These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
10. Functional characterization of a germline ETV6 variant associated with inherited thrombocytopenia, acute lymphoblastic leukemia, and salivary gland carcinoma in childhood. Yoshino H; Nishiyama Y; Kamma H; Chiba T; Fujiwara M; Karaho T; Kogashiwa Y; Morio T; Yan K; Bessho F; Takagi M Int J Hematol; 2020 Aug; 112(2):217-222. PubMed ID: 32367453 [TBL] [Abstract][Full Text] [Related]
11. Molecular basis of ETV6-mediated predisposition to childhood acute lymphoblastic leukemia. Nishii R; Baskin-Doerfler R; Yang W; Oak N; Zhao X; Yang W; Hoshitsuki K; Bloom M; Verbist K; Burns M; Li Z; Lin TN; Qian M; Moriyama T; Gastier-Foster JM; Rabin KR; Raetz E; Mullighan C; Pui CH; Yeoh AE; Zhang J; Metzger ML; Klco JM; Hunger SP; Newman S; Wu G; Loh ML; Nichols KE; Yang JJ Blood; 2021 Jan; 137(3):364-373. PubMed ID: 32693409 [TBL] [Abstract][Full Text] [Related]
12. Junk SV; Klein N; Schreek S; Zimmermann M; Möricke A; Bleckmann K; Alten J; Dagdan E; Cario G; Kratz CP; Schrappe M; Stanulla M Haematologica; 2019 Sep; 104(9):e402-e405. PubMed ID: 31289210 [No Abstract] [Full Text] [Related]
13. Expression profile of wild-type ETV6 in childhood acute leukaemia. Patel N; Goff LK; Clark T; Ford AM; Foot N; Lillington D; Hing S; Pritchard-Jones K; Jones LK; Saha V Br J Haematol; 2003 Jul; 122(1):94-8. PubMed ID: 12823350 [TBL] [Abstract][Full Text] [Related]
14. Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders. Latger-Cannard V; Philippe C; Bouquet A; Baccini V; Alessi MC; Ankri A; Bauters A; Bayart S; Cornillet-Lefebvre P; Daliphard S; Mozziconacci MJ; Renneville A; Ballerini P; Leverger G; Sobol H; Jonveaux P; Preudhomme C; Nurden P; Lecompte T; Favier R Orphanet J Rare Dis; 2016 Apr; 11():49. PubMed ID: 27112265 [TBL] [Abstract][Full Text] [Related]
15. Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting Järviaho T; Bang B; Zachariadis V; Taylan F; Moilanen J; Möttönen M; Smith CIE; Harila-Saari A; Niinimäki R; Nordgren A Blood Adv; 2019 Sep; 3(18):2722-2731. PubMed ID: 31519648 [TBL] [Abstract][Full Text] [Related]
16. Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. Ellinghaus E; Stanulla M; Richter G; Ellinghaus D; te Kronnie G; Cario G; Cazzaniga G; Horstmann M; Panzer Grümayer R; Cavé H; Trka J; Cinek O; Teigler-Schlegel A; ElSharawy A; Häsler R; Nebel A; Meissner B; Bartram T; Lescai F; Franceschi C; Giordan M; Nürnberg P; Heinzow B; Zimmermann M; Schreiber S; Schrappe M; Franke A Leukemia; 2012 May; 26(5):902-9. PubMed ID: 22076464 [TBL] [Abstract][Full Text] [Related]
17. ETV6 in hematopoiesis and leukemia predisposition. Hock H; Shimamura A Semin Hematol; 2017 Apr; 54(2):98-104. PubMed ID: 28637624 [TBL] [Abstract][Full Text] [Related]
18. Functional analysis of germline Kozubik KS; Radova L; Reblova K; Smida M; Zaliova Kubricanova M; Baloun J; Pesova M; Vrzalova Z; Folber F; Mejstrikova S; Pospisilova S; Doubek M Platelets; 2021 Aug; 32(6):838-841. PubMed ID: 32819174 [TBL] [Abstract][Full Text] [Related]
19. Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: a combined PCR and Southern blotting analysis. O'Connor HE; Butler TA; Clark R; Swanton S; Harrison CJ; Secker-Walker LM; Foroni L Leukemia; 1998 Jul; 12(7):1099-106. PubMed ID: 9665196 [TBL] [Abstract][Full Text] [Related]
20. Functional damaging germline variants in ETV6, IKZF1, PAX5 and RUNX1 predisposing to B-cell precursor acute lymphoblastic leukemia. Wagener R; Elitzur S; Brozou T; Borkhardt A Eur J Med Genet; 2023 Apr; 66(4):104725. PubMed ID: 36764385 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]