-
1
-
-
0026646745
-
Clinical significance of the del(20q) chromosome in hematologic disorders
-
Aatola, M., Armstrong, E., Teerenhovi, I., & Borgstrom, G.H. (1992) Clinical significance of the del(20q) chromosome in hematologic disorders. Cancer Genetics and Cytogenetics, 62, 75-80.
-
(1992)
Cancer Genetics and Cytogenetics
, vol.62
, pp. 75-80
-
-
Aatola, M.1
Armstrong, E.2
Teerenhovi, I.3
Borgstrom, G.H.4
-
2
-
-
0026348155
-
Clonality of cell populations in refractory anaemia uising combined approach of gene loss and X-linked restriction fragment length polymorphism-methylation analyses
-
Abrahamson, G., Boultwood, J., Madden, J., Kelly, S., Oscier, D.G., Rack, K., Buckle, V.J. & Wainscoat, J.S. (1991) Clonality of cell populations in refractory anaemia uising combined approach of gene loss and X-linked restriction fragment length polymorphism-methylation analyses. British Journal of Haematology. 79. 550-555.
-
(1991)
British Journal of Haematology
, vol.79
, pp. 550-555
-
-
Abrahamson, G.1
Boultwood, J.2
Madden, J.3
Kelly, S.4
Oscier, D.G.5
Rack, K.6
Buckle, V.J.7
Wainscoat, J.S.8
-
3
-
-
10244226926
-
A YAC contig spanning the region of chromosome 20q that is detected in myeloproliferative disorders
-
Aldred, M.A., Humphray, S.J., Gwillian, R., Bench, A., Bentley, D.R. & Green, A.R. (1996) A YAC contig spanning the region of chromosome 20q that is detected in myeloproliferative disorders, HGM' 96 Abstract Book, p. 2.
-
(1996)
HGM' 96 Abstract Book
, pp. 2
-
-
Aldred, M.A.1
Humphray, S.J.2
Gwillian, R.3
Bench, A.4
Bentley, D.R.5
Green, A.R.6
-
4
-
-
0022998535
-
Cytogenetic evidence for partially committed myeloid progenitor cell origin of chronic myelomonocytic leukaemia and juvenile chronic myeloid leukaemia
-
Amenomori, T., Tomonaga, M., Yoshida, Y., Kuriyama, K., Matsuo, T., Jinnai, I., Ichimaru, M., Omiya, A. & Tsuji, Y. (1986) Cytogenetic evidence for partially committed myeloid progenitor cell origin of chronic myelomonocytic leukaemia and juvenile chronic myeloid leukaemia. British Journal of Haematology, 64, 539-546.
-
(1986)
British Journal of Haematology
, vol.64
, pp. 539-546
-
-
Amenomori, T.1
Tomonaga, M.2
Yoshida, Y.3
Kuriyama, K.4
Matsuo, T.5
Jinnai, I.6
Ichimaru, M.7
Omiya, A.8
Tsuji, Y.9
-
5
-
-
10244245182
-
hHNF-4B and HNF-4C gene loci map to chromosome 20q12-q13.2 and are closely linked
-
Argyrokastritis, A., Kamakari, S., Kapsetaki, M., Kritis, A., Talianidis, I. & Moschonas, N.K. (1996) hHNF-4B and HNF-4C gene loci map to chromosome 20q12-q13.2 and are closely linked. HGM' 96 Abstract Book, p. 4.
-
(1996)
HGM' 96 Abstract Book
, pp. 4
-
-
Argyrokastritis, A.1
Kamakari, S.2
Kapsetaki, M.3
Kritis, A.4
Talianidis, I.5
Moschonas, N.K.6
-
7
-
-
0029842073
-
Interstitial deletion constitutes the main mechanism for loss of heterozygosity on chromosome 20q in polycythemia vera
-
in press
-
Asimakopoulos, F.A., Gilbert, J.G.R., Aldred, M.A., Pearson, T.C. & Green, A.R. (1996a) Interstitial deletion constitutes the main mechanism for loss of heterozygosity on chromosome 20q in polycythemia vera. Blood, in press.
-
(1996)
Blood
-
-
Asimakopoulos, F.A.1
Gilbert, J.G.R.2
Aldred, M.A.3
Pearson, T.C.4
Green, A.R.5
-
8
-
-
0030043357
-
Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes
-
Asimakopoulos, F.A., Holloway, T.L., Nacheva, E.P., Scott, M.A., Fenaux, P. & Green, A.R. (1996b) Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes, Blood 87, 1561-1570.
-
(1996)
Blood
, vol.87
, pp. 1561-1570
-
-
Asimakopoulos, F.A.1
Holloway, T.L.2
Nacheva, E.P.3
Scott, M.A.4
Fenaux, P.5
Green, A.R.6
-
9
-
-
0028116531
-
Molecular analysis of chromosome 20 deletions associated with myeloproliferative disorders and myelodysplastic syndromes
-
Asimakopoulos, F.A., White, N., Nacheva, E. & Green, A.R. (1994) Molecular analysis of chromosome 20 deletions associated with myeloproliferative disorders and myelodysplastic syndromes. Blood, 84, 3086-3094.
-
(1994)
Blood
, vol.84
, pp. 3086-3094
-
-
Asimakopoulos, F.A.1
White, N.2
Nacheva, E.3
Green, A.R.4
-
10
-
-
0030043164
-
The human CD40 gene lies within chromosome 20q deletions associated with myeloid malignancies
-
Asimakopoulos, F.A., White, N.J., Nacheva, E.P. & Green, A.R. (1996c) The human CD40 gene lies within chromosome 20q deletions associated with myeloid malignancies. British Journal of Haematology, 92, 127-130.
-
(1996)
British Journal of Haematology
, vol.92
, pp. 127-130
-
-
Asimakopoulos, F.A.1
White, N.J.2
Nacheva, E.P.3
Green, A.R.4
-
11
-
-
0026696107
-
Murine chromosomal location of four hepatocyte enriched transcription factors: HNF-3a, HNF-33, HF-3 , and HNF-4
-
Avraham, K.B., Prezioso, V.R., Chen, W.S., Lai, E., Sladek, F.M., Zhong, W., Darnell, J.E., Jr, Jenkins, N.A. & Copeland, N.G. (1992) Murine chromosomal location of four hepatocyte enriched transcription factors: HNF-3a, HNF-33, HF-3 , and HNF-4. Genomics, 13, 264-268.
-
(1992)
Genomics
, vol.13
, pp. 264-268
-
-
Avraham, K.B.1
Prezioso, V.R.2
Chen, W.S.3
Lai, E.4
Sladek, F.M.5
Zhong, W.6
Darnell Jr., J.E.7
Jenkins, N.A.8
Copeland, N.G.9
-
12
-
-
0027954472
-
The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders
-
Campbell, L.J. & Garson, O.M. (1994) The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders. Leukemia, 8, 67-71.
-
(1994)
Leukemia
, vol.8
, pp. 67-71
-
-
Campbell, L.J.1
Garson, O.M.2
-
13
-
-
0026780475
-
Clonal lymphocytes are detectable in only some cases of MDS
-
Culligan, D.J., Cachia, P., Whittaker, J., Jacobs, A. & Padua, R.A. (1992) Clonal lymphocytes are detectable in only some cases of MDS. British Journal of Haematology, 81, 346-352.
-
(1992)
British Journal of Haematology
, vol.81
, pp. 346-352
-
-
Culligan, D.J.1
Cachia, P.2
Whittaker, J.3
Jacobs, A.4
Padua, R.A.5
-
14
-
-
0021254497
-
Hematologic manifestations associated with deletions of the long arm of chromosome 20
-
Davis, M.P., Dewald, G.W., Pierre, R.V. & Hoagland, H.C. (1984) Hematologic manifestations associated with deletions of the long arm of chromosome 20. Cancer Genetics and Cytogenetics, 12, 63-71.
-
(1984)
Cancer Genetics and Cytogenetics
, vol.12
, pp. 63-71
-
-
Davis, M.P.1
Dewald, G.W.2
Pierre, R.V.3
Hoagland, H.C.4
-
15
-
-
0023726101
-
Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: A report on 47 cases
-
Demory, J.L., Dupriez, B., Fenaux, P., Lai, J.L., Beuscart, R., Jouet, J.P., Deminatti, M. & Bauters, F. (1988) Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: a report on 47 cases. Blood, 72, 855-859.
-
(1988)
Blood
, vol.72
, pp. 855-859
-
-
Demory, J.L.1
Dupriez, B.2
Fenaux, P.3
Lai, J.L.4
Beuscart, R.5
Jouet, J.P.6
Deminatti, M.7
Bauters, F.8
-
16
-
-
0029154197
-
Chromosome abnormalities in the myeloproliferative disorders
-
Dewald, G.W. & Wright, P.I. (1995) Chromosome abnormalities in the myeloproliferative disorders. Seminars in Oncology. 22, 341-354.
-
(1995)
Seminars in Oncology
, vol.22
, pp. 341-354
-
-
Dewald, G.W.1
Wright, P.I.2
-
17
-
-
0025904546
-
Chromosome studies in 104 patients with polycythemia vera
-
Diez-Martin, J.L., Graham, D.L., Pettit, R.M. & Dewald, G.W. (1991) Chromosome studies in 104 patients with polycythemia vera. Mayo Clinic Proceedings, 66, 287-299.
-
(1991)
Mayo Clinic Proceedings
, vol.66
, pp. 287-299
-
-
Diez-Martin, J.L.1
Graham, D.L.2
Pettit, R.M.3
Dewald, G.W.4
-
18
-
-
0030004485
-
Heterozygous embryonic lethality induced by target inactivation of the VEGF gene
-
Ferrara, N., Carver-Moore, K., Chen, H., Dowd, M., Lu, L., O'Shea, K.S., Powell-Braxton, L., Hillan, K.J. & Moore, M.W. (1996) Heterozygous embryonic lethality induced by target inactivation of the VEGF gene, Nature, 380, 439-442.
-
(1996)
Nature
, vol.380
, pp. 439-442
-
-
Ferrara, N.1
Carver-Moore, K.2
Chen, H.3
Dowd, M.4
Lu, L.5
O'Shea, K.S.6
Powell-Braxton, L.7
Hillan, K.J.8
Moore, M.W.9
-
19
-
-
0028058986
-
Human haploinsufficiency; one for sorrow, two for joy
-
Fisher, E. & Scambler, P. (1994) Human haploinsufficiency; one for sorrow, two for joy. Nature Genetics. 7, 5-7.
-
(1994)
Nature Genetics
, vol.7
, pp. 5-7
-
-
Fisher, E.1
Scambler, P.2
-
20
-
-
0029922403
-
Pathogenesis of polycythaemia vera
-
Green, A.R. (1996) Pathogenesis of polycythaemia vera. Lancet, 347, 844-845.
-
(1996)
Lancet
, vol.347
, pp. 844-845
-
-
Green, A.R.1
-
21
-
-
0029935705
-
The most unkindest cut of all
-
Hartl, D.L. (1996) The most unkindest cut of all. Nature Genetics, 12, 227-229.
-
(1996)
Nature Genetics
, vol.12
, pp. 227-229
-
-
Hartl, D.L.1
-
22
-
-
0028072991
-
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma
-
Herman, J.G., Latif, F., Weng, Y., Lerman, M.I., Zbar, B., Liu, S., Samid, D., Duan, D.S.R., Gnarra, J.R., Linehan, W.M. & Baylin, S.B. (1994) Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma, Proceedings of the National Academy of Sciences of the United States of America, 91, 9700-9704.
-
(1994)
Proceedings of the National Academy of Sciences of the United States of America
, vol.91
, pp. 9700-9704
-
-
Herman, J.G.1
Latif, F.2
Weng, Y.3
Lerman, M.I.4
Zbar, B.5
Liu, S.6
Samid, D.7
Duan, D.S.R.8
Gnarra, J.R.9
Linehan, W.M.10
Baylin, S.B.11
-
23
-
-
0028144840
-
Molecular heterogeneity at the breakpoints of smaller 20q deletions
-
Hollings, P.E. (1994) Molecular heterogeneity at the breakpoints of smaller 20q deletions. Genes, Chromosomes and Cancer. 11, 21-28.
-
(1994)
Genes, Chromosomes and Cancer
, vol.11
, pp. 21-28
-
-
Hollings, P.E.1
-
24
-
-
0028855736
-
Deletion 20q in association with Philadelphia chromosome positive acute lymphoblastic leukemia: Report of two cases
-
Hollings, P.E., Benjes, S.M., Rosman, I. & Fitzgerald, P.H. (1995) Deletion 20q in association with Philadelphia chromosome positive acute lymphoblastic leukemia: report of two cases. Cancer Genetics and Cytogenetics, 79, 32-35.
-
(1995)
Cancer Genetics and Cytogenetics
, vol.79
, pp. 32-35
-
-
Hollings, P.E.1
Benjes, S.M.2
Rosman, I.3
Fitzgerald, P.H.4
-
25
-
-
0024509491
-
Clonal analysis of myelodysplastic syndromes: Evidence of multipotent stem cell origin
-
Janssen, J.W.G., Buschle, M., Layton, M., Drexler, H.G., Lyons, J., van den Berghe, H., Heimpel, H., Kubarek, B., Kleihauer, E., Mufti, G.J. & Bartram, C.R. (1989) Clonal analysis of myelodysplastic syndromes: evidence of multipotent stem cell origin. Blood, 73, 248-254.
-
(1989)
Blood
, vol.73
, pp. 248-254
-
-
Janssen, J.W.G.1
Buschle, M.2
Layton, M.3
Drexler, H.G.4
Lyons, J.5
Van Den Berghe, H.6
Heimpel, H.7
Kubarek, B.8
Kleihauer, E.9
Mufti, G.J.10
Bartram, C.R.11
-
26
-
-
0011134388
-
RAS gene mutations in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders and myelodysplastic syndromes
-
Janssen, J.W.G., Steenvoorden, A.C.M., Lyons, J., Anger, B., Bohlke, J.U., Bos, J.L., Seliger, H. & Bartram, C.R. (1987) RAS gene mutations in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders and myelodysplastic syndromes. Proceedings of the National Academy of Sciences of the United States of America, 84, 9228-9232.
-
(1987)
Proceedings of the National Academy of Sciences of the United States of America
, vol.84
, pp. 9228-9232
-
-
Janssen, J.W.G.1
Steenvoorden, A.C.M.2
Lyons, J.3
Anger, B.4
Bohlke, J.U.5
Bos, J.L.6
Seliger, H.7
Bartram, C.R.8
-
27
-
-
0027378164
-
Cytogenetic deletion maps of hematologic neoplasms: Circumstantial evidence for tumor suppressor loci
-
Johansson, B., Mertens, F. & Mitelman, F. (1993) Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes, Chromosomes and Cancer. 8, 205-218.
-
(1993)
Genes, Chromosomes and Cancer
, vol.8
, pp. 205-218
-
-
Johansson, B.1
Mertens, F.2
Mitelman, F.3
-
28
-
-
0013951833
-
The chromosomes in polycythaemia vera
-
Kay, H.E., Lawler, S.D. & Millard, R.E. (1966) The chromosomes in polycythaemia vera. British Journal of Haematology, 12, 507-528.
-
(1966)
British Journal of Haematology
, vol.12
, pp. 507-528
-
-
Kay, H.E.1
Lawler, S.D.2
Millard, R.E.3
-
29
-
-
0023098320
-
Monosomy 7 in granulocytes and monocytes in myelodysplastic syndrome
-
Kere, J., Ruutu, T., Lachtinen, R. & de la Chapelle, A. (1987) Monosomy 7 in granulocytes and monocytes in myelodysplastic syndrome. New England Journal of Medicine, 316, 499-503.
-
(1987)
New England Journal of Medicine
, vol.316
, pp. 499-503
-
-
Kere, J.1
Ruutu, T.2
Lachtinen, R.3
De La Chapelle, A.4
-
30
-
-
0022393713
-
Cytogenetic studies in 174 consecutive patients with preleukemia or meylodysplastic syndromes
-
Knapp, R.H., Dewald, G.W. & Pierre, R.V. (1985) Cytogenetic studies in 174 consecutive patients with preleukemia or meylodysplastic syndromes, Mayo Clinic Proceedings, 60, 507-516.
-
(1985)
Mayo Clinic Proceedings
, vol.60
, pp. 507-516
-
-
Knapp, R.H.1
Dewald, G.W.2
Pierre, R.V.3
-
31
-
-
0028235669
-
Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms
-
Knuutila, S., Teerenhovi, L., Larramendy, M.L., Elonen, E., Franssila, K.O., Nylund, S.J., Timonen, T., Heinonen, K., Mahlamaki, E., Winqvist, R. & Ruutu, T. (1994) Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms. Genes, Chromosomes and Cancer, 10, 95-102.
-
(1994)
Genes, Chromosomes and Cancer
, vol.10
, pp. 95-102
-
-
Knuutila, S.1
Teerenhovi, L.2
Larramendy, M.L.3
Elonen, E.4
Franssila, K.O.5
Nylund, S.J.6
Timonen, T.7
Heinonen, K.8
Mahlamaki, E.9
Winqvist, R.10
Ruutu, T.11
-
32
-
-
0027533768
-
Myeloid but not lymphoid cells carry the 5q deletion: Polymerase chain reaction analysis of loss of heterozygosity using mini-repeat sequences on highly purified cell fractions
-
Kroef, M.J., Fibbe, W.E., Mout, R., Jansen, R.P., Haak, H.L., Wessels, J.W., Van Kamp, H., Willemze, R. & Landegent, J.E. (1993) Myeloid but not lymphoid cells carry the 5q deletion: polymerase chain reaction analysis of loss of heterozygosity using mini-repeat sequences on highly purified cell fractions. Blood, 81, 1849-1854.
-
(1993)
Blood
, vol.81
, pp. 1849-1854
-
-
Kroef, M.J.1
Fibbe, W.E.2
Mout, R.3
Jansen, R.P.4
Haak, H.L.5
Wessels, J.W.6
Van Kamp, H.7
Willemze, R.8
Landegent, J.E.9
-
33
-
-
0023632578
-
Cytogenetic evidence for involvement of B lymphocytes in acquired idiopathic sideroblastic anemias
-
Lawrence, H.J., Broudy, V-.C., Magenis, R.E., Olson, S., Tomar, D., Barton, S., Fitchen, J.H. & Bagby, G.C., Jr (1987) Cytogenetic evidence for involvement of B lymphocytes in acquired idiopathic sideroblastic anemias. Blood, 70, 1003-1005.
-
(1987)
Blood
, vol.70
, pp. 1003-1005
-
-
Lawrence, H.J.1
Broudy, V.-C.2
Magenis, R.E.3
Olson, S.4
Tomar, D.5
Barton, S.6
Fitchen, J.H.7
Bagby Jr., G.C.8
-
34
-
-
0022337348
-
c-src is consistently conserved in the chromsomal deletion (20q)I observed in myeloid disorders
-
Le Beau, M.M., Westbrook, C.A., Diaz, M.O. & Rowley, J.D. (1985) c-src is consistently conserved in the chromsomal deletion (20q)I observed in myeloid disorders. Proceedings of the National Academy of Sciences of the United States of America, 82, 6692-6696.
-
(1985)
Proceedings of the National Academy of Sciences of the United States of America
, vol.82
, pp. 6692-6696
-
-
Le Beau, M.M.1
Westbrook, C.A.2
Diaz, M.O.3
Rowley, J.D.4
-
35
-
-
0027186443
-
DNA topoisomerase I is involved in both repression and activation of transcription
-
Merino, A., Madden, K.R., Lane, W.S., Champoux, J.J. & Reinberg, D. (1993) DNA topoisomerase I is involved in both repression and activation of transcription. Nature, 365, 227-232.
-
(1993)
Nature
, vol.365
, pp. 227-232
-
-
Merino, A.1
Madden, K.R.2
Lane, W.S.3
Champoux, J.J.4
Reinberg, D.5
-
36
-
-
0029011539
-
5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers
-
Merlo, A., Herman, J.G., Mao, L., Lee, D.J., Gabrielson, E., Burger, P.C., Baylin, S.B. & Sidransky, D. (1995) 5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers. Nature Medicine, 1, 686-692.
-
(1995)
Nature Medicine
, vol.1
, pp. 686-692
-
-
Merlo, A.1
Herman, J.G.2
Mao, L.3
Lee, D.J.4
Gabrielson, E.5
Burger, P.C.6
Baylin, S.B.7
Sidransky, D.8
-
37
-
-
0025848934
-
Karyotypic patterns in chronic myeloproliferative disorders: Report on 74 cases and review of the literature
-
Mertens, F., Johansson, B., Heim, S., Kristofferson, U. & Mitelman, F. (1991) Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature. Leukemia, 5, 214-220.
-
(1991)
Leukemia
, vol.5
, pp. 214-220
-
-
Mertens, F.1
Johansson, B.2
Heim, S.3
Kristofferson, U.4
Mitelman, F.5
-
39
-
-
0024458410
-
Localization of the SRC oncogene to chromosome hand 20q 11.2 and loss of this gene with deletion (20q) in two leukemic patients
-
Morris, C.M., Honeybone, L.M. & Hollings, P.E. (1989) Localization of the SRC oncogene to chromosome hand 20q 11.2 and loss of this gene with deletion (20q) in two leukemic patients. Blood, 74, 1768-1773.
-
(1989)
Blood
, vol.74
, pp. 1768-1773
-
-
Morris, C.M.1
Honeybone, L.M.2
Hollings, P.E.3
-
40
-
-
0026536685
-
Chromosomal deletions in the myelodysplastic syndrome
-
Mufti, G.J. (1992) Chromosomal deletions in the myelodysplastic syndrome. Leukemia Research, 16, 35-41.
-
(1992)
Leukemia Research
, vol.16
, pp. 35-41
-
-
Mufti, G.J.1
-
41
-
-
0029031073
-
Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes
-
Nacheva, E., Holloway, T., Carter, N., Grace, C., White, N. & Green, A.R. (1995) Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes. Cancer Genetics and Cytogenetics, 80, 87-94.
-
(1995)
Cancer Genetics and Cytogenetics
, vol.80
, pp. 87-94
-
-
Nacheva, E.1
Holloway, T.2
Carter, N.3
Grace, C.4
White, N.5
Green, A.R.6
-
42
-
-
0026525853
-
Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity for chromosomes 5 and 7 in malignant myeloid disorders
-
Neuman. W.L., Rubin, C.M., Rios, R.B., Larson, R.A., Le Beau, M.M., Rowley, J.D., Vardiman, J.W., Schwartz, J.L. & Farber, R.A. (1992) Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity for chromosomes 5 and 7 in malignant myeloid disorders. Blood, 79, 1501-1510.
-
(1992)
Blood
, vol.79
, pp. 1501-1510
-
-
Neuman, W.L.1
Rubin, C.M.2
Rios, R.B.3
Larson, R.A.4
Le Beau, M.M.5
Rowley, J.D.6
Vardiman, J.W.7
Schwartz, J.L.8
Farber, R.A.9
-
43
-
-
0027507360
-
The turnover of B-cell populations
-
Osmond, D.G. (1993) The turnover of B-cell populations. Immunology Today, 14, 34-37.
-
(1993)
Immunology Today
, vol.14
, pp. 34-37
-
-
Osmond, D.G.1
-
44
-
-
0029022770
-
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
-
Petrij, F., Giles, R.H., Dauwerse, H.G., Saris, J.J., Hennekam, R.C.M., Masuno, M., Tommerup, N., van Ommen, G.-J.B., Goodman, R.H., Peters, D.J.M. & Breuning, M.H. (1995) Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature, 376, 348-352.
-
(1995)
Nature
, vol.376
, pp. 348-352
-
-
Petrij, F.1
Giles, R.H.2
Dauwerse, H.G.3
Saris, J.J.4
Hennekam, R.C.M.5
Masuno, M.6
Tommerup, N.7
Van Ommen, G.-J.B.8
Goodman, R.H.9
Peters, D.J.M.10
Breuning, M.H.11
-
45
-
-
0027980131
-
Evolving understanding of the cellular defect in polycythemia vera: Implications for its clinical diagnosis and molecular pathophysiology
-
Prchal, J.T. & Prchal, J.F. (1994) Evolving understanding of the cellular defect in polycythemia vera: implications for its clinical diagnosis and molecular pathophysiology. Blood, 83, 1-4.
-
(1994)
Blood
, vol.83
, pp. 1-4
-
-
Prchal, J.T.1
Prchal, J.F.2
-
46
-
-
0018138805
-
A common progenitor for human myeloid and lymphoid cells
-
Prchal, J.T., Throckmorton, D.W., Carroll, A.J.D., Fuson, E.W., Gams, R.A. & Prchal, J.F. (1978) A common progenitor for human myeloid and lymphoid cells, Nature, 274, 590-591.
-
(1978)
Nature
, vol.274
, pp. 590-591
-
-
Prchal, J.T.1
Throckmorton, D.W.2
Carroll, A.J.D.3
Fuson, E.W.4
Gams, R.A.5
Prchal, J.F.6
-
47
-
-
0027970838
-
Chromosomal translocations in human cancer
-
Rabbitts, T.H. (1994) Chromosomal translocations in human cancer. Nature, 372, 143-149.
-
(1994)
Nature
, vol.372
, pp. 143-149
-
-
Rabbitts, T.H.1
-
48
-
-
0029562967
-
Chromosome engineering in mice
-
Ramirez-Solis, R., Liu, P. & Bradley, A. (1995) Chromosome engineering in mice, Nature, 378, 720-724.
-
(1995)
Nature
, vol.378
, pp. 720-724
-
-
Ramirez-Solis, R.1
Liu, P.2
Bradley, A.3
-
49
-
-
0021250450
-
Evidence fora multistep pathogenesis of a myelodysplastic syndrome
-
Raskind, W.H., Tirumali, N., Jacobson, R., Singer, J. & Fialkow, P.J. (1984) Evidence fora multistep pathogenesis of a myelodysplastic syndrome. Bood, 63, 1318-1323.
-
(1984)
Bood
, vol.63
, pp. 1318-1323
-
-
Raskind, W.H.1
Tirumali, N.2
Jacobson, R.3
Singer, J.4
Fialkow, P.J.5
-
50
-
-
0029020851
-
Apoptosis in bone marrow biopsy samples involving stromal and hematopoietic cells in 50 patients with myelodysplastic syndromes
-
Raza, A., Gezer, S., Mundle, S., Gao, X-Z., Alvi, S., Borok, R., Rifkin, S., Iftikhar, A., Shetty, V., Parcharidou, A., Loew, J., Marcus, B., Khan, Z., Chaney, C., Showel, J., Gregory, S. & Preisler, H. (1995a) Apoptosis in bone marrow biopsy samples involving stromal and hematopoietic cells in 50 patients with myelodysplastic syndromes. Blood, 86, 268-276.
-
(1995)
Blood
, vol.86
, pp. 268-276
-
-
Raza, A.1
Gezer, S.2
Mundle, S.3
Gao, X.-Z.4
Alvi, S.5
Borok, R.6
Rifkin, S.7
Iftikhar, A.8
Shetty, V.9
Parcharidou, A.10
Loew, J.11
Marcus, B.12
Khan, Z.13
Chaney, C.14
Showel, J.15
Gregory, S.16
Preisler, H.17
-
51
-
-
0028930939
-
Simultaneous assessment of cell kinetics and programmed cell death in bone marrow biopsies of myelodysplastics reveals extensive apoptosis as the probable basis for ineffective hematopoiesis
-
Raza, A., Mundle, S., Iftikhar, A., Gregory, S., Marcus, B., Khan, Z., Alvi, S., Shetty, V., Dameron, S., Wright, V., Adler, S., Loew, J.M. Shott, S., All, S.N. & Preisler, H. (1995b) Simultaneous assessment of cell kinetics and programmed cell death in bone marrow biopsies of myelodysplastics reveals extensive apoptosis as the probable basis for ineffective hematopoiesis. American Journal of Hematology. 48, 143-154.
-
(1995)
American Journal of Hematology
, vol.48
, pp. 143-154
-
-
Raza, A.1
Mundle, S.2
Iftikhar, A.3
Gregory, S.4
Marcus, B.5
Khan, Z.6
Alvi, S.7
Shetty, V.8
Dameron, S.9
Wright, V.10
Adler, S.11
Loew, J.M.12
Shott, S.13
All, S.N.14
Preisler, H.15
-
52
-
-
0015262981
-
Identity of the abnormal F group chromosome associated with polycythemia vera
-
Reeves, B.R., Lobb, D.S. & Lawler, S.D. (1972) Identity of the abnormal F group chromosome associated with polycythemia vera. Human Genetics, 14, 159-161.
-
(1972)
Human Genetics
, vol.14
, pp. 159-161
-
-
Reeves, B.R.1
Lobb, D.S.2
Lawler, S.D.3
-
53
-
-
0023092651
-
A chromosomal profile of polycythemia
-
Rege-Cambrin, G., Mecucci, C. & Tricot, G. (1987) A chromosomal profile of polycythemia. Cancer Genetics and Cytoaenetics, 25, 233-245.
-
(1987)
Cancer Genetics and Cytoaenetics
, vol.25
, pp. 233-245
-
-
Rege-Cambrin, G.1
Mecucci, C.2
Tricot, G.3
-
54
-
-
0024403320
-
Studies of inositol phospholipid-specific phospholipase C
-
Rhee, S.G., Suh, P.-G., Ruy, S.-H. & Lee, S.Y. (1989) Studies of inositol phospholipid-specific phospholipase C. Science, 244, 546-550.
-
(1989)
Science
, vol.244
, pp. 546-550
-
-
Rhee, S.G.1
Suh, P.-G.2
Ruy, S.-H.3
Lee, S.Y.4
-
55
-
-
0027375437
-
Molecular genetics of myeloid leukemia: Identification of the commonly deleted segment of chromosome 20
-
Roulston, D., Espinosa, R., Stoffel, M. Bell, G.I. & Le Beau, M.M. (1993) Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20. Blood, 82, 3424-3429.
-
(1993)
Blood
, vol.82
, pp. 3424-3429
-
-
Roulston, D.1
Espinosa, R.2
Stoffel, M.3
Bell, G.I.4
Le Beau, M.M.5
-
56
-
-
0029411032
-
Myelin genes: Getting the dosage right
-
Scherer, S.S. & Chance, P.F. (1995) Myelin genes: getting the dosage right. Nature Genetics, 11, 226-228.
-
(1995)
Nature Genetics
, vol.11
, pp. 226-228
-
-
Scherer, S.S.1
Chance, P.F.2
-
57
-
-
0025731630
-
Absence of allelic loss on chromosome 5q by RFLP analysis in preleukemia
-
Shepherd, L., Cameron, C., Galbraith, P., Windsor, S. & Lillicrap, D. (1991) Absence of allelic loss on chromosome 5q by RFLP analysis in preleukemia. Leukemia Research, 15, 297-303.
-
(1991)
Leukemia Research
, vol.15
, pp. 297-303
-
-
Shepherd, L.1
Cameron, C.2
Galbraith, P.3
Windsor, S.4
Lillicrap, D.5
-
58
-
-
0021036334
-
Chronic myelomonocytic leukemia with a chromosome abnormality (46,XY.20q-) in all dividing myeloid cells
-
Shinohara, T., Takuwa, N., Morishita, K., Ieka, R., Yokota, J., Nakayama, E., Asano, S. & Miwa, S. (1983) Chronic myelomonocytic leukemia with a chromosome abnormality (46,XY.20q-) in all dividing myeloid cells. American Journal of Hematology, 15, 289-293.
-
(1983)
American Journal of Hematology
, vol.15
, pp. 289-293
-
-
Shinohara, T.1
Takuwa, N.2
Morishita, K.3
Ieka, R.4
Yokota, J.5
Nakayama, E.6
Asano, S.7
Miwa, S.8
-
59
-
-
0025690311
-
Liverenriched transcription factor HNF-4 is a novel member of the steroid hormone receptor superfamily
-
Sladek, F.M., Zhong, W., Lai, E. & Darnell, J.E., Jr (1990) Liverenriched transcription factor HNF-4 is a novel member of the steroid hormone receptor superfamily. Genes and Development, 4, 2353-2365.
-
(1990)
Genes and Development
, vol.4
, pp. 2353-2365
-
-
Sladek, F.M.1
Zhong, W.2
Lai, E.3
Darnell Jr., J.E.4
-
60
-
-
9244258538
-
A yeast artificial chromosome based map of the region of chromosome 20 containing the diabetes susceptibility gene, MODY1, and a myeloid leukemia related gene
-
Stoffel, M., Le Beau, M.M., Espinosa, R., Bohlander, S.F., Le Paslier, D., Cohen, D., Xiang, K.S., Cox, N.J., Fajans, S.S. & Bell, G.I. (1996) A yeast artificial chromosome based map of the region of chromosome 20 containing the diabetes susceptibility gene, MODY1, and a myeloid leukemia related gene, Proceedings of the National Academy of Sciences of the United States of America, 93, 3937-3941.
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, pp. 3937-3941
-
-
Stoffel, M.1
Le Beau, M.M.2
Espinosa, R.3
Bohlander, S.F.4
Le Paslier, D.5
Cohen, D.6
Xiang, K.S.7
Cox, N.J.8
Fajans, S.S.9
Bell, G.I.10
-
61
-
-
0023713372
-
A prospective long-term cytogenetic study in polycythemia vera in relation to treatment and clinical course
-
Swolin, B., Weinfeld, A. & Westin, J. (1988) A prospective long-term cytogenetic study in polycythemia vera in relation to treatment and clinical course, Blood, 72, 386-395.
-
(1988)
Blood
, vol.72
, pp. 386-395
-
-
Swolin, B.1
Weinfeld, A.2
Westin, J.3
-
62
-
-
10244266548
-
Clinical characteristics of patients with 20q-chromosome deletion
-
Tandon, R., Tuason, L., Hoeltge, G. & Lichtin, A. (1995) Clinical characteristics of patients with 20q-chromosome deletion. Blood, 86, (Suppl. 1), 333.
-
(1995)
Blood
, vol.86
, Issue.1 SUPPL.
, pp. 333
-
-
Tandon, R.1
Tuason, L.2
Hoeltge, G.3
Lichtin, A.4
-
63
-
-
0025319860
-
Clonal studies in the myelodysplastic syndrome using X-linked restriction fragment length polymorphisms
-
Tefferi, A., Thibodeau, S.N. & Solberg, L.A., Jr (1990) Clonal studies in the myelodysplastic syndrome using X-linked restriction fragment length polymorphisms. Blood, 75, 1770-1773.
-
(1990)
Blood
, vol.75
, pp. 1770-1773
-
-
Tefferi, A.1
Thibodeau, S.N.2
Solberg Jr., L.A.3
-
64
-
-
0018215209
-
Deletion of the long arm of chromsome 20 [del(20)(q,11)] in myeloid disorders
-
Testa, J.R., Kinealey, A., Rowley, J.D., Golde, D.W. & Potter, D. (1978) Deletion of the long arm of chromsome 20 [del(20)(q,11)] in myeloid disorders. Blood, 52, 868-877.
-
(1978)
Blood
, vol.52
, pp. 868-877
-
-
Testa, J.R.1
Kinealey, A.2
Rowley, J.D.3
Golde, D.W.4
Potter, D.5
-
65
-
-
0027410946
-
Clonality in myelodysplastic syndromes: Demonstration of pluripotent stem cell origin using X-linked restriction fragment length polymorphisms
-
Tsukamoto, N., Morita, K., Maehara, T., Okamoto, K., Karasawa, M., Omine, M. & Naruse, T. (1993) Clonality in myelodysplastic syndromes: demonstration of pluripotent stem cell origin using X-linked restriction fragment length polymorphisms. British Journal of Haematology, 83, 589-594.
-
(1993)
British Journal of Haematology
, vol.83
, pp. 589-594
-
-
Tsukamoto, N.1
Morita, K.2
Maehara, T.3
Okamoto, K.4
Karasawa, M.5
Omine, M.6
Naruse, T.7
-
66
-
-
0026781966
-
Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: Analysis by X-linked restriction fragment length polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene
-
van Kamp, H., Fibbe, W.E., Jansen, R.P., van der Keur, M., de Graaf, E., Willemze, R. & Landegent, J.E. (1992) Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: analysis by X-linked restriction fragment length polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene. Blood, 80, 1774-1780.
-
(1992)
Blood
, vol.80
, pp. 1774-1780
-
-
Kamp, H.1
Fibbe, W.E.2
Jansen, R.P.3
Van Der Keur, M.4
De Graaf, E.5
Willemze, R.6
Landegent, J.E.7
-
68
-
-
0027426034
-
De novo myelodysplastic syndrome (MDS) with deletion of the long arm of chromosome 20: A subtype of MDS with distinct hematological and prognostic features?
-
Watlel, F., Lai, J.L., Hebbar, M., Preudhomme, C., Grahek, D., Morel, P., Bauters, F. & Fenaux, P. (1993) De novo myelodysplastic syndrome (MDS) with deletion of the long arm of chromosome 20: a subtype of MDS with distinct hematological and prognostic features? Leukemia Research, 17, 921-926.
-
(1993)
Leukemia Research
, vol.17
, pp. 921-926
-
-
Watlel, F.1
Lai, J.L.2
Hebbar, M.3
Preudhomme, C.4
Grahek, D.5
Morel, P.6
Bauters, F.7
Fenaux, P.8
-
69
-
-
0028295411
-
Deletion of chromosome 20q in myelodysplasia can occur in a multipotent precursor of both myeloid cells and B cells
-
White, N.J., Nacheva, E., Asimakopoulos, F.A., Paul, B. & Green, A.R. (1994) Deletion of chromosome 20q in myelodysplasia can occur in a multipotent precursor of both myeloid cells and B cells. Blood, 83, 2809-2816.
-
(1994)
Blood
, vol.83
, pp. 2809-2816
-
-
White, N.J.1
Nacheva, E.2
Asimakopoulos, F.A.3
Paul, B.4
Green, A.R.5
-
70
-
-
0029618925
-
Apoptosis in myelodysplasia: A paradox or paradigm
-
Yoshida, Y., Anzai, N. & Kawabata, H. (1995) Apoptosis in myelodysplasia: a paradox or paradigm. Leukemia Research, 19, 887-891.
-
(1995)
Leukemia Research
, vol.19
, pp. 887-891
-
-
Yoshida, Y.1
Anzai, N.2
Kawabata, H.3
|