77 related articles for article (PubMed ID: 11342320)
1. Fish demonstrates treatment-related chromosome damage in myeloid but not plasma cells in primary systemic amyloidosis.
Fonseca R; Rajkumar SV; Ahmann GJ; Jalal SM; Hoyer JD; Gertz MA; Kyle RA; Greipp PR; Dewald GW
Leuk Lymphoma; 2000 Oct; 39(3-4):391-5. PubMed ID: 11342320
[TBL] [Abstract][Full Text] [Related]
2. Chromosomal abnormalities in systemic amyloidosis.
Fonseca R; Ahmann GJ; Jalal SM; Dewald GW; Larson DR; Therneau TM; Gertz MA; Kyle RA; Greipp PR
Br J Haematol; 1998 Dec; 103(3):704-10. PubMed ID: 9858220
[TBL] [Abstract][Full Text] [Related]
3. Risk stratification of plasma cell neoplasm: insights from plasma cell-specific cytoplasmic immunoglobulin fluorescence in situ hybridization (cIg FISH) vs. conventional FISH.
Dong H; Yang HS; Jagannath S; Stephenson CF; Brenholz P; Mazumder A; Chari A
Clin Lymphoma Myeloma Leuk; 2012 Oct; 12(5):366-74. PubMed ID: 22658896
[TBL] [Abstract][Full Text] [Related]
4. Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis.
Granzow M; Hegenbart U; Hinderhofer K; Hose D; Seckinger A; Bochtler T; Hemminki K; Goldschmidt H; Schönland SO; Jauch A
Haematologica; 2017 Jul; 102(7):1281-1290. PubMed ID: 28341732
[TBL] [Abstract][Full Text] [Related]
5. Clonal cell lineage involvement in myelodysplastic syndromes studied by fluorescence in situ hybridization and morphology.
Bernell P; Jacobsson B; Nordgren A; Hast R
Leukemia; 1996 Apr; 10(4):662-8. PubMed ID: 8618444
[TBL] [Abstract][Full Text] [Related]
6. Detection of chromosome 13 deletions by fluorescent in situ hybridization.
VanWier S; Fonseca R
Methods Mol Med; 2005; 113():59-69. PubMed ID: 15968095
[TBL] [Abstract][Full Text] [Related]
7. Abnormal FISH in patients with immunoglobulin light chain amyloidosis is a risk factor for cardiac involvement and for death.
Warsame R; Kumar SK; Gertz MA; Lacy MQ; Buadi FK; Hayman SR; Leung N; Dingli D; Lust JA; Ketterling RP; Lin Y; Russell S; Hwa L; Kapoor P; Go RS; Zeldenrust SR; Kyle RA; Rajkumar SV; Dispenzieri A
Blood Cancer J; 2015 May; 5(5):e310. PubMed ID: 25933374
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic aberrations in patients with multiple myeloma studied by interphase fluorescence in situ hybridization.
Chen L; Li J; Xu W; Qiu H; Zhu Y; Zhang Y; Duan L; Qian S; Lu H
Exp Oncol; 2007 Jun; 29(2):116-20. PubMed ID: 17704743
[TBL] [Abstract][Full Text] [Related]
9. Interphase cytogenetics by fluorescent in situ hybridization (FISH) for characterization of monosomy-7-associated myeloid disorders.
Baurmann H; Cherif D; Berger R
Leukemia; 1993 Mar; 7(3):384-91. PubMed ID: 8445944
[TBL] [Abstract][Full Text] [Related]
10. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
11. Unbalanced translocation der(1;7)(q10;p10) defines a unique clinicopathological subgroup of myeloid neoplasms.
Sanada M; Uike N; Ohyashiki K; Ozawa K; Lili W; Hangaishi A; Kanda Y; Chiba S; Kurokawa M; Omine M; Mitani K; Ogawa S
Leukemia; 2007 May; 21(5):992-7. PubMed ID: 17315020
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of the recurrent unbalanced translocation der(1;7)(q10;p10).
Wang L; Ogawa S; Hangaishi A; Qiao Y; Hosoya N; Nanya Y; Ohyashiki K; Mizoguchi H; Hirai H
Blood; 2003 Oct; 102(7):2597-604. PubMed ID: 12816870
[TBL] [Abstract][Full Text] [Related]
13. Translocation t(11;14) and survival of patients with light chain (AL) amyloidosis.
Bryce AH; Ketterling RP; Gertz MA; Lacy M; Knudson RA; Zeldenrust S; Kumar S; Hayman S; Buadi F; Kyle RA; Greipp PR; Lust JA; Russell S; Rajkumar SV; Fonseca R; Dispenzieri A
Haematologica; 2009 Mar; 94(3):380-6. PubMed ID: 19211640
[TBL] [Abstract][Full Text] [Related]
14. Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias.
Brizard F; Brizard A; Guilhot F; Tanzer J; Berger R
Leukemia; 1994 Jun; 8(6):1005-11. PubMed ID: 8207973
[TBL] [Abstract][Full Text] [Related]
15. Der(16)t(1;16)(q10;p10) in multiple myeloma: a new non-random abnormality that is frequently associated with Burkitt's-type translocations.
Mugneret F; Sidaner I; Favre B; Manone L; Maynadié M; Caillot D; Solary E
Leukemia; 1995 Feb; 9(2):277-81. PubMed ID: 7869764
[TBL] [Abstract][Full Text] [Related]
16. [Application Value of CD138 MACS-FISH in the Genetic Diagnosis of Plasma Cell Dyscrasia].
Mei JG; Li HQ; Cao HQ; Shao JJ; Zhai YP
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2016 Oct; 24(5):1437-1442. PubMed ID: 27784371
[TBL] [Abstract][Full Text] [Related]
17. Cytogenetic clonality analysis in myelodysplastic syndrome: monosomy 7 can be demonstrated in the myeloid and in the lymphoid lineage.
van Lom K; Hagemeijer A; Smit E; Hählen K; Groeneveld K; Löwenberg B
Leukemia; 1995 Nov; 9(11):1818-21. PubMed ID: 7475268
[TBL] [Abstract][Full Text] [Related]
18. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
Beyer V; Castagné C; Mühlematter D; Parlier V; Gmür J; Hess U; Kovacsovics T; Meyer-Monard S; Tichelli A; Tobler A; Jacky E; Schanz U; Bargetzi M; Hagemeijer A; de Witte T; van Melle G; Jotterand M
Cancer Genet Cytogenet; 2004 Jul; 152(1):29-41. PubMed ID: 15193439
[TBL] [Abstract][Full Text] [Related]
19. Deletion(20q) as the sole abnormality in plasma cell myeloma is not associated with plasma cells as identified by cIg FISH.
White JS; Zordan A; Batzios C; Campbell LJ
Cancer Genet; 2012 Dec; 205(12):644-52. PubMed ID: 23200818
[TBL] [Abstract][Full Text] [Related]
20. [Combined use of molecular cytogenetic techniques to detect a small chromosomal translocation].
Xie YJ; Chen BJ; Wu JZ; Chen Z; Lin SB; Fang Q
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct; 28(5):568-71. PubMed ID: 21983737
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
