-
1
-
-
0027769876
-
A new regulation motif in cell-cycle control causing specific inhibition of cyclin D/CDK4
-
Serrano M, Hannon GJ, Beach D: A new regulation motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature 366:704, 1993
-
(1993)
Nature
, vol.366
, pp. 704
-
-
Serrano, M.1
Hannon, G.J.2
Beach, D.3
-
2
-
-
0028275733
-
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
-
Nobori T, Miura K, Wu DJ, Lois A, Takabayashi K, Carson DA: Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature 368:753, 1994
-
(1994)
Nature
, vol.368
, pp. 753
-
-
Nobori, T.1
Miura, K.2
Wu, D.J.3
Lois, A.4
Takabayashi, K.5
Carson, D.A.6
-
3
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb A, Gruis NA, Weaver-Feldhaus J, Liu Q, Harshman K, Tavtigian SV, Stockert E, Day RS III, Johnson BE, Skolnick MH: A cell cycle regulator potentially involved in genesis of many tumor types. Science 264:436, 1994
-
(1994)
Science
, vol.264
, pp. 436
-
-
Kamb, A.1
Gruis, N.A.2
Weaver-Feldhaus, J.3
Liu, Q.4
Harshman, K.5
Tavtigian, S.V.6
Stockert, E.7
Day III, R.S.8
Johnson, B.E.9
Skolnick, M.H.10
-
4
-
-
0028775245
-
P21 inhibits cyclin shock
-
Pines J: P21 inhibits cyclin shock. Nature 369:520, 1994
-
(1994)
Nature
, vol.369
, pp. 520
-
-
Pines, J.1
-
5
-
-
0028059330
-
Frequent somatic mutations and homozygous deletions of the p 16 (MTS1) gene in pancreatic adenocarcinoma
-
Caldas C, Hahn SA, Da Costa LT, Redston MS, Schutte M, Seymour AB, Weinstein CL, Hruban RH, Yeo CJ, Kern SE: Frequent somatic mutations and homozygous deletions of the p 16 (MTS1) gene in pancreatic adenocarcinoma. Nature Genet 8:27, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 27
-
-
Caldas, C.1
Hahn, S.A.2
Da Costa, L.T.3
Redston, M.S.4
Schutte, M.5
Seymour, A.B.6
Weinstein, C.L.7
Hruban, R.H.8
Yeo, C.J.9
Kern, S.E.10
-
6
-
-
0028070985
-
p16 gene in uncultured tumours
-
Spruck CH, Gonzalez-Zulueta M, Shibata A, Simoneau AR, Lin MF, Gonzales F, Tsal YC, Jones PA: p16 gene in uncultured tumours. Nature 370:183, 1994
-
(1994)
Nature
, vol.370
, pp. 183
-
-
Spruck, C.H.1
Gonzalez-Zulueta, M.2
Shibata, A.3
Simoneau, A.R.4
Lin, M.F.5
Gonzales, F.6
Tsal, Y.C.7
Jones, P.A.8
-
7
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian C, Struewing JP, Goldstein AM, Higgins PAT, Ally DS, Sheahan MD, Clark WH, Tucker MA, Dracopoli NC: Germline p16 mutations in familial melanoma. Nature Genet 8:15, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 15
-
-
Hussussian, C.1
Struewing, J.P.2
Goldstein, A.M.3
Higgins, P.A.T.4
Ally, D.S.5
Sheahan, M.D.6
Clark, W.H.7
Tucker, M.A.8
Dracopoli, N.C.9
-
8
-
-
0021799508
-
Lymphoblastic leukemia with lymphomatous features associated with abnormalities of the short arm of chromosome 9
-
Chilcote RR, Brown E, Rowley JD: Lymphoblastic leukemia with lymphomatous features associated with abnormalities of the short arm of chromosome 9. N Engl J Med 313:286, 1985
-
(1985)
N Engl J Med
, vol.313
, pp. 286
-
-
Chilcote, R.R.1
Brown, E.2
Rowley, J.D.3
-
9
-
-
0023091250
-
Lack of association between abnormalities of the chromosome 9 short arm and either "lymphomatous" features or T cell phenotype in childhood acute lymphocytic leukemia
-
Carroll AJ, Castleberry RP, Crist WM: Lack of association between abnormalities of the chromosome 9 short arm and either "lymphomatous" features or T cell phenotype in childhood acute lymphocytic leukemia. Blood 69:735, 1987
-
(1987)
Blood
, vol.69
, pp. 735
-
-
Carroll, A.J.1
Castleberry, R.P.2
Crist, W.M.3
-
10
-
-
0001122795
-
Homozygous deletion in the alpha- and beta 1 interferon genes in human leukemia and derived cell lines
-
Diaz MO, Ziemin S, Le Beau MM, Pitha P, Smith SD, Chilcote RR, Rowley JD: Homozygous deletion in the alpha- and beta 1 interferon genes in human leukemia and derived cell lines. Proc Natl Acad Sci USA 85:5259, 1988
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 5259
-
-
Diaz, M.O.1
Ziemin, S.2
Le Beau, M.M.3
Pitha, P.4
Smith, S.D.5
Chilcote, R.R.6
Rowley, J.D.7
-
11
-
-
0025023615
-
Deletions of interferon genes in acute lymphoblastic leukemia
-
Diaz MO, Rubin CM, Harden A, Ziemin S, Larson RA, Le Beau MM, Rowley JD: Deletions of interferon genes in acute lymphoblastic leukemia. N Engl J Med 322:77, 1990
-
(1990)
N Engl J Med
, vol.322
, pp. 77
-
-
Diaz, M.O.1
Rubin, C.M.2
Harden, A.3
Ziemin, S.4
Larson, R.A.5
Le Beau, M.M.6
Rowley, J.D.7
-
12
-
-
0017162163
-
Proposals for the classification of acute leukemias
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton D, Gralnick H, Sultan C: Proposals for the classification of acute leukemias. Br J Haematol 33:451, 1976
-
(1976)
Br J Haematol
, vol.33
, pp. 451
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.5
Gralnick, H.6
Sultan, C.7
-
13
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton D, Gralnick H, Sultan C: Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 51:189, 1982
-
(1982)
Br J Haematol
, vol.51
, pp. 189
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.5
Gralnick, H.6
Sultan, C.7
-
15
-
-
0026537641
-
Longitudinal analysis of point mutations of the N-ras proto-oncogene in patients with myelodysplasia using archived blood smears
-
Van Kamp H, De Pijper C, Verlaan de Vries M, Bos J, Leeksma C, Kerkhofs H, Willemze R, Fibbe W, Landegent J: Longitudinal analysis of point mutations of the N-ras proto-oncogene in patients with myelodysplasia using archived blood smears. Blood 79:1266, 1992
-
(1992)
Blood
, vol.79
, pp. 1266
-
-
Van Kamp, H.1
De Pijper, C.2
Verlaan De Vries, M.3
Bos, J.4
Leeksma, C.5
Kerkhofs, H.6
Willemze, R.7
Fibbe, W.8
Landegent, J.9
-
16
-
-
0004136246
-
-
Cold Spring Harbor, NY, Cold Spring Harbor Laboratory
-
Maniatis T, Fritsh E, Sambrook J: Molecular Cloning: A Laboratory Manual. Cold Spring Harbor, NY, Cold Spring Harbor Laboratory, 1982
-
(1982)
Molecular Cloning: A Laboratory Manual
-
-
Maniatis, T.1
Fritsh, E.2
Sambrook, J.3
-
17
-
-
0028279317
-
Absence of rearrangement of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes and acute myeloid leukemia
-
Quesnel B, Preudhomme C, Vanrumbeke M, Vachee A, Lai JL, Fenaux P: Absence of rearrangement of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes and acute myeloid leukemia. Leukemia 8:878, 1994
-
(1994)
Leukemia
, vol.8
, pp. 878
-
-
Quesnel, B.1
Preudhomme, C.2
Vanrumbeke, M.3
Vachee, A.4
Lai, J.L.5
Fenaux, P.6
-
18
-
-
0026096185
-
p53 gene mutations in acute myeloid leukemia with 17p monosomy
-
Fenaux P, Jonveaux P, Quiquandon I, Lai JL, Pignon JM, Loucheux-Lefebvre MH, Bauters F, Berger R, Kerckaert JP: p53 gene mutations in acute myeloid leukemia with 17p monosomy. Blood 78:1652, 1991
-
(1991)
Blood
, vol.78
, pp. 1652
-
-
Fenaux, P.1
Jonveaux, P.2
Quiquandon, I.3
Lai, J.L.4
Pignon, J.M.5
Loucheux-Lefebvre, M.H.6
Bauters, F.7
Berger, R.8
Kerckaert, J.P.9
-
19
-
-
0027489384
-
Clinical implications of the p53 tumor-suppressor gene
-
Harris CC, Hollstein M: Clinical implications of the p53 tumor-suppressor gene. N Engl J Med 329:1318, 1993
-
(1993)
N Engl J Med
, vol.329
, pp. 1318
-
-
Harris, C.C.1
Hollstein, M.2
|