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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

385 related articles for article (PubMed ID: 29264741)

  • 1. Rearrangement of VPS13B, a causative gene of Cohen syndrome, in a case of RUNX1-RUNX1T1 leukemia with t(8;12;21).
    Abe A; Yamamoto Y; Katsumi A; Okamoto A; Tokuda M; Inaguma Y; Yamamoto K; Yanada M; Kanie T; Tomita A; Akatsuka Y; Okamoto M; Kameyama T; Mayeda A; Emi N
    Int J Hematol; 2018 Aug; 108(2):208-212. PubMed ID: 29264741
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Myeloid neoplasms with t(16;21)(q24;q22)/RUNX1-RUNX1T3 mimics acute myeloid leukemia with RUNX1-RUNX1T1.
    Liu H; Wang SA; Schlette EJ; Xu J; Jorgensen JL; Cameron Yin C; Li S; Jeffrey Medeiros L; Tang G
    Ann Hematol; 2018 Oct; 97(10):1775-1783. PubMed ID: 29872884
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transformation into acute myeloid leukemia with t(8;21)(q22;q22.1); RUNX1::RUNX1T1 from JAK2-mutated essential thrombocythemia: a case report.
    Asou C; Sakamoto T; Suzuki K; Okuda I; Osaki A; Abe R; Ito Y; Kakegawa E; Miyakawa Y; Terui Y; Nakamura Y
    J Med Case Rep; 2024 Aug; 18(1):372. PubMed ID: 39154170
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel Four-Way t(8;14;15;21)(q22;q22;q15;q22.1) Translocation Variant in Acute Myeloid Leukemia with
    Tsuge N; Ogasawara F; Kondo T; Yoshida S; Kojima K
    Turk J Haematol; 2024 May; 41(2):128-129. PubMed ID: 38488305
    [No Abstract]   [Full Text] [Related]  

  • 5. First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations.
    Rejeb I; Jilani H; Elaribi Y; Hizem S; Hila L; Zillahrdt JL; Chelly J; Benjemaa L
    BMC Med Genet; 2017 Nov; 18(1):134. PubMed ID: 29149870
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The dynamics of RUNX1-RUNX1T1 transcript levels after allogeneic hematopoietic stem cell transplantation predict relapse in patients with t(8;21) acute myeloid leukemia.
    Qin YZ; Wang Y; Xu LP; Zhang XH; Chen H; Han W; Chen YH; Wang FR; Wang JZ; Chen Y; Mo XD; Zhao XS; Chang YJ; Liu KY; Huang XJ
    J Hematol Oncol; 2017 Feb; 10(1):44. PubMed ID: 28166825
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A favorable clinical course of acute myeloid leukemia with t (6;21;8)(p23;q22;q22)].
    Wada A; Doki N; Otsuka Y; Adachi H; Konuma R; Kishida Y; Konishi T; Yamada Y; Nagata A; Nagata R; Marumo A; Noguchi Y; Mukae J; Toya T; Igarashi A; Najima Y; Kobayashi T; Harada H; Harada Y; Sakamaki H; Ohashi K
    Rinsho Ketsueki; 2022; 63(2):104-107. PubMed ID: 35264498
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel VPS13B mutation in Cohen syndrome: a case report and review of literature.
    Momtazmanesh S; Rayzan E; Shahkarami S; Rohlfs M; Klein C; Rezaei N
    BMC Med Genet; 2020 Jun; 21(1):140. PubMed ID: 32605629
    [TBL] [Abstract][Full Text] [Related]  

  • 9. t(2;2;21;8)(p21;q37;q22;q22), a novel four-way complex translocation involving variant t(8;21) in case of acute myeloid leukemia : A case report and literature review.
    Han B; Jing Y; Bi X; Lin Y; Li H; Li H; Ru K; Yang S
    Cancer Genet; 2024 Jun; 284-285():1-4. PubMed ID: 38460349
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new complex translocation (8;22;21)(q22;q12;q22) in RUNX1/RUNX1T1 acute myeloid leukaemia.
    Tay Za K; Shanmugam H; Chin EFM
    Malays J Pathol; 2019 Dec; 41(3):333-338. PubMed ID: 31901918
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Salmon-coloured granules in residual acute myeloid leukaemia with t(8;21)(q22;q22.1); RUNX1-RUNX1T1.
    Chen D; Chen W
    Br J Haematol; 2021 May; 193(4):691. PubMed ID: 33386742
    [No Abstract]   [Full Text] [Related]  

  • 12. A novel homozygous nonsense mutation of VPS13B associated with previously unreported features of Cohen syndrome.
    Koehler K; Schuelke M; Hell AK; Schittkowski M; Huebner A; Brockmann K
    Am J Med Genet A; 2020 Mar; 182(3):570-575. PubMed ID: 31825161
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Acute myeloid leukemia with del(X)(p21) and cryptic RUNX1/RUNX1T1 from ins(8;21)(q22;q22q22) revealed by atypical FISH signals.
    Jang JH; Yoo EH; Kim HJ; Kim DH; Jung CW; Kim SH
    Ann Clin Lab Sci; 2010; 40(1):80-4. PubMed ID: 20124335
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Novel VPS13B Mutation Identified by Whole-Exome Sequencing in Iranian Patients with Cohen Syndrome.
    Karimzadeh MR; Omidi F; Sahebalzamani A; Saeidi K
    J Mol Neurosci; 2021 Dec; 71(12):2566-2574. PubMed ID: 34041686
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Case report: two novel VPS13B mutations in a Chinese family with Cohen syndrome and hyperlinear palms.
    Zhao S; Luo Z; Xiao Z; Li L; Zhao R; Yang Y; Zhong Y
    BMC Med Genet; 2019 Nov; 20(1):187. PubMed ID: 31752730
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a Cryptic t(8;20;21)(q22;p13;q22) Resulting in RUNX1T1/RUNX1 Fusion in a Patient with Newly Diagnosed Acute Myeloid Leukemia.
    Macke EL; Meyer RG; Hoppman NL; Ketterling RP; Greipp PT; Xu X; Baughn LB; Shafer DA; He RR; Peterson JF
    Lab Med; 2022 Jul; 53(4):e87-e90. PubMed ID: 34791328
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional and clinical characterization of the alternatively spliced isoform AML1-ETO9a in adult patients with translocation t(8;21)(q22;q22.1) acute myeloid leukemia (AML).
    Agrawal M; Schwarz P; Giaimo BD; Bedzhov I; Corbacioglu A; Weber D; Gaidzik VI; Jahn N; Rücker FG; Schroeder T; Kindler T; Wattad M; Götze K; Lübbert M; Salwender H; Ringhoffer M; Lange E; Koller E; Thol F; Heuser M; Ganser A; Bullinger L; Paschka P; Döhner H; Geiger H; Borggrefe T; Döhner K; Oswald F
    Leukemia; 2020 Feb; 34(2):630-634. PubMed ID: 31462736
    [No Abstract]   [Full Text] [Related]  

  • 18. Characterization of bone marrow mast cells in acute myeloid leukemia with t(8;21) (q22;q22); RUNX1-RUNX1T1.
    Pullarkat ST; Pullarkat V; Lagoo A; Brynes R; Weiss LM; Bedell V; Chen W; Huang Q; Gaal K; Weisenburger DD; Kim YS
    Leuk Res; 2013 Nov; 37(11):1572-5. PubMed ID: 24035334
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in the VPS13B Gene in Iranian Patients with Different Phenotypes of Cohen Syndrome.
    Alipour N; Salehpour S; Tonekaboni SH; Rostami M; Bahari S; Yassaee V; Miryounesi M; Ghafouri-Fard S
    J Mol Neurosci; 2020 Jan; 70(1):21-25. PubMed ID: 31444703
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis.
    Yamato G; Shiba N; Yoshida K; Shiraishi Y; Hara Y; Ohki K; Okubo J; Okuno H; Chiba K; Tanaka H; Kinoshita A; Moritake H; Kiyokawa N; Tomizawa D; Park MJ; Sotomatsu M; Taga T; Adachi S; Tawa A; Horibe K; Arakawa H; Miyano S; Ogawa S; Hayashi Y
    Genes Chromosomes Cancer; 2017 May; 56(5):382-393. PubMed ID: 28063196
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.