Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 31 Records) |
| Query Trace: Leukemia and NF1[original query] |
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| Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia. Pediatric research 2009 Mar 65 (3): 334-40. Yoshida Nao, Yagasaki Hiroshi, Xu Yinyan, Matsuda Kazuyuki, Yoshimi Ayami, Takahashi Yoshiyuki, Hama Asahito, Nishio Nobuhiro, Muramatsu Hideki, Watanabe Nobuhiro, Matsumoto Kimikazu, Kato Koji, Ueyama Junichi, Inada Hiroko, Goto Hiroaki, Yabe Miharu, Kudo Kazuko, Mimaya Junichi, Kikuchi Akira, Manabe Atsushi, Koike Kenichi, Kojima Sei |
| Genome wide molecular analysis of minimally differentiated acute myeloid leukemia. Haematologica 2009 Nov 94 (11): 1546-54. Silva Fernando P G, Almeida Inês, Morolli Bruno, Brouwer-Mandema Geeske, Wessels Hans, Vossen Rolf, Vrieling Harry, Marijt Erik W A, Valk Peter J M, Kluin-Nelemans Hanneke C, Sperr Wolfgang R, Ludwig Wolf-Dieter, Giphart-Gassler Micheli |
| Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype. Haematologica 2009 Feb 94 (2): 213-23. Akagi Tadayuki, Ogawa Seishi, Dugas Martin, Kawamata Norihiko, Yamamoto Go, Nannya Yasuhito, Sanada Masashi, Miller Carl W, Yung Amanda, Schnittger Susanne, Haferlach Torsten, Haferlach Claudia, Koeffler H Phill |
| Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia. Haematologica 2010 Sep 95 (9): 1481-8. Okamoto Ryoko, Ogawa Seishi, Nowak Daniel, Kawamata Norihiko, Akagi Tadayuki, Kato Motohiro, Sanada Masashi, Weiss Tamara, Haferlach Claudia, Dugas Martin, Ruckert Christian, Haferlach Torsten, Koeffler H Phill |
| CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia. Blood 2011 May 117 (21): e198-206. Makishima Hideki, Jankowska Anna M, McDevitt Michael A, O'Keefe Christine, Dujardin Simon, Cazzolli Heather, Przychodzen Bartlomiej, Prince Courtney, Nicoll John, Siddaiah Harish, Shaik Mohammed, Szpurka Hadrian, Hsi Eric, Advani Anjali, Paquette Ronald, Maciejewski Jaroslaw |
| Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms. Genes, chromosomes & cancer 2012 Aug 51 (8): 743-55. Brecqueville Mandy, Rey Jérôme, Bertucci François, Coppin Emilie, Finetti Pascal, Carbuccia Nadine, Cervera Nathalie, Gelsi-Boyer Véronique, Arnoulet Christine, Gisserot Olivier, Verrot Denis, Slama Borhane, Vey Norbert, Mozziconacci Marie-Joelle, Birnbaum Daniel, Murati An |
| Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations? Human genomics 2012 6 (1): 1. Alkindy A, Chuzhanova N, Kini U, Cooper DN, Upadhyaya M |
| Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia. American journal of hematology 2013 Apr 88 (4): 306-11. Boudry-Labis Elise, Roche-Lestienne Catherine, Nibourel Olivier, Boissel Nicolas, Terre Christine, Perot Christine, Eclache Virginie, Gachard Nathalie, Tigaud Isabelle, Plessis Ghislaine, Cuccuini Wendy, Geffroy Sandrine, Villenet Céline, Figeac Martin, Leprêtre Frederic, Renneville Aline, Cheok Meyling, Soulier Jean, Dombret Hervé, Preudhomme Claude, |
| Low frequency of mutations in Chinese with acute myeloid leukemia: Different disease or different aetiology? Leukemia research 2015 Jun 39 (6): 646-8. Yin Jiawei, Xie Xiaoli, Zhang Fan, Chen Zheng, Hu Chenxi, Su Guangsong, Liu Hong, Zheng Yanwen, He Chao, Shen Hongjie, Qiu Qiaocheng, He Jun, Pan Zhirong, Gale Robert Peter, Wu Depei, Yin B |
| Are the methylenetetrahydrofolate reductase 1298 and 677 gene polymorphisms related to optic glioma and hamartoma risk in neurofibromatosis type 1 patients? The Turkish journal of pediatrics 2016 58 (2): 152-158. Tany?ld?z Hikmet Gül?ah, Ye?il ?ule, Bozkurt Ceyhun, Çand?r Mehmet Onur, Akp?nar-Tekgündüz Sibel, Toprak ?ule, Yüksel Deniz, ?ahin Gürs |
| Genetic variations of bone marrow mesenchymal stromal cells derived from acute leukemia and myelodysplastic syndrome by targeted deep sequencing. Leukemia research 2017 Sep 62 23-28. Azuma Kenko, Umezu Tomohiro, Imanishi Satoshi, Asano Michiyo, Yoshizawa Seiichiro, Katagiri Seiichiro, Ohyashiki Kazuma, Ohyashiki Junko |
| NF1 mutations are recurrent in adult acute myeloid leukemia and confer poor outcome. Leukemia 2018 6 32 (12): 2536-2545. Eisfeld Ann-Kathrin, Kohlschmidt Jessica, Mrózek Krzysztof, Mims Alice, Walker Christopher J, Blachly James S, Nicolet Deedra, Orwick Shelley, Maharry Sophia E, Carroll Andrew J, Powell Bayard L, Kolitz Jonathan E, Wang Eunice S, Stone Richard M, de la Chapelle Albert, Byrd John C, Bloomfield Clara |
| Association of mutations with morphological dysplasia in de novo acute myeloid leukemia without 2016 WHO Classification-defined cytogenetic abnormalities. Haematologica 2018 Jan . Weinberg Olga K, Gibson Christopher J, Blonquist Traci M, Neuberg Donna, Pozdnyakova Olga, Kuo Frank, Ebert Benjamin L, Hasserjian Robert |
| The Profile of Immunophenotype and Genotype Aberrations in Subsets of Pediatric T-Cell Acute Lymphoblastic Leukemia. Frontiers in oncology 2019 9 316. Noronha Elda Pereira, Marques Luísa Vieira Codeço, Andrade Francianne Gomes, Thuler Luiz Claudio Santos, Terra-Granado Eugênia, Pombo-de-Oliveira Maria S, |
| Estimated number of adult survivors of childhood cancer in United States with cancer-predisposing germline variants. Pediatric blood & cancer 2019 11 67 (2): e28047. Wilson Carmen L, Wang Zhaoming, Liu Qi, Ehrhardt Matthew J, Mostafavi Roya, Easton John, Mulder Heather, Hedges Dale J, Wang Shuoguo, Rusch Michael, Edmonson Michael, Levy Shawn, Lanctot Jennifer Q, Currie Kelsey, Lear Matthew, Patel Aman, Sapkota Yadav, Brooke Russell J, Moon Wonjong, Chang Ti-Cheng, Chen Wenan, Kesserwan Chimene A, Wu Gang, Nichols Kim E, Hudson Melissa M, Zhang Jinghui, Robison Leslie L, Yasui Yuta |
| Acute Myeloid Leukemia with t(8;16)(p11.2;p13.3)/ KAT6A-CREBBP in a Patient with an NF1 Germline Mutation and Clinical Presentation Mimicking Acute Promyelocytic Leukemia. Journal of the Association of Genetic Technologists 2020 9 46 (3): 135-139. Donnelly Liam, Rankins Casey, Bruno Ximena Jordan, McKinnon Wendy, Devitt Katherine, Gardner Juli-An |
| The mutational landscape of histiocytic sarcoma associated with lymphoid malignancy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2020 9 34 (2): 336-347. Egan Caoimhe, Lack Justin, Skarshaug Shannon, Pham Thu Anh, Abdullaev Zied, Xi Liqiang, Pack Svetlana, Pittaluga Stefania, Jaffe Elaine S, Raffeld Ma |
| Steroid receptor-associated and regulated protein is a biomarker in predicting the clinical outcome and treatment response in malignancies. Cancer reports (Hoboken, N.J.) 2020 Jul e1267. Naderi A |
| Juvenile myelomonocytic leukemia - A bona fide RASopathy syndrome. Best practice & research. Clinical haematology 2020 5 33 (2): 101171. Lasho Terra, Patnaik Mrinal |
| Mutations predictive of hyperactive Ras signaling correlate with inferior survival across high-risk pediatric acute leukemia. Translational pediatrics 2020 3 9 (1): 43-50. Ney Gina M, Anderson Bailey, Bender Jonathan, Kumar-Sinha Chandan, Wu Yi-Mi, Vats Pankaj, Cieslik Marcin, Robinson Dan R, Li Qing, Chinnaiyan Arul M, Mody Raj |
| Ras pathway mutation feature in the same individuals at diagnosis and relapse of childhood acute lymphoblastic leukemia. Translational pediatrics 2020 Feb 9 (1): 4-12. Zhang Hong-Hong, Wang Hong-Sheng, Qian Xiao-Wen, Zhu Xiao-Hua, Miao Hui, Yu Yi, Meng Jian-Hua, Le Jun, Jiang Jun-Ye, Cao Ping, Jiang Wen-Jing, Wang Ping, Fu Yang, Li Jun, Qian Mao-Xiang, Zhai Xiao-W |
| [Clinical Characteristics and Prognostic Significance of BCOR/BCORL1 Gene Mutation in Patients with Myelodysplastic Syndromes]. Zhongguo shi yan xue ye xue za zhi 2020 Dec 28 (6): 2004-2010. Cen Yan-Xia, Li Y |
| Clinical findings and mutational spectrum of neurofibromatosis type 1 patients in a single center of south part of Turkey. Turkish journal of medical sciences 2021 Aug . Demir Gündo?an Begümhan, Tu? Bozdo?an Sevcan, Ayhan Yavuz Selim, Müjde Cem, Bi?gin Atil, Çitak Elvan Ça?l |
| Mutational landscape of Juvenile Myelomonocytic Leukemia (JMML)-A real-world context. International journal of laboratory hematology 2021 Aug . Nathany Shrinidhi, Chatterjee Gaurav, Ghai Shruti, Moulik Nirmalya Roy, Shetty Dhanalaxmi, Subramanian P G, Tembhare Prashant, Gujral Sumeet, Dhamne Chetan, Banavali Sripad, Narula Gaurav, Patkar Nikh |
| Implications of mosaicism in variant interpretation: A case of a de novo homozygous NF1 variant. European journal of medical genetics 2021 5 64 (7): 104236. Alghamdi Malak, Monies Dorota, Alsohime Fahad, Temsah Hani, Almodaihsh Fahad, Aldawasri Mana, Alsultan Abdulrahman, Alkuraya Fowzan |
| Juvenile xanthogranuloma in Noonan syndrome. American journal of medical genetics. Part A 2021 5 185 (10): 3048-3052. Ali Marwan M, Gilliam Amy E, Ruben Beth S, Tidyman William E, Rauen Katherine |
| Genomic landscape of B-other acute lymphoblastic leukemia in an adult retrospective cohort with a focus on BCR-ABL1-like subtype. Acta oncologica (Stockholm, Sweden) 2021 3 60 (6): 760-770. Hrabovsky Stepan, Vrzalova Zuzana, Stika Jiri, Jelinkova Hana, Jarosova Marie, Navrkalova Veronika, Martenek Jiri, Folber Frantisek, Salek Cyril, Horacek Jan M, Pospisilova Sarka, Mayer Jiri, Doubek Micha |
| Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia. Haematologica 2021 Mar . Kaburagi Taeko, Yamato Genki, Shiba Norio, Yoshida Kenichi, Hara Yusuke, Tabuchi Ken, Shiraishi Yuichi, Ohki Kentaro, Sotomatsu Manabu, Arakawa Hirokazu, Matsuo Hidemasa, Shimada Akira, Taki Tomohiko, Kiyokawa Nobutaka, Tomizawa Daisuke, Horibe Keizo, Miyano Satoru, Taga Takashi, Adachi Souichi, Ogawa Seishi, Hayashi Yasuhi |
| Novel Germline PHD2 Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia. Medicina (Kaunas, Lithuania) 2022 Aug 58 (8): . Provenzano Aldesia, Chetta Massimiliano, De Filpo Giuseppina, Cantini Giulia, La Barbera Andrea, Nesi Gabriella, Santi Raffaella, Martinelli Serena, Rapizzi Elena, Luconi Michaela, Maggi Mario, Mannelli Massimo, Ercolino Tonino, Canu Letiz |
| TP53 copy number and protein expression inform mutation status across risk categories in acute myeloid leukemia. Blood 2022 4 140 (1): 58-72. Tashakori Mehrnoosh, Kadia Tapan, Loghavi Sanam, Daver Naval, Kanagal-Shamanna Rashmi, Pierce Sherry, Sui Dawen, Wei Peng, Khodakarami Farnoosh, Tang Zhenya, Routbort Mark, Bivins Carol A, Jabbour Elias J, Medeiros L Jeffrey, Bhalla Kapil, Kantarjian Hagop M, Ravandi Farhad, Khoury Joseph |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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