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Items: 1 to 20 of 358

1.

Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q.

Gao Q, Horwitz M, Roulston D, Hagos F, Zhao N, Freireich EJ, Golomb HM, Olopade OI.

Genes Chromosomes Cancer. 2000 Jun;28(2):164-72.

PMID:
10825001
2.

Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation.

Liu TX, Becker MW, Jelinek J, Wu WS, Deng M, Mikhalkevich N, Hsu K, Bloomfield CD, Stone RM, DeAngelo DJ, Galinsky IA, Issa JP, Clarke MF, Look AT.

Nat Med. 2007 Jan;13(1):78-83. Epub 2006 Dec 10.

PMID:
17159988
3.
4.
5.
6.

Deletions of chromosome 5 in malignant myeloid disorders.

Le Beau MM.

Cancer Surv. 1992;15:143-59. Review.

PMID:
1451109
7.

FISH investigation of 5q and 7q deletions in MDS/AML reveals hidden translocations, insertions and fragmentations of the same chromosomes.

Lessard M, Herry A, Berthou C, Léglise MC, Abgrall JF, Morice P, Flandrin G.

Leuk Res. 1998 Apr;22(4):303-12.

PMID:
9669835
8.

dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53.

Wang P, Spielberger RT, Thangavelu M, Zhao N, Davis EM, Iannantuoni K, Larson RA, Le Beau MM.

Genes Chromosomes Cancer. 1997 Nov;20(3):282-91.

PMID:
9365836
9.

Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions.

Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, Berthou C, De Braekeleer M.

Cancer Genet Cytogenet. 2007 Jun;175(2):125-31.

PMID:
17556068
10.

Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.

Boultwood J, Fidler C, Lewis S, MacCarthy A, Sheridan H, Kelly S, Oscier D, Buckle VJ, Wainscoat JS.

Blood. 1993 Nov 1;82(9):2611-6.

11.

Absence of point mutations within the AML-1 gene in patients with MDS/AML and loss of chromosome 5q or 7.

Ferrari T, Weber B, Pils S, Harbott J, Borkhardt A.

Ann Hematol. 2001 Feb;80(2):72-3.

PMID:
11261327
12.

Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias.

Fischer K, Fröhling S, Scherer SW, McAllister Brown J, Scholl C, Stilgenbauer S, Tsui LC, Lichter P, Döhner H.

Blood. 1997 Mar 15;89(6):2036-41.

13.

Cytogenetic analysis of de novo acute myeloid leukemia with trilineage myelodysplasia in comparison with myelodysplastic syndrome evolving to acute myeloid leukemia.

Tamura S, Takemoto Y, Hashimoto-Tamaoki T, Mimura K, Sugahara Y, Senoh J, Furuyama JI, Kakishita E.

Int J Oncol. 1998 Jun;12(6):1259-62.

PMID:
9592183
14.

Loss of heterozygosity on chromosome 5 in adults with acute lymphoblastic leukemia.

Faderl S, Gidel C, Kantarjian HM, Manshouri T, Keating M, Albitar M.

Leuk Res. 2001 Jan;25(1):39-43.

PMID:
11137559
15.

Delineation of multiple deleted regions in 7q in myeloid disorders.

Tosi S, Scherer SW, Giudici G, Czepulkowski B, Biondi A, Kearney L.

Genes Chromosomes Cancer. 1999 Aug;25(4):384-92.

PMID:
10398433
16.

Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?

Lessard M, Hélias C, Struski S, Perrusson N, Uettwiller F, Mozziconacci MJ, Lafage-Pochitaloff M, Dastugue N, Terré C, Brizard F, Cornillet-Lefebvre P, Mugneret F, Barin C, Herry A, Luquet I, Desangles F, Michaux L, Verellen-Dumoulin C, Perrot C, Van den Akker J, Lespinasse J, Eclache V, Berger R; Groupe Francophone de Cytogénétique Hématologique.

Cancer Genet Cytogenet. 2007 Jul 1;176(1):1-21.

PMID:
17574959
17.

Familial myeloid leukemia associated with loss of the long arm of chromosome 5.

Olopade OI, Roulston D, Baker T, Narvid S, Le Beau MM, Freireich EJ, Larson RA, Golomb HM.

Leukemia. 1996 Apr;10(4):669-74.

PMID:
8618445
18.

Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.

Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.

Eur J Haematol. 2007 Jun;78(6):457-67. Epub 2007 Mar 28.

PMID:
17391336
19.

New complex t(2;11;17)(p21;q23;q11), a variant form of t(2;11), associated with del(5)(q23q32) in myelodysplastic syndrome-derived acute myeloblastic leukemia.

Yamamoto K, Nagata K, Morita Y, Inagaki K, Hamaguchi H.

Cancer Genet Cytogenet. 2002 Sep;137(2):119-23. Review.

PMID:
12393282

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