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Results 1 to 25 of 14166

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Co-expression of two FAB-specific chromosome changes, t(15;17) and t(8;21), in a case of acute promyelocytic leukemiaMOVAFAGH, A; VARMA, N; VARMA, S et al.Annals of hematology (Print). 1996, Vol 72, Num 6, pp 375-378, issn 0939-5555, 3 p.Article

Clonal Genetic alterations in the lungs of current and former smokersMAO, L; JIN SOO LEE; KEMP, B. L et al.Journal of the National Cancer Institute. 1997, Vol 89, Num 12, pp 857-862, issn 0027-8874Article

A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignanciesZHONG CHEN; RICHKIND, K; ROHERTY, S et al.Cancer genetics and cytogenetics. 1999, Vol 113, Num 2, pp 162-165, issn 0165-4608Article

Clinical and biologic implications of recurrent genomic aberrations in myelomaFONSECA, Rafael; BLOOD, Emily; BAILEY, Richard J et al.Blood. 2003, Vol 101, Num 11, pp 4569-4575, issn 0006-4971, 7 p.Article

Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesotheliomaBJÖRKQVIST, A.-M; TAMMILEHTO, L; ANTTILA, S et al.British journal of cancer. 1997, Vol 75, Num 4, pp 523-527, issn 0007-0920Article

Allelic losses at chromosomes 1p, 2p, 6p, 10p, 13q, 17p, and 21q significantly correlate with the chromophobe subtype of renal cell carcinomaSCHWERDTLE, R. F; STÖRKEL, S; NEUHAUS, C et al.Cancer research (Baltimore). 1996, Vol 56, Num 13, pp 2927-2930, issn 0008-5472Article

Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1, and CBFB-MYH11 acute myeloid leukemiasOMMEN, Hans Beier; SCHNITTGER, Susanne; JOVANOVIC, Jelena V et al.Blood. 2010, Vol 115, Num 2, pp 198-205, issn 0006-4971, 8 p.Article

A new variant translocation of t(15;17) in a patient with acute promyelocytic leukemia (M3) : t(15;19;17)(q22;p13;q12)SAITOH, K; MIURA, I; MIURA, A. B et al.Cancer genetics and cytogenetics. 1998, Vol 102, Num 1, pp 15-18, issn 0165-4608Article

Translocation (6;9;22)(p25;q34;q11.2) identified by FISH in acute leukemiaGONZALEZ, G. J. R; NOTOHAMIPRODJO, M.Cancer genetics and cytogenetics. 1996, Vol 92, Num 1, pp 82-84, issn 0165-4608Article

Cytogenetic findings in reactive lymphoid hyperplasia: Significance of non-clonal t(3;14) and t(3;22)AU, Wing Y; HORSMAN, Douglas E; CONNORS, Joseph M et al.American journal of hematology. 2002, Vol 70, Num 2, pp 133-138, issn 0361-8609Article

Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2)LIJUN ZHANG; MULVIHILL, John J; KINASEWITZ, Gary T et al.Cancer genetics and cytogenetics. 2002, Vol 133, Num 2, pp 148-151, issn 0165-4608Article

Primary effusion lymphomas exhibit complex and recurrent cytogenetic abnormalitiesWILSON, Kathleen S; MCKENNA, Robert W; KROFT, Steven H et al.British journal of haematology. 2002, Vol 116, Num 1, pp 113-121, issn 0007-1048Article

Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocationsMADAN, K; NIEUWINT, A. W. M; VAN BEVER, Y et al.Human genetics. 1997, Vol 99, Num 6, pp 806-815, issn 0340-6717Article

Translocation (8;12;21)(q22.1;q24.1;q22.1) : A new masked type of t(8;21)(q22;q22) in a patient with acute myeloid leukemiaSAITOH, K; MIURA, I; SAITO, M et al.Cancer genetics and cytogenetics. 1997, Vol 96, Num 2, pp 111-114, issn 0165-4608Article

Isolated trisomy of chromosomes 8, 11, 13 and 21 is an adverse prognostic factor in adults with de novo acute myeloid leukemia: Results from Cancer and Leukemia Group B 8461FARAG, Sherif S; ARCHER, Kellie J; LARSON, Richard A et al.International journal of oncology. 2002, Vol 21, Num 5, pp 1041-1051, issn 1019-6439Article

Complex translocation (6;21;8), a variant of t(8;21), with trisomy 4 in a patient with acute myelogenous leukemia (M2)SHINAGAWA, A; KOMATSU, T; NINOMIYA, H et al.Cancer genetics and cytogenetics. 1999, Vol 109, Num 1, pp 72-75, issn 0165-4608Article

Jumping translocations of 3q in acute promyelocytic leukemiaBATANIAN, J. R; DUNPHY, C. H; WALL, D. A et al.Cancer genetics and cytogenetics. 1999, Vol 108, Num 2, pp 149-153, issn 0165-4608Article

Correlation of cytogenetic abnormalities with the outcome of patients with uveal melanomaWHITE, V. A; CHAMBERS, J. D; COURTRIGHT, P. D et al.Cancer. 1998, Vol 83, Num 2, pp 354-359, issn 0008-543XConference Paper

MLL/ENL fusion in congenital acute lymphoblastic leukemia with a unique t(11;18;19)HORSTMANN, M; ARGYRIOU-TIRITA, A; BORKHARDT, A et al.Cancer genetics and cytogenetics. 1996, Vol 88, Num 2, pp 103-109, issn 0165-4608Article

Missense mutations in PML-RARA are critical for the lack of responsiveness to arsenic triode treatmentGOTO, Emi; TOMITA, Akihiro; HAYAKAWA, Fumihiko et al.Blood. 2011, Vol 118, Num 6, pp 1600-1609, issn 0006-4971, 10 p.Article

Autophagy contributes to therapy-induced degradation of the PML/RARA oncoproteinISAKSON, Pauline; BJØRAS, Magnar; OVE BØE, Stig et al.Blood. 2010, Vol 116, Num 13, pp 2324-2331, issn 0006-4971, 8 p.Article

Complex chromosome 4, 9, and 22 rearrangement in a patient presenting with AML-FAB M2MARTIN, E. S; JOSEPH, A; AHMAD, M. A et al.Cancer genetics and cytogenetics. 1997, Vol 93, Num 2, pp 119-124, issn 0165-4608Article

Complex chromosome rearrangement involving chromosomes 1, 4 and 16 revealed by fluorescence in situ hybridizationJOHANNESSON, T; EHLERS, S; WAHLSTRÖM, J et al.Clinical genetics. 1997, Vol 51, Num 4, pp 281-285, issn 0009-9163Article

Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22→pter and trisomy 10p11.2→pter and 11q21 analysed by dual and triple colour fishSTANKIEWICZ, P; KOSTYK, E; BOCIAN, E et al.Journal of medical genetics. 1997, Vol 34, Num 8, pp 696-699, issn 0022-2593Article

Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22) : an additional deletion in 9q is an adverse prognostic factorSCHOCH, C; HAASE, D; LÖFFLER, H et al.Leukemia. 1996, Vol 10, Num 8, pp 1288-1295, issn 0887-6924Article

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