Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: RARS[original query] |
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High incidence of hemochromatosis gene mutations in the myelodysplastic syndrome: the Budapest Study on 50 patients. Acta haematologica 2003 109 (2): 64-7. Várkonyi Judit, Tarkovács Gábor, Karádi István, Andrikovics Hajnalka, Varga Ferenc, Varga Fatime, Demeter Judit, Tordai Atti |
Structural variants in the retinoid receptor genes in patients with schizophrenia and other psychiatric diseases. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005 Feb 133B (1): 50-3. Feng Jinong, Chen Jiesheng, Yan Jin, Jones Ian R, Craddock Nick, Cook Edwin H, Goldman David, Heston Leonard L, Sommer Steve |
Hemochromatosis-associated gene mutations in patients with myelodysplastic syndromes with refractory anemia with ringed sideroblasts. American journal of hematology 2007 Dec 82 (12): 1076-9. Nearman Zachary P, Szpurka Hadrian, Serio Bianca, Warshawksy Ilka, Theil Karl, Lichtin Alan, Sekeres Mikkael A, Maciejewski Jaroslaw |
A comparative study of molecular mutations in 381 patients with myelodysplastic syndrome and in 4130 patients with acute myeloid leukemia. Haematologica 2007 Jun 92 (6): 744-52. Bacher Ulrike, Haferlach Torsten, Kern Wolfgang, Haferlach Claudia, Schnittger Susan |
Connexin 26 and 30 genes mutations in patients with chronic rhinosinusitis. The Laryngoscope 2008 Feb 118 (2): 310-3. BuSaba Nicolas Y, Cunningham Michael |
JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Haematologica 2008 Jan 93 (1): 34-40. Schmitt-Graeff Annette H, Teo Soon-Siong, Olschewski Manfred, Schaub Franz, Haxelmans Sabine, Kirn Andreas, Reinecke Petra, Germing Ulrich, Skoda Radek |
Abnormal expression of C3ORF9 gene in patients with myelodysplastic syndromes. International journal of immunopathology and pharmacology 0 22 (3): 787-93. Karadonta A-V, Alexandrakis M G, Kourelis T V, Manola A, Garlemou K, Stathakis N E, Kyriakou |
JAK2 V617F mutation in myelodysplastic syndrome, myelodysplastic syndrome/myeloproliferative neoplasm, unclassifiable, refractory anemia with ring sideroblasts with thrombocytosis, and acute myeloid leukemia. The Korean journal of hematology 2010 Mar 45 (1): 46-50. Jekarl Dong Wook, Han Sang Bong, Kim Myungshin, Lim Jihyang, Oh Eun-Jee, Kim Yonggoo, Kim Hee-Je, Min Woo-Sung, Han Kyung |
Acquired mutation of the tyrosine kinase JAK2V617F in Egyptian patients with myeloid disorders. Genetic testing and molecular biomarkers 0 15 (1-2): 17-21. Ayad Mona Wagdy, Nafea Dal |
Association of retinoic acid receptor genes with meningomyelocele. Birth defects research. Part A, Clinical and molecular teratology 2011 Jan 91 (1): 39-43. Tran Phong X, Au Kit Sing, Morrison Alanna C, Fletcher Jack M, Ostermaier Kathryn K, Tyerman Gayle H, Northrup Ho |
High frequency of human leukocyte antigen class II DRB1*1602 haplotype in Greek patients with myelodysplastic syndrome and of DRB1*1501 in the low-risk subgroup. Human immunology 2012 Mar 73 (3): 278-81. Kritikou-Griva Elpiniki, Spyropoulou-Vlachou Maria, Tsagarakis Nikolaos J, Goumakou Eleni, Vrani Vasiliki, Galanopoulos Athanasios, Papadhimitriou Stefanos I, Androutsos George, Paterakis George, Stavropoulos-Giokas Catheri |
Age, JAK2(V617F) and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis. Leukemia 2013 Sep 27 (9): 1826-31. Broséus J, Alpermann T, Wulfert M, Florensa Brichs L, Jeromin S, Lippert E, Rozman M, Lifermann F, Grossmann V, Haferlach T, Germing U, Luño E, Girodon F, Schnittger S, |
Clinical significance of SF3B1 mutations in Korean patients with myelodysplastic syndromes and myelodysplasia/myeloproliferative neoplasms with ring sideroblasts. Annals of hematology 2014 Apr 93 (4): 603-8. Seo Ja Young, Lee Ki-O, Kim Sun-Hee, Kim Kihyun, Jung Chul Won, Jang Jun Ho, Kim Hee-J |
SF3B1 mutations in patients with myelodysplastic syndromes: the mutation is stable during disease evolution. American journal of hematology 2014 Aug 89 (8): E109-15. Lin Chien-Chin, Hou Hsin-An, Chou Wen-Chien, Kuo Yuan-Yeh, Wu Shang-Ju, Liu Chieh-Yu, Chen Chien-Yuan, Tseng Mei-Hsuan, Huang Chi-Fei, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Huang Shang-Yi, Hsu Szu-Chun, Ko Bor-Sheng, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
Potentially functional polymorphisms in aminoacyl-tRNA synthetases genes are associated with breast cancer risk in a Chinese population. Molecular carcinogenesis 2015 Jul 54 (7): 577-83. He Yisha, Gong Jianhang, Wang Yanru, Qin Zhenzhen, Jiang Yue, Ma Hongxia, Jin Guangfu, Chen Jiaping, Hu Zhibin, Guan Xiaoxiang, Shen Hongbi |
Deregulation of genes related to iron and mitochondrial metabolism in refractory anemia with ring sideroblasts. PloS one 2015 10 (5): e0126555. del Rey Mónica, Benito Rocío, Fontanillo Celia, Campos-Laborie Francisco J, Janusz Kamila, Velasco-Hernández Talía, Abáigar María, Hernández María, Cuello Rebeca, Borrego Daniel, Martín-Zanca Dionisio, De Las Rivas Javier, Mills Ken I, Hernández-Rivas Jesús |
SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts. Blood 2015 Jul 126 (2): 233-41. Malcovati Luca, Karimi Mohsen, Papaemmanuil Elli, Ambaglio Ilaria, Jädersten Martin, Jansson Monika, Elena Chiara, Gallì Anna, Walldin Gunilla, Della Porta Matteo G, Raaschou-Jensen Klas, Travaglino Erica, Kallenbach Klaus, Pietra Daniela, Ljungström Viktor, Conte Simona, Boveri Emanuela, Invernizzi Rosangela, Rosenquist Richard, Campbell Peter J, Cazzola Mario, Hellström Lindberg E |
Clinical Evaluation of Cisplatin Sensitivity of Germline Polymorphisms in Neoadjuvant Chemotherapy for Urothelial Cancer. Clinical genitourinary cancer 2016 Mar . O'Donnell Peter H, Alanee Shaheen, Stratton Kelly L, Garcia-Grossman Ilana R, Cao Hongyuan, Ostrovnaya Irina, Plimack Elizabeth R, Manschreck Christopher, Ganshert Cory, Smith Norm D, Steinberg Gary D, Vijai Joseph, Offit Kenneth, Stadler Walter M, Bajorin Dean |
Predictors of survival in refractory anemia with ring sideroblasts and thrombocytosis (RARS-T) and the role of next-generation sequencing. American journal of hematology 2016 Feb . Patnaik Mrinal M, Lasho Terra L, Finke Christy M, Hanson Curtis A, King Rebecca L, Ketterling Rhett P, Gangat Naseema, Tefferi Ayal |
Association of DARS gene polymorphisms with the risk of isolated ventricular septal defects in the Chinese Han population. Italian journal of pediatrics 2016 Nov 42 (1): 102. Feng Yu, Chen Runsen, Mo Xumi |
Negative impact on clinical outcome of the mutational co-occurrence of SF3B1 and DNMT3A in refractory anemia with ring sideroblasts (RARS). Leukemia & lymphoma 2016 Oct 1-8. Martín Iván, Such Esperanza, Navarro Blanca, Vicente Ana, López-Pavía María, Ibáñez Mariam, Tormo Mar, Villamón Eva, Gómez-Seguí Inés, Luna Irene, Oltra Silvestre, Pedrola Laia, Sanz Miguel Angel, Cervera Jose, Sanz Guiller |
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients. PloS one 2018 2 13 (2): e0188869. Ji Haoran, Li Dongxiao, Wu Ye, Zhang Quanli, Gu Qiang, Xie Han, Ji Taoyun, Wang Huifang, Zhao Lu, Zhao Haijuan, Yang Yanling, Feng Hongchun, Xiong Hui, Ji Jinhua, Yang Zhixian, Kou Liping, Li Ming, Bao Xinhua, Chang Xingzhi, Zhang Yuehua, Li Li, Li Huijuan, Niu Zhengping, Wu Xiru, Xiao Jiangxi, Jiang Yuwu, Wang Jingm |
[Gene mutations from 511 myelodysplastic syndromes patients performed by targeted gene sequencing]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2018 1 38 (12): 1012-1016. Li B, Wang J Y, Liu J Q, Shi Z X, Peng S L, Huang H J, Qin T J, Xu Z F, Zhang Y, Fang L W, Zhang H L, Hu N B, Pan L J, Qu S Q, Xiao Z |
Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients. Neuropediatrics 2019 2 50 (2): 130-134. Rezaei Zahra, Hosseinpour Sareh, Ashrafi Mahmoud Reza, Mahdieh Nejat, Alizadeh Houman, Mohammadpour Masoud, Khosroshahi Nahideh, Amanat Man, Tavasoli Ali Re |
Impact of HFE gene variants on iron overload, overall survival and leukemia-free survival in myelodysplastic syndromes. American journal of cancer research 2021 4 11 (3): 955-967. Schneeweiss-Gleixner Mathias, Greiner Georg, Herndlhofer Susanne, Schellnegger Julia, Krauth Maria-Theresa, Gleixner Karoline V, Wimazal Friedrich, Steinhauser Corinna, Kundi Michael, Thalhammer Renate, Schwarzinger Ilse, Hoermann Gregor, Esterbauer Harald, Födinger Manuela, Valent Peter, Sperr Wolfgang |
Myelodysplastic/myeloproliferative neoplasms with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T): Mayo-Moffitt collaborative study of 158 patients. Blood cancer journal 2022 2 12 (2): 26. Mangaonkar Abhishek A, Lasho Terra L, Ketterling Rhett P, Reichard Kaaren K, Gangat Naseema, Al-Kali Aref, Begna Kebede H, Pardanani Animesh, Al Ali Najla H, Talati Chetasi, Sallman David, Padron Eric, Patnaik Mrinal M, Tefferi Ayalew, Komrokji Ra |
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- Page last updated:Apr 16, 2024
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