Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 88 Records) |
| Query Trace: Wilms Tumor and WT1[original query] |
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| Prognostic Impact of WT-1 and Survivin Gene Expression in Acute Myeloid Leukemia Patients. Clinical laboratory 2019 Apr 65 (4): . Adnan-Awad Shady, Meligui Yomna M El, Salem Salem Eid, Salaheldin Omina, Ayoub Mahmoud A, Kamel Mahmoud |
| Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort. European journal of medical genetics 2020 9 63 (11): 104047. Sun Shuzhen, Xu Linan, Bi Yunli, Wang Jing, Zhang Zhiqing, Tang Xiaoshan, Cao Qi, Zhai Yihui, Chen Jing, Fang Xiaoyan, Liu Jialu, Fang Ye, Xiang Tianchao, Qian Yanyan, Wu Bingbing, Wang Huijun, Zhou Wenhao, Shen Jian, Dong Kuiran, Liu Xiaorong, Zheng Bixia, Zhang Aihua, Wang Xiaowen, Wu Yubing, Ma Duan, Shen Qian, Rao Jia, Xu Ho |
| A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977?kb deletion in the 11p13 region. BMC medical genomics 2020 9 13 (Suppl 8): 130. Vasilyeva Tatyana A, Marakhonov Andrey V, Minzhenkova Marina E, Markova Zhanna G, Petrova Nika V, Sukhanova Natella V, Koshkin Philipp A, Pyankov Denis V, Kanivets Ilya V, Korostelev Sergey A, Krynskaya Irina A, Shilova Nadezhda V, Kutsev Sergey I, Kadyshev Vitaly V, Zinchenko Rena |
| Refractory Hypertension in Infantile-Onset Denys-Drash Syndrome. The Tohoku journal of experimental medicine 2020 9 252 (1): 45-51. Nishi Kentaro, Kamei Koichi, Ogura Masao, Sato Mai, Murakoshi Miki, Kamae Chikako, Suzuki Ryutaro, Kanamori Toru, Nagano China, Nozu Kandai, Ishikura Kenji, Ito Shuic |
| Association between the Wilms tumor-1 rs16754 polymorphism and acute myeloid leukemia: A MOOSE-compliant meta-analysis. Medicine 2020 Jul 99 (27): e20713. Yu Xin, Zhang Yuan, Liu Shuang, Mu Yu, Shang Fengjia, Zhang N |
| Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (WT1) gene. Proceedings of the National Academy of Sciences of the United States of America 2020 6 117 (24): 13680-13688. Eozenou Caroline, Gonen Nitzan, Touzon Maria Sol, Jorgensen Anne, Yatsenko Svetlana A, Fusee Leila, Kamel Alaa K, Gellen Balazs, Guercio Gabriela, Singh Priti, Witchel Selma, Berman Andrea J, Mainpal Rana, Totonchi Mehdi, Mohseni Meybodi Anahita, Askari Masomeh, Merel-Chali Tiphanie, Bignon-Topalovic Joelle, Migale Roberta, Costanzo Mariana, Marino Roxana, Ramirez Pablo, Perez Garrido Natalia, Berensztein Esperanza, Mekkawy Mona K, Schimenti John C, Bertalan Rita, Mazen Inas, McElreavey Ken, Belgorosky Alicia, Lovell-Badge Robin, Rajkovic Aleksandar, Bashamboo A |
| Analysis of pre-chemotherapy WBC, PLT, monocyte, hemoglobin, and MPV levels in acute myeloid leukemia patients with WT1, FLT3, or NPM gene mutations. Medicine 2020 Apr 99 (14): e19627. Merdin Alparslan, Dal Mehmet Sinan, Çakar Merih Kizil, Yildiz Jale, Ulu Bahar Uncu, Batgi Hikmetullah, Tetik Ay?egül, Seçilmi? Sema, Darçin Tahir, ?ahin Derya, Bakirta? Mehmet, Ba?çi Semih, Yi?eno?lu Tu?çe Nur, Baysal Nuran Ahu, ?skender Dicle, Altunta? Fev |
| 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 |
| Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations. Cancers 2020 12 13 (1): . Royer-Pokora Brigitte, Busch Maike Anna, Tenbusch Sarah, Schmidt Mathias, Beier Manfred, Woods Andrew D, Thiele Holger, Mora Jau |
| Hotspots mutational analysis of Wilms tumor 1 gene in acute myeloid leukaemia; prevalence and clinical correlation in North Indian population. American journal of blood research 2020 10 (5): 179-189. Haider Imran, Kumar Chandan, Jain Garima, Bakhshi Sameer, Kumar Lalit, Chopra Anita, Ranjan Amar, Tanwar Pran |
| Auxiliary genetic analysis in a Chinese adolescent NPH family by single nucleotide polymorphism screening. Molecular medicine reports 2020 1 21 (3): 1115-1124. Tang Chunrong, Zhou Daoyuan, Tan Rongshao, Zhong Xiaoshi, Xiao Xiao, Qin Danping, Liu Yun, Hu Jianguang, Liu Y |
| WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2021 8 16 (1): 46-54. Ferrari Maria T M, Watanabe Andreia, da Silva Thatiane E, Gomes Nathalia L, Batista Rafael L, Nishi Mirian Y, de Paula Leila C P, Costa Eduardo C, Costa Elaine M F, Cukier Priscilla, Onuchic Luiz F, Mendonca Berenice B, Domenice Sorah |
| Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants. Kidney international reports 2021 8 6 (8): 2114-2121. Nagano China, Takaoka Yutaka, Kamei Koichi, Hamada Riku, Ichikawa Daisuke, Tanaka Kazuki, Aoto Yuya, Ishiko Shinya, Rossanti Rini, Sakakibara Nana, Okada Eri, Horinouchi Tomoko, Yamamura Tomohiko, Tsuji Yurika, Noguchi Yuko, Ishimori Shingo, Nagase Hiroaki, Ninchoji Takeshi, Iijima Kazumoto, Nozu Kand |
| Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. JNCI cancer spectrum 2021 7 5 (2): . Kim Jung, Gianferante Matthew, Karyadi Danielle M, Hartley Stephen W, Frone Megan N, Luo Wen, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Dean Michael, Yeager Meredith, Zhu Bin, Song Lei, Sampson Joshua N, Yasui Yutaka, Leisenring Wendy M, Brodie Seth A, de Andrade Kelvin C, Fortes Fernanda P, Goldstein Alisa M, Khincha Payal P, Machiela Mitchell J, McMaster Mary L, Nickerson Michael L, Oba Leatrisse, Pemov Alexander, Pinheiro Maisa, Rotunno Melissa, Santiago Karina, Wegman-Ostrosky Talia, Diver W Ryan, Teras Lauren, Freedman Neal D, Hicks Belynda D, Zhu Bin, Wang Mingyi, Jones Kristine, Hutchinson Amy A, Dagnall Casey, Savage Sharon A, Tucker Margaret A, Chanock Stephen J, Morton Lindsay M, Stewart Douglas R, Mirabello Li |
| New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report. Medicine 2021 6 100 (19): e25864. Akramov Nail R, Shavaliev Rafael F, Osipova Ilsiya |
| Novel combined variants of WT1 and TET2 in a refractory and recurrent AML patient. BMC medical genomics 2021 (1): 158. Ma Qiang, Guo Yixian, Lan Xiaoxi, Wang Guoxiang, Sun Wanli |
| A novel WT1 gene mutation in a chinese girl with denys-drash syndrome. Journal of clinical laboratory analysis 2021 5 35 (5): e23769. Wang Faliang, Cai Jiabin, Wang Jinhu, He Min, Mao Junqing, Zhu Kun, Zhao Manli, Guan Zhonghai, Li Linjie, Jin Hongchuan, Shu Qia |
| 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 |
| Friend or foe? The case of Wilms' Tumor 1 (WT1) mutations in acute myeloid leukemia. Blood cells, molecules & diseases 2021 2 88 102549. Awada Hassan, Durmaz Arda, Gurnari Carmelo, Kishtagari Ashwin, Zawit Misam, Pagliuca Simona, Visconte Valer |
| Genomic landscape of T-cell lymphoblastic lymphoma. Chinese journal of cancer research = Chung-kuo yen cheng yen chiu 2022 6 34 (2): 83-94. Li Zhaoming, Song Yue, Zhang Mingzhi, Wei Yiming, Ruan Ha |
| Detection of TET2 Mutation in Patients with De Novo Acute Myeloid Leukemia: A Mutation Analysis of 51 Iranian Patients. Asian Pacific journal of cancer prevention : APJCP 2022 3 23 (3): 803-806. Chehreghani Zahra, Sadeghian Mohammad Hadi, Ayatollahi Hossein, Bagheri Parisa, Zafari Zahra, Rezazadeh Omid, Arbab Jafari Pour |
| Incidence and Prognostic Impact of WT-1 Gene Exon7 and 9 Mutations in Acute Promyelocytic Leukemia. International journal of hematology-oncology and stem cell research 2022 10 16 (2): 74-80. Nejatifar Fatemeh, Rostami Shahrbano, Chahardouli Barham, Kasaeian Amir, Vaezi Mohammad, Kamranzadeh Hossein, Mousavi Seied Asadollah, Farbod Abolfazl, Alimoghaddam Kamran, Ghavamzadeh Ardesh |
| Frequency and clinical impact of WT1 mutations in the context of CEBPA-mutated acute myeloid leukemia. Hematology (Amsterdam, Netherlands) 2022 Dec 27 (1): 994-1002. Wang Ting, Hua Haiying, Wang Zheng, Wang Biao, Cao Liujun, Qin Wei, Wu Pin, Cai Xiaohui, Chao Hongying, Lu XuZha |
| Wilms' tumor 1 expression combined with genetic mutations for prognostic assessment in MDS. Leukemia & lymphoma 2023 3 1-9. Pan Danqi, Zhao Wenshu, Jiang Qianli, Yin Changxin, He Han, Liao Libin, Ye Jieyu, Dai M |
| Inter-Ethnic Variations in the Clinical, Pathological, and Molecular Characteristics of Wilms Tumor. Cancers 2024 9 16 (17): . Kia Teng Lim, Amos H P L |
| WT1 And DNMT3A Mutations in Prognostic Significance of Acute Myeloid Leukemia: A Meta-Analysis. Cancer biotherapy & radiopharmaceuticals 2024 8 . Shiyue Ma, Lingjian Tang, Hui Tang, Chaoli Wu, Xue Pu, Jun Yang, Ninhong N |
| WT1 gene mutations impact post-transplant relapse in myelodysplastic syndrome with excess blasts 2 patients. Annals of hematology 2024 7 . Wenwen Guo, Haixiao Zhang, Mingyang Wang, Yawei Zheng, Yigeng Cao, Xiaoyu Zhang, Weihua Zhai, Rongli Zhang, Donglin Yang, Jialin Wei, Yi He, Qiaoling Ma, Yonghui Xia, Aiming Pang, Sizhou Feng, Mingzhe Han, Erlie Jia |
| Evaluation of pathogenicity of WT1 intron variants by in vitro splicing analysis. Clinical and experimental nephrology 2024 6 . Seiya Inoue, Atsushi Kondo, Yuta Inoki, Yuta Ichikawa, Yu Tanaka, Chika Ueda, Hideaki Kitakado, Ryota Suzuki, Eri Okada, Nana Sakakibara, Tomoko Horinouchi, Kandai No |
| A distinct subgroup of AML resembling the APL immunophenotype is associated with DIC. BMC cancer 2024 12 24 (1): 1576. Pan Li, Li Liu, Fuling Zh |
| Clinical Characterization of a National Cohort of Patients With Germline WT1 Variants Including Late-Onset Phenotypes. Kidney international reports 2024 12 9 (12): 3570-3579. Sophie E van Peer, Roland P Kuiper, Janna A Hol, Sanne Egging, Bert van der Zwaag, Marc R Lilien, M Paola Lombardi, Marry M van den Heuvel-Eibrink, Marjolijn C J Jongma |
- Page last reviewed:Feb 1, 2024
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