37 results on '"Xue, Yongquan"'
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2. The characteristics and prognostic analysis in 213 myeloid malignancy patients with del(20q): a report of a single-center case series
3. Establishment and characterization of a new human acute myelomonocytic leukemia cell line JIH-3
4. Acute promyelocytic leukemia with a STAT5b-RARα fusion transcript defined by array-CGH, FISH, and RT-PCR
5. The utility of fluorescence in situ hybridization analysis in diagnosing myelodysplastic syndromes is limited to cases with karyotype failure
6. Establishment and characterization of a novel acute myeloid leukemia cell line, JIH-4, carrying a t(16;21)(p11.2;q22) and expressing the FUS-ERG fusion
7. A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia
8. A novel t(5;11)(q31;p15) involving the NUP98 gene on 11p15 is associated with a loss of the EGR1 gene on 5q31 in a patient with acute myeloid leukemia
9. Y-chromosome loss as the sole karyotypic anomaly with 3′RARα submicroscopic deletion in a case of M3r subtype of acute promyelocytic leukemia
10. The significance of bone marrow cell morphology and its correlation with cytogenetic features in the diagnosis of MDS-RA patients
11. Tetraploid clone characterized by two t(15;17) in five cases of acute promyelocytic leukemia
12. Translocation (14;14)(q11;q32) with simultaneous involvement of the IGH and CEBPE genes in B-lineage acute lymphoblastic leukemia
13. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration
14. Isodicentric 20q− in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2)
15. Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia
16. CytCD79a expression in acute leukemia with t(8;21): biphenotypic or myeloid leukemia?
17. A novel t(4;12)(q11;q13) in a patient with acute myeloid leukemia
18. Dicentric (7;9)(p11;p11) is a rare but recurrent abnormality in acute lymphoblastic leukemia: a study of 7 cases
19. Y-chromosome loss in acute promyelocytic leukemia
20. Generation of the NUP98-TOP1 fusion transcript by the t(11;20) (p15;q11) in a case of acute monocytic leukemia
21. Constitutional Robertsonian translocations in (9;22)-positive chronic myelogenous leukemia
22. AML1 and ETO genes implicated in an acute myeloblastic leukemia patient with t(8;19)
23. Biosynthesis and Combinatorial Biosynthesis of Pikromycin-Related Macrolides in Streptomyces venezuelae
24. The Streptomyces venezuelae pikAV gene contains a transcription unit essential for expression of enzymes involved in glycosylation of narbonolide and 10-deoxymethynolide
25. Mechanisms of molecular recognition in the pikromycin polyketide synthase
26. Two Cases of AML (M2) with a t(8;19)(q22;q13)
27. Genetic architecture of the polyketide synthases for methymycin and pikromycin series macrolides
28. A rare variant translocation t(3;8)(q29;q22) without AML1/ETO fusion transcript in a case of oligoblastic leukemia
29. Hydroxylation of macrolactones YC-17 and narbomycin is mediated by the pikC-encoded cytochrome P450 in Streptomyces venezuelae
30. A Case of Acute Megakaryocytic Leukemia Presenting as Peripheral Acute Leukemia with Complex Karyotypic Abnormalities
31. Translocation t(7;11)(P15;P15) in a patient with therapy-related acute myeloid leukemia following bimolane and ICRF-154 treatment for psoriasis
32. An isochromosome of the long arm of chromosome 18 in a patient with myelodysplastic syndrome with myelofibrosis
33. Translocation (8;21) in oligoblastic leukemia: Is this a true myelodysplastic syndrome?
34. Acquired amegakaryocytic thrombocytopenic purpura with a Philadelphia chromosome
35. Complex karyotypic abnormalities including t(8;22) in a patient with chronic lymphocytic leukemia
36. Specific chromosomal translocations and therapy related leukemia induced by bimolane therapy for psoriasis
37. A case of basophilic leukemia bearing simultaneous translocations t(8;21) and t(9;22)
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