Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and PPM1D[original query] |
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Prognostic Mutations in Myelodysplastic Syndrome after Stem-Cell Transplantation. The New England journal of medicine 2017 02 376 (6): 536-547. Lindsley R Coleman, Saber Wael, Mar Brenton G, Redd Robert, Wang Tao, Haagenson Michael D, Grauman Peter V, Hu Zhen-Huan, Spellman Stephen R, Lee Stephanie J, Verneris Michael R, Hsu Katharine, Fleischhauer Katharina, Cutler Corey, Antin Joseph H, Neuberg Donna, Ebert Benjamin |
Diagnosis of Li-Fraumeni Syndrome: Differentiating TP53 germline mutations from clonal hematopoiesis: Results of the observational AGO-TR1 trial. Human mutation 2018 Sep . Weber-Lassalle Konstantin, Harter Philipp, Hauke Jan, Ernst Corinna, Kommoss Stefan, Marmé Frederik, Weber-Lassalle Nana, Prieske Katharina, Dietrich Dimo, Borde Julika, Pohl-Rescigno Esther, Reuss Alexander, Ataseven Beyhan, Engel Christoph, Stingl Julia C, Schmutzler Rita K, Hahnen Er |
A high prevalence of myeloid malignancies in progeria with Werner syndrome is associated with p53 insufficiency. Experimental hematology 2022 3 109 11-17. Kato Hisaya, Maezawa Yoshiro, Nishijima Dai, Iwamoto Eisuke, Takeda June, Kanamori Takashi, Yamaga Masaya, Mishina Tatsuzo, Takeda Yusuke, Izumi Shintaro, Hino Yutaro, Nishi Hiroyuki, Ishiko Jun, Takeuchi Masahiro, Kaneko Hiyori, Koshizaka Masaya, Mimura Naoya, Kuzuya Masafumi, Sakaida Emiko, Takemoto Minoru, Shiraishi Yuichi, Miyano Satoru, Ogawa Seishi, Iwama Atsushi, Sanada Masashi, Yokote Kouta |
Low-Frequency PPM1D Gene Mutations Affect Treatment Response to CD19-Targeted CAR T-Cell Therapy in Large B-Cell Lymphoma. Current oncology (Toronto, Ont.) 2023 12 30 (12): 10463-10476. Katja Seipel, Michèle Frey, Henning Nilius, Dilara Akhoundova, Yara Banz, Ulrike Bacher, Thomas Pab |
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- Page last updated:Apr 22, 2024
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