Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 12 (of 12 Records) |
Query Trace: Pure Red Cell Aplasia[original query] |
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The association of anti-r-HuEpo-associated pure red cell aplasia with HLA-DRB1*09-DQB1*0309. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2009 May 24 (5): 1545-9. Praditpornsilpa Kearkiat, Kupatawintu Pawinee, Mongkonsritagoon Wichean, Supasyndh Ouppatham, Jootar Saengsuree, Intarakumthornchai Tanin, Pongskul Cholatip, Prasithsirikul Wisit, Achavanuntakul Bunlersak, Ruangkarnchanasetr Prajej, Laohavinij Sudsawat, Eiam-Ong Somch |
Case-control study of the association between select HLA genes and anti-erythropoietin antibody-positive pure red-cell aplasia. Pharmacogenomics 2008 Feb 9 (2): 157-67. Fijal Bonnie, Ricci Deborah, Vercammen Els, Palmer Peter A, Fotiou Fotis, Fife Daniel, Lindholm Anders, Broderick Erin, Francke Stephan, Wu Xiaodong, Colaianne James, Cohen Nadi |
STAT3 gene mutations and their association with pure red cell aplasia in large granular lymphocyte leukemia. Cancer science 2014 Mar 105 (3): 342-6. Ishida Fumihiro, Matsuda Kazuyuki, Sekiguchi Nodoka, Makishima Hideki, Taira Chiaki, Momose Kayoko, Nishina Sayaka, Senoo Noriko, Sakai Hitoshi, Ito Toshiro, Kwong Yok-L |
STAT3 mutations are frequent in T-cell large granular lymphocytic leukemia with pure red cell aplasia. Journal of hematology & oncology 2013 6 (1): 82. Qiu Zhi-Yuan, Fan Lei, Wang Li, Qiao Chun, Wu Yu-Jie, Zhou Jian-Feng, Xu Wei, Li Jian-Yo |
A cluster of Epoetin-associated pure red cell aplasia: clinical features and the possible association of HLA-DRB1*12:02. Pharmacogenomics 2016 Jun . Tan Chuen Wen, Tan-Koi Wei-Chuen, Ng Jennifer, Chan Choong Meng, Hwang William Ying Kh |
Cell size variations of large granular lymphocyte leukemia: Implication of a small cell subtype of granular lymphocyte leukemia with STAT3 mutations. Leukemia research 2016 Apr 45 8-13. Tanahashi Takahiro, Sekiguchi Nodoka, Matsuda Kazuyuki, Takezawa Yuka, Ito Toshiro, Kobayashi Hikaru, Ichikawa Naoaki, Nishina Sayaka, Senoo Noriko, Sakai Hitoshi, Nakazawa Hideyuki, Ishida Fumihi |
Identification of mutations in patients with acquired pure red cell aplasia. Acta biochimica et biophysica Sinica 2018 5 50 (7): 685-692. Zhang Xinchao, Shi Yi, Song Lingjun, Shen Chang, Cai Qi, Zhang Zhou, Wu Jun, Fu Guohui, Shen Weiw |
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 |
Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2). The Journal of allergy and clinical immunology 2020 1 145 (6): 1664-1672.e10. Lee Pui Y, Kellner Erinn S, Huang Yuelong, Furutani Elissa, Huang Zhengping, Bainter Wayne, Alosaimi Mohammed F, Stafstrom Kelsey, Platt Craig D, Stauber Tali, Raz Somech, Tirosh Irit, Weiss Aaron, Jordan Michael B, Krupski Christa, Eleftheriou Despina, Brogan Paul, Sobh Ali, Baz Zeina, Lefranc Gerard, Irani Carla, Kilic Sara S, El-Owaidy Rasha, Lokeshwar M R, Pimpale Pallavi, Khubchandani Raju, Chambers Eugene P, Chou Janet, Geha Raif S, Nigrovic Peter A, Zhou Qi |
The Glucocorticoid Receptor Polymorphism Landscape in Patients With Diamond Blackfan Anemia Reveals an Association Between Two Clinically Relevant Single Nucleotide Polymorphisms and Time to Diagnosis. Frontiers in physiology 2021 12 745032. Lonetti Annalisa, Indio Valentina, Dianzani Irma, Ramenghi Ugo, Da Costa Lydie, Pospíšilová Dagmar, Migliaccio Anna Ri |
Clonal hematopoiesis in adult pure red cell aplasia. Scientific reports 2021 1 11 (1): 2253. Fujishima Naohito, Kohmaru Junki, Koyota Souichi, Kuba Keiji, Saga Tomoo, Omokawa Ayumi, Moritoki Yuki, Ueki Shigeharu, Ishida Fumihiro, Nakao Shinji, Matsuda Akira, Ohta Akiko, Tohyama Kaoru, Yamasaki Hiroshi, Usuki Kensuke, Nakashima Yasuhiro, Sato Shinya, Miyazaki Yasushi, Nannya Yasuhito, Ogawa Seishi, Sawada Kenichi, Mitani Kinuko, Hirokawa Mako |
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 |
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