BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

298 related articles for article (PubMed ID: 34621053)

  • 1. Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes.
    Sahoo SS; Pastor VB; Goodings C; Voss RK; Kozyra EJ; Szvetnik A; Noellke P; Dworzak M; Starý J; Locatelli F; Masetti R; Schmugge M; De Moerloose B; Catala A; Kállay K; Turkiewicz D; Hasle H; Buechner J; Jahnukainen K; Ussowicz M; Polychronopoulou S; Smith OP; Fabri O; Barzilai S; de Haas V; Baumann I; Schwarz-Furlan S; ; Niewisch MR; Sauer MG; Burkhardt B; Lang P; Bader P; Beier R; Müller I; Albert MH; Meisel R; Schulz A; Cario G; Panda PK; Wehrle J; Hirabayashi S; Derecka M; Durruthy-Durruthy R; Göhring G; Yoshimi-Noellke A; Ku M; Lebrecht D; Erlacher M; Flotho C; Strahm B; Niemeyer CM; Wlodarski MW
    Nat Med; 2021 Oct; 27(10):1806-1817. PubMed ID: 34621053
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7.
    Yoshida M; Tanase-Nakao K; Shima H; Shirai R; Yoshida K; Osumi T; Deguchi T; Mori M; Arakawa Y; Takagi M; Miyamura T; Sakaguchi K; Toyoda H; Ishida H; Sakata N; Imamura T; Kawahara Y; Morimoto A; Koike T; Yagasaki H; Ito S; Tomizawa D; Kiyokawa N; Narumi S; Kato M
    Br J Haematol; 2020 Dec; 191(5):835-843. PubMed ID: 32770553
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes.
    Sahoo SS; Kozyra EJ; Wlodarski MW
    Best Pract Res Clin Haematol; 2020 Sep; 33(3):101197. PubMed ID: 33038986
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Outcomes of Hematopoietic Cell Transplantation in Patients with Germline SAMD9/SAMD9L Mutations.
    Ahmed IA; Farooqi MS; Vander Lugt MT; Boklan J; Rose M; Friehling ED; Triplett B; Lieuw K; Saldana BD; Smith CM; Schwartz JR; Goyal RK
    Biol Blood Marrow Transplant; 2019 Nov; 25(11):2186-2196. PubMed ID: 31306780
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pediatric MDS and bone marrow failure-associated germline mutations in SAMD9 and SAMD9L impair multiple pathways in primary hematopoietic cells.
    Thomas ME; Abdelhamed S; Hiltenbrand R; Schwartz JR; Sakurada SM; Walsh M; Song G; Ma J; Pruett-Miller SM; Klco JM
    Leukemia; 2021 Nov; 35(11):3232-3244. PubMed ID: 33731850
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cord Blood Transplantation in 2 Infants Presenting Monosomy 7 Clonal Hematopoiesis: SAMD9 / SAMD9L Germline Mutation.
    Hirai M; Yagasaki H; Kanezawa K; Ueno M; Shimozawa K; Imai K; Morio T; Kato M; Gocho Y; Narumi S; Ebihara Y; Morioka I
    J Pediatr Hematol Oncol; 2023 Mar; 45(2):e290-e293. PubMed ID: 36730951
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes.
    Wong JC; Bryant V; Lamprecht T; Ma J; Walsh M; Schwartz J; Del Pilar Alzamora M; Mullighan CG; Loh ML; Ribeiro R; Downing JR; Carroll WL; Davis J; Gold S; Rogers PC; Israels S; Yanofsky R; Shannon K; Klco JM
    JCI Insight; 2018 Jul; 3(14):. PubMed ID: 30046003
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiorgan failure with abnormal receptor metabolism in mice mimicking Samd9/9L syndromes.
    Nagamachi A; Kanai A; Nakamura M; Okuda H; Yokoyama A; Shinriki S; Matsui H; Inaba T
    J Clin Invest; 2021 Feb; 131(4):. PubMed ID: 33373325
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The genomic landscape of pediatric myelodysplastic syndromes.
    Schwartz JR; Ma J; Lamprecht T; Walsh M; Wang S; Bryant V; Song G; Wu G; Easton J; Kesserwan C; Nichols KE; Mullighan CG; Ribeiro RC; Klco JM
    Nat Commun; 2017 Nov; 8(1):1557. PubMed ID: 29146900
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents.
    Wlodarski MW; Hirabayashi S; Pastor V; Starý J; Hasle H; Masetti R; Dworzak M; Schmugge M; van den Heuvel-Eibrink M; Ussowicz M; De Moerloose B; Catala A; Smith OP; Sedlacek P; Lankester AC; Zecca M; Bordon V; Matthes-Martin S; Abrahamsson J; Kühl JS; Sykora KW; Albert MH; Przychodzien B; Maciejewski JP; Schwarz S; Göhring G; Schlegelberger B; Cseh A; Noellke P; Yoshimi A; Locatelli F; Baumann I; Strahm B; Niemeyer CM;
    Blood; 2016 Mar; 127(11):1387-97; quiz 1518. PubMed ID: 26702063
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies.
    Davidsson J; Puschmann A; Tedgård U; Bryder D; Nilsson L; Cammenga J
    Leukemia; 2018 May; 32(5):1106-1115. PubMed ID: 29535429
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Revertant somatic mosaicism as a cause of cancer.
    Inaba T; Nagamachi A
    Cancer Sci; 2021 Apr; 112(4):1383-1389. PubMed ID: 33583097
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Generation of heterozygous SAMD9 CRISPR/Cas9-edited iPSC line (ESi086-A-3), carrying p.I1567M mutation.
    Pera J; Castaño J; Casamitjana J; Giorgetti A; Romero-Moya D
    Stem Cell Res; 2022 Oct; 64():102906. PubMed ID: 36087523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Predisposition and progression of myelodysplastic syndromes].
    Makishima H
    Rinsho Ketsueki; 2021; 62(4):278-288. PubMed ID: 33967153
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Germline loss-of-function
    Nagata Y; Narumi S; Guan Y; Przychodzen BP; Hirsch CM; Makishima H; Shima H; Aly M; Pastor V; Kuzmanovic T; Radivoyevitch T; Adema V; Awada H; Yoshida K; Li S; Sole F; Hanna R; Jha BK; LaFramboise T; Ogawa S; Sekeres MA; Wlodarski MW; Cammenga J; Maciejewski JP
    Blood; 2018 Nov; 132(21):2309-2313. PubMed ID: 30322869
    [No Abstract]   [Full Text] [Related]  

  • 16. The International Consensus Classification (ICC) of hematologic neoplasms with germline predisposition, pediatric myelodysplastic syndrome, and juvenile myelomonocytic leukemia.
    Rudelius M; Weinberg OK; Niemeyer CM; Shimamura A; Calvo KR
    Virchows Arch; 2023 Jan; 482(1):113-130. PubMed ID: 36445482
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Novel germline SAMD9 mutation in an elderly patient with myelodysplastic syndrome].
    Uchida T; Fujii T; Ohara S; Imai Y; Inoue M; Harada Y; Harada H; Hagihara M
    Rinsho Ketsueki; 2022; 63(8):865-869. PubMed ID: 36058856
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MDS-associated mutations in germline GATA2 mutated patients with hematologic manifestations.
    McReynolds LJ; Yang Y; Yuen Wong H; Tang J; Zhang Y; Mulé MP; Daub J; Palmer C; Foruraghi L; Liu Q; Zhu J; Wang W; West RR; Yohe ME; Hsu AP; Hickstein DD; Townsley DM; Holland SM; Calvo KR; Hourigan CS
    Leuk Res; 2019 Jan; 76():70-75. PubMed ID: 30578959
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A familial
    Rahim MQ; Rahrig A; Overholt K; Conboy E; Czader M; Saraf AJ
    Cold Spring Harb Mol Case Stud; 2023 Apr; 9(2):. PubMed ID: 37160314
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Monosomy 7 in Pediatric Myelodysplastic Syndromes.
    Wlodarski MW; Sahoo SS; Niemeyer CM
    Hematol Oncol Clin North Am; 2018 Aug; 32(4):729-743. PubMed ID: 30047423
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.