230 related articles for article (PubMed ID: 24030261)
1. ANKRD26-related thrombocytopenia and myeloid malignancies.
Noris P; Favier R; Alessi MC; Geddis AE; Kunishima S; Heller PG; Giordano P; Niederhoffer KY; Bussel JB; Podda GM; Vianelli N; Kersseboom R; Pecci A; Gnan C; Marconi C; Auvrignon A; Cohen W; Yu JC; Iguchi A; Miller Imahiyerobo A; Boehlen F; Ghalloussi D; De Rocco D; Magini P; Civaschi E; Biino G; Seri M; Savoia A; Balduini CL
Blood; 2013 Sep; 122(11):1987-9. PubMed ID: 24030261
[No Abstract] [Full Text] [Related]
2. A missense mutation in ANKRD26 segregates with thrombocytopenia.
Al Daama SA; Housawi YH; Dridi W; Sager M; Otieno FG; Hou C; Vasquez L; Kim C; Tian L; Sleiman P; Hakonarson H
Blood; 2013 Jul; 122(3):461-2. PubMed ID: 23869080
[No Abstract] [Full Text] [Related]
3. BCR-ABL+ Chronic Myeloid Leukemia Arising in a Family With Inherited ANKRD26-Related Thrombocytopenia.
Tsumura AM; Druker BJ; Brewer D; Press R; Braun TP
JCO Precis Oncol; 2021; 5():. PubMed ID: 34250402
[No Abstract] [Full Text] [Related]
4. 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]
5. 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]
6. Relation between mutations in the 5' UTR of ANKRD26 gene and inherited thrombocytopenia with predisposition to myeloid malignancies. An Egyptian study.
Zidan NI; AbdElmonem DM; Elsheikh HM; Metwally EA; Mokhtar WA; Osman GM
Platelets; 2021 Jul; 32(5):642-650. PubMed ID: 32659145
[TBL] [Abstract][Full Text] [Related]
7. Philadelphia chromosome positive myelodysplastic syndrome and acute myelogenous leukemia.
Advani AS
Leuk Res; 2004 Jun; 28(6):545-6. PubMed ID: 15120928
[No Abstract] [Full Text] [Related]
8. Mutations of the RAS genes in childhood acute myeloid leukemia, myelodysplastic syndrome and juvenile chronic myelocytic leukemia.
Sheng XM; Kawamura M; Ohnishi H; Ida K; Hanada R; Kojima S; Kobayashi M; Bessho F; Yanagisawa M; Hayashi Y
Leuk Res; 1997 Aug; 21(8):697-701. PubMed ID: 9379676
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Spectrum of 5'UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected.
Ferrari S; Lombardi AM; Putti MC; Bertomoro A; Cortella I; Barzon I; Girolami A; Fabris F
Platelets; 2017 Sep; 28(6):621-624. PubMed ID: 28277066
[No Abstract] [Full Text] [Related]
11. Absence of BRAF V600E mutation in a cohort of 402 patients with various chronic and acute myeloid neoplasms.
Trifa AP; Popp RA; Cucuianu A; Coadă CA; Urian LG; Militaru MS; Bănescu C; Dima D; Farcaş MF; Crişan TO; Petrov L; Gug C; Pop IV
Leuk Lymphoma; 2012 Dec; 53(12):2496-7. PubMed ID: 22339435
[No Abstract] [Full Text] [Related]
12. Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemia.
Boultwood J; Pellagatti A; Watkins F; Campbell LJ; Esoof N; Cross NC; Eagleton H; Littlewood TJ; Fidler C; Wainscoat JS
Br J Haematol; 2004 Aug; 126(4):508-11. PubMed ID: 15287943
[TBL] [Abstract][Full Text] [Related]
13. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21.
Preudhomme C; Warot-Loze D; Roumier C; Grardel-Duflos N; Garand R; Lai JL; Dastugue N; Macintyre E; Denis C; Bauters F; Kerckaert JP; Cosson A; Fenaux P
Blood; 2000 Oct; 96(8):2862-9. PubMed ID: 11023523
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Myeloid neoplasm with t(3;8)(q26;q24): report of six cases and review of the literature.
Xu X; Su M; Levy NB; Mohtashamian A; Monaghan S; Kaur P; Zaremba C; Garcia R; Broome HE; Dell'Aquila ML; Wang HY
Leuk Lymphoma; 2014 Nov; 55(11):2532-7. PubMed ID: 24397594
[TBL] [Abstract][Full Text] [Related]
20. High frequency of MEFV gene mutations in patients with myeloid neoplasm.
Oktenli C; Sayan O; Celik S; Erikci AA; Tunca Y; Terekeci HM; Umur EE; Sanisoglu YS; Torun D; Tangi F; Sahan B; Nalbant S
Int J Hematol; 2010 Jun; 91(5):758-61. PubMed ID: 20437121
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
