Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: Abnormalities and WT1[original query] |
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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, |
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 |
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 |
Topographic molecular profile of pheochromocytomas: role of somatic down-regulation of mismatch repair. The Journal of clinical endocrinology and metabolism 2006 1 91 (3): 1150-8. Blanes Alfredo, Sanchez-Carrillo Juan J, Diaz-Cano Salvador |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
Combined Genetic and Chromosomal Characterization of Wilms Tumors Identifies Chromosome 12 Gain as a Potential New Marker Predicting a Favorable Outcome. Neoplasia (New York, N.Y.) 2018 12 21 (1): 117-131. Haruta Masayuki, Arai Yasuhito, Okita Hajime, Tanaka Yukichi, Takimoto Tetsuya, Sugino Ryuichi P, Yamada Yasuhiro, Kamijo Takehiko, Oue Takaharu, Fukuzawa Masahiro, Koshinaga Tsugumichi, Kaneko Yasuhi |
What biologic factors predict for transformation to AML? Best practice & research. Clinical haematology 2018 11 31 (4): 341-345. Bejar Rafa |
Genetic Characterization and Prognostic Relevance of Acquired Uniparental Disomies in Cytogenetically Normal Acute Myeloid Leukemia. Clinical cancer research : an official journal of the American Association for Cancer Research 2019 8 25 (21): 6524-6531. Walker Christopher J, Kohlschmidt Jessica, Eisfeld Ann-Kathrin, Mrózek Krzysztof, Liyanarachchi Sandya, Song Chi, Nicolet Deedra, Blachly James S, Bill Marius, Papaioannou Dimitrios, Oakes Christopher C, Giacopelli Brian, Genutis Luke K, Maharry Sophia E, Orwick Shelley, Archer Kellie J, Powell Bayard L, Kolitz Jonathan E, Uy Geoffrey L, Wang Eunice S, Carroll Andrew J, Stone Richard M, Byrd John C, de la Chapelle Albert, Bloomfield Clara |
Methylation Statuses of H19DMR and KvDMR at WT2 in Wilms Tumors in Taiwan. Pathology oncology research : POR 2020 3 26 (4): 2153-2159. Lu Meng-Yao, Wang Wen-Chung, Hou Tai-Cheng, Kuo Chen-Yun, Lai Yen-Che |
Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations. Internal medicine (Tokyo, Japan) 2021 5 60 (23): 3785-3788. Murakami Ken, Yamaguchi Yuuta, Kida Yuko, Morikawa Yoichiro, Ujiie Hidetoshi, Sugahara Hiroyuki, Nannya Yasuhito, Ogawa Seishi, Kanakura Yuzu |
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. American journal of medical genetics. Part A 2021 3 185 (6): 1666-1677. Mazen Inas, Mekkawy Mona, Kamel Alaa, Essawi Mona, Hassan Heba, Abdel-Hamid Mohamed, Amr Khalda, Soliman Hala, El-Ruby Mona, Torky Ahmed, El Gammal Mona, Elaidy Aya, Bashamboo Anu, McElreavey Kenne |
[Clinical Characteristics of Acute Myeloid Leukemia Patients with RUNX1 Gene Mutation]. Zhongguo shi yan xue ye xue za zhi 2021 Oct 29 (5): 1411-1416. Ni Zeng-Feng, Ma Li-Jie, Shi Li-Li, Shen Pan-Li, Zhao Jian-Qia |
Molecular evaluation of gene mutation profiles and copy number variations in pediatric acute myeloid leukemia. Leukemia research 2022 9 122 106954. Meena Jagdish Prasad, Pathak Nivedita, Gupta Aditya Kumar, Bakhshi Sameer, Gupta Ritu, Makkar Harshita, Seth Rach |
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 |
Novel variants in the PAX6 gene related to isolated aniridia. Congenital anomalies 2023 5 . Katarzyna Kuchalska, Anna Wawrocka, Maciej R Krawczyns |
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- Page last updated:Mar 25, 2024
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