BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

351 related articles for article (PubMed ID: 29535429)

  • 1. 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]  

  • 2. 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]  

  • 3. [Association between SAMD9/SAMD9L and hematological malignancies].
    Narumi S; Hasegawa T
    Rinsho Ketsueki; 2018; 59(11):2475-2480. PubMed ID: 30531146
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Of gains and losses: SAMD9/SAMD9L and monosomy 7 in myelodysplastic syndrome.
    Cammenga J
    Exp Hematol; 2024 Apr; 134():104217. PubMed ID: 38649131
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gain-of-function
    Tesi B; Davidsson J; Voss M; Rahikkala E; Holmes TD; Chiang SCC; Komulainen-Ebrahim J; Gorcenco S; Rundberg Nilsson A; Ripperger T; Kokkonen H; Bryder D; Fioretos T; Henter JI; Möttönen M; Niinimäki R; Nilsson L; Pronk CJ; Puschmann A; Qian H; Uusimaa J; Moilanen J; Tedgård U; Cammenga J; Bryceson YT
    Blood; 2017 Apr; 129(16):2266-2279. PubMed ID: 28202457
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 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 Neuropathology of MIRAGE Syndrome.
    Viaene AN; Harding BN
    J Neuropathol Exp Neurol; 2020 Apr; 79(4):458-462. PubMed ID: 32106287
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L.
    Chen DH; Below JE; Shimamura A; Keel SB; Matsushita M; Wolff J; Sul Y; Bonkowski E; Castella M; Taniguchi T; Nickerson D; Papayannopoulou T; Bird TD; Raskind WH
    Am J Hum Genet; 2016 Jun; 98(6):1146-1158. PubMed ID: 27259050
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7.
    Nagamachi A; Matsui H; Asou H; Ozaki Y; Aki D; Kanai A; Takubo K; Suda T; Nakamura T; Wolff L; Honda H; Inaba T
    Cancer Cell; 2013 Sep; 24(3):305-17. PubMed ID: 24029230
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SAMD9L autoinflammatory or ataxia pancytopenia disease mutations activate cell-autonomous translational repression.
    Russell AJ; Gray PE; Ziegler JB; Kim YJ; Smith S; Sewell WA; Goodnow CC
    Proc Natl Acad Sci U S A; 2021 Aug; 118(34):. PubMed ID: 34417303
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Discovery of MIRAGE syndrome.
    Narumi S
    Pediatr Int; 2022 Jan; 64(1):e15283. PubMed ID: 35972063
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Emerging phenotypes linked to variants in
    Suntharalingham JP; Ishida M; Del Valle I; Stalman SE; Solanky N; Wakeling E; Moore GE; Achermann JC; Buonocore F
    Front Endocrinol (Lausanne); 2022; 13():953707. PubMed ID: 36060959
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A novel germline
    Cheah JJC; Brown AL; Schreiber AW; Feng J; Babic M; Moore S; Young CC; Fine M; Phillips K; Guandalini M; Wilson P; Poplawski N; Hahn CN; Scott HS
    Haematologica; 2019 Jul; 104(7):e318-e321. PubMed ID: 30923096
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 18.