-
1
-
-
0034670036
-
The molecular biology of chronic myeloid leukemia
-
Deininger M.W.N., Goldman J.M., and Melo J.V. The molecular biology of chronic myeloid leukemia. Blood 96 (2000) 3343-3356
-
(2000)
Blood
, vol.96
, pp. 3343-3356
-
-
Deininger, M.W.N.1
Goldman, J.M.2
Melo, J.V.3
-
2
-
-
0141528828
-
Chronic myeloid leukemia: advances in biology and new approaches to treatment
-
Goldman J.M., and Melo J.V. Chronic myeloid leukemia: advances in biology and new approaches to treatment. N Engl J Med 349 (2003) 1451-1464
-
(2003)
N Engl J Med
, vol.349
, pp. 1451-1464
-
-
Goldman, J.M.1
Melo, J.V.2
-
3
-
-
0034655511
-
A FISH study of variant Philadelphia rearrangements
-
Reddy K.S., and Sulcova V. A FISH study of variant Philadelphia rearrangements. Cancer Genet Cytogenet 118 (2000) 121-131
-
(2000)
Cancer Genet Cytogenet
, vol.118
, pp. 121-131
-
-
Reddy, K.S.1
Sulcova, V.2
-
4
-
-
33847149254
-
On the genesis and prognosis of variant translocations in chronic myeloid leukemia
-
Gorusu M., Benn P., Li Z., and Fang M. On the genesis and prognosis of variant translocations in chronic myeloid leukemia. Cancer Genet Cytogenet 173 (2007) 97-106
-
(2007)
Cancer Genet Cytogenet
, vol.173
, pp. 97-106
-
-
Gorusu, M.1
Benn, P.2
Li, Z.3
Fang, M.4
-
5
-
-
38849131989
-
A masked BCR/ABL rearrangement in a case of chronic myeloid leukemia with translocation t(3;9)(p14;q34)
-
Bennour A., Sennana H., Laatiri M.A., Khelif A., and Saad A. A masked BCR/ABL rearrangement in a case of chronic myeloid leukemia with translocation t(3;9)(p14;q34). Cancer Genet Cytogenet 181 (2008) 72-74
-
(2008)
Cancer Genet Cytogenet
, vol.181
, pp. 72-74
-
-
Bennour, A.1
Sennana, H.2
Laatiri, M.A.3
Khelif, A.4
Saad, A.5
-
6
-
-
33646490448
-
A Ph-negative chronic myeloid leukemia with a complex BCR/ABL rearrangement and a t(6;9)(p21;q34.1)
-
Todorić-Zivanović B., Marisavljević D., Surace C., Cemerikić V., Marković O., Krtolica K., Tatomirović Z., Cikota B., Magić Z., and Rocchi M. A Ph-negative chronic myeloid leukemia with a complex BCR/ABL rearrangement and a t(6;9)(p21;q34.1). Cancer Genet Cytogenet 166 (2006) 180-185
-
(2006)
Cancer Genet Cytogenet
, vol.166
, pp. 180-185
-
-
Todorić-Zivanović, B.1
Marisavljević, D.2
Surace, C.3
Cemerikić, V.4
Marković, O.5
Krtolica, K.6
Tatomirović, Z.7
Cikota, B.8
Magić, Z.9
Rocchi, M.10
-
7
-
-
0142248373
-
Genesis of variant Philadelphia chromosome translocations in chronic myelocytic leukemia
-
Naumann S., and Decker H.J. Genesis of variant Philadelphia chromosome translocations in chronic myelocytic leukemia. Cancer Genet Cytogenet 147 (2003) 18-22
-
(2003)
Cancer Genet Cytogenet
, vol.147
, pp. 18-22
-
-
Naumann, S.1
Decker, H.J.2
-
8
-
-
0026317492
-
Complex chromosomal translocations in the Philadelphia chromosome leukemias: serial translocations or a concerted genomic rearrangements?
-
Fitzgerald P.H., and Morris C.M. Complex chromosomal translocations in the Philadelphia chromosome leukemias: serial translocations or a concerted genomic rearrangements?. Cancer Genet Cytogenet 57 (1991) 143-151
-
(1991)
Cancer Genet Cytogenet
, vol.57
, pp. 143-151
-
-
Fitzgerald, P.H.1
Morris, C.M.2
-
9
-
-
41749098088
-
Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL or BCR deletion status or response to imatinib therapy
-
Fi-LMC Group
-
Soenen V., Viguié F., Laï J.L., Andrieux J., Corm S., Roche-Lestienne C., and Fi-LMC Group. Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL or BCR deletion status or response to imatinib therapy. Cancer Genet Cytogenet 182 (2008) 95-102
-
(2008)
Cancer Genet Cytogenet
, vol.182
, pp. 95-102
-
-
Soenen, V.1
Viguié, F.2
Laï, J.L.3
Andrieux, J.4
Corm, S.5
Roche-Lestienne, C.6
-
10
-
-
0032831959
-
Clinical implications of fluorescence in situ hybridization analysis in 13 chronic myeloid leukemia cases: Ph-negative and variant Ph-positive
-
Yehuda O., Abeliovich D., Ben-Neriah S., Sverdlin I., Cohen R., Varadi G., Orr R., Ashkenazi Y.J., Heyd J., Lugassy G., and Ben Yehuda D. Clinical implications of fluorescence in situ hybridization analysis in 13 chronic myeloid leukemia cases: Ph-negative and variant Ph-positive. Cancer Genet Cytogenet 114 (1999) 100-107
-
(1999)
Cancer Genet Cytogenet
, vol.114
, pp. 100-107
-
-
Yehuda, O.1
Abeliovich, D.2
Ben-Neriah, S.3
Sverdlin, I.4
Cohen, R.5
Varadi, G.6
Orr, R.7
Ashkenazi, Y.J.8
Heyd, J.9
Lugassy, G.10
Ben Yehuda, D.11
-
11
-
-
0025939293
-
Entire ABL gene is joined to 5′- BCR in some patients with Philadelphia-positive leukemia
-
Morris C.M., Heisterkamp N., Groffen J., and Fitzgerald P.H. Entire ABL gene is joined to 5′- BCR in some patients with Philadelphia-positive leukemia. Blood 78 (1991) 1078-1084
-
(1991)
Blood
, vol.78
, pp. 1078-1084
-
-
Morris, C.M.1
Heisterkamp, N.2
Groffen, J.3
Fitzgerald, P.H.4
-
12
-
-
0025075367
-
Complex translocations, simple variant translocations and Ph-negative cases in chronic myelogenous leukaemia
-
Huret J.L. Complex translocations, simple variant translocations and Ph-negative cases in chronic myelogenous leukaemia. Hum Genet 85 (1990) 565-568
-
(1990)
Hum Genet
, vol.85
, pp. 565-568
-
-
Huret, J.L.1
-
13
-
-
0034842032
-
Chronic myelogenous leukemia: laboratory diagnosis and monitoring
-
Wang Y.L., Bagg A., Pear W., Nowel P.C., and Hess J.L. Chronic myelogenous leukemia: laboratory diagnosis and monitoring. Genes Chromosomes Cancer 32 (2001) 97-111
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 97-111
-
-
Wang, Y.L.1
Bagg, A.2
Pear, W.3
Nowel, P.C.4
Hess, J.L.5
-
14
-
-
33646832041
-
Molecular cytogenetic characterization of deletions on der(9) in chronic myelocytic leukemia
-
Zagaria A., Anelli L., Albano F., Vicari L., Schiavone E.M., Annunziata M., Pane F., Liso V., Rocchi M., and Specchia G. Molecular cytogenetic characterization of deletions on der(9) in chronic myelocytic leukemia. Cancer Genet Cytogenet 167 (2006) 97-102
-
(2006)
Cancer Genet Cytogenet
, vol.167
, pp. 97-102
-
-
Zagaria, A.1
Anelli, L.2
Albano, F.3
Vicari, L.4
Schiavone, E.M.5
Annunziata, M.6
Pane, F.7
Liso, V.8
Rocchi, M.9
Specchia, G.10
-
15
-
-
33749152100
-
Deletion size characterization of der(9) deletions in Philadelphia-positive chronic myeloid leukemia
-
Douet-Guilbert N., Morel F., Quemener S., Maguer A., Le Bris M.J., Morice P., Berthou C., and De Braekeleer M. Deletion size characterization of der(9) deletions in Philadelphia-positive chronic myeloid leukemia. Cancer Genet Cytogenet 170 (2006) e89-e92
-
(2006)
Cancer Genet Cytogenet
, vol.170
-
-
Douet-Guilbert, N.1
Morel, F.2
Quemener, S.3
Maguer, A.4
Le Bris, M.J.5
Morice, P.6
Berthou, C.7
De Braekeleer, M.8
-
16
-
-
12944295358
-
Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia
-
Sinclair P.B., Nacheva E.P., Leversha M., Telford N., Chang J., Reid A., Bench A., Champion K., Huntly B., and Green A.R. Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia. Blood 95 (2000) 738-743
-
(2000)
Blood
, vol.95
, pp. 738-743
-
-
Sinclair, P.B.1
Nacheva, E.P.2
Leversha, M.3
Telford, N.4
Chang, J.5
Reid, A.6
Bench, A.7
Champion, K.8
Huntly, B.9
Green, A.R.10
-
17
-
-
0035885928
-
Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia
-
Huntly B.J., Reid A.G., Bench A.J., Campbell L.J., Telford N., Shepherd P., Szer J., Prince H.M., Turner P., Grace C., Nacheva E.P., and Green A.R. Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia. Blood 98 (2001) 1732-1738
-
(2001)
Blood
, vol.98
, pp. 1732-1738
-
-
Huntly, B.J.1
Reid, A.G.2
Bench, A.J.3
Campbell, L.J.4
Telford, N.5
Shepherd, P.6
Szer, J.7
Prince, H.M.8
Turner, P.9
Grace, C.10
Nacheva, E.P.11
Green, A.R.12
-
18
-
-
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., and 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
-
19
-
-
0042638382
-
Imatinib improves but may not fully reverse the poor prognosis of patients with CML with derivative chromosome 9 deletions
-
Huntly B.J., Guilhot F., Reid A.G., Vassiliou G., Hennig E., Franke C., Byrne J., Brizard A., Niederwieser D., Freeman-Edward J., Cuthbert G., Bown N., Clark R.E., Nacheva E.P., Green A.R., and Deininger M.W. Imatinib improves but may not fully reverse the poor prognosis of patients with CML with derivative chromosome 9 deletions. Blood 102 (2003) 2205-2212
-
(2003)
Blood
, vol.102
, pp. 2205-2212
-
-
Huntly, B.J.1
Guilhot, F.2
Reid, A.G.3
Vassiliou, G.4
Hennig, E.5
Franke, C.6
Byrne, J.7
Brizard, A.8
Niederwieser, D.9
Freeman-Edward, J.10
Cuthbert, G.11
Bown, N.12
Clark, R.E.13
Nacheva, E.P.14
Green, A.R.15
Deininger, M.W.16
-
20
-
-
15444350807
-
Selective inhibition of cell proliferation and BCR-ABL phosphorylation in acute lymphoblastic leukemia cells expressing Mr 190,000 BCR-ABL protein by a tyrosine kinase inhibitor (CGP-57148)
-
Beran M., Cao X., Estrov Z., Jeha S., Jin G., O'Brien S., Talpaz M., Arlinghaus R.B., Lydon N.B., and Kantarjian H. Selective inhibition of cell proliferation and BCR-ABL phosphorylation in acute lymphoblastic leukemia cells expressing Mr 190,000 BCR-ABL protein by a tyrosine kinase inhibitor (CGP-57148). Clin Cancer Res 4 (1998) 1661-1672
-
(1998)
Clin Cancer Res
, vol.4
, pp. 1661-1672
-
-
Beran, M.1
Cao, X.2
Estrov, Z.3
Jeha, S.4
Jin, G.5
O'Brien, S.6
Talpaz, M.7
Arlinghaus, R.B.8
Lydon, N.B.9
Kantarjian, H.10
-
21
-
-
0029947186
-
Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells
-
Druker B.J., Tamura S., Buchdunger E., Ohno S., Segal G.M., Fanning S., Zimmermann J., and Lydon N.B. Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells. Nat Med 2 (1996) 561-566
-
(1996)
Nat Med
, vol.2
, pp. 561-566
-
-
Druker, B.J.1
Tamura, S.2
Buchdunger, E.3
Ohno, S.4
Segal, G.M.5
Fanning, S.6
Zimmermann, J.7
Lydon, N.B.8
-
23
-
-
41749115965
-
Deletions adjacent to BCR and ABL1 breakpoints occur in a substantial minority of chronic myeloid leukemia patients with masked Philadelphia rearrangements
-
De Melo V.A., Milojkovic D., Marin D., Apperley J.F., Nacheva E.P., and Reid A.G. Deletions adjacent to BCR and ABL1 breakpoints occur in a substantial minority of chronic myeloid leukemia patients with masked Philadelphia rearrangements. Cancer Genet Cytogenet 182 (2008) 111-115
-
(2008)
Cancer Genet Cytogenet
, vol.182
, pp. 111-115
-
-
De Melo, V.A.1
Milojkovic, D.2
Marin, D.3
Apperley, J.F.4
Nacheva, E.P.5
Reid, A.G.6
-
24
-
-
0018222170
-
A variant chromosomal translocation found in a series of 24 patients with Philadelphia positive chronic granulocytic leukaemia
-
Lyall J.M., Brodie G.N., and Garson O.M. A variant chromosomal translocation found in a series of 24 patients with Philadelphia positive chronic granulocytic leukaemia. Aust N Z J Med 8 (1978) 288-289
-
(1978)
Aust N Z J Med
, vol.8
, pp. 288-289
-
-
Lyall, J.M.1
Brodie, G.N.2
Garson, O.M.3
-
25
-
-
0019501570
-
A complex variant Philadelphia (Ph1) chromosome translocation involving chromosomes no. 11, 14, and 22 in a case of chronic myelogenous leukemia
-
Kolitz J.E., Schulman P., Kardon N., Budman D.R., Vinciguerra V.P., Broekman A., and Degnan T.J. A complex variant Philadelphia (Ph1) chromosome translocation involving chromosomes no. 11, 14, and 22 in a case of chronic myelogenous leukemia. Cancer Genet Cytogenet 4 (1981) 185-188
-
(1981)
Cancer Genet Cytogenet
, vol.4
, pp. 185-188
-
-
Kolitz, J.E.1
Schulman, P.2
Kardon, N.3
Budman, D.R.4
Vinciguerra, V.P.5
Broekman, A.6
Degnan, T.J.7
-
26
-
-
0019446816
-
Significance of non-standard Philadelphia chromosomes in chronic granulocytic leukaemia
-
Potter A.M., Watmore A.E., Cooke P., Lilleyman J.S., and Sokol R.J. Significance of non-standard Philadelphia chromosomes in chronic granulocytic leukaemia. Br J Cancer 44 (1981) 51-54
-
(1981)
Br J Cancer
, vol.44
, pp. 51-54
-
-
Potter, A.M.1
Watmore, A.E.2
Cooke, P.3
Lilleyman, J.S.4
Sokol, R.J.5
-
27
-
-
0020274979
-
Variant Philadelphia chromosome translocations in two patients with chronic myelogenous leukemia
-
Testa J.R., Jumamoy L.M., and Wiernik P.H. Variant Philadelphia chromosome translocations in two patients with chronic myelogenous leukemia. Cancer Genet Cytogenet 7 (1982) 79-84
-
(1982)
Cancer Genet Cytogenet
, vol.7
, pp. 79-84
-
-
Testa, J.R.1
Jumamoy, L.M.2
Wiernik, P.H.3
-
28
-
-
0021262126
-
The incidence, type, and subsequent evolution of 14 variant Ph1 translocations in 180 South African patients with Ph1-positive chronic myeloid leukemia
-
Bernstein R., Pinto M.R., Wallace C., Penfold G., and Mendelow B. The incidence, type, and subsequent evolution of 14 variant Ph1 translocations in 180 South African patients with Ph1-positive chronic myeloid leukemia. Cancer Genet Cytogenet 12 (1984) 225-238
-
(1984)
Cancer Genet Cytogenet
, vol.12
, pp. 225-238
-
-
Bernstein, R.1
Pinto, M.R.2
Wallace, C.3
Penfold, G.4
Mendelow, B.5
-
29
-
-
0023192225
-
Variant Philadelphia translocations in chronic myeloid leukemia
-
De Braekeleer M. Variant Philadelphia translocations in chronic myeloid leukemia. Cytogenet Cell Genet 44 (1987) 215-222
-
(1987)
Cytogenet Cell Genet
, vol.44
, pp. 215-222
-
-
De Braekeleer, M.1
-
30
-
-
29244452674
-
Jumping translocation of 17q11∼qter and 3q25∼q28 duplication in a variant Philadelphia t(9;14;22)(q34;q32;q11) in a childhood chronic myelogenous leukemia
-
Haltrich I., Kost-Alimova M., Kovacs G., Krivan G., Tamaska J., Klein G., Fekete G., and Imreh S. Jumping translocation of 17q11∼qter and 3q25∼q28 duplication in a variant Philadelphia t(9;14;22)(q34;q32;q11) in a childhood chronic myelogenous leukemia. Cancer Genet Cytogenet 164 (2006) 74-80
-
(2006)
Cancer Genet Cytogenet
, vol.164
, pp. 74-80
-
-
Haltrich, I.1
Kost-Alimova, M.2
Kovacs, G.3
Krivan, G.4
Tamaska, J.5
Klein, G.6
Fekete, G.7
Imreh, S.8
-
31
-
-
0033953991
-
Complex chromosome rearrangements may locate the bcr/abl fusion gene sites other than 22q11
-
Sessarego M., Fugazza G., Bruzzone R., Ballestrero A., Miglino M., and Bacigalupo A. Complex chromosome rearrangements may locate the bcr/abl fusion gene sites other than 22q11. Haematologica 85 (2000) 35-39
-
(2000)
Haematologica
, vol.85
, pp. 35-39
-
-
Sessarego, M.1
Fugazza, G.2
Bruzzone, R.3
Ballestrero, A.4
Miglino, M.5
Bacigalupo, A.6
-
32
-
-
13844281267
-
A complex translocation (9;22;16)(q34;q11.2;p13) in chronic myelocytic leukemia
-
Espinoza J.P.M., Cárdenas V.J.P., Jiménez E.A.V., Angulo M.G., Flores M.A.E., and García J.R.G. A complex translocation (9;22;16)(q34;q11.2;p13) in chronic myelocytic leukemia. Cancer Genet Cytogenet 157 (2005) 175-177
-
(2005)
Cancer Genet Cytogenet
, vol.157
, pp. 175-177
-
-
Espinoza, J.P.M.1
Cárdenas, V.J.P.2
Jiménez, E.A.V.3
Angulo, M.G.4
Flores, M.A.E.5
García, J.R.G.6
-
33
-
-
35948977724
-
Poor prognosis chronic myeloid leukemia with a complex variant Philadelphia translocation, t(9;10;22)(q34;q24;q11)
-
Buda G., Orciuolo E., Cecconi N., Galimberti S., Cervetti G., and Petrini M. Poor prognosis chronic myeloid leukemia with a complex variant Philadelphia translocation, t(9;10;22)(q34;q24;q11). Leuk Res 31 (2007) 1765-1766
-
(2007)
Leuk Res
, vol.31
, pp. 1765-1766
-
-
Buda, G.1
Orciuolo, E.2
Cecconi, N.3
Galimberti, S.4
Cervetti, G.5
Petrini, M.6
-
34
-
-
18444401418
-
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia
-
Loncarevic I.F., Römer J., Starke H., Heller A., Bleck C., Ziegler M., Fiedler W., Liehr T., Clement J.H., and Claussen U. Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia. Genes Chromosomes Cancer 34 (2002) 193-200
-
(2002)
Genes Chromosomes Cancer
, vol.34
, pp. 193-200
-
-
Loncarevic, I.F.1
Römer, J.2
Starke, H.3
Heller, A.4
Bleck, C.5
Ziegler, M.6
Fiedler, W.7
Liehr, T.8
Clement, J.H.9
Claussen, U.10
-
35
-
-
0038353973
-
Survival implications of molecular heterogeneity in variant Philadelphia-positive chronic myeloid leukaemia
-
Reid A.G., Huntly B.J., Grace C., Green A.R., and Nacheva E.P. Survival implications of molecular heterogeneity in variant Philadelphia-positive chronic myeloid leukaemia. Br J Haematol 121 (2003) 419-427
-
(2003)
Br J Haematol
, vol.121
, pp. 419-427
-
-
Reid, A.G.1
Huntly, B.J.2
Grace, C.3
Green, A.R.4
Nacheva, E.P.5
-
36
-
-
21744442745
-
Breakpoints of variant 9;22 translocations in chronic myeloid leukemia locate preferentially in the CG-richest regions of the genome
-
Fisher A.M., Strike P., Scott C., and Moorman A.V. Breakpoints of variant 9;22 translocations in chronic myeloid leukemia locate preferentially in the CG-richest regions of the genome. Genes Chromosomes Cancer 43 (2005) 383-389
-
(2005)
Genes Chromosomes Cancer
, vol.43
, pp. 383-389
-
-
Fisher, A.M.1
Strike, P.2
Scott, C.3
Moorman, A.V.4
-
37
-
-
0035827373
-
The sequence of the human genome
-
[Erratum in: Science 2001;292:1838]
-
Venter J.C., Adams M.D., Myers E.W., Li P.W., Mural R.J., Sutton G.G., Smith H.O., Yandell M., Evans C.A., Holt R.A., Gocayne J.D., Amanatides P., Ballew R.M., Huson D.H., Wortman J.R., Zhang Q., Kodira C.D., Zheng X.H., Chen L., Skupski M., Subramanian G., Thomas P.D., Zhang J., Gabor Miklos G.L., Nelson C., Broder S., Clark A.G., Nadeau J., McKusick V.A., Zinder N., Levine A.J., Roberts R.J., Simon M., Slayman C., Hunkapiller M., Bolanos R., Delcher A., Dew I., Fasulo D., Flanigan M., Florea L., Halpern A., Hannenhalli S., Kravitz S., Levy S., Mobarry C., Reinert K., Remington K., Abu-Threideh J., Beasley E., Biddick K., Bonazzi V., Brandon R., Cargill M., Chandramouliswaran I., Charlab R., Chaturvedi K., Deng Z., Di Francesco V., Dunn P., Eilbeck K., Evangelista C., Gabrielian A.E., Gan W., Ge W., Gong F., Gu Z., Guan P., Heiman T.J., Higgins M.E., Ji R.R., Ke Z., Ketchum K.A., Lai Z., Lei Y., Li Z., Li J., Liang Y., Lin X., Lu F., Merkulov G.V., Milshina N., Moore H.M., Naik A.K., Narayan V.A., Neelam B., Nusskern D., Rusch D.B., Salzberg S., Shao W., Shue B., Sun J., Wang Z., Wang A., Wang X., Wang J., Wei M., Wides R., Xiao C., Yan C., Yao A., Ye J., Zhan M., Zhang W., Zhang H., Zhao Q., Zheng L., Zhong F., Zhong W., Zhu S., Zhao S., Gilbert D., Baumhueter S., Spier G., Carter C., Cravchik A., Woodage T., Ali F., An H., Awe A., Baldwin D., Baden H., Barnstead M., Barrow I., Beeson K., Busam D., Carver A., Center A., Cheng M.L., Curry L., Danaher S., Davenport L., Desilets R., Dietz S., Dodson K., Doup L., Ferriera S., Garg N., Gluecksmann A., Hart B., Haynes J., Haynes C., Heiner C., Hladun S., Hostin D., Houck J., Howland T., Ibegwam C., Johnson J., Kalush F., Kline L., Koduru S., Love A., Mann F., May D., McCawley S., McIntosh T., McMullen I., Moy M., Moy L., Murphy B., Nelson K., Pfannkoch C., Pratts E., Puri V., Qureshi H., Reardon M., Rodriguez R., Rogers Y.H., Romblad D., Ruhfel B., Scott R., Sitter C., Smallwood M., Stewart E., Strong R., Suh E., Thomas R., Tint N.N., Tse S., Vech C., Wang G., Wetter J., Williams S., Williams M., Windsor S., Winn-Deen E., Wolfe K., Zaveri J., Zaveri K., Abril J.F., Guigó R., Campbell M.J., Sjolander K.V., Karlak B., Kejariwal A., Mi H., Lazareva B., Hatton T., Narechania A., Diemer K., Muruganujan A., Guo N., Sato S., Bafna V., Istrail S., Lippert R., Schwartz R., Walenz B., Yooseph S., Allen D., Basu A., Baxendale J., Blick L., Caminha M., Carnes-Stine J., Caulk P., Chiang Y.H., Coyne M., Dahlke C., Mays A., Dombroski M., Donnelly M., Ely D., Esparham S., Fosler C., Gire H., Glanowski S., Glasser K., Glodek A., Gorokhov M., Graham K., Gropman B., Harris M., Heil J., Henderson S., Hoover J., Jennings D., Jordan C., Jordan J., Kasha J., Kagan L., Kraft C., Levitsky A., Lewis M., Liu X., Lopez J., Ma D., Majoros W., McDaniel J., Murphy S., Newman M., Nguyen T., Nguyen N., Nodell M., Pan S., Peck J., Peterson M., Rowe W., Sanders R., Scott J., Simpson M., Smith T., Sprague A., Stockwell T., Turner R., Venter E., Wang M., Wen M., Wu D., Wu M., Xia A., Zandieh A., and Zhu X. The sequence of the human genome. [Erratum in: Science 2001;292:1838]. Science 292 (2001) 1838
-
(2001)
Science
, vol.292
, pp. 1838
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
Smith, H.O.7
Yandell, M.8
Evans, C.A.9
Holt, R.A.10
Gocayne, J.D.11
Amanatides, P.12
Ballew, R.M.13
Huson, D.H.14
Wortman, J.R.15
Zhang, Q.16
Kodira, C.D.17
Zheng, X.H.18
Chen, L.19
Skupski, M.20
Subramanian, G.21
Thomas, P.D.22
Zhang, J.23
Gabor Miklos, G.L.24
Nelson, C.25
Broder, S.26
Clark, A.G.27
Nadeau, J.28
McKusick, V.A.29
Zinder, N.30
Levine, A.J.31
Roberts, R.J.32
Simon, M.33
Slayman, C.34
Hunkapiller, M.35
Bolanos, R.36
Delcher, A.37
Dew, I.38
Fasulo, D.39
Flanigan, M.40
Florea, L.41
Halpern, A.42
Hannenhalli, S.43
Kravitz, S.44
Levy, S.45
Mobarry, C.46
Reinert, K.47
Remington, K.48
Abu-Threideh, J.49
Beasley, E.50
Biddick, K.51
Bonazzi, V.52
Brandon, R.53
Cargill, M.54
Chandramouliswaran, I.55
Charlab, R.56
Chaturvedi, K.57
Deng, Z.58
Di Francesco, V.59
Dunn, P.60
Eilbeck, K.61
Evangelista, C.62
Gabrielian, A.E.63
Gan, W.64
Ge, W.65
Gong, F.66
Gu, Z.67
Guan, P.68
Heiman, T.J.69
Higgins, M.E.70
Ji, R.R.71
Ke, Z.72
Ketchum, K.A.73
Lai, Z.74
Lei, Y.75
Li, Z.76
Li, J.77
Liang, Y.78
Lin, X.79
Lu, F.80
Merkulov, G.V.81
Milshina, N.82
Moore, H.M.83
Naik, A.K.84
Narayan, V.A.85
Neelam, B.86
Nusskern, D.87
Rusch, D.B.88
Salzberg, S.89
Shao, W.90
Shue, B.91
Sun, J.92
Wang, Z.93
Wang, A.94
Wang, X.95
Wang, J.96
Wei, M.97
Wides, R.98
Xiao, C.99
Yan, C.100
Yao, A.101
Ye, J.102
Zhan, M.103
Zhang, W.104
Zhang, H.105
Zhao, Q.106
Zheng, L.107
Zhong, F.108
Zhong, W.109
Zhu, S.110
Zhao, S.111
Gilbert, D.112
Baumhueter, S.113
Spier, G.114
Carter, C.115
Cravchik, A.116
Woodage, T.117
Ali, F.118
An, H.119
Awe, A.120
Baldwin, D.121
Baden, H.122
Barnstead, M.123
Barrow, I.124
Beeson, K.125
Busam, D.126
Carver, A.127
Center, A.128
Cheng, M.L.129
Curry, L.130
Danaher, S.131
Davenport, L.132
Desilets, R.133
Dietz, S.134
Dodson, K.135
Doup, L.136
Ferriera, S.137
Garg, N.138
Gluecksmann, A.139
Hart, B.140
Haynes, J.141
Haynes, C.142
Heiner, C.143
Hladun, S.144
Hostin, D.145
Houck, J.146
Howland, T.147
Ibegwam, C.148
Johnson, J.149
Kalush, F.150
Kline, L.151
Koduru, S.152
Love, A.153
Mann, F.154
May, D.155
McCawley, S.156
McIntosh, T.157
McMullen, I.158
Moy, M.159
Moy, L.160
Murphy, B.161
Nelson, K.162
Pfannkoch, C.163
Pratts, E.164
Puri, V.165
Qureshi, H.166
Reardon, M.167
Rodriguez, R.168
Rogers, Y.H.169
Romblad, D.170
Ruhfel, B.171
Scott, R.172
Sitter, C.173
Smallwood, M.174
Stewart, E.175
Strong, R.176
Suh, E.177
Thomas, R.178
Tint, N.N.179
Tse, S.180
Vech, C.181
Wang, G.182
Wetter, J.183
Williams, S.184
Williams, M.185
Windsor, S.186
Winn-Deen, E.187
Wolfe, K.188
Zaveri, J.189
Zaveri, K.190
Abril, J.F.191
Guigó, R.192
Campbell, M.J.193
Sjolander, K.V.194
Karlak, B.195
Kejariwal, A.196
Mi, H.197
Lazareva, B.198
Hatton, T.199
Narechania, A.200
Diemer, K.201
Muruganujan, A.202
Guo, N.203
Sato, S.204
Bafna, V.205
Istrail, S.206
Lippert, R.207
Schwartz, R.208
Walenz, B.209
Yooseph, S.210
Allen, D.211
Basu, A.212
Baxendale, J.213
Blick, L.214
Caminha, M.215
Carnes-Stine, J.216
Caulk, P.217
Chiang, Y.H.218
Coyne, M.219
Dahlke, C.220
Mays, A.221
Dombroski, M.222
Donnelly, M.223
Ely, D.224
Esparham, S.225
Fosler, C.226
Gire, H.227
Glanowski, S.228
Glasser, K.229
Glodek, A.230
Gorokhov, M.231
Graham, K.232
Gropman, B.233
Harris, M.234
Heil, J.235
Henderson, S.236
Hoover, J.237
Jennings, D.238
Jordan, C.239
Jordan, J.240
Kasha, J.241
Kagan, L.242
Kraft, C.243
Levitsky, A.244
Lewis, M.245
Liu, X.246
Lopez, J.247
Ma, D.248
Majoros, W.249
McDaniel, J.250
Murphy, S.251
Newman, M.252
Nguyen, T.253
Nguyen, N.254
Nodell, M.255
Pan, S.256
Peck, J.257
Peterson, M.258
Rowe, W.259
Sanders, R.260
Scott, J.261
Simpson, M.262
Smith, T.263
Sprague, A.264
Stockwell, T.265
Turner, R.266
Venter, E.267
Wang, M.268
Wen, M.269
Wu, D.270
Wu, M.271
Xia, A.272
Zandieh, A.273
Zhu, X.274
more..
-
38
-
-
0033962962
-
Alu and translisin recognition site sequences flanking translocation sites in a novel type of chimeric bcr-abl transcript suggest a possible general mechanism for bcr-abl breakpoints
-
Martinelli G., Terragna C., Amabile M., Montefusco V., Testoni N., Ottaviani E., de Vivo A., Mianulli A., Saglio G., and Tura S. Alu and translisin recognition site sequences flanking translocation sites in a novel type of chimeric bcr-abl transcript suggest a possible general mechanism for bcr-abl breakpoints. Hematologica 85 (2000) 40-46
-
(2000)
Hematologica
, vol.85
, pp. 40-46
-
-
Martinelli, G.1
Terragna, C.2
Amabile, M.3
Montefusco, V.4
Testoni, N.5
Ottaviani, E.6
de Vivo, A.7
Mianulli, A.8
Saglio, G.9
Tura, S.10
-
39
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong A., Gudbjartsson D.F., Sainz J., Jonsdottir G.M., Gudjonsson S.A., Richardsson B., Sigurdardottir S., Barnard J., Hallbeck B., Masson G., Shlien A., Palsson S.T., Frigge M.L., Thorgeirsson T.E., Gulcher J.R., and Stefansson K. A high-resolution recombination map of the human genome. Nat Genet 31 (2002) 241-247
-
(2002)
Nat Genet
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
Shlien, A.11
Palsson, S.T.12
Frigge, M.L.13
Thorgeirsson, T.E.14
Gulcher, J.R.15
Stefansson, K.16
-
40
-
-
4444258534
-
Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibers
-
Gilbert N., Boyle S., Fiegler H., Woodfine K., Carter N.P., and Bickmore W.A. Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibers. Cell 118 (2004) 555-566
-
(2004)
Cell
, vol.118
, pp. 555-566
-
-
Gilbert, N.1
Boyle, S.2
Fiegler, H.3
Woodfine, K.4
Carter, N.P.5
Bickmore, W.A.6
-
41
-
-
0141854009
-
The human transcriptome map reveals extremes in gene density, intron length, GC content, and repeat pattern for domains of highly and weakly expressed genes
-
Versteeg R., van Schaik B.D., van Batenburg M.F., Roos M., Monajemi R., Caron H., Bussemaker H.J., and van Kampen A.H. The human transcriptome map reveals extremes in gene density, intron length, GC content, and repeat pattern for domains of highly and weakly expressed genes. Genome Res 13 (2003) 1998-2004
-
(2003)
Genome Res
, vol.13
, pp. 1998-2004
-
-
Versteeg, R.1
van Schaik, B.D.2
van Batenburg, M.F.3
Roos, M.4
Monajemi, R.5
Caron, H.6
Bussemaker, H.J.7
van Kampen, A.H.8
-
42
-
-
0031898431
-
The BCR gene recombines preferentially with Alu elements in complex BCR-ABL translocations of chronic myeloid leukaemia
-
Jeffs A.R., Benjes S.M., Smith T.L., Sowerby S.J., and Morris C.M. The BCR gene recombines preferentially with Alu elements in complex BCR-ABL translocations of chronic myeloid leukaemia. Hum Mol Genet 7 (1998) 767-776
-
(1998)
Hum Mol Genet
, vol.7
, pp. 767-776
-
-
Jeffs, A.R.1
Benjes, S.M.2
Smith, T.L.3
Sowerby, S.J.4
Morris, C.M.5
-
43
-
-
11144357159
-
Results of imatinib mesylate therapy in chronic myelogenous leukaemia with variant Philadelphia chromosome
-
El-Zimaity M.M., Kantarjian H., Talpaz M., O'Brien S., Giles F., Garcia-Manero G., Verstovsek S., Thomas D., Ferrajoli A., Hayes K., Nebiyou Bekele B., Zhou X., Rios M.B., Glassman A.B., and Cortes J.E. Results of imatinib mesylate therapy in chronic myelogenous leukaemia with variant Philadelphia chromosome. Br J Haematol 125 (2004) 187-195
-
(2004)
Br J Haematol
, vol.125
, pp. 187-195
-
-
El-Zimaity, M.M.1
Kantarjian, H.2
Talpaz, M.3
O'Brien, S.4
Giles, F.5
Garcia-Manero, G.6
Verstovsek, S.7
Thomas, D.8
Ferrajoli, A.9
Hayes, K.10
Nebiyou Bekele, B.11
Zhou, X.12
Rios, M.B.13
Glassman, A.B.14
Cortes, J.E.15
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