BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 32944898)

  • 1. A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome.
    Ferrari S; Regazzo D; Omenetto E; Scaroni C; Semenzato G; Fabris F; Vianello F
    Aging Clin Exp Res; 2021 Jul; 33(7):1987-1992. PubMed ID: 32944898
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults.
    Babushok DV; Bessler M; Olson TS
    Leuk Lymphoma; 2016; 57(3):520-36. PubMed ID: 26693794
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ANKRD26-Related Thrombocytopenia and Predisposition to Myeloid Neoplasms.
    Sullivan MJ; Palmer EL; Botero JP
    Curr Hematol Malig Rep; 2022 Oct; 17(5):105-112. PubMed ID: 35751752
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia.
    Melazzini F; Palombo F; Balduini A; De Rocco D; Marconi C; Noris P; Gnan C; Pippucci T; Bozzi V; Faleschini M; Barozzi S; Doubek M; Di Buduo CA; Kozubik KS; Radova L; Loffredo G; Pospisilova S; Alfano C; Seri M; Balduini CL; Pecci A; Savoia A
    Haematologica; 2016 Nov; 101(11):1333-1342. PubMed ID: 27365488
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inherited thrombocytopenia and platelet disorders with germline predisposition to myeloid neoplasia.
    Galera P; Dulau-Florea A; Calvo KR
    Int J Lab Hematol; 2019 May; 41 Suppl 1():131-141. PubMed ID: 31069978
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Platelet transcriptome analysis in patients with germline RUNX1 mutations.
    Palma-Barqueros V; Bastida JM; López Andreo MJ; Zámora-Cánovas A; Zaninetti C; Ruiz-Pividal JF; Bohdan N; Padilla J; Teruel-Montoya R; Marín-Quilez A; Revilla N; Sánchez-Fuentes A; Rodriguez-Alen A; Benito R; Vicente V; Iturbe T; Greinacher A; Lozano ML; Rivera J; ;
    J Thromb Haemost; 2023 May; 21(5):1352-1365. PubMed ID: 36736831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence and natural history of variants in the
    Vyas H; Alcheikh A; Lowe G; Stevenson WS; Morgan NV; Rabbolini DJ
    Platelets; 2022 Nov; 33(8):1107-1112. PubMed ID: 35587581
    [No Abstract]   [Full Text] [Related]  

  • 8. Hereditary Predispositions to Myelodysplastic Syndrome.
    Bannon SA; DiNardo CD
    Int J Mol Sci; 2016 May; 17(6):. PubMed ID: 27248996
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic predisposition syndromes: when should they be considered in the work-up of MDS?
    Babushok DV; Bessler M
    Best Pract Res Clin Haematol; 2015 Mar; 28(1):55-68. PubMed ID: 25659730
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia.
    Marconi C; Canobbio I; Bozzi V; Pippucci T; Simonetti G; Melazzini F; Angori S; Martinelli G; Saglio G; Torti M; Pastan I; Seri M; Pecci A
    J Hematol Oncol; 2017 Jan; 10(1):18. PubMed ID: 28100250
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases.
    Zaninetti C; Santini V; Tiniakou M; Barozzi S; Savoia A; Pecci A
    J Thromb Haemost; 2017 Dec; 15(12):2388-2392. PubMed ID: 28976612
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation.
    Bluteau D; Balduini A; Balayn N; Currao M; Nurden P; Deswarte C; Leverger G; Noris P; Perrotta S; Solary E; Vainchenker W; Debili N; Favier R; Raslova H
    J Clin Invest; 2014 Feb; 124(2):580-91. PubMed ID: 24430186
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical and genetic background of familial myelodysplasia and acute myeloid leukemia].
    Király PA; Kállay K; Marosvári D; Benyó G; Szőke A; Csomor J; Bödör C
    Orv Hetil; 2016 Feb; 157(8):283-9. PubMed ID: 26876264
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inherited Thrombocytopenia Caused by Germline
    Kewan T; Noss R; Godley LA; Rogers HJ; Carraway HE
    J Investig Med High Impact Case Rep; 2020; 8():2324709620938941. PubMed ID: 32618208
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombo-cytopenia.
    Necchi V; Balduini A; Noris P; Barozzi S; Sommi P; di Buduo C; Balduini CL; Solcia E; Pecci A
    Thromb Haemost; 2013 Feb; 109(2):263-71. PubMed ID: 23223974
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Germline ETV6 mutations and predisposition to hematological malignancies.
    Feurstein S; Godley LA
    Int J Hematol; 2017 Aug; 106(2):189-195. PubMed ID: 28555414
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.
    Ouchi-Uchiyama M; Sasahara Y; Kikuchi A; Goi K; Nakane T; Ikeno M; Noguchi Y; Uike N; Miyajima Y; Matsubara K; Koh K; Sugita K; Imaizumi M; Kure S
    Pediatr Blood Cancer; 2015 Dec; 62(12):2082-8. PubMed ID: 26175287
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectrum of clinical and genetic features of patients with inherited platelet disorder with suspected predisposition to hematological malignancies: a nationwide survey in Japan.
    Yoshimi A; Toya T; Nannya Y; Takaoka K; Kirito K; Ito E; Nakajima H; Hayashi Y; Takahashi T; Moriya-Saito A; Suzuki K; Harada H; Komatsu N; Usuki K; Ichikawa M; Kurokawa M
    Ann Oncol; 2016 May; 27(5):887-95. PubMed ID: 26884589
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26.
    Homan CC; Scott HS; Brown AL
    Blood; 2023 Mar; 141(13):1533-1543. PubMed ID: 36626254
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel phenotypes observed in patients with
    Karastaneva A; Nebral K; Schlagenhauf A; Baschin M; Palankar R; Juch H; Heitzer E; Speicher MR; Höfler G; Grigorow I; Urban C; Benesch M; Greinacher A; Haas OA; Seidel MG
    J Med Genet; 2020 Jun; 57(6):427-433. PubMed ID: 31704777
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.