HuGE Literature Finder
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| Integrated clinical genotype-phenotype characteristics of early T-cell precursor acute lymphoblastic leukemia. Cancer 2022 Oct . Ye Matthew T, Wang Yi, Zuo Zhuang, Calin Steliana, He Hua, Tang Zhenya, Jabbour Elias J, Borthakur Gautam, Zhang Yizhuo, Yang Yaling, You M Jam |
| The genetics and clinical characteristics of children morphologically diagnosed as acute promyelocytic leukemia. Leukemia 2019 Jun 33 (6): 1387-1399. Zhao Jie, Liang Jian-Wei, Xue Hui-Liang, Shen Shu-Hong, Chen Jing, Tang Yan-Jing, Yu Li-Sha, Liang Huan-Huan, Gu Long-Jun, Tang Jing-Yan, Li Ben-Sha |
| Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome. Frontiers in genetics 2018 9 214. Abid Aiysha, Shahid Saba, Shakoor Madiha, Lanewala Ali A, Hashmi Seema, Khaliq Shaguf |
| A high incidence of WT1 abnormality in bilateral Wilms tumours in Japan, and the penetrance rates in children with WT1 germline mutation. British journal of cancer 2015 Mar 112 (6): 1121-33. Kaneko Y, Okita H, Haruta M, Arai Y, Oue T, Tanaka Y, Horie H, Hinotsu S, Koshinaga T, Yoneda A, Ohtsuka Y, Taguchi T, Fukuzawa |
| The prognostic effect of high diagnostic WT1 gene expression in pediatric AML depends on WT1 SNP rs16754 status: report from the Children's Oncology Group. Pediatric blood & cancer 2014 Jan 61 (1): 81-8. Ho Phoenix A, Alonzo Todd A, Gerbing Robert B, Kuhn Julia, Pollard Jessica A, Hirsch Betsy, Raimondi Susana C, Gamis Alan S, Meshinchi Sohe |
| Immunophenotypic analysis of ovarian endometrioid adenocarcinoma: correlation with KRAS mutation and the presence of endometriosis. Pathology 2013 Oct 45 (6): 559-66. Stewart Colin J R, Walsh Michael D, Budgeon Charley A, Crook Maxine L, Buchanan Daniel |
| WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group. International journal of hematology 2013 Oct 98 (4): 437-45. Sano Hirozumi, Shimada Akira, Tabuchi Ken, Taki Tomohiko, Murata Chisato, Park Myoung-ja, Ohki Kentaro, Sotomatsu Manabu, Adachi Souichi, Tawa Akio, Kobayashi Ryoji, Horibe Keizo, Tsuchida Masahiro, Hanada Ryoji, Tsukimoto Ichiro, Hayashi Yasuhi |
| Core binding factor acute myeloid leukaemia and c-KIT mutations. Oncology reports 2013 May 29 (5): 1867-72. Riera Ludovica, Marmont Filippo, Toppino Daniela, Frairia Chiara, Sismondi Francesca, Audisio Ernesta, Di Bello Cristiana, D'Ardia Stefano, Di Celle Paola Francia, Messa Emanuela, Inghirami Giorgio, Vitolo Umberto, Pich Achil |
| High WT1 mRNA expression after induction chemotherapy and FLT3-ITD have prognostic impact in pediatric acute myeloid leukemia: a study of the Japanese Childhood AML Cooperative Study Group. International journal of hematology 2012 Oct 96 (4): 469-76. Shimada Akira, Taki Tomohiko, Koga Daisuke, Tabuchi Ken, Tawa Akio, Hanada Ryoji, Tsuchida Masahiro, Horibe Keizo, Tsukimoto Ichiro, Adachi Souichi, Kojima Seiji, Hayashi Yasuhi |
| Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children. Cancer science 2012 Jun 103 (6): 1129-35. Haruta Masayuki, Arai Yasuhito, Watanabe Naoki, Fujiwara Yuiko, Honda Shohei, Ohshima Junjiro, Kasai Fumio, Nakadate Hisaya, Horie Hiroshi, Okita Hajime, Hata Jun-Ichi, Fukuzawa Masahiro, Kaneko Yasuhi |
| Genetic and epigenetic similarities and differences between childhood and adult AML. Pediatric blood & cancer 2012 Apr 58 (4): 525-31. Juhl-Christensen Caroline, Ommen Hans Beier, Aggerholm Anni, Lausen Birgitte, Kjeldsen Eigil, Hasle Henrik, Hokland Pet |
| Gene mutation patterns and their prognostic impact in a cohort of 1185 patients with acute myeloid leukemia. Blood 2011 Nov 118 (20): 5593-603. Shen Yang, Zhu Yong-Mei, Fan Xing, Shi Jing-Yi, Wang Qin-Rong, Yan Xiao-Jing, Gu Zhao-Hui, Wang Yan-Yan, Chen Bing, Jiang Chun-Lei, Yan Han, Chen Fei-Fei, Chen Hai-Min, Chen Zhu, Jin Jie, Chen Sai-Ju |
| Transcription factor mutations in myelodysplastic/myeloproliferative neoplasms. Haematologica 2010 Sep 95 (9): 1473-80. Ernst Thomas, Chase Andrew, Zoi Katerina, Waghorn Katherine, Hidalgo-Curtis Claire, Score Joannah, Jones Amy, Grand Francis, Reiter Andreas, Hochhaus Andreas, Cross Nicholas C |
| Eye involvement in children with primary focal segmental glomerulosclerosis. Pediatric nephrology (Berlin, Germany) 2008 Mar 23 (3): 421-7. Ozaltin Fatih, Heeringa Saskia, Poyraz Ceren Erdogan, Bilginer Yelda, Kadayifcilar Sibel, Besbas Nesrin, Topaloglu Rezan, Ozen Seza, Hildebrandt Friedhelm, Bakkaloglu Ays |
| WT1 gene analysis in sporadic early-onset and bilateral wilms tumor patients without associated abnormalities. Journal of pediatric hematology/oncology 2005 Apr 27 (4): 197-201. Perotti Daniela, Mondini Patrizia, Terenziani Monica, Spreafico Filippo, Collini Paola, Fossati-Bellani Franca, Radice Pao |
| Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2004 Oct 22 (20): 4140-6. Little Suzanne E, Hanks Sandra P, King-Underwood Linda, Jones Chris, Rapley Elizabeth A, Rahman Nazneen, Pritchard-Jones Kat |
| Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome. Kidney international 2004 Aug 66 (2): 564-70. Ruf Rainer G, Schultheiss Michael, Lichtenberger Anne, Karle Stephanie M, Zalewski Isabella, Mucha Bettina, Everding Anne Schulze, Neuhaus Thomas, Patzer Ludwig, Plank Christian, Haas Johannes P, Ozaltin Fatih, Imm Anita, Fuchshuber Arno, Bakkaloglu Aysin, Hildebrandt Friedhelm, |
| Clinical, Pathologic, and Genetic Features of Wilms Tumors With WTX Gene Mutation. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 20 (2): 105-111. Alexandrescu Sanda, Akhavanfard Sara, Harris Marian H, Vargas Sara |
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- Page last updated:Jan 26, 2023
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