Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Abnormalities and STAT3[original query] |
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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 |
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 |
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 |
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 |
[Genetic analysis and its clinical implication in adult T-cell leukemia/lymphoma]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2018 10 59 (10): 2127-2135. Kogure Yasunori, Kataoka Keisu |
IL6R-STAT3-ADAR1 (P150) interplay promotes oncogenicity in multiple myeloma with 1q21 amplification. Haematologica 2019 8 105 (5): 1391-1404. Teoh Phaik Ju, Chung Tae-Hoon, Chng Pamela Y Z, Toh Sabrina H M, Chng Wee J |
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 Marlène, Abou Chahla Wadih, Barlogis Vincent, Bertrand Yves, Pellier Isabelle, Colomb Bottollier 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 Frédéric, |
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 |
Characteristics of genetic alterations of peripheral T-cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG). British journal of haematology 2021 7 194 (4): 718-729. Ohki Kentaro, Kiyokawa Nobutaka, Watanabe Satoru, Iwafuchi Hideto, Nakazawa Astuko, Ishiwata Keisuke, Ogata-Kawata Hiroko, Nakabayashi Kazuhiko, Okamura Kohji, Tanaka Fumiko, Fukano Reiji, Hata Kenichiro, Mori Tetsuya, Moriya Saito Akiko, Hayashi Yasuhide, Taga Takashi, Sekimizu Masahiro, Kobayashi Ryoji, |
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 |
T cell clonal expansion and STAT3 mutations: a characteristic feature of acquired chronic T cell-mediated pure red cell aplasia. International journal of hematology 2022 3 115 (6): 816-825. Kawakami Fumihiro, Kawakami Toru, Yamane Taku, Maruyama Masae, Kobayashi Jun, Nishina Sayaka, Sakai Hitoshi, Higuchi Yumiko, Hamanaka Kazutoshi, Hirokawa Makoto, Nakao Shinji, Nakazawa Hideyuki, Ishida Fumihi |
The genetic polymorphisms of immune-related genes contribute to the susceptibility and survival of lymphoma. Cancer medicine 2023 6 . Chaoyang Gu, Can Can, Jinting Liu, Yihong Wei, Xinyu Yang, Xiaodong Guo, Ruiqing Wang, Wenbo Jia, Wancheng Liu, Daoxin |
Genetic diagnosis of inborn errors of immunity using clinical exome sequencing. Frontiers in immunology 2023 6 14 1178582. Soon Sung Kwon, Youn Keong Cho, Seungmin Hahn, Jiyoung Oh, Dongju Won, Saeam Shin, Ji-Man Kang, Jong Gyun Ahn, Seung-Tae Lee, Jong Rak Ch |
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- Page last updated:Apr 16, 2024
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