HuGE Literature Finder
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| Are angiotensin converting enzyme (ACE1/ACE2) gene variants associated with the clinical severity of COVID-19 pneumonia? A single-center cohort study. Anatolian journal of cardiology 2022 02 26 (2): 133-140. Ba?tu? Serdal, Çavdarl? Bü?ranur, Ba?tu? Aliye, ?encan ?rfan, Tunçez Ebru, Yak???k Çak?r Esra, Kemirtlek Nizamettin, Sakar Cihad, Erdem Deniz, Güleç Ceylan Gülay, Özkoçak Turan I??l, Kazanc?o?lu Sümeyye, Bodur Hürr |
| Co-occurrence of KIT and NRAS mutations defines an adverse prognostic core-binding factor acute myeloid leukemia. Leukemia & lymphoma 2021 May 1-10. Jin Huimin, Zhu Yu, Hong Ming, Wu Yujie, Qiu Hairong, Wang Rong, Jin Hui, Sun Qian, Fu Jianxin, Li Jianyong, Qian Sixuan, Qiao Ch |
| Secondary cytogenetic abnormalities in core-binding factor AML harboring inv(16) vs t(8;21). Blood advances 2021 May 5 (10): 2481-2489. Han Se Young, Mrózek Krzysztof, Voutsinas Jenna, Wu Qian, Morgan Elizabeth A, Vestergaard Hanne, Ohgami Robert, Kluin Philip M, Kristensen Thomas Kielsgaard, Pullarkat Sheeja, Møller Michael Boe, Schiefer Ana-Iris, Baughn Linda B, Kim Young, Czuchlewski David, Hilberink Jacobien R, Horny Hans-Peter, George Tracy I, Dolan Michelle, Ku Nam K, Arana Yi Cecilia, Pullarkat Vinod, Kohlschmidt Jessica, Salhotra Amandeep, Soma Lori, Bloomfield Clara D, Chen Dong, Sperr Wolfgang R, Marcucci Guido, Cho Christina, Akin Cem, Gotlib Jason, Broesby-Olsen Sigurd, Larson Melissa, Linden Michael A, Deeg H Joachim, Hoermann Gregor, Perales Miguel-Angel, Hornick Jason L, Litzow Mark R, Nakamura Ryotaro, Weisdorf Daniel, Borthakur Gautam, Huls Gerwin, Valent Peter, Ustun Celalettin, Yeung Cecilia C |
| RAS/RAF mutations and their associations with epigenetic alterations for distinct pathways in Vietnamese colorectal cancer. Pathology, research and practice 2020 Feb 152898. Ta To Van, Nguyen Quang Ngoc, Chu Ha Hoang, Truong Van-Long, Vuong Linh Di |
| [Significance of detecting minimal/measurable residual disease utilizing genetic mutations in acute myeloid leukemia]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2020 61 (8): 965-970. Yamaguchi Hiro |
| [Cytogenetic, kariopathological and morphological abnormalities of spermatozoa and urothelial cells in human granulocytic anaplasmosis depending on polymorphism of the gene of DNA ligase IV]. Urologiia (Moscow, Russia : 1999) 2019 Apr (1): 84-89. Ilyinskikh N N, Ilyinskikh E N, Subbotin A M, Kostromeeva M |
| D816 mutation of the KIT gene in core binding factor acute myeloid leukemia is associated with poorer prognosis than other KIT gene mutations. Annals of hematology 2017 Jul . Yui Shunsuke, Kurosawa Saiko, Yamaguchi Hiroki, Kanamori Heiwa, Ueki Toshimitsu, Uoshima Nobuhiko, Mizuno Ishikazu, Shono Katsuhiro, Usuki Kensuke, Chiba Shigeru, Nakamura Yukinori, Yanada Masamitsu, Kanda Junya, Tajika Kenji, Gomi Seiji, Fukunaga Keiko, Wakita Satoshi, Ryotokuji Takeshi, Fukuda Takahiro, Inokuchi Koi |
| Mastocytosis among elderly patients: A multicenter retrospective French study on 53 patients. Medicine 2016 Jun 95 (24): e3901. Rouet Audrey, Aouba Achille, Damaj Gandhi, Soucié Erinn, Hanssens Katia, Chandesris Marie-Olivia, Livideanu Cristina Bulai, Dutertre Marine, Durieu Isabelle, Grandpeix-Guyodo Catherine, Barète Stéphane, Bachmeyer Claude, Soria Angèle, Frenzel Laurent, Fain Olivier, Grosbois Bernard, de Gennes Christian, Hamidou Mohamed, Arlet Jean-Benoit, Launay David, Lavigne Christian, Arock Michel, Lortholary Olivier, Dubreuil Patrice, Hermine Olivier, Georgin-Lavialle Soph |
| A SNaPshot of potentially personalized care: Molecular diagnostics in gynecologic cancer. Gynecologic oncology 2016 Apr 141 (1): 108-12. Penson R T, Sales E, Sullivan L, Borger D R, Krasner C N, Goodman A K, Del Carmen M G, Growdon W B, Schorge J O, Boruta D M, Castro C M, Dizon D S, Birrer M |
| High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome. Leukemia 2014 Jul 28 (7): 1449-58. Krauth M-T, Eder C, Alpermann T, Bacher U, Nadarajah N, Kern W, Haferlach C, Haferlach T, Schnittger |
| 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 |
| MET and EGFR mutations identified in ALK-rearranged pulmonary adenocarcinoma: molecular analysis of 25 ALK-positive cases. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2013 May 8 (5): 574-81. Boland Jennifer M, Jang Jin Sung, Li Jun, Lee Adam M, Wampfler Jason A, Erickson-Johnson Michele R, Soares Ibere, Yang Ping, Jen Jin, Oliveira Andre M, Yi Eunhee |
| 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 |
| Single nucleotide polymorphism array lesions, TET2, DNMT3A, ASXL1 and CBL mutations are present in systemic mastocytosis. PloS one 2012 7 (8): e43090. Traina Fabiola, Visconte Valeria, Jankowska Anna M, Makishima Hideki, O'Keefe Christine L, Elson Paul, Han Yingchun, Hsieh Fred H, Sekeres Mikkael A, Mali Raghuveer Singh, Kalaycio Matt, Lichtin Alan E, Advani Anjali S, Duong Hien K, Copelan Edward, Kapur Reuben, Olalla Saad Sara T, Maciejewski Jaroslaw P, Tiu Ramon |
| 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 |
| Melanoma hyperpigmentation is strongly associated with KIT alterations. The American Journal of dermatopathology 2009 Oct 31 (7): 619-25. Wu Julie M, Alvarez Hector, García Patricia, Rojas Pamela L, Wong Grace, Maitra Anirban, Antonescu Cristina, Montgomery Elizabeth |
| Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells. Haematologica 2009 Sep 94 (9): 1301-6. Akagi Tadayuki, Shih Lee-Yung, Ogawa Seishi, Gerss Joachim, Moore Stephen R, Schreck Rhona, Kawamata Norihiko, Liang Der-Cherng, Sanada Masashi, Nannya Yasuhito, Deneberg Stefan, Zachariadis Vasilios, Nordgren Ann, Song Jee Hoon, Dugas Martin, Lehmann Sören, Koeffler H Phill |
| Mutations in KIT and RAS are frequent events in pediatric core-binding factor acute myeloid leukemia. Leukemia 2005 Sep 19 (9): 1536-42. Goemans B F, Zwaan C M, Miller M, Zimmermann M, Harlow A, Meshinchi S, Loonen A H, Hählen K, Reinhardt D, Creutzig U, Kaspers G J L, Heinrich M |
| The complexity of KIT gene mutations and chromosome rearrangements and their clinical correlation in gastrointestinal stromal (pacemaker cell) tumors. The American journal of pathology 2002 1 160 (1): 15-22. Andersson Johanna, Sjögren Helene, Meis-Kindblom Jeanne M, Stenman Göran, Aman Pierre, Kindblom Lars-Gunn |
| KRAS mutations and M2PK upregulation in stool samples from individuals with positive fecal occult blood tests screened for colorectal cancer. Tumori 0 100 (2): 122-7. Battaglia Paolo, Baritono Elisabetta, Remo Andrea, Vendraminelli Roberto, Conti Anton |
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- Page last updated:Feb 01, 2023
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