BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Bone cancer AND PBX1, P40424, 5087 AND Diagnosis
11 results:

  • 1. High frequency of heat shock protein 27 overexpression is a highly effective, high-coverage marker for minimal residual disease detection in children with B-cell acute lymphoblastic leukemia.
    Chou SW; Su YH; Lu MY; Chang HH; Yang YL; Lin DT; Lin KH; Coustan-Smith E; Jou ST
    Pediatr Blood Cancer; 2023 Jan; 70(1):e29990. PubMed ID: 36250996
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Genetic features of B-cell lymphoblastic lymphoma with TCF3-pbx1.
    Shirai R; Osumi T; Sato-Otsubo A; Nakabayashi K; Mori T; Yoshida M; Yoshida K; Kohri M; Ishihara T; Yasue S; Imamura T; Endo M; Miyamoto S; Ohki K; Sanada M; Kiyokawa N; Ogawa S; Yoshioka T; Hata K; Takagi M; Kato M
    Cancer Rep (Hoboken); 2022 Sep; 5(9):e1559. PubMed ID: 34553842
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Co-occurrence of TCF3-pbx1 gene fusion, and chromosomal aberration in a pediatric pre-B cell acute lymphoblastic leukemia with clitoris swelling: A case report and literature review.
    He GQ; Guo X; Jiang MY; Xu RR; Dai YL; Luo L; Gao J
    Medicine (Baltimore); 2021 Feb; 100(8):e24802. PubMed ID: 33663097
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. A novel PAX5 rearrangement in TCF3-pbx1 acute lymphoblastic leukemia: a case report.
    Barbosa TC; Lopes BA; Blunck CB; Mansur MB; Deyl AVS; Emerenciano M; Pombo-de-Oliveira MS
    BMC Med Genomics; 2018 Dec; 11(1):122. PubMed ID: 30563523
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients.
    Busse TM; Roth JJ; Wilmoth D; Wainwright L; Tooke L; Biegel JA
    Genes Chromosomes Cancer; 2017 Oct; 56(10):730-749. PubMed ID: 28597942
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. [Clinical significance of glucocorticoid induction test in Chinese childhood acute lymphoblastic leukemia].
    Fan JJ; Chai YH; Hu SY; He HL; Zhao WL; Wang Y; Li J; Lu J; Xiao PF; Sun YN; Wang W; Cao L
    Zhonghua Er Ke Za Zhi; 2013 Jul; 51(7):523-6. PubMed ID: 24267134
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Genetic evaluation of childhood acute lymphoblastic leukemia in Iraq using FTA cards.
    Al-Kzayer LF; Sakashita K; Matsuda K; Al-Hadad SA; Al-Jadiry MF; Abed WM; Abdulkadhim JM; Al-Shujairi TA; Hasan JG; Al-Abdullah HM; Al-Ani MH; Saber PA; Inoshita T; Kamata M; Koike K
    Pediatr Blood Cancer; 2012 Sep; 59(3):461-7. PubMed ID: 22238115
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. EWSR1-POU5F1 fusion in soft tissue myoepithelial tumors. A molecular analysis of sixty-six cases, including soft tissue, bone, and visceral lesions, showing common involvement of the EWSR1 gene.
    Antonescu CR; Zhang L; Chang NE; Pawel BR; Travis W; Katabi N; Edelman M; Rosenberg AE; Nielsen GP; Dal Cin P; Fletcher CD
    Genes Chromosomes Cancer; 2010 Dec; 49(12):1114-24. PubMed ID: 20815032
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. [The genetic diagnosis of hematopoietic malignancy by polymerase chain reaction method].
    Yokota H; Kitamura K
    Rinsho Byori; 2000 Aug; 48(8):708-15. PubMed ID: 11064593
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Recurrence of childhood acute lymphoblastic leukemia presenting as a tumor of the middle ear: a case report.
    Millot F; Klossek JM; Brizard F; Brizard A; Vandermarq P; Babin P; Guilhot F
    J Pediatr Hematol Oncol; 1997; 19(4):351-3. PubMed ID: 9256837
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analyses.
    Izraeli S; Janssen JW; Haas OA; Harbott J; Brok-Simoni F; Walther JU; Kovar H; Henn T; Ludwig WD; Reiter A
    Leukemia; 1993 May; 7(5):671-8. PubMed ID: 8483319
    [TBL] [Abstract] [Full Text] [Related]  


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