Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Syndrome and STAT3[original query] |
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| STAT3 single-nucleotide polymorphisms and STAT3 mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma families. European journal of human genetics : EJHG 2009 Mar 17 (3): 352-6. Wjst Matthias, Lichtner Peter, Meitinger Thomas, Grimbacher Bo |
| Dietary saturated fat modulates the association between STAT3 polymorphisms and abdominal obesity in adults. The Journal of nutrition 2009 Nov 139 (11): 2011-7. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Field Martyn R, Peloso Gina M, Shen Jian, McManus Ross, Hercberg Serge, Lairon Denis, Planells Richard, Roche Helen |
| 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 |
| STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility. Genes and immunity 2010 Apr 11 (3): 264-8. Cénit M C, Alcina A, Márquez A, Mendoza J L, Díaz-Rubio M, de las Heras V, Izquierdo G, Arroyo R, Fernández O, de la Concha E G, Matesanz F, Urcelay |
| GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation. Journal of hepatology 2012 Jan 56 (1): 184-91. Nault Jean Charles, Fabre Monique, Couchy Gabrielle, Pilati Camilla, Jeannot Emmanuelle, Tran Van Nhieu Jeanne, Saint-Paul Marie-Christine, De Muret Anne, Redon Marie-José, Buffet Catherine, Salenave Sylvie, Balabaud Charles, Prevot Sophie, Labrune Philippe, Bioulac-Sage Paulette, Scoazec Jean-Yves, Chanson Philippe, Zucman-Rossi Jessi |
| 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 |
| JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population. Investigative ophthalmology & visual science 2013 May 54 (5): 3360-5. Hu Ke, Hou Shengping, Li Fuzhen, Xiang Qin, Kijlstra Aize, Yang Peize |
| Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation. The Journal of allergy and clinical immunology 2013 Dec 132 (6): 1388-96. Siegel Andrea M, Stone Kelly D, Cruse Glenn, Lawrence Monica G, Olivera Ana, Jung Mi-yeon, Barber John S, Freeman Alexandra F, Holland Steven M, O'Brien Michelle, Jones Nina, Nelson Celeste G, Wisch Laura B, Kong Heidi H, Desai Avanti, Farber Orly, Gilfillan Alasdair M, Rivera Juan, Milner Joshua |
| Molecular Genetic Advances in Uveitis. Progress in molecular biology and translational science 2015 134 283-98. Hou Shengping, Kijlstra Aize, Yang Peize |
| Functional characterization of two new STAT3 mutations associated with hyper-IgE syndrome in a Mexican cohort. Clinical genetics 2015 Aug . Alcántara-Montiel Julio C, Staines-Boone Tamara, López-Herrera Gabriela, Espinosa-Rosales Francisco, Espinosa-Padilla Sara E, Hernández-Rivas Rosaura, Santos-Argumedo Leopol |
| TH17 Cells in STAT3 Related Hyper-IgE Syndrome. Indian journal of pediatrics 2016 May . Sharma Sudha, Saikia Biman, Goel Shubham, Rawat Amit, Minz Ranjana W, Suri Deepti, Chhabra Seema, Singh Surj |
| Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency. The Journal of allergy and clinical immunology 2017 9 141 (4): 1450-1458. Abolhassani Hassan, Chou Janet, Bainter Wayne, Platt Craig D, Tavassoli Mahmood, Momen Tooba, Tavakol Marzieh, Eslamian Mohammad Hossein, Gharagozlou Mohammad, Movahedi Masoud, Ghadami Mohsen, Hamidieh Amir Ali, Azizi Gholamreza, Yazdani Reza, Afarideh Mohsen, Ghajar Alireza, Havaei Arash, Chavoshzadeh Zahra, Mahdaviani Seyed Alireza, Cheraghi Taher, Behniafard Nasrin, Amin Reza, Aleyasin Soheila, Faridhosseini Reza, Jabbari-Azad Farahzad, Nabavi Mohammamd, Bemanian Mohammad Hassan, Arshi Saba, Molatefi Rasol, Sherkat Roya, Mansouri Mahboubeh, Mesdaghi Mehrnaz, Babaie Delara, Mohammadzadeh Iraj, Ghaffari Javad, Shafiei Alireza, Kalantari Najmeddin, Ahanchian Hamid, Khoshkhui Maryam, Soheili Habib, Dabbaghzadeh Abbas, Shirkani Afshin, Nasiri Kalmarzi Rasoul, Mortazavi Seyed Hamidreza, Tafaroji Javad, Khalili Abbas, Mohammadi Javad, Negahdari Babak, Joghataei Mohammad-Taghi, Al-Ramadi Basel K, Picard Capucine, Parvaneh Nima, Rezaei Nima, Chatila Talal A, Massaad Michel J, Keles Sevgi, Hammarström Lennart, Geha Raif S, Aghamohammadi Asgh |
| Somatic STAT3 mutations in Felty syndrome: an implication for a common pathogenesis with large granular lymphocyte leukemia. Haematologica 2017 Dec . Savola Paula, Brück Oscar, Olson Thomas, Kelkka Tiina, Kauppi Markku J, Kovanen Panu E, Kytölä Soili, Sokka-Isler Tuulikki, Loughran Thomas P, Leirisalo-Repo Marjatta, Mustjoki Sa |
| Th17 pathway signatures in a large Indian cohort of Guillain Barré syndrome. Journal of neuroimmunology 2018 Oct 323 125-130. Debnath Monojit, Nagappa Madhu, Subbanna Manjula, Sundaravadivel Pandarisamy, Talukdar Pinku Mani, Shivakumar Venkataram, Wahatule Rahul, Dutta Debprasad, Binukumar B, Sinha Sanjib, Bindu Parayil Sankaran, Periyavan Sundar, Umamaheswara Rao G S, Taly Arun |
| Frequent STAT3 mutations in CD8 T cells from patients with pure red cell aplasia. Blood advances 2018 10 2 (20): 2704-2712. Kawakami Toru, Sekiguchi Nodoka, Kobayashi Jun, Imi Tatsuya, Matsuda Kazuyuki, Yamane Taku, Nishina Sayaka, Senoo Yasushi, Sakai Hitoshi, Ito Toshiro, Koizumi Tomonobu, Hirokawa Makoto, Nakao Shinji, Nakazawa Hideyuki, Ishida Fumihi |
| Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations. Clinical immunology (Orlando, Fla.) 2018 1 188 52-57. Besnard Caroline, Levy Eva, Aladjidi Nathalie, Stolzenberg Marie-Claude, Magerus-Chatinet Aude, Alibeu Olivier, Nitschke Patrick, Blanche Stéphane, Hermine Olivier, Jeziorski Eric, Landman-Parker Judith, Leverger Guy, Mahlaoui Nizar, Michel Gérard, Pellier Isabelle, Suarez Felipe, Thuret Isabelle, de Saint-Basile Geneviève, Picard Capucine, Fischer Alain, Neven Bénédicte, Rieux-Laucat Frédéric, Quartier Pierre, |
| 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, |
| Analysis of a single-institution cohort of patients with Felty's syndrome and T-cell large granular lymphocytic leukemia in the setting of rheumatoid arthritis. Rheumatology international 2020 12 41 (1): 147-156. Gorodetskiy Vadim Romanovich, Sidorova Yulia Vladimirovna, Kupryshina Natalia Alexandrovna, Vasilyev Vladimir Ivanovich, Probatova Natalya Alexandrovna, Ryzhikova Natalya Valerievna, Sudarikov Andrey Borisovi |
| Innate immune response analysis in COVID-19 and kawasaki disease reveals MIS-C predictors. Journal of the Formosan Medical Association = Taiwan yi zhi 2021 7 121 (3): 623-632. Yang Chin-An, Huang Ya-Ling, Chiang Bor-Lu |
| Molecular Analysis of the Kidney From a Patient With COVID-19-Associated Collapsing Glomerulopathy. Kidney medicine 2021 5 3 (4): 653-658. Meliambro Kristin, Li Xuezhu, Salem Fadi, Yi Zhengzi, Sun Zeguo, Chan Lili, Chung Miriam, Chancay Jorge, Vy Ha My T, Nadkarni Girish, Wong Jenny S, Fu Jia, Lee Kyung, Zhang Weijia, He John C, Campbell Kirk |
| Exome Sequencing of 21 Bardet-Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians. Obesity (Silver Spring, Md.) 2021 2 29 (4): 748-754. Day Samantha E, Muller Yunhua L, Koroglu Cigdem, Kobes Sayuko, Wiedrich Kim, Mahkee Darin, Kim Hye In, Van Hout Cris, Gosalia Nehal, Ye Bin, , Shuldiner Alan R, Knowler William C, Hanson Robert L, Bogardus Clifton, Baier Leslie |
| Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3. Journal of clinical immunology 2021 1 41 (4): 780-790. Tanita Kay, Sakura Fumiaki, Nambu Ryusuke, Tsumura Miyuki, Imanaka Yusuke, Ohnishi Hidenori, Kato Zenichiro, Pan Jie, Hoshino Akihiro, Suzuki Koji, Yasutomi Motoko, Umetsu Shuichiro, Okada Chizuru, Takagi Masatoshi, Imai Kohsuke, Ohara Osamu, Muise Alexo M, Okada Satoshi, Morio Tomohiro, Kanegane Hiroka |
| HELQ and EGR3 expression correlate with IGHV mutation status and prognosis in chronic lymphocytic leukemia. Journal of translational medicine 2021 1 19 (1): 42. Guo Chao, Gao Ya-Yue, Ju Qian-Qian, Zhang Chun-Xia, Gong Ming, Li Zhen-Li |
| Clinical Study of the Relationship between Sjögren Syndrome and T-Cell Large Granular Lymphocytic Leukemia: Single-Center Experience. International journal of molecular sciences 2022 11 23 (21): . Gorodetskiy Vadim, Vasilyev Vladimir, Sidorova Yulia, Biderman Bella, Kupryshina Natalia, Vagida Murad, Ryzhikova Natalya, Sudarikov Andr |
| Prevalence of STAT3 mutations in patients with rheumatoid arthritis-associated T-cell large granular lymphocytic leukaemia and Felty syndrome. Clinical and experimental rheumatology 2023 7 . Vadim Gorodetskiy, Yulia Sidorova, Bella Biderman, Natalya Ryzhikova, Vladimir Vasilyev, Andrey Sudarik |
| Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the literature. Molecular genetics & genomic medicine 2023 3 e2166. Buki Gergely, Szalai Renata, Pinter Adrienn, Hadzsiev Kinga, Melegh Bela, Rauch Tibor, Bene Jud |
| Autoimmunity-Associated SNP rs3024505 Disrupts STAT3 Binding in B Cells, Leading to IL10 Dysregulation. International journal of molecular sciences 2024 9 25 (18): . Aksinya N Uvarova, Elina A Zheremyan, Alina S Ustiugova, Matvey M Murashko, Elvina A Bogomolova, Denis E Demin, Ekaterina M Stasevich, Dmitry V Kuprash, Kirill V Korne |
| Gamma-delta T-cell large granular lymphocytic leukemia in the setting of rheumatologic diseases. Frontiers in cell and developmental biology 2024 8 12 1434676. Vadim Gorodetskiy, Yulia Sidorova, Bella Biderman, Natalia Kupryshina, Natalya Ryzhikova, Andrey Sudarik |
- Page last reviewed:Feb 1, 2024
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