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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 5, 2023. (Total: 217663Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Monosomy and TET2[original query]
Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases.
Haematologica 2012 Dec 97 (12): 1890-4.
Schnittger Susanne, Bacher Ulrike, Alpermann Tamara, Reiter Andreas, Ulke Madlen, Dicker Frank, Eder Christiane, Kohlmann Alexander, Grossmann Vera, Kowarsch Andreas, Kern Wolfgang, Haferlach Claudia, Haferlach Torst
The enigma of monosomy 7.
Blood 2018 4 131 (26): 2891-2898.
Inaba Toshiya, Honda Hiroaki, Matsui Hirota
Homogeneously staining region (hsr) on chromosome 11 is highly specific for KMT2A amplification in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS).
Cancer genetics 2019 Jul 238 18-22.
Sakhdari Ali, Tang Zhenya, Ok Chi Young, Bueso-Ramos Carlos E, Medeiros L Jeffrey, Huh Yang
ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome.
Blood advances 2021 9 6 (3): 793-807.
West Robert R, Calvo Katherine R, Embree Lisa J, Wang Weixin, Tuschong Laura M, Bauer Thomas R, Tillo Desiree, Lack Justin, Droll Stephenie, Hsu Amy P, Holland Steven M, Hickstein Dennis
Prognostic impact of the adverse molecular-genetic profile on long-term outcomes following allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia.
Bone marrow transplantation 2021 Mar .
Daher-Reyes Georgina, Kim TaeHyung, Novitzky-Basso Igor, Kim Kyuoung Ha, Smith Adam, Stockley Tracy, Capochichi Jose-Mario, Al-Shaibani Zeyad, Pasic Ivan, Law Arjun, Lam Wilson, Michelis Fotios V, Gerbitz Armin, Viswabandya Auro, Lipton Jeffrey, Kumar Rajat, Mattsson Jonas, Schimmer Aaron, McNamara Caroline, Murphy Tracy, Maze Dawn, Gupta Vikas, Sibai Hassan, Chan Steven, Yee Karen, Minden Mark, Zhang Zhaolei, Schuh Andre, Kim Dennis D
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