-
1
-
-
0025833975
-
Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias
-
Ziemin-van der Poel S., McCabe N.R., Gill H.J., Espinosa R. III, Patel Y., Harden A., Rubinelli P., Smith S.D., LeBeau M.M., Rowley J.D., Diaz M.O. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias. Proc Natl Acad Sci USA. 88:1991;10735-10739
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 10735-10739
-
-
Ziemin-Van Der Poel, S.1
McCabe, N.R.2
Gill, H.J.3
Espinosa III, R.4
Patel, Y.5
Harden, A.6
Rubinelli, P.7
Smith, S.D.8
Lebeau, M.M.9
Rowley, J.D.10
Diaz, M.O.11
-
2
-
-
0032717039
-
The role of chromosome translocations in leukemogenesis
-
Rowley J.D. The role of chromosome translocations in leukemogenesis. Semin Hematol. 36:1999;59-72
-
(1999)
Semin Hematol
, vol.36
, pp. 59-72
-
-
Rowley, J.D.1
-
3
-
-
0033788685
-
Location and function of critical genes in leukemogenesis inferred from cytogenetic abnormalities in hematologic malignancies
-
Bernard O.A., Berger R. Location and function of critical genes in leukemogenesis inferred from cytogenetic abnormalities in hematologic malignancies. Semin Hematol. 37:2000;412-419
-
(2000)
Semin Hematol
, vol.37
, pp. 412-419
-
-
Bernard, O.A.1
Berger, R.2
-
4
-
-
0033788513
-
Clinical implications of recurring chromosomal and associated molecular abnormalities in acute lymphoblastic leukemia
-
Ferrando A.A., Look A.T. Clinical implications of recurring chromosomal and associated molecular abnormalities in acute lymphoblastic leukemia. Semin Hematol. 37:2000;381-395
-
(2000)
Semin Hematol
, vol.37
, pp. 381-395
-
-
Ferrando, A.A.1
Look, A.T.2
-
5
-
-
0034970067
-
An atlas of chromosomes in hematological malignancies. Example: 11q23 and MLL partners
-
Huret J.L., Dessen P., Bernheim A. An atlas of chromosomes in hematological malignancies. Example: 11q23 and MLL partners. Leukemia. 15:2001;987-989
-
(2001)
Leukemia
, vol.15
, pp. 987-989
-
-
Huret, J.L.1
Dessen, P.2
Bernheim, A.3
-
6
-
-
0031895538
-
Hematological malignancies with a deletion of 11q23: Cytogenetic and clinical aspects. European 11q23 Workshop participants
-
Harbott J., Mancini M., Verellen-Dumoulin C., Moorman A.V., Secker-Walker L.M. Hematological malignancies with a deletion of 11q23: cytogenetic and clinical aspects. European 11q23 Workshop participants. Leukemia. 12:1998;823-827
-
(1998)
Leukemia
, vol.12
, pp. 823-827
-
-
Harbott, J.1
Mancini, M.2
Verellen-Dumoulin, C.3
Moorman, A.V.4
Secker-Walker, L.M.5
-
7
-
-
0034517778
-
11q23 abnormalities in patients with acute myelogenous leukemia and myelodysplastic syndrome as detected by molecular and cytogenetic analyses
-
Ibrahim S., Estey E.H., Pierce S., Glassman A., Keating M., O'Brien S., Kantarjian H.M., Albitar M. 11q23 abnormalities in patients with acute myelogenous leukemia and myelodysplastic syndrome as detected by molecular and cytogenetic analyses. Am J Clin Pathol. 114:2000;793-797
-
(2000)
Am J Clin Pathol
, vol.114
, pp. 793-797
-
-
Ibrahim, S.1
Estey, E.H.2
Pierce, S.3
Glassman, A.4
Keating, M.5
O'Brien, S.6
Kantarjian, H.M.7
Albitar, M.8
-
8
-
-
0033518112
-
Identification of three distinct regions of deletion on the long arm of chromosome 11 in childhood acute lymphoblastic leukemia
-
Takeuchi S., Cho S.K., Seriu T., Koike M., Bartram C.R., Reiter A., Schrappe M., Takeuchi C., Taguchi H., Koeffler H.P. Identification of three distinct regions of deletion on the long arm of chromosome 11 in childhood acute lymphoblastic leukemia. Oncogene. 18:1999;7387-7388
-
(1999)
Oncogene
, vol.18
, pp. 7387-7388
-
-
Takeuchi, S.1
Cho, S.K.2
Seriu, T.3
Koike, M.4
Bartram, C.R.5
Reiter, A.6
Schrappe, M.7
Takeuchi, C.8
Taguchi, H.9
Koeffler, H.P.10
-
9
-
-
0031920586
-
Myelodysplastic syndromes associated with 11q23 abnormalities. European 11q23 Workshop participants
-
Bain B.J., Moorman A.V., Johansson B., Mehta A.B., Secker-Walker L.M. Myelodysplastic syndromes associated with 11q23 abnormalities. European 11q23 Workshop participants. Leukemia. 12:1998;834-839
-
(1998)
Leukemia
, vol.12
, pp. 834-839
-
-
Bain, B.J.1
Moorman, A.V.2
Johansson, B.3
Mehta, A.B.4
Secker-Walker, L.M.5
-
10
-
-
0037238249
-
Interphase fluorescence in situ hybridization analysis of del(11)(q23) and del(17)(p13) in chronic lymphocytic leukemia. A study of 40 early-onset patients
-
Doneda L., Montillo M., Intropido L., Tedeschi A., Morra E., Larizza L. Interphase fluorescence in situ hybridization analysis of del(11)(q23) and del(17)(p13) in chronic lymphocytic leukemia. a study of 40 early-onset patients. Cancer Genet Cytogenet. 140:2003;31-36
-
(2003)
Cancer Genet Cytogenet
, vol.140
, pp. 31-36
-
-
Doneda, L.1
Montillo, M.2
Intropido, L.3
Tedeschi, A.4
Morra, E.5
Larizza, L.6
-
11
-
-
0034727833
-
Genomic aberrations and survival in chronic lymphocytic leukemia
-
Dohner H., Stilgenbauer S., Benner A., Leupolt E., Krober A., Bullinger L., Dohner K., Bentz M., Lichter P. Genomic aberrations and survival in chronic lymphocytic leukemia. N Engl J Med. 343:2000;1910-1916
-
(2000)
N Engl J Med
, vol.343
, pp. 1910-1916
-
-
Dohner, H.1
Stilgenbauer, S.2
Benner, A.3
Leupolt, E.4
Krober, A.5
Bullinger, L.6
Dohner, K.7
Bentz, M.8
Lichter, P.9
-
12
-
-
0035035480
-
11q deletions in hematological malignancies
-
Monni O., Knuutila S. 11q deletions in hematological malignancies. Leuk Lymphoma. 40:2001;259-266
-
(2001)
Leuk Lymphoma
, vol.40
, pp. 259-266
-
-
Monni, O.1
Knuutila, S.2
-
13
-
-
1842328565
-
11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis
-
Dohner H., Stilgenbauer S., James M.R., Benner A., Weilguni T., Bentz M., Fischer K., Hunstein W., Lichter P. 11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis. Blood. 89:1997;2516-2522
-
(1997)
Blood
, vol.89
, pp. 2516-2522
-
-
Dohner, H.1
Stilgenbauer, S.2
James, M.R.3
Benner, A.4
Weilguni, T.5
Bentz, M.6
Fischer, K.7
Hunstein, W.8
Lichter, P.9
-
14
-
-
0029969111
-
Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-923.1 in lymphoproliferative disorders
-
Stilgenbauer S., Liebisch P., James M.R., Schroder M., Schlegelberger B., Fischer K., Bentz M., Lichter P., Dohner H. Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-923.1 in lymphoproliferative disorders. Proc Natl Acad Sci USA. 93:1996;11837-11841
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 11837-11841
-
-
Stilgenbauer, S.1
Liebisch, P.2
James, M.R.3
Schroder, M.4
Schlegelberger, B.5
Fischer, K.6
Bentz, M.7
Lichter, P.8
Dohner, H.9
-
15
-
-
0033013993
-
Discontinuous deletions at 11q23 in B cell chronic lymphocytic leukemia
-
Zhu Y., Monni O., El-Rifai W., Siitonen S.M., Vilpo L., Vilpo J., Knuutila S. Discontinuous deletions at 11q23 in B cell chronic lymphocytic leukemia. Leukemia. 13:1999;708-712
-
(1999)
Leukemia
, vol.13
, pp. 708-712
-
-
Zhu, Y.1
Monni, O.2
El-Rifai, W.3
Siitonen, S.M.4
Vilpo, L.5
Vilpo, J.6
Knuutila, S.7
-
16
-
-
0034213319
-
Allelic loss in the progression of myelodysplastic syndrome
-
Mori N., Morosetti R., Hoflehner E., Lubbert M., Mizoguchi H., Koeffler H.P. Allelic loss in the progression of myelodysplastic syndrome. Cancer Res. 60:2000;3039-3042
-
(2000)
Cancer Res
, vol.60
, pp. 3039-3042
-
-
Mori, N.1
Morosetti, R.2
Hoflehner, E.3
Lubbert, M.4
Mizoguchi, H.5
Koeffler, H.P.6
-
18
-
-
0032532095
-
Deficiency of the ATM protein expression defines an aggressive subgroup of B-cell chronic lymphocytic leukemia
-
Starostik P., Manshouri T., O'Brien S., Freireich E., Kantarjian H., Haidar M., Lerner S., Keating M., Albitar M. Deficiency of the ATM protein expression defines an aggressive subgroup of B-cell chronic lymphocytic leukemia. Cancer Res. 58:1998;4552-4557
-
(1998)
Cancer Res
, vol.58
, pp. 4552-4557
-
-
Starostik, P.1
Manshouri, T.2
O'Brien, S.3
Freireich, E.4
Kantarjian, H.5
Haidar, M.6
Lerner, S.7
Keating, M.8
Albitar, M.9
-
19
-
-
0033513587
-
Inactivation of ataxia telangiectasia mutated gene in B-cell chronic lymphocytic leukaemia
-
Stankovic T., Weber P., Stewart G., Bedenham T., Murray J., Byrd P.J., Moss P.A., Taylor A.M. Inactivation of ataxia telangiectasia mutated gene in B-cell chronic lymphocytic leukaemia. Lancet. 353:1999;26-29
-
(1999)
Lancet
, vol.353
, pp. 26-29
-
-
Stankovic, T.1
Weber, P.2
Stewart, G.3
Bedenham, T.4
Murray, J.5
Byrd, P.J.6
Moss, P.A.7
Taylor, A.M.8
-
20
-
-
0032944319
-
ATM mutations in B-cell chronic lymphocytic leukemia
-
Bullrich F., Rasio D., Kitada S., Starostik P., Kipps T., Keating M., Albitar M., Reed J.C., Croce C.M. ATM mutations in B-cell chronic lymphocytic leukemia. Cancer Res. 59:1999;24-27
-
(1999)
Cancer Res
, vol.59
, pp. 24-27
-
-
Bullrich, F.1
Rasio, D.2
Kitada, S.3
Starostik, P.4
Kipps, T.5
Keating, M.6
Albitar, M.7
Reed, J.C.8
Croce, C.M.9
-
21
-
-
0033566329
-
Somatic ATM mutations indicate a pathogenic role of ATM in B-cell chronic lymphocytic leukemia
-
Schaffner C., Stilgenbauer S., Rappold G.A., Dohner H., Lichter P. Somatic ATM mutations indicate a pathogenic role of ATM in B-cell chronic lymphocytic leukemia. Blood. 94:1999;748-753
-
(1999)
Blood
, vol.94
, pp. 748-753
-
-
Schaffner, C.1
Stilgenbauer, S.2
Rappold, G.A.3
Dohner, H.4
Lichter, P.5
-
22
-
-
0032847004
-
Linkage analysis for ATM in familial B cell chronic lymphocytic leukaemia
-
Bevan S., Catovsky D., Marossy A., Matutes E., Popat S., Antonovic P., Bell A., Berrebi A., Gaminara E., Quabeck K., Ribeiro I., Mauro F.R., Stark P., Sykes H., van Dongen J., Wimperis J., Wright S., Yuille M.R., Houlston R.S. Linkage analysis for ATM in familial B cell chronic lymphocytic leukaemia. Leukemia. 13:1999;1497-1500
-
(1999)
Leukemia
, vol.13
, pp. 1497-1500
-
-
Bevan, S.1
Catovsky, D.2
Marossy, A.3
Matutes, E.4
Popat, S.5
Antonovic, P.6
Bell, A.7
Berrebi, A.8
Gaminara, E.9
Quabeck, K.10
Ribeiro, I.11
Mauro, F.R.12
Stark, P.13
Sykes, H.14
Van Dongen, J.15
Wimperis, J.16
Wright, S.17
Yuille, M.R.18
Houlston, R.S.19
-
23
-
-
0037100516
-
ATM mutations are rare in familial chronic lymphocytic leukemia
-
Yuille M.R., Condie A., Hudson C.D., Bradshaw P.S., Stone E.M., Matutes E., Catovsky D., Houlston R.S. ATM mutations are rare in familial chronic lymphocytic leukemia. Blood. 100:2002;603-609
-
(2002)
Blood
, vol.100
, pp. 603-609
-
-
Yuille, M.R.1
Condie, A.2
Hudson, C.D.3
Bradshaw, P.S.4
Stone, E.M.5
Matutes, E.6
Catovsky, D.7
Houlston, R.S.8
-
24
-
-
0035383839
-
Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis
-
Kolomietz E., Al-Maghrabi J., Brennan S., Karaskova J., Minkin S., Lipton J., Squire J.A. Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis. Blood. 97:2001;3581-3588
-
(2001)
Blood
, vol.97
, pp. 3581-3588
-
-
Kolomietz, E.1
Al-Maghrabi, J.2
Brennan, S.3
Karaskova, J.4
Minkin, S.5
Lipton, J.6
Squire, J.A.7
-
25
-
-
0032715401
-
Rapid and sensitive detection of all types of MLL gene translocations with a single FISH probe set
-
van der Burg M., Beverloo H.B., Langerak A.W., Wijsman J., van Drunen E., Slater R., van Dongen J.J. Rapid and sensitive detection of all types of MLL gene translocations with a single FISH probe set. Leukemia. 13:1999;2107-2113
-
(1999)
Leukemia
, vol.13
, pp. 2107-2113
-
-
Van Der Burg, M.1
Beverloo, H.B.2
Langerak, A.W.3
Wijsman, J.4
Van Drunen, E.5
Slater, R.6
Van Dongen, J.J.7
-
26
-
-
0025633261
-
Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: Identification of 11q23 translocation breakpoints with a yeast artificial chromosome
-
Rowley J.D., Diaz M.O., Espinosa R. 3rd, Patel Y.D., van Melle E., Ziemin S., Taillon-Miller P., Lichter P., Evans G.A., Kersey J.H., Ward D.C., Domes P.H., Le Beau M.M. Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome. Proc Natl Acad Sci USA. 87:1990;9358-9362
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 9358-9362
-
-
Rowley, J.D.1
Diaz, M.O.2
Espinosa III, R.3
Patel, Y.D.4
Van Melle, E.5
Ziemin, S.6
Taillon-Miller, P.7
Lichter, P.8
Evans, G.A.9
Kersey, J.H.10
Ward, D.C.11
Domes, P.H.12
Le Beau, M.M.13
-
27
-
-
0033844375
-
Sensitivity of FISH in detection of MLL translocations
-
Cuthbert G., Thompson K., Breese G., McCullough S., Bown N. Sensitivity of FISH in detection of MLL translocations. Genes Chromosomes Cancer. 29:2000;180-185
-
(2000)
Genes Chromosomes Cancer
, vol.29
, pp. 180-185
-
-
Cuthbert, G.1
Thompson, K.2
Breese, G.3
McCullough, S.4
Bown, N.5
-
28
-
-
6744221199
-
A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias
-
von Bergh A., Emanuel B., van Zelderen-Bhola S., Smetsers T., van Soest R., Stul M., Vranckx H., Schuuring E., Hagemeijer A., Kluin P. A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias. Genes Chromosomes Cancer. 28:2000;14-22
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 14-22
-
-
Von Bergh, A.1
Emanuel, B.2
Van Zelderen-Bhola, S.3
Smetsers, T.4
Van Soest, R.5
Stul, M.6
Vranckx, H.7
Schuuring, E.8
Hagemeijer, A.9
Kluin, P.10
-
29
-
-
0029025482
-
Loss of heterozygosity on chromosome 11q in breast cancer
-
Tomlinson I.P., Strickland J.E., Lee A.S., Bromley L., Evans M.F., Morton J., McGee J.O. Loss of heterozygosity on chromosome 11q in breast cancer. J Clin Pathol. 48:1995;424-428
-
(1995)
J Clin Pathol
, vol.48
, pp. 424-428
-
-
Tomlinson, I.P.1
Strickland, J.E.2
Lee, A.S.3
Bromley, L.4
Evans, M.F.5
Morton, J.6
McGee, J.O.7
-
30
-
-
0033817281
-
Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
-
Lee A.S., Seo Y.C., Chang A., Tohari S., Eu K.W., Seow-Choen F., McGee J.O. Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma. Br J Cancer. 83:2000;750-755
-
(2000)
Br J Cancer
, vol.83
, pp. 750-755
-
-
Lee, A.S.1
Seo, Y.C.2
Chang, A.3
Tohari, S.4
Eu, K.W.5
Seow-Choen, F.6
McGee, J.O.7
-
31
-
-
0032934560
-
Refined mapping of two regions of loss of heterozygosity on chromosome band 11q23 in lung cancer
-
Wang S.S., Virmani A., Gazdar A.F., Minna J.D., Evans G.A. Refined mapping of two regions of loss of heterozygosity on chromosome band 11q23 in lung cancer. Genes Chromosomes Cancer. 25:1999;154-159
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 154-159
-
-
Wang, S.S.1
Virmani, A.2
Gazdar, A.F.3
Minna, J.D.4
Evans, G.A.5
-
32
-
-
0030046994
-
Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomach
-
Baffa R., Negrini M., Mandes B., Rugge M., Ranzani G.N., Hirohashi S., Croce C.M. Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomach. Cancer Res. 56:1996;268-272
-
(1996)
Cancer Res
, vol.56
, pp. 268-272
-
-
Baffa, R.1
Negrini, M.2
Mandes, B.3
Rugge, M.4
Ranzani, G.N.5
Hirohashi, S.6
Croce, C.M.7
-
33
-
-
0030019840
-
Refinement of two chromosome 11q regions of loss of heterozygosity in ovarian cancer
-
Davis M., Hitchcock A., Foulkes W.D., Campbell I.G. Refinement of two chromosome 11q regions of loss of heterozygosity in ovarian cancer. Cancer Res. 56:1996;741-744
-
(1996)
Cancer Res
, vol.56
, pp. 741-744
-
-
Davis, M.1
Hitchcock, A.2
Foulkes, W.D.3
Campbell, I.G.4
-
34
-
-
0032516209
-
Allelic deletion at 11q23.3-q25 is an early event in cervical neoplasia
-
Evans M.F., Koreth J., Bakkenist C.J., Herrington C.S., McGee J.O. Allelic deletion at 11q23.3-q25 is an early event in cervical neoplasia. Oncogene. 16:1998;2557-2564
-
(1998)
Oncogene
, vol.16
, pp. 2557-2564
-
-
Evans, M.F.1
Koreth, J.2
Bakkenist, C.J.3
Herrington, C.S.4
McGee, J.O.5
-
35
-
-
0034987675
-
Loss of heterozygosity at 11q23.3 in vasculoinvasive and metastatic squamous cell carcinoma of the cervix
-
O'Sullivan M.J., Rader J.S., Gerhard D.S., Li Y., Trinkaus K.M., Gersell D.J., Huettner P.C. Loss of heterozygosity at 11q23.3 in vasculoinvasive and metastatic squamous cell carcinoma of the cervix. Hum Pathol. 32:2001;475-478
-
(2001)
Hum Pathol
, vol.32
, pp. 475-478
-
-
O'Sullivan, M.J.1
Rader, J.S.2
Gerhard, D.S.3
Li, Y.4
Trinkaus, K.M.5
Gersell, D.J.6
Huettner, P.C.7
-
36
-
-
0029948389
-
Loss of heterozygosity on the long arm of chromosome 11 in nasopharyngeal carcinoma
-
Hui A.B., Lo K.W., Leung S.F., Choi P.H., Fong Y., Lee J.C., Huang D.P. Loss of heterozygosity on the long arm of chromosome 11 in nasopharyngeal carcinoma. Cancer Res. 56:1996;3225-3229
-
(1996)
Cancer Res
, vol.56
, pp. 3225-3229
-
-
Hui, A.B.1
Lo, K.W.2
Leung, S.F.3
Choi, P.H.4
Fong, Y.5
Lee, J.C.6
Huang, D.P.7
-
37
-
-
0035162463
-
Loss of heterozygosity and its correlation with clinical outcome and Epstein-Barr virus infection in nasopharyngeal carcinoma
-
Shao J.Y., Huang X.M., Yu X.J., Huang L.X., Wu Q.L., Xia J.C., Wang H.Y., Feng Q.S., Ren Z.F., Ernberg I., Hu L.F., Zeng Y.X. Loss of heterozygosity and its correlation with clinical outcome and Epstein-Barr virus infection in nasopharyngeal carcinoma. Anticancer Res. 21:2001;3021-3029
-
(2001)
Anticancer Res
, vol.21
, pp. 3021-3029
-
-
Shao, J.Y.1
Huang, X.M.2
Yu, X.J.3
Huang, L.X.4
Wu, Q.L.5
Xia, J.C.6
Wang, H.Y.7
Feng, Q.S.8
Ren, Z.F.9
Ernberg, I.10
Hu, L.F.11
Zeng, Y.X.12
|