194 related articles for article (PubMed ID: 37738626)
21. 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]
22. The clinical heterogeneity of
Tang C; Rabbolini DJ; Morel-Kopp MC; Connor DE; Crispin P; Ward CM; Stevenson WS
Res Pract Thromb Haemost; 2020 Jan; 4(1):106-110. PubMed ID: 31989091
[TBL] [Abstract][Full Text] [Related]
23. MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.
Antony-Debré I; Bluteau D; Itzykson R; Baccini V; Renneville A; Boehlen F; Morabito M; Droin N; Deswarte C; Chang Y; Leverger G; Solary E; Vainchenker W; Favier R; Raslova H
Blood; 2012 Sep; 120(13):2719-22. PubMed ID: 22677128
[TBL] [Abstract][Full Text] [Related]
24. A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder.
Almazni I; Chudakou P; Dawson-Meadows A; Downes K; Freson K; Mason J; Page P; Reay K; Myers B; Morgan NV;
Platelets; 2022 Feb; 33(2):320-323. PubMed ID: 33616470
[TBL] [Abstract][Full Text] [Related]
25. Role of RUNX1 in hematological malignancies.
Sood R; Kamikubo Y; Liu P
Blood; 2017 Apr; 129(15):2070-2082. PubMed ID: 28179279
[TBL] [Abstract][Full Text] [Related]
26. Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency.
Del Carpio-Cano F; Mao G; Goldfinger LE; Wurtzel J; Guan L; Alam MA; Lee K; Poncz M; Rao AK
Blood Adv; 2024 Apr; 8(7):1699-1714. PubMed ID: 38330198
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant.
Lamolda M; Montes R; Simón I; Perales S; Martínez-Navajas G; Lopez-Onieva L; Ríos-Pelegrina R; Del Moral RG; Griñan-Lison C; Marchal JA; Lozano ML; Ramos-Mejia V; Rivera J; Bastida JM; Real PJ
Stem Cell Res; 2019 Dec; 41():101603. PubMed ID: 31698193
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Germline RUNX1 translocation in familial platelet disorder with propensity to myeloid malignancies.
Sakurai M; Nannya Y; Yamazaki R; Yamaguchi K; Koda Y; Abe R; Yokoyama K; Ogawa S; Mori T
Ann Hematol; 2022 Jan; 101(1):237-239. PubMed ID: 33462643
[No Abstract] [Full Text] [Related]
31. Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy.
Owen CJ; Toze CL; Koochin A; Forrest DL; Smith CA; Stevens JM; Jackson SC; Poon MC; Sinclair GD; Leber B; Johnson PR; Macheta A; Yin JA; Barnett MJ; Lister TA; Fitzgibbon J
Blood; 2008 Dec; 112(12):4639-45. PubMed ID: 18723428
[TBL] [Abstract][Full Text] [Related]
32. [Familial platelet disorder with predisposition to myeloid leukemia (FPD/AML): a case report and literature review].
Zhang RR; Chen XJ; Ren YY; Yang WY; Zhu XF
Zhonghua Xue Ye Xue Za Zhi; 2021 Apr; 42(4):308-312. PubMed ID: 33979975
[No Abstract] [Full Text] [Related]
33. Inherited predisposition to acute myeloid leukemia.
Godley LA
Semin Hematol; 2014 Oct; 51(4):306-21. PubMed ID: 25311743
[TBL] [Abstract][Full Text] [Related]
34. A novel RUNX1 mutation in a kindred with familial platelet disorder with propensity to acute myeloid leukaemia: male predominance of affected individuals.
Langabeer SE; Owen CJ; McCarron SL; Fitzgibbon J; Smith OP; O'Marcaigh A; Browne P
Eur J Haematol; 2010 Dec; 85(6):552-3. PubMed ID: 20722699
[No Abstract] [Full Text] [Related]
35. Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets.
Glembotsky AC; Bluteau D; Espasandin YR; Goette NP; Marta RF; Marin Oyarzun CP; Korin L; Lev PR; Laguens RP; Molinas FC; Raslova H; Heller PG
J Thromb Haemost; 2014 May; 12(5):761-72. PubMed ID: 24606315
[TBL] [Abstract][Full Text] [Related]
36. B-cell acute lymphoblastic leukemia in patients with germline RUNX1 mutations.
Six KA; Gerdemann U; Brown AL; Place AE; Cantor AB; Kutny MA; Avagyan S
Blood Adv; 2021 Aug; 5(16):3199-3202. PubMed ID: 34424323
[TBL] [Abstract][Full Text] [Related]
37. Development of hairy cell leukemia in familial platelet disorder with predisposition to acute myeloid leukemia.
Toya T; Yoshimi A; Morioka T; Arai S; Ichikawa M; Usuki K; Kurokawa M
Platelets; 2014; 25(4):300-2. PubMed ID: 23971860
[TBL] [Abstract][Full Text] [Related]
38. Genomic Landscape of Patients with Germline
Yu K; Deuitch N; Merguerian M; Cunningham L; Davis J; Bresciani E; Diemer J; Andrews E; Young A; Donovan F; Sood R; Craft K; Chong S; Chandrasekharappa S; Mullikin J; Liu PP
bioRxiv; 2023 Jan; ():. PubMed ID: 36789433
[TBL] [Abstract][Full Text] [Related]
39. Familial myelodysplasia and acute myeloid leukaemia--a review.
Owen C; Barnett M; Fitzgibbon J
Br J Haematol; 2008 Jan; 140(2):123-32. PubMed ID: 18173751
[TBL] [Abstract][Full Text] [Related]
40. AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.
Taketani T; Taki T; Takita J; Tsuchida M; Hanada R; Hongo T; Kaneko T; Manabe A; Ida K; Hayashi Y
Genes Chromosomes Cancer; 2003 Sep; 38(1):1-7. PubMed ID: 12874780
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
