemallaz Elodie, Fouyssac Fanny, Blouin Pascale, Thomas Caroline, Cheikh Nathalie, Dore Eric, Pondarre Corinne, Plantaz Dominique, Jeziorski Eric, Millot Frédéric, Garcelon Nicolas, Ducassou Stéphane, Perel Yves, Leblanc Thierry, Neven Bénédicte, Fischer Alain, Rieux-Laucat Frédér |
| STAT3 mutations indicate the presence of subclinical T-cell clones in a subset of aplastic anemia and myelodysplastic syndrome patients. Blood 2013 Oct 122 (14): 2453-9. Jerez Andres, Clemente Michael J, Makishima Hideki, Rajala Hanna, Gómez-Seguí Ines, Olson Thomas, McGraw Kathy, Przychodzen Bartlomiej, Kulasekararaj Austin, Afable Manuel, Husseinzadeh Holleh D, Hosono Naoko, LeBlanc Francis, Lagström Sonja, Zhang Dan, Ellonen Pekka, Tichelli André, Nissen Catherine, Lichtin Alan E, Wodnar-Filipowicz Aleksandra, Mufti Ghulam J, List Alan F, Mustjoki Satu, Loughran Thomas P, Maciejewski Jaroslaw |
| Paucity of genotype-phenotype correlations in STAT3 mutation positive Hyper IgE Syndrome (HIES). Clinical immunology (Orlando, Fla.) 2011 Apr 139 (1): 75-84. Heimall Jennifer, Davis Joie, Shaw Pamela A, Hsu Amy P, Gu Wenjuan, Welch Pam, Holland Steven M, Freeman Alexandra |
| Reduced appetite and body mass index with delayed puberty in a mother and son: association with a rare novel sequence variant in the leptin gene. European journal of endocrinology / European Federation of Endocrine Societies 2011 Apr 164 (4): 521-7. Murray P G, Read A, Banerjee I, Whatmore A J, Pritchard L E, Davies R A, Brennand J, White A, Ross R J, Clayton P |
| Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome. The Journal of allergy and clinical immunology 2009 Aug 124 (2): 342-8, 348.e1-5. Al Khatib Shadi, Keles Sevgi, Garcia-Lloret Maria, Karakoc-Aydiner Elif, Reisli Ismail, Artac Hasibe, Camcioglu Yildiz, Cokugras Haluk, Somer Ayper, Kutukculer Necil, Yilmaz Mustafa, Ikinciogullari Aydan, Yegin Olcay, Yüksek Mutlu, Genel Ferah, Kucukosmanoglu Ercan, Baki Ali, Bahceciler Nerin N, Rambhatla Anupama, Nickerson Derek W, McGhee Sean, Barlan Isil B, Chatila Tal |
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- Page last updated:Jan 26, 2023
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