BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

258 related articles for article (PubMed ID: 26280900)

  • 1. Germline duplication of ATG2B and GSKIP predisposes to familial myeloid malignancies.
    Saliba J; Saint-Martin C; Di Stefano A; Lenglet G; Marty C; Keren B; Pasquier F; Valle VD; Secardin L; Leroy G; Mahfoudhi E; Grosjean S; Droin N; Diop M; Dessen P; Charrier S; Palazzo A; Merlevede J; Meniane JC; Delaunay-Darivon C; Fuseau P; Isnard F; Casadevall N; Solary E; Debili N; Bernard OA; Raslova H; Najman A; Vainchenker W; Bellanné-Chantelot C; Plo I
    Nat Genet; 2015 Oct; 47(10):1131-40. PubMed ID: 26280900
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Germline ATG2B/GSKIP-containing 14q32 duplication predisposes to early clonal hematopoiesis leading to myeloid neoplasms.
    Pegliasco J; Hirsch P; Marzac C; Isnard F; Meniane JC; Deswarte C; Pellet P; Lemaitre C; Leroy G; Rabadan Moraes G; Guermouche H; Schmaltz-Panneau B; Pasquier F; Colas C; Benusiglio PR; Bera O; Bourhis JH; Brissot E; Caron O; Chraibi S; Cony-Makhoul P; Delaunay-Darivon C; Lapusan S; de Fontbrune FS; Fuseau P; Najman A; Vainchenker W; Delhommeau F; Micol JB; Plo I; Bellanné-Chantelot C
    Leukemia; 2022 Jan; 36(1):126-137. PubMed ID: 34172895
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germline duplication of ATG2B and GSKIP genes is not required for the familial myeloid malignancy syndrome associated with the duplication of chromosome 14q32.
    Babushok DV; Stanley NL; Morrissette JJD; Lieberman DB; Olson TS; Chou ST; Hexner EO
    Leukemia; 2018 Dec; 32(12):2720-2723. PubMed ID: 30087419
    [No Abstract]   [Full Text] [Related]  

  • 4. Loss of
    Sakai SS; Hasegawa A; Ishimura R; Tamura N; Kageyama S; Komatsu-Hirota S; Abe M; Ling Y; Okuda S; Funayama M; Kikkawa M; Miura Y; Sakimura K; Narita I; Waguri S; Shimizu R; Komatsu M
    Mol Cell Biol; 2022 Jan; 42(1):e0002421. PubMed ID: 34748402
    [TBL] [Abstract][Full Text] [Related]  

  • 5.
    Pegliasco J; Schmaltz-Panneau B; Martin JE; Chraibi S; Khalife-Hachem S; Salviat F; Pasquier F; Willekens C; Lopez M; Ben-Ali A; Bera O; Caron O; Castilla-Llorent C; Cotteret S; Bourdin C; Saada V; Auger N; de Botton S; Vainchenker W; Fuseau P; Helias P; Benabdelali R; Marzac C; Meniane JC; Plo I; Bellanné-Chantelot C; Micol JB
    Leuk Lymphoma; 2021 Jul; 62(7):1770-1773. PubMed ID: 33554699
    [No Abstract]   [Full Text] [Related]  

  • 6. Advances in understanding the pathogenesis of familial myeloproliferative neoplasms.
    Rumi E; Cazzola M
    Br J Haematol; 2017 Sep; 178(5):689-698. PubMed ID: 28444727
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial Acute Myeloid Leukemia and Myelodysplasia in Hungary.
    Király AP; Kállay K; Gángó A; Kellner Á; Egyed M; Szőke A; Kiss R; Vályi-Nagy I; Csomor J; Matolcsy A; Bödör C
    Pathol Oncol Res; 2018 Jan; 24(1):83-88. PubMed ID: 28357685
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. ATG2B and GSKIP: 2 new genes predisposing to myeloid malignancies.
    Plo I; Bellanné-Chantelot C; Vainchenker W
    Mol Cell Oncol; 2016 Mar; 3(2):e1094564. PubMed ID: 27308616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myelodysplastic syndromes and acute leukemia with genetic predispositions: a new challenge for hematologists.
    Duployez N; Lejeune S; Renneville A; Preudhomme C
    Expert Rev Hematol; 2016 Dec; 9(12):1189-1202. PubMed ID: 27819178
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations.
    Meggendorfer M; Bacher U; Alpermann T; Haferlach C; Kern W; Gambacorti-Passerini C; Haferlach T; Schnittger S
    Leukemia; 2013 Sep; 27(9):1852-60. PubMed ID: 23628959
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Expanding the role of the splicing USB1 gene from Poikiloderma with Neutropenia to acquired myeloid neoplasms.
    Negri G; Crescenzi B; Colombo EA; Fontana L; Barba G; Arcioni F; Gervasini C; Mecucci C; Larizza L
    Br J Haematol; 2015 Nov; 171(4):557-65. PubMed ID: 26306619
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Role of ASXL1 mutation in myeloid malignancies].
    Sheng MY; Zhou Y; Xu MJ; Yang FC
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2014 Aug; 22(4):1183-7. PubMed ID: 25130853
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Germline genetic factors in the pathogenesis of myeloproliferative neoplasms.
    Bellanné-Chantelot C; Rabadan Moraes G; Schmaltz-Panneau B; Marty C; Vainchenker W; Plo I
    Blood Rev; 2020 Jul; 42():100710. PubMed ID: 32532454
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia.
    Cardoso SR; Ryan G; Walne AJ; Ellison A; Lowe R; Tummala H; Rio-Machin A; Collopy L; Al Seraihi A; Wallis Y; Page P; Akiki S; Fitzgibbon J; Vulliamy T; Dokal I
    Leukemia; 2016 Oct; 30(10):2083-2086. PubMed ID: 27133828
    [No Abstract]   [Full Text] [Related]  

  • 18. Myeloid Neoplasms with Germline Predisposition: A New Provisional Entity Within the World Health Organization Classification.
    Czuchlewski DR; Peterson LC
    Surg Pathol Clin; 2016 Mar; 9(1):165-76. PubMed ID: 26940275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants.
    Rio-Machin A; Vulliamy T; Hug N; Walne A; Tawana K; Cardoso S; Ellison A; Pontikos N; Wang J; Tummala H; Al Seraihi AFH; Alnajar J; Bewicke-Copley F; Armes H; Barnett M; Bloor A; Bödör C; Bowen D; Fenaux P; Green A; Hallahan A; Hjorth-Hansen H; Hossain U; Killick S; Lawson S; Layton M; Male AM; Marsh J; Mehta P; Mous R; Nomdedéu JF; Owen C; Pavlu J; Payne EM; Protheroe RE; Preudhomme C; Pujol-Moix N; Renneville A; Russell N; Saggar A; Sciuccati G; Taussig D; Toze CL; Uyttebroeck A; Vandenberghe P; Schlegelberger B; Ripperger T; Steinemann D; Wu J; Mason J; Page P; Akiki S; Reay K; Cavenagh JD; Plagnol V; Caceres JF; Fitzgibbon J; Dokal I
    Nat Commun; 2020 Feb; 11(1):1044. PubMed ID: 32098966
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recent advances in the application of induced pluripotent stem cell technology to the study of myeloid malignancies.
    Tatwavedi D; Pellagatti A; Boultwood J
    Adv Biol Regul; 2024 Jan; 91():100993. PubMed ID: 37827894
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.