-
1
-
-
0028948958
-
A reciprocal translocation (1;15)(36.2;q24) in a neuroblastoma cell line is accompanied by DNA duplication and may signal the site of a putative tumor suppressor gene
-
Amler LC, Corvi R, Praml C, Savelyeva L, Le Paslier D, Schwab M (1995a) A reciprocal translocation (1;15)(36.2;q24) in a neuroblastoma cell line is accompanied by DNA duplication and may signal the site of a putative tumor suppressor gene. Oncogene 10:1095-1101.
-
(1995)
Oncogene
, vol.10
, pp. 1095-1101
-
-
Amler, L.C.1
Corvi, R.2
Praml, C.3
Savelyeva, L.4
Le Paslier, D.5
Schwab, M.6
-
2
-
-
0029055020
-
Reciprocal translocation at 1p36.2/D1S160 in a neuroblastoma cell line: Isolation of a YAC clone at the break
-
Amler LC, Corvi R, Praml C, Savelyeva L, Le Paslier D, Schwab M (1995b) Reciprocal translocation at 1p36.2/D1S160 in a neuroblastoma cell line: Isolation of a YAC clone at the break. Europ J Cancer 31A:527-530.
-
(1995)
Europ J Cancer
, vol.31 A
, pp. 527-530
-
-
Amler, L.C.1
Corvi, R.2
Praml, C.3
Savelyeva, L.4
Le Paslier, D.5
Schwab, M.6
-
3
-
-
0025642707
-
Disruption of the human SCL locus by "illegitimate" V-(D)-J recombinase activity
-
Aplan PD, Lombardi DP, Ginsberg AM, Cossman J, Bertness VL, Kirsch IR (1990) Disruption of the human SCL locus by "illegitimate" V-(D)-J recombinase activity. Science 250:1426-1429.
-
(1990)
Science
, vol.250
, pp. 1426-1429
-
-
Aplan, P.D.1
Lombardi, D.P.2
Ginsberg, A.M.3
Cossman, J.4
Bertness, V.L.5
Kirsch, I.R.6
-
4
-
-
0026765020
-
Disruption of the SCL gene by a t(1;3) translocation in a patient with T-cell acute lymphoblastic leukemia
-
Aplan PD, Raimondi SC, Kirsch IR (1992) Disruption of the SCL gene by a t(1;3) translocation in a patient with T-cell acute lymphoblastic leukemia. J Exp Med 176:1301-1310.
-
(1992)
J Exp Med
, vol.176
, pp. 1301-1310
-
-
Aplan, P.D.1
Raimondi, S.C.2
Kirsch, I.R.3
-
5
-
-
0028968174
-
-
Aplan PD, Johnson BE, Russel E, Chervinsky DS, Kirsch IR (1995) Cancer Res 55:1917-1921.
-
(1995)
Cancer Res
, vol.55
, pp. 1917-1921
-
-
Aplan, P.D.1
Johnson, B.E.2
Russel, E.3
Chervinsky, D.S.4
Kirsch, I.R.5
-
6
-
-
0028936363
-
High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: The precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs
-
Ariyama T, Inazawa J, Ezaki T, Nakamura Y, Horii A, Abe T (1995) High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: The precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs. Genomics 25: 114-123.
-
(1995)
Genomics
, vol.25
, pp. 114-123
-
-
Ariyama, T.1
Inazawa, J.2
Ezaki, T.3
Nakamura, Y.4
Horii, A.5
Abe, T.6
-
7
-
-
0022573439
-
Chromosome 1 aberrations in cancer
-
Atkin NB (1986) Chromosome 1 aberrations in cancer. Cancer Genet Cytogenet 21:279-285.
-
(1986)
Cancer Genet Cytogenet
, vol.21
, pp. 279-285
-
-
Atkin, N.B.1
-
8
-
-
0018687329
-
Chromosome 1 in 26 carcinomas of the cervix uteri: Structural and numerical changes
-
Atkin NB, Baker MC (1979) Chromosome 1 in 26 carcinomas of the cervix uteri: Structural and numerical changes. Cancer 44:604-613.
-
(1979)
Cancer
, vol.44
, pp. 604-613
-
-
Atkin, N.B.1
Baker, M.C.2
-
9
-
-
0021986687
-
Cytogenetic study of ten carcinomas of the bladder: Involvement of chromosomes 1 and 11
-
Atkin NB, Baker MC (1985) Cytogenetic study of ten carcinomas of the bladder: Involvement of chromosomes 1 and 11. Cancer Genet Cytogenet 15:253-268.
-
(1985)
Cancer Genet Cytogenet
, vol.15
, pp. 253-268
-
-
Atkin, N.B.1
Baker, M.C.2
-
10
-
-
0026166356
-
Dissociation of suppression of tumorigenicity and differentiation in vitro effected by transfer of single human chromosomes into human neuroblastoma cells
-
Bader SA, Fasching C, Brodeur GM, Stanbridge EJ (1991) Dissociation of suppression of tumorigenicity and differentiation in vitro effected by transfer of single human chromosomes into human neuroblastoma cells. Cell Growth & Differentiation 2:245-255.
-
(1991)
Cell Growth & Differentiation
, vol.2
, pp. 245-255
-
-
Bader, S.A.1
Fasching, C.2
Brodeur, G.M.3
Stanbridge, E.J.4
-
11
-
-
0029029543
-
Characterization of add(I)(p36) in non-Hodgkin lymphomas by fluorescence in situ hybridization
-
Bajalica S, Brøndum-Nielsen K, Sørensen A-G, Tinggaard Pedersen N, Kristoffersson U, Åkerman M, Anderson M, Pisa P, Nordenskjöld M (1995) Characterization of add(I)(p36) in non-Hodgkin lymphomas by fluorescence in situ hybridization. Genes Chromosom Cancer 13:34-39.
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 34-39
-
-
Bajalica, S.1
Brøndum-Nielsen, K.2
Sørensen, A.-G.3
Tinggaard Pedersen, N.4
Kristoffersson, U.5
Åkerman, M.6
Anderson, M.7
Pisa, P.8
Nordenskjöld, M.9
-
13
-
-
0022542636
-
Cutaneous malignant melanoma and familial dysplastic nevi: Evidence for autosomal dominance and pleiotropy
-
Bale SJ, Chakravarti A, Greene MH (1986) Cutaneous malignant melanoma and familial dysplastic nevi: Evidence for autosomal dominance and pleiotropy. Am J Hum Genet 38:188-196.
-
(1986)
Am J Hum Genet
, vol.38
, pp. 188-196
-
-
Bale, S.J.1
Chakravarti, A.2
Greene, M.H.3
-
14
-
-
9544252604
-
Linkage analysis of melanoma and dysplastic nevus syndrome with polymorphic loci on human chromosome 1p
-
Bale SJ, Dracopoli NC, Greene MH, Gerhard DS, Housman DE (1987) Linkage analysis of melanoma and dysplastic nevus syndrome with polymorphic loci on human chromosome 1p. Cytogenet Cell Genet 46:575.
-
(1987)
Cytogenet Cell Genet
, vol.46
, pp. 575
-
-
Bale, S.J.1
Dracopoli, N.C.2
Greene, M.H.3
Gerhard, D.S.4
Housman, D.E.5
-
15
-
-
0024320151
-
Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p
-
Bale SJ, Dracopoli NC, Tucker MA, Clark Jr WH, Fraser M, Stanger BZ, Green P, Donis-Keller H, Housman DE, Greene MH (1989) Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p. New Engl J Med 320:1367-1372.
-
(1989)
New Engl J Med
, vol.320
, pp. 1367-1372
-
-
Bale, S.J.1
Dracopoli, N.C.2
Tucker, M.A.3
Clark Jr., W.H.4
Fraser, M.5
Stanger, B.Z.6
Green, P.7
Donis-Keller, H.8
Housman, D.E.9
Greene, M.H.10
-
16
-
-
0026544724
-
Cytogenetic findings in three primary hepatocellular carcinomas
-
Bardi G, Johansson B, Pandis N, Heim S, Mandahl N, Andrén-Sandberg Å, Hägerstrand I, Mitelman F (1992) Cytogenetic findings in three primary hepatocellular carcinomas. Cancer Genet Cytogenet 58:191-195.
-
(1992)
Cancer Genet Cytogenet
, vol.58
, pp. 191-195
-
-
Bardi, G.1
Johansson, B.2
Pandis, N.3
Heim, S.4
Mandahl, N.5
Andrén-Sandberg, Å.6
Hägerstrand, I.7
Mitelman, F.8
-
17
-
-
0027500221
-
Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features
-
Bardi G, Johansson B, Pandis N, Bak-Jensen E, Orndal C, Heim S, Mandahl N, Andrén-Sandberg Å, Mitelman F (1993a) Cytogenetic aberrations in colorectal adenocarcinomas and their correlation with clinicopathologic features. Cancer 71:306-314.
-
(1993)
Cancer
, vol.71
, pp. 306-314
-
-
Bardi, G.1
Johansson, B.2
Pandis, N.3
Bak-Jensen, E.4
Orndal, C.5
Heim, S.6
Mandahl, N.7
Andrén-Sandberg, Å.8
Mitelman, F.9
-
18
-
-
0027382019
-
Cytogenetic analysis of 52 colorectal carcinomas: Non-random aberration pattern and correlation with pathologic parameters
-
Bardi G, Johansson B, Pandis N, Mandahl N, Bak-Jensen E, Lindstrom C, Tornqvist A, Frederiksen H, Andren-Sandberg A, Mitelman F, Heim S (1993b) Cytogenetic analysis of 52 colorectal carcinomas: Non-random aberration pattern and correlation with pathologic parameters. Int J Cancer 55:422-428.
-
(1993)
Int J Cancer
, vol.55
, pp. 422-428
-
-
Bardi, G.1
Johansson, B.2
Pandis, N.3
Mandahl, N.4
Bak-Jensen, E.5
Lindstrom, C.6
Tornqvist, A.7
Frederiksen, H.8
Andren-Sandberg, A.9
Mitelman, F.10
Heim, S.11
-
19
-
-
0027157843
-
Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis
-
Bardi G, Pandis N, Fenger C, Kronborg O, Bomme L, Heim S (1993c) Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis. Cancer Res 53:1895-1898.
-
(1993)
Cancer Res
, vol.53
, pp. 1895-1898
-
-
Bardi, G.1
Pandis, N.2
Fenger, C.3
Kronborg, O.4
Bomme, L.5
Heim, S.6
-
20
-
-
0027190815
-
Karyotypic abnormalities in tumours of the pancreas
-
Bardi G, Johansson B, Pandis N, Mandahl N, Bak-Jensen E, Andrén-Sandberg Å, Mitelman F, Heim S (1993d) Karyotypic abnormalities in tumours of the pancreas. Br J Cancer 67:1106-1112.
-
(1993)
Br J Cancer
, vol.67
, pp. 1106-1112
-
-
Bardi, G.1
Johansson, B.2
Pandis, N.3
Mandahl, N.4
Bak-Jensen, E.5
Andrén-Sandberg, Å.6
Mitelman, F.7
Heim, S.8
-
21
-
-
0028809085
-
Karyotypic characterization of colorectal adenocarcinomas
-
Bardi G, Sukhikh T, Pandis N, Fenger C, Kronborg O, Heim S (1995) Karyotypic characterization of colorectal adenocarcinomas. Genes Chromosom Cancer 12:97-109.
-
(1995)
Genes Chromosom Cancer
, vol.12
, pp. 97-109
-
-
Bardi, G.1
Sukhikh, T.2
Pandis, N.3
Fenger, C.4
Kronborg, O.5
Heim, S.6
-
22
-
-
0027441214
-
Translocation junctions cluster at the distal short arm of chromosome 1 (1p36.1-2) in human neuroblastoma cells
-
Barker PE, Savelyeva L, Schwab M (1993) Translocation junctions cluster at the distal short arm of chromosome 1 (1p36.1-2) in human neuroblastoma cells. Oncogene 8:3353-3358.
-
(1993)
Oncogene
, vol.8
, pp. 3353-3358
-
-
Barker, P.E.1
Savelyeva, L.2
Schwab, M.3
-
23
-
-
0028793259
-
Determination and regional assignement of grouped sets of microclones in chromosome 1pter-p35
-
Barnas CM, Onyango P, Ellmeier W, Lengauer C, Kleiner E, Henn T, Brunner C, Stapleton P, Weith A (1995) Determination and regional assignement of grouped sets of microclones in chromosome 1pter-p35. Genomics 29:607-615.
-
(1995)
Genomics
, vol.29
, pp. 607-615
-
-
Barnas, C.M.1
Onyango, P.2
Ellmeier, W.3
Lengauer, C.4
Kleiner, E.5
Henn, T.6
Brunner, C.7
Stapleton, P.8
Weith, A.9
-
24
-
-
0021153546
-
Tumorigenicity of human HT1080 fibrosarcoma x normal fibroblast hybrids: Chromosome dosage dependency
-
Benedict WF, Weissman BE, Mark C, Stanbridge EJ (1984) Tumorigenicity of human HT1080 fibrosarcoma x normal fibroblast hybrids: Chromosome dosage dependency. Cancer Res 44:3471-3479.
-
(1984)
Cancer Res
, vol.44
, pp. 3471-3479
-
-
Benedict, W.F.1
Weissman, B.E.2
Mark, C.3
Stanbridge, E.J.4
-
25
-
-
0028037272
-
Genetics of seven Dutch familial atypical multiple Mole-melanoma syndrome families: A review of linkage results including chromosomes 1 and 9
-
Bergman W, Gruis NA, Sandkuijl LA, Frants RR (1994) Genetics of seven Dutch familial atypical multiple Mole-melanoma syndrome families: A review of linkage results including chromosomes 1 and 9. J Invest Dermatol 5:122S-125S.
-
(1994)
J Invest Dermatol
, vol.5
-
-
Bergman, W.1
Gruis, N.A.2
Sandkuijl, L.A.3
Frants, R.R.4
-
26
-
-
0025851073
-
Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5′ part of the tal-1 gene
-
Bernard O, Lecointe N, Jonveaux P, Souyri M, Mauchauffé M, Berger R, Larsen CJ, Mathieu-Mahul D (1991) Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5′ part of the tal-1 gene. Oncogene 6:1477-1488.
-
(1991)
Oncogene
, vol.6
, pp. 1477-1488
-
-
Bernard, O.1
Lecointe, N.2
Jonveaux, P.3
Souyri, M.4
Mauchauffé, M.5
Berger, R.6
Larsen, C.J.7
Mathieu-Mahul, D.8
-
27
-
-
0029018546
-
Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations
-
Bernard O, Berger R (1995) Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations. Genes Chromosom Cancer 13:75-85.
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 75-85
-
-
Bernard, O.1
Berger, R.2
-
28
-
-
0028215338
-
A novel gene, AF-1p, fused to HRX in t(1;11)(q23), is not related to AF-4, AF-9 nor ENL
-
Bernard O, Mauchauffe M, Mecucci C, van den Berghe H, Berger R (1994) A novel gene, AF-1p, fused to HRX in t(1;11)(q23), is not related to AF-4, AF-9 nor ENL. Oncogene 9:1039-1045.
-
(1994)
Oncogene
, vol.9
, pp. 1039-1045
-
-
Bernard, O.1
Mauchauffe, M.2
Mecucci, C.3
Van Den Berghe, H.4
Berger, R.5
-
29
-
-
0001800304
-
Overview: Biology of neuroblastoma
-
Pochedly C (ed): Boca Raton, CRC Press
-
Berthold F (1990) Overview: Biology of neuroblastoma. In Pochedly C (ed): Neuroblastoma: Tumor biology and therapy. pp. 1-27. Boca Raton, CRC Press.
-
(1990)
Neuroblastoma: Tumor Biology and Therapy
, pp. 1-27
-
-
Berthold, F.1
-
30
-
-
0025339162
-
Loss of heterozygosity of the L-myc oncogene in human breast tumors
-
Bièche I, Champème M-H, Merlo G, Larsen C-J, Callahan R, Lidereau R (1990) Loss of heterozygosity of the L-myc oncogene in human breast tumors. Hum Genet 85:101-105.
-
(1990)
Hum Genet
, vol.85
, pp. 101-105
-
-
Bièche, I.1
Champème, M.-H.2
Merlo, G.3
Larsen, C.-J.4
Callahan, R.5
Lidereau, R.6
-
31
-
-
0027155128
-
Two distinct regions involved in 1p deletion in human primary breast cancer
-
Bièche I, Champème M-H, Matifas F, Crop CS, Callahan R, Lidereau R (1993) Two distinct regions involved in 1p deletion in human primary breast cancer. Cancer Res 53:1900-1994.
-
(1993)
Cancer Res
, vol.53
, pp. 1900-1994
-
-
Bièche, I.1
Champème, M.-H.2
Matifas, F.3
Crop, C.S.4
Callahan, R.5
Lidereau, R.6
-
32
-
-
0028382419
-
Mise en évidence de deux régions délétées sur le bras court du chromosome 1 dans les tumeurs du sein
-
Bièche I, Champème M-H, Matifas F, Callahan R, Lidereau R (1994) Mise en évidence de deux régions délétées sur le bras court du chromosome 1 dans les tumeurs du sein. Bull Cancer 81:108-113.
-
(1994)
Bull Cancer
, vol.81
, pp. 108-113
-
-
Bièche, I.1
Champème, M.-H.2
Matifas, F.3
Callahan, R.4
Lidereau, R.5
-
33
-
-
0026340855
-
Chromosomal translocation t(1;13)(p36;q14) in a case of rhabdomyosarcoma
-
Biegel JA, Meek RS, Parmiter AH, Conard K, Emanuel BS (1991) Chromosomal translocation t(1;13)(p36;q14) in a case of rhabdomyosarcoma. Genes Chromosom Cancer 3:483-484.
-
(1991)
Genes Chromosom Cancer
, vol.3
, pp. 483-484
-
-
Biegel, J.A.1
Meek, R.S.2
Parmiter, A.H.3
Conard, K.4
Emanuel, B.S.5
-
34
-
-
0027476712
-
Constitutional 1p36 deletion in a child with neuroblastoma
-
Biegel JA, White PS, Marshall HN, Fujimori M, Zackai EH, Scher CD, Brodeur GM, Emanuel BS (1993) Constitutional 1p36 deletion in a child with neuroblastoma. Am J Hum Genet 52:176-182.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 176-182
-
-
Biegel, J.A.1
White, P.S.2
Marshall, H.N.3
Fujimori, M.4
Zackai, E.H.5
Scher, C.D.6
Brodeur, G.M.7
Emanuel, B.S.8
-
35
-
-
0024323447
-
Molecular characterization of the lymphoid V(D)J recombination activity
-
Blackwell TK, Alt FW (1989) Molecular characterization of the lymphoid V(D)J recombination activity. J Biol Chem 264:10327-10330.
-
(1989)
J Biol Chem
, vol.264
, pp. 10327-10330
-
-
Blackwell, T.K.1
Alt, F.W.2
-
36
-
-
0022409280
-
T(1;3)(p36;q21) in acute nonlymphocytic leukemia: A new cytogenetic-clinopathologic association
-
Bloomfield CD, Garson M, Volin L, Knuutila S, de la Chapelle A (1985) t(1;3)(p36;q21) in acute nonlymphocytic leukemia: a new cytogenetic-clinopathologic association. Blood 66:1409-1413.
-
(1985)
Blood
, vol.66
, pp. 1409-1413
-
-
Bloomfield, C.D.1
Garson, M.2
Volin, L.3
Knuutila, S.4
De La Chapelle, A.5
-
37
-
-
0026620034
-
Chromosome 1 alterations in breast cancer: Allelic loss on 1p and 1q is related to lymphogenic metastases and poor prognosis
-
Borg Å, Zhang Q-X, Olsson H, Wenngren E (1992) Chromosome 1 alterations in breast cancer: Allelic loss on 1p and 1q is related to lymphogenic metastases and poor prognosis. Genes Chromosom Cancer 5:311-320.
-
(1992)
Genes Chromosom Cancer
, vol.5
, pp. 311-320
-
-
Borg, Å.1
Zhang, Q.-X.2
Olsson, H.3
Wenngren, E.4
-
38
-
-
0019819011
-
Break points in chromosome #1 abnormalities of 218 human neoplasms
-
Brito-Babapulle V, Atkin NB (1981) Break points in chromosome #1 abnormalities of 218 human neoplasms. Cancer Genet Cytogenet 4:215-225.
-
(1981)
Cancer Genet Cytogenet
, vol.4
, pp. 215-225
-
-
Brito-Babapulle, V.1
Atkin, N.B.2
-
39
-
-
0019777535
-
Cytogenetic features of human neuroblastomas and cell lines
-
Brodeur GM, Green AA, Hayes FA, Williams KJ, Williams DL, Tsiatis AA (1981) Cytogenetic features of human neuroblastomas and cell lines. Cancer Res 41:4678-4686.
-
(1981)
Cancer Res
, vol.41
, pp. 4678-4686
-
-
Brodeur, G.M.1
Green, A.A.2
Hayes, F.A.3
Williams, K.J.4
Williams, D.L.5
Tsiatis, A.A.6
-
40
-
-
0025151168
-
Site-specific recombination of the tal-1 gene is a common occurrence in human T cell leukemia
-
Brown L, Cheng J-T, Chen Q, Siciliano MJ, Crist W, Buchanan G, Baer R (1990) Site-specific recombination of the tal-1 gene is a common occurrence in human T cell leukemia. EMBO J 9:3343-3351.
-
(1990)
EMBO J
, vol.9
, pp. 3343-3351
-
-
Brown, L.1
Cheng, J.-T.2
Chen, Q.3
Siciliano, M.J.4
Crist, W.5
Buchanan, G.6
Baer, R.7
-
41
-
-
0024332123
-
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma
-
Buetow KH, Murray JC, Israel JL, London WT, Smith M, Kew M, Blanquet V, Brechot C, Redeker A, Govindarajh S (1989) Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proc Natl Acad Sci USA 86: 8852-8856.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 8852-8856
-
-
Buetow, K.H.1
Murray, J.C.2
Israel, J.L.3
London, W.T.4
Smith, M.5
Kew, M.6
Blanquet, V.7
Brechot, C.8
Redeker, A.9
Govindarajh, S.10
-
42
-
-
0027965590
-
Molecular analysis of the T-cell acute lymphoblastic leukemia-associated t(1;7)(p34;q34) that fuses LCK and TCRB
-
Burnett RC, Thirman MJ, Rowley JD, Diaz MO (1994) Molecular analysis of the T-cell acute lymphoblastic leukemia-associated t(1;7)(p34;q34) that fuses LCK and TCRB. Blood 84:1232-1236.
-
(1994)
Blood
, vol.84
, pp. 1232-1236
-
-
Burnett, R.C.1
Thirman, M.J.2
Rowley, J.D.3
Diaz, M.O.4
-
43
-
-
0025338277
-
Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome 1p36
-
Cannon-Albright LA, Goldgar DE, Wright EC, Turco A, Jost M, Meyer LJ, Piepkorn M, Zone JJ, Skolnick MH (1990) Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome 1p36. Am J Hum Genet 46:912-918.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 912-918
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Wright, E.C.3
Turco, A.4
Jost, M.5
Meyer, L.J.6
Piepkorn, M.7
Zone, J.J.8
Skolnick, M.H.9
-
44
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22
-
Cannon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, Fountain JW, et al. (1992) Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science 258:1148-1152.
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
Lewis, C.M.4
Anderson, D.E.5
Fountain, J.W.6
-
45
-
-
84970049889
-
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification
-
Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R (1993) Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification. Nature Genet 4:187-190.
-
(1993)
Nature Genet
, vol.4
, pp. 187-190
-
-
Caron, H.1
Van Sluis, P.2
Van Hoeve, M.3
De Kraker, J.4
Bras, J.5
Slater, R.6
Mannens, M.7
Voûte, P.A.8
Westerveld, A.9
Versteeg, R.10
-
46
-
-
0028128737
-
Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity
-
Caron H, van Sluis P, van Roy N, de Kraker J, Speleman F, Voûte PA, Westerveld A, Slater R, Versteeg R (1994) Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity. Am J Hum Genet 55:341-347.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 341-347
-
-
Caron, H.1
Van Sluis, P.2
Van Roy, N.3
De Kraker, J.4
Speleman, F.5
Voûte, P.A.6
Westerveld, A.7
Slater, R.8
Versteeg, R.9
-
47
-
-
34447491255
-
Allelic loss of chromosome 1p identifies neuroblastoma patients at high risk of an unfavourable outcome
-
in press
-
Caron H, van Sluis P, de Kraker J, Bökkerink J, Egeler M, Laureys G, Slater R, Westerveld A, Voûte PA, Versteeg R (1995) Allelic loss of chromosome 1p identifies neuroblastoma patients at high risk of an unfavourable outcome. N Engl J Med (in press).
-
(1995)
N Engl J Med
-
-
Caron, H.1
Van Sluis, P.2
De Kraker, J.3
Bökkerink, J.4
Egeler, M.5
Laureys, G.6
Slater, R.7
Westerveld, A.8
Voûte, P.A.9
Versteeg, R.10
-
48
-
-
0025040167
-
The t(1;14) (p34;q11) is nonrandom and restricted to T-cell acute lymphoblastic leukemia: A pediatric oncology group study
-
Carroll AJ, Crist WM, Link MP, Amylon MD, Pullen DJ, Ragab AH, Buchanan GR, Wimmer RS, Vietti TJ (1990) The t(1;14) (p34;q11) is nonrandom and restricted to T-cell acute lymphoblastic leukemia: A pediatric oncology group study. Blood 76: 1220-1224.
-
(1990)
Blood
, vol.76
, pp. 1220-1224
-
-
Carroll, A.J.1
Crist, W.M.2
Link, M.P.3
Amylon, M.D.4
Pullen, D.J.5
Ragab, A.H.6
Buchanan, G.R.7
Wimmer, R.S.8
Vietti, T.J.9
-
49
-
-
0024457239
-
Chromosomal changes in human primary testicular nonseminomatous germ cell tumors
-
Castedo SMMJ, de Jong B, Oosterhuis JW, Seruca R, Idenburg VJS, Dam A, te Meerman G, Koops HS, Sleijfer DT (1989) Chromosomal changes in human primary testicular nonseminomatous germ cell tumors. Cancer Res 49:5696-5701.
-
(1989)
Cancer Res
, vol.49
, pp. 5696-5701
-
-
Castedo, S.M.M.J.1
De Jong, B.2
Oosterhuis, J.W.3
Seruca, R.4
Idenburg, V.J.S.5
Dam, A.6
Te Meerman, G.7
Koops, H.S.8
Sleijfer, D.T.9
-
51
-
-
0025014636
-
The tal gene undergoes chromosome translocation in T cell leukemia and potentially encodes a helix-loop-helix protein
-
Chen Q, Cheng J-T, Tsai L-H, Schneider N, Buchanan G, Carroll A, Crist W, Ozanne B, Siciliano MJ, Baer R (1990) The tal gene undergoes chromosome translocation in T cell leukemia and potentially encodes a helix-loop-helix protein. EMBO J 9:415-424.
-
(1990)
EMBO J
, vol.9
, pp. 415-424
-
-
Chen, Q.1
Cheng, J.-T.2
Tsai, L.-H.3
Schneider, N.4
Buchanan, G.5
Carroll, A.6
Crist, W.7
Ozanne, B.8
Siciliano, M.J.9
Baer, R.10
-
52
-
-
0027280613
-
Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas
-
Cheng JM, Hiemstra JL, Schneider SS, Naumova A, Cheung N-KV, Cohn SL, Diller L, Sapienza C, Brodeur GM (1993) Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas. Nature Genetics 4:191-194.
-
(1993)
Nature Genetics
, vol.4
, pp. 191-194
-
-
Cheng, J.M.1
Hiemstra, J.L.2
Schneider, S.S.3
Naumova, A.4
Cheung, N.-K.V.5
Cohn, S.L.6
Diller, L.7
Sapienza, C.8
Brodeur, G.M.9
-
53
-
-
0028815356
-
Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification
-
Cheng NC, Van Roy N, Chan A, Beitsma M, Westerveld A, Speleman F, Versteeg R (1995) Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification. Oncogene 10:291-297.
-
(1995)
Oncogene
, vol.10
, pp. 291-297
-
-
Cheng, N.C.1
Van Roy, N.2
Chan, A.3
Beitsma, M.4
Westerveld, A.5
Speleman, F.6
Versteeg, R.7
-
54
-
-
0030026542
-
A human modifier for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1
-
Cheng NC, Chan AJK, Beitsma MM, Speleman F, Westerveld A, Versteeg R (1996) A human modifier for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1. Hum Molec Genet 5:309-317.
-
(1996)
Hum Molec Genet
, vol.5
, pp. 309-317
-
-
Cheng, N.C.1
Chan, A.J.K.2
Beitsma, M.M.3
Speleman, F.4
Westerveld, A.5
Versteeg, R.6
-
55
-
-
0023835841
-
Tumour karyotype discriminates between good and bad prognostic outcome in neueroblastoma
-
Christiansen H, Lampert F (1988) Tumour karyotype discriminates between good and bad prognostic outcome in neueroblastoma. Br J Cancer 57:121-126.
-
(1988)
Br J Cancer
, vol.57
, pp. 121-126
-
-
Christiansen, H.1
Lampert, F.2
-
56
-
-
0029061595
-
Comparison of DNA aneuploidy, chromosome 1 abnormalities, MYCN amplification and CD44 expression as prognostic factors in neuroblastoma
-
Christiansen H, Sahin K, Berthold F, Hero B, Terpe H-J, Lampert F (1995) Comparison of DNA aneuploidy, chromosome 1 abnormalities, MYCN amplification and CD44 expression as prognostic factors in neuroblastoma. Europ J Cancer 31A, 541-544.
-
(1995)
Europ J Cancer
, vol.31 A
, pp. 541-544
-
-
Christiansen, H.1
Sahin, K.2
Berthold, F.3
Hero, B.4
Terpe, H.-J.5
Lampert, F.6
-
57
-
-
0028927796
-
Sensitive detection of numerical and structural aberrations of chromosome 1 in neuroblastoma by interphase fluorescence in situ hybridization. Comparison with restriction fragment length polymorphism and conventional cytogenetic analyses
-
Combaret V, Turc-Carel C, Thiesse P, Rebillard A-C, Frappaz D, Haus O, Philip T, Favrot MC (1995) Sensitive detection of numerical and structural aberrations of chromosome 1 in neuroblastoma by interphase fluorescence in situ hybridization. Comparison with restriction fragment length polymorphism and conventional cytogenetic analyses. Int J Cancer 61:185-191.
-
(1995)
Int J Cancer
, vol.61
, pp. 185-191
-
-
Combaret, V.1
Turc-Carel, C.2
Thiesse, P.3
Rebillard, A.-C.4
Frappaz, D.5
Haus, O.6
Philip, T.7
Favrot, M.C.8
-
58
-
-
0026551788
-
Chromosome 1 in human colorectal tumors
-
Couturier-Turpin M-H, Esnous C, Louvel A, Poirier Y, Couturier D (1992) Chromosome 1 in human colorectal tumors. Hum Genet 88:431-438.
-
(1992)
Hum Genet
, vol.88
, pp. 431-438
-
-
Couturier-Turpin, M.-H.1
Esnous, C.2
Louvel, A.3
Poirier, Y.4
Couturier, D.5
-
59
-
-
0029010785
-
Frequent loss of chromosome arm 1p DNA in parathyroid adenomas
-
Cryns VL, Yi SM, Tahara H, Gaz RD, Arnold A (1995) Frequent loss of chromosome arm 1p DNA in parathyroid adenomas. Genes Chromosom Cancer 13:9-17.
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 9-17
-
-
Cryns, V.L.1
Yi, S.M.2
Tahara, H.3
Gaz, R.D.4
Arnold, A.5
-
60
-
-
0028364374
-
Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma
-
Davis RJ, D'Cruz CM, Lovell MA, Biegel JA, Barr FG (1994) Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma. Cancer Res 54:2869-2872.
-
(1994)
Cancer Res
, vol.54
, pp. 2869-2872
-
-
Davis, R.J.1
D'Cruz, C.M.2
Lovell, M.A.3
Biegel, J.A.4
Barr, F.G.5
-
61
-
-
0026080951
-
Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma
-
Devilee P, van Vliet M, Bardoel A, Kievits T, Kuipers-Dijkshoorn N, Pearson PL, Cornelisse CJ (1991) Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma. Cancer Res 51:1020-1025.
-
(1991)
Cancer Res
, vol.51
, pp. 1020-1025
-
-
Devilee, P.1
Van Vliet, M.2
Bardoel, A.3
Kievits, T.4
Kuipers-Dijkshoorn, N.5
Pearson, P.L.6
Cornelisse, C.J.7
-
62
-
-
0027363063
-
Genetic identification of Mom1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
-
Dietrich WF, Lander ES, Smith JS, Moser AR, Gould KA, Luongo C, Borenstein N, Dove W (1993) Genetic identification of Mom1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse. Cell 75:631-639.
-
(1993)
Cell
, vol.75
, pp. 631-639
-
-
Dietrich, W.F.1
Lander, E.S.2
Smith, J.S.3
Moser, A.R.4
Gould, K.A.5
Luongo, C.6
Borenstein, N.7
Dove, W.8
-
63
-
-
0026317567
-
Variant translocations of chromosome 13 in alveolar rhabdomyosarcoma
-
Douglass EC, Rowe ST, Valentine M, Parham DM, Berkow R, Bowman WP, Maurer HM (1991) Variant translocations of chromosome 13 in alveolar rhabdomyosarcoma. Genes Chromosom Cancer 3:480-482.
-
(1991)
Genes Chromosom Cancer
, vol.3
, pp. 480-482
-
-
Douglass, E.C.1
Rowe, S.T.2
Valentine, M.3
Parham, D.M.4
Berkow, R.5
Bowman, W.P.6
Maurer, H.M.7
-
64
-
-
0013513408
-
Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression
-
Dracopoli NC, Harnett P, Bale SJ, Stanger BZ, Tucker MA, Housman DE, Kefford RF (1989) Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression. Proc Natl Acad Sci USA 86:4614-4618.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 4614-4618
-
-
Dracopoli, N.C.1
Harnett, P.2
Bale, S.J.3
Stanger, B.Z.4
Tucker, M.A.5
Housman, D.E.6
Kefford, R.F.7
-
65
-
-
0025981877
-
The CEPH consortium linkage map of human chromosome 1
-
Dracopoli NC, O'Connell P, Elsner TI, Lalouel J-M, White RL, Buetow KH, Nishimura DY, Murray JC, Helms C, Mishra SK, Donis-Keller H, Hall JM, Lee MK, King M-C, Attwood J, Morton NE, Robson EB, Mahtani M, Willard HF, Royle NJ, Patel I, Jeffreys AJ, Verga V, Jenkins T, Weber JL, Mitchell AL, Bale AE (1991) The CEPH consortium linkage map of human chromosome 1. Genomics 9:686-700.
-
(1991)
Genomics
, vol.9
, pp. 686-700
-
-
Dracopoli, N.C.1
O'Connell, P.2
Elsner, T.I.3
Lalouel, J.-M.4
White, R.L.5
Buetow, K.H.6
Nishimura, D.Y.7
Murray, J.C.8
Helms, C.9
Mishra, S.K.10
Donis-Keller, H.11
Hall, J.M.12
Lee, M.K.13
King, M.-C.14
Attwood, J.15
Morton, N.E.16
Robson, E.B.17
Mahtani, M.18
Willard, H.F.19
Royle, N.J.20
Patel, I.21
Jeffreys, A.J.22
Verga, V.23
Jenkins, T.24
Weber, J.L.25
Mitchell, A.L.26
Bale, A.E.27
more..
-
66
-
-
0028311249
-
Report of the first international workshop on human chromosome 1 mapping 1994
-
Dracopoli NC, Bruns GAP, Brodeur GM, Landes GM, Matise TC, Seldin MF, Vance JM, Weith A (1994) Report of the first international workshop on human chromosome 1 mapping 1994. Cytogenetic Cell Genet 67:144-165.
-
(1994)
Cytogenetic Cell Genet
, vol.67
, pp. 144-165
-
-
Dracopoli, N.C.1
Bruns, G.A.P.2
Brodeur, G.M.3
Landes, G.M.4
Matise, T.C.5
Seldin, M.F.6
Vance, J.M.7
Weith, A.8
-
68
-
-
0026749965
-
Mutually exclusive expression of a helix-loop-helix gene and N-myc in human neuroblastomas and in normal development
-
Ellmeier W, Aguzzi A, Kleiner E, Kurzbauer R, Weith A (1992) Mutually exclusive expression of a helix-loop-helix gene and N-myc in human neuroblastomas and in normal development. EMBO J 11:2563-2571.
-
(1992)
EMBO J
, vol.11
, pp. 2563-2571
-
-
Ellmeier, W.1
Aguzzi, A.2
Kleiner, E.3
Kurzbauer, R.4
Weith, A.5
-
69
-
-
0028086524
-
Identification of human DAN gene, mapping to the putative neuroblastoma tumor suppressor locus
-
Enomoto H, Ozaki T, Takahashi E-I, Nomura N, Tabata S, Takahashi H, Ohnuma N, Tanabe M, Iwai J, Yoshido H, Matsunaga T, Sakiyama S (1994) Identification of human DAN gene, mapping to the putative neuroblastoma tumor suppressor locus. Oncogene 9:2785-2791.
-
(1994)
Oncogene
, vol.9
, pp. 2785-2791
-
-
Enomoto, H.1
Ozaki, T.2
Takahashi, E.-I.3
Nomura, N.4
Tabata, S.5
Takahashi, H.6
Ohnuma, N.7
Tanabe, M.8
Iwai, J.9
Yoshido, H.10
Matsunaga, T.11
Sakiyama, S.12
-
70
-
-
0023196534
-
Cytogenetic studies of four human lung adenocarcinoma cell lines
-
Fan Y-S, Li P (1987) Cytogenetic studies of four human lung adenocarcinoma cell lines. Cancer Genet Cytogenet 26:317-325.
-
(1987)
Cancer Genet Cytogenet
, vol.26
, pp. 317-325
-
-
Fan, Y.-S.1
Li, P.2
-
71
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon ER, Vogelstein B (1990) A genetic model for colorectal tumorigenesis. Cell 61:759-767.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
72
-
-
0029017337
-
A gene for susceptibility to small intestinal cancer, ssic1, maps to the distal part of mouse chromosome 4
-
Fijneman RJA, Demant P (1995) A gene for susceptibility to small intestinal cancer, ssic1, maps to the distal part of mouse chromosome 4. Cancer Res 55:3179-3182.
-
(1995)
Cancer Res
, vol.55
, pp. 3179-3182
-
-
Fijneman, R.J.A.1
Demant, P.2
-
73
-
-
0345347904
-
Involvement of the TCL5 gene on human chromosome 1 in T-cell leukemia and melanoma
-
Finger LR, Kagan J, Christopher G, Kurtzberg J, Hershfield MS, Nowell PC, Croce CM (1989) Involvement of the TCL5 gene on human chromosome 1 in T-cell leukemia and melanoma. Proc Natl Acad Sci USA 86:5039-5043.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 5039-5043
-
-
Finger, L.R.1
Kagan, J.2
Christopher, G.3
Kurtzberg, J.4
Hershfield, M.S.5
Nowell, P.C.6
Croce, C.M.7
-
74
-
-
0025889062
-
c-tal, a helix-loop-helix protein, is juxtaposed to the T-cell receptor -B chain gene by a reciprocal chromosomal translocation: T(1;7) (p32;q35)
-
Fitzgerald TJ, Neale GAM, Raimondi S, Goorha RM (1991) c-tal, a helix-loop-helix protein, is juxtaposed to the T-cell receptor -B chain gene by a reciprocal chromosomal translocation: t(1;7) (p32;q35). Blood 78:2686-3695.
-
(1991)
Blood
, vol.78
, pp. 2686-3695
-
-
Fitzgerald, T.J.1
Neale, G.A.M.2
Raimondi, S.3
Goorha, R.M.4
-
75
-
-
0024670859
-
Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-mycamplification
-
Fong C-T, Dracopoli NC, White PS, Merrill PT, Griffith RC, Housman DE, Brodeur GM (1989) Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-mycamplification. Proc Natl Acad Sci USA 86:3753-3757.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 3753-3757
-
-
Fong, C.-T.1
Dracopoli, N.C.2
White, P.S.3
Merrill, P.T.4
Griffith, R.C.5
Housman, D.E.6
Brodeur, G.M.7
-
76
-
-
0026769255
-
Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas
-
Fong C-T, White PS, Peterson K, Sapienza C, Cavenee WK, Kern SE, Vogelstein B, Cantor AB, Look AT, Brodeur GM (1992) Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas. Cancer Res 52:1780-1785.
-
(1992)
Cancer Res
, vol.52
, pp. 1780-1785
-
-
Fong, C.-T.1
White, P.S.2
Peterson, K.3
Sapienza, C.4
Cavenee, W.K.5
Kern, S.E.6
Vogelstein, B.7
Cantor, A.B.8
Look, A.T.9
Brodeur, G.M.10
-
78
-
-
0026022684
-
Allelotype study of primary hepatocellular carcinoma
-
Fujiimori M, Tokino T, Hino O, Kitagawa T, Imamura T, Okamoto E, Mitsunobu M, Ishikawa T, Nakagama H, Harada H, Yagura M, Matsubara K, Nakamura Y (1991) Allelotype study of primary hepatocellular carcinoma. Cancer Res 51:89-93.
-
(1991)
Cancer Res
, vol.51
, pp. 89-93
-
-
Fujiimori, M.1
Tokino, T.2
Hino, O.3
Kitagawa, T.4
Imamura, T.5
Okamoto, E.6
Mitsunobu, M.7
Ishikawa, T.8
Nakagama, H.9
Harada, H.10
Yagura, M.11
Matsubara, K.12
Nakamura, Y.13
-
79
-
-
0028790325
-
The 1p deletion is not a reliable marker for the prognosis of patients with neuroblastoma
-
Gehring M, Berthold F, Edler L, Schwab M, Amler LC (1995) The 1p deletion is not a reliable marker for the prognosis of patients with neuroblastoma. Cancer Res 55:5366-5369.
-
(1995)
Cancer Res
, vol.55
, pp. 5366-5369
-
-
Gehring, M.1
Berthold, F.2
Edler, L.3
Schwab, M.4
Amler, L.C.5
-
81
-
-
0029021505
-
Recurrent deletions involving chromosome 1, 5, 17, and 18 in colorectal carcinoma: Possible role in biological and clinical behavior of tumors
-
Gerdes H, Chen Q, Elahi AH, Sircar A, Goldberg E, Winawer D, Urmacher C, Winawer SJ, Jhanwar SC (1995) Recurrent deletions involving chromosome 1, 5, 17, and 18 in colorectal carcinoma: possible role in biological and clinical behavior of tumors. Anticancer Res 15:13-24.
-
(1995)
Anticancer Res
, vol.15
, pp. 13-24
-
-
Gerdes, H.1
Chen, Q.2
Elahi, A.H.3
Sircar, A.4
Goldberg, E.5
Winawer, D.6
Urmacher, C.7
Winawer, S.J.8
Jhanwar, S.C.9
-
82
-
-
0020314732
-
Abnormalities of chromosome 1p in human neuroblastoma tumors and cell lines
-
Gilbert F, Balaban G, Moorhead P, Bianchi D, Schlesinger H (1982) Abnormalities of chromosome 1p in human neuroblastoma tumors and cell lines. Cancer Genet Cytogenet 7:33-42.
-
(1982)
Cancer Genet Cytogenet
, vol.7
, pp. 33-42
-
-
Gilbert, F.1
Balaban, G.2
Moorhead, P.3
Bianchi, D.4
Schlesinger, H.5
-
83
-
-
0021683414
-
Human neuroblastomas and abnormalities of chromosomes 1 and 17
-
Gilbert F, Feder M, Balaban G, Brangman D, Lurie DK, Podolsky R, Rinaldt V, Vinikoor N, Weisband J (1984) Human neuroblastomas and abnormalities of chromosomes 1 and 17. Cancer Res 44:5444-5449.
-
(1984)
Cancer Res
, vol.44
, pp. 5444-5449
-
-
Gilbert, F.1
Feder, M.2
Balaban, G.3
Brangman, D.4
Lurie, D.K.5
Podolsky, R.6
Rinaldt, V.7
Vinikoor, N.8
Weisband, J.9
-
84
-
-
0027370901
-
Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity
-
Goldstein AM, Dracopoli NC, Ho EC, Fraser MC, Kearns KS, Bale SJ, McBride OW, Clark Jr WJ, Tucker MA (1993) Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity. Am J Hum Genet 52:537-550.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 537-550
-
-
Goldstein, A.M.1
Dracopoli, N.C.2
Ho, E.C.3
Fraser, M.C.4
Kearns, K.S.5
Bale, S.J.6
McBride, O.W.7
Clark Jr., W.J.8
Tucker, M.A.9
-
85
-
-
0028013327
-
Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity
-
Goldstein AM, Dracopoli NC, Engelstein M, Fraser MC, Clark WH Jr, Tucker MA (1994) Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity. Am J Hum Genet 54:489-496.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 489-496
-
-
Goldstein, A.M.1
Dracopoli, N.C.2
Engelstein, M.3
Fraser, M.C.4
Clark Jr., W.H.5
Tucker, M.A.6
-
86
-
-
0002941239
-
The herditary variant of malignant melanoma
-
Clark WH Jr, Goldman LI, Mastrangelo MJ (eds): New York, Grune & Stratton
-
Greene MH, Fraumeni JF Jr (1979) The herditary variant of malignant melanoma. In: Clark WH Jr, Goldman LI, Mastrangelo MJ (eds): Human Malignant Melanoma, pp. 139-166. New York, Grune & Stratton.
-
(1979)
Human Malignant Melanoma
, pp. 139-166
-
-
Greene, M.H.1
Fraumeni Jr., J.F.2
-
87
-
-
0021063979
-
Familial cutaneous malignant melanoma: Autosomal dominant trait possibly linked to the Rh locus
-
Greene MH, Goldin LR, Clark Jr WH et al. (1983) Familial cutaneous malignant melanoma: autosomal dominant trait possibly linked to the Rh locus. Proc Natl Acad Sci USA 80:6071-6075.
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 6071-6075
-
-
Greene, M.H.1
Goldin, L.R.2
Clark Jr., W.H.3
-
89
-
-
0025348509
-
Locus for susceptibility to melanoma on chromosome 1p
-
Gruis NA, Bergman W, Frants RR (1990) Locus for susceptibility to melanoma on chromosome 1p. N Engl J Med 322:853-854.
-
(1990)
N Engl J Med
, vol.322
, pp. 853-854
-
-
Gruis, N.A.1
Bergman, W.2
Frants, R.R.3
-
90
-
-
0026774858
-
A comprehensive genetic linkage map of the human genome
-
Guyer M, Cann H (1992) A comprehensive genetic linkage map of the human genome. Science 258:67-86.
-
(1992)
Science
, vol.258
, pp. 67-86
-
-
Guyer, M.1
Cann, H.2
-
91
-
-
0028231090
-
The 1993-94 Généthon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M, Weissenbach J (1994) The 1993-94 Généthon human genetic linkage map. Nature Genetics 7:246-249.
-
(1994)
Nature Genetics
, vol.7
, pp. 246-249
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
92
-
-
0028875562
-
Allelotype of pancreatic adenocarcinoma using xenograft enrichment
-
Hahn S, Seymour AB, Hoque ATMS, Schutte M, da Costa LT, Redston M, Caldas C, Weinstein CL, Fischer A, Yeo CJ, Hruban RH, Kern SE (1995) Allelotype of pancreatic adenocarcinoma using xenograft enrichment. Cancer Res 55:4670-4675.
-
(1995)
Cancer Res
, vol.55
, pp. 4670-4675
-
-
Hahn, S.1
Seymour, A.B.2
Hoque, A.T.M.S.3
Schutte, M.4
Da Costa, L.T.5
Redston, M.6
Caldas, C.7
Weinstein, C.L.8
Fischer, A.9
Yeo, C.J.10
Hruban, R.H.11
Kern, S.E.12
-
93
-
-
0026656607
-
Rearrangements of chromosome 1p in breast cancer correlates with poor prognostic features
-
Hainsworth PJ, Raphael KL, Stillwell RG, Bennett RC, Garson OM (1992) Rearrangements of chromosome 1p in breast cancer correlates with poor prognostic features. Br J Cancer 66:131-135.
-
(1992)
Br J Cancer
, vol.66
, pp. 131-135
-
-
Hainsworth, P.J.1
Raphael, K.L.2
Stillwell, R.G.3
Bennett, R.C.4
Garson, O.M.5
-
94
-
-
0024121491
-
Localization of the human JUN protooncogene to chromosome region 1p31-32
-
Haluska FG, Huebner K, Isobe M, Nishimura T, Croce CM, Vogt PK (1988) Localization of the human JUN protooncogene to chromosome region 1p31-32. Proc Natl Acad Sci USA 85:2215-2218
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 2215-2218
-
-
Haluska, F.G.1
Huebner, K.2
Isobe, M.3
Nishimura, T.4
Croce, C.M.5
Vogt, P.K.6
-
95
-
-
0025870449
-
Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma. A marker of neural crest origins?
-
Harnett PR, Kearsley JH, Hayward NK, Dracopoli NC, Kefford RF (1991) Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma. A marker of neural crest origins? Cancer Genet Cytogenet 54:109-113.
-
(1991)
Cancer Genet Cytogenet
, vol.54
, pp. 109-113
-
-
Harnett, P.R.1
Kearsley, J.H.2
Hayward, N.K.3
Dracopoli, N.C.4
Kefford, R.F.5
-
96
-
-
34447492536
-
-
in press
-
Hashimoto N, Ichikawa D, Arakawa Y, Date K, Ueda S, Nakagawa Y, Horii A, Nakamura Y, Abe T, Inazawa J (1995) Frequent deletions of chromosome 1p in oligodendroglial tumors revealed by double-target fluorescence in situ hybridization and microsatellite analysis (in press).
-
(1995)
Frequent Deletions of Chromosome 1p in Oligodendroglial Tumors Revealed by Double-target Fluorescence in Situ Hybridization and Microsatellite Analysis
-
-
Hashimoto, N.1
Ichikawa, D.2
Arakawa, Y.3
Date, K.4
Ueda, S.5
Nakagawa, Y.6
Horii, A.7
Nakamura, Y.8
Abe, T.9
Inazawa, J.10
-
97
-
-
0024501461
-
Cytogenetic findings and prognosis in neuroblastoma with emphasis on marker chromosome 1
-
Hayashi Y, Kanda N, Inaba T, Hanada R, Nagahara N, Muchi H, Yamamoto K (1989) Cytogenetic findings and prognosis in neuroblastoma with emphasis on marker chromosome 1. Cancer 63: 126-132.
-
(1989)
Cancer
, vol.63
, pp. 126-132
-
-
Hayashi, Y.1
Kanda, N.2
Inaba, T.3
Hanada, R.4
Nagahara, N.5
Muchi, H.6
Yamamoto, K.7
-
100
-
-
0021358995
-
Conversion of a stem cell leukemia from a T-lymphoid to a myeloid phenotype induced by the adenosine deaminase inhibitor 2́-deoxycoformycin
-
Hershfield MS, Kurtzberg J, Harden E, Moore JO, Whang-Peng J, Haynes BF (1984) Conversion of a stem cell leukemia from a T-lymphoid to a myeloid phenotype induced by the adenosine deaminase inhibitor 2́-deoxycoformycin. Proc Natl Acad Sci USA 81:253-257.
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 253-257
-
-
Hershfield, M.S.1
Kurtzberg, J.2
Harden, E.3
Moore, J.O.4
Whang-Peng, J.5
Haynes, B.F.6
-
101
-
-
0028824273
-
Allelic loss of distal chromosome 4 in mouse lung tumors localizes a putative tumor suppressor gene to a region homologous with human chromosome 1p36
-
Herzog CR, Wang Y, You M (1995) Allelic loss of distal chromosome 4 in mouse lung tumors localizes a putative tumor suppressor gene to a region homologous with human chromosome 1p36. Oncogene 11:1811-1815.
-
(1995)
Oncogene
, vol.11
, pp. 1811-1815
-
-
Herzog, C.R.1
Wang, Y.2
You, M.3
-
102
-
-
0028819584
-
Allelic imbalance on chromosome 1 in human breast cancer. II. microsatellite repeat analysis
-
Hoggard N, Brintnell B, Howell A, Weissenbach J, Varley J (1995a) Allelic imbalance on chromosome 1 in human breast cancer. II. microsatellite repeat analysis. Genes Chromosom Cancer 12:24-31.
-
(1995)
Genes Chromosom Cancer
, vol.12
, pp. 24-31
-
-
Hoggard, N.1
Brintnell, B.2
Howell, A.3
Weissenbach, J.4
Varley, J.5
-
103
-
-
0028829767
-
Identification and cloning of yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer
-
Hoggard N, Hey Y, Brintnell B, James L, Jones D, Mitchell E, Weissenbach J, Varley J (1995b) Identification and cloning of yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer. Genomics 30:233-243.
-
(1995)
Genomics
, vol.30
, pp. 233-243
-
-
Hoggard, N.1
Hey, Y.2
Brintnell, B.3
James, L.4
Jones, D.5
Mitchell, E.6
Weissenbach, J.7
Varley, J.8
-
104
-
-
0025157874
-
Molecular evaluation of abnormalities of the short arm of chromosome 1 in neuroblastoma
-
Hunt JD, Tereba A (1990) Molecular evaluation of abnormalities of the short arm of chromosome 1 in neuroblastoma. Genes Chromosom Cancer 2:137-146.
-
(1990)
Genes Chromosom Cancer
, vol.2
, pp. 137-146
-
-
Hunt, J.D.1
Tereba, A.2
-
105
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian CT, Struewing JP, Goldstein A, Higgins PAT, Ally DS, Sheahan MD, Clark WH, Tucker MA, Dracopoli NC (1994) Germline p16 mutations in familial melanoma. Nature Genet 18: 15-21.
-
(1994)
Nature Genet
, vol.18
, pp. 15-21
-
-
Hussussian, C.T.1
Struewing, J.P.2
Goldstein, A.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
-
106
-
-
0029054735
-
Tumor suppressor activity of the gene encoding mammary-derived growth inhibitor
-
Huynh HT, Larsson C, Narod S, Pollak M (1995) Tumor suppressor activity of the gene encoding mammary-derived growth inhibitor. Cancer Res 55:2225-2231.
-
(1995)
Cancer Res
, vol.55
, pp. 2225-2231
-
-
Huynh, H.T.1
Larsson, C.2
Narod, S.3
Pollak, M.4
-
107
-
-
0024609569
-
A gene for the suppression of anchorage independence is located in rat chromosome 5 bands q22-23, and the rat alpha-interferon locus maps at the same region
-
Islam MQ, Szpirer J, Szpirer C, Islam K, Dasnoy J-F, Levan G (1989) A gene for the suppression of anchorage independence is located in rat chromosome 5 bands q22-23, and the rat alpha-interferon locus maps at the same region. J Cell Sciences 92:147-162.
-
(1989)
J Cell Sciences
, vol.92
, pp. 147-162
-
-
Islam, M.Q.1
Szpirer, J.2
Szpirer, C.3
Islam, K.4
Dasnoy, J.-F.5
Levan, G.6
-
109
-
-
0026100469
-
Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1
-
Järvelä I, Schleutker J, Haataja L, Santavuori P, Puhakka L, Manninen T, Palotie A, Sandkuijl LA, Renlund M, White R, Aula P, Peltonen L (1991) Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1. Genomics 9:170-173.
-
(1991)
Genomics
, vol.9
, pp. 170-173
-
-
Järvelä, I.1
Schleutker, J.2
Haataja, L.3
Santavuori, P.4
Puhakka, L.5
Manninen, T.6
Palotie, A.7
Sandkuijl, L.A.8
Renlund, M.9
White, R.10
Aula, P.11
Peltonen, L.12
-
110
-
-
0023772997
-
Isochromosome i(8q) or i(9q) in three adenocarcinomas of the lung
-
Jin Y-S, Mandahl N, Heim S, Schuller H, Mitelman F (1988) Isochromosome i(8q) or i(9q) in three adenocarcinomas of the lung. Cancer Genet Cytogenet 33:11-17.
-
(1988)
Cancer Genet Cytogenet
, vol.33
, pp. 11-17
-
-
Jin, Y.-S.1
Mandahl, N.2
Heim, S.3
Schuller, H.4
Mitelman, F.5
-
111
-
-
0028991951
-
Waldenström's macroglobulinemia with the AML/MDS-associated t(1;3)(p36;q21)
-
Johansson B, Waldenström J, Hasselblom S, Mitelman F (1995) Waldenström's macroglobulinemia with the AML/MDS-associated t(1;3)(p36;q21). Leukemia 9, 1136-1138.
-
(1995)
Leukemia
, vol.9
, pp. 1136-1138
-
-
Johansson, B.1
Waldenström, J.2
Hasselblom, S.3
Mitelman, F.4
-
112
-
-
0023681795
-
Myc family DNA amplification in small cell lung cancer patients' tumors and corresponding cell lines
-
Johnson BE, Makuch RW, Simmons AD, Gazdar AF, Burch D, Cashell AW (1988) Myc family DNA amplification in small cell lung cancer patients' tumors and corresponding cell lines. Cancer Res 48:5163-5166.
-
(1988)
Cancer Res
, vol.48
, pp. 5163-5166
-
-
Johnson, B.E.1
Makuch, R.W.2
Simmons, A.D.3
Gazdar, A.F.4
Burch, D.5
Cashell, A.W.6
-
113
-
-
0026042304
-
Rearrangements of the tal-1 locus as clonal markers for T cell acute lymphoblastic leukemia
-
Jonsson OF, Kitchens RL, Baer RJ, Buchanan GR, Smith RG (1991) Rearrangements of the tal-1 locus as clonal markers for T cell acute lymphoblastic leukemia. J Clin Invest 87:2029-2035.
-
(1991)
J Clin Invest
, vol.87
, pp. 2029-2035
-
-
Jonsson, O.F.1
Kitchens, R.L.2
Baer, R.J.3
Buchanan, G.R.4
Smith, R.G.5
-
114
-
-
0017366014
-
The analysis of malignancy by cell fusion. VII. Cytogenetic analysis of hybrids between malignant and diploid cells and of tumours derived from them
-
Jonasson J, Povey S, Harris H (1977) The analysis of malignancy by cell fusion. VII. Cytogenetic analysis of hybrids between malignant and diploid cells and of tumours derived from them. J Cell Sci 24:217-254.
-
(1977)
J Cell Sci
, vol.24
, pp. 217-254
-
-
Jonasson, J.1
Povey, S.2
Harris, H.3
-
115
-
-
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 III RS, Johnson BE, Skolnick MH (1994a) A cell cycle regulator potentially involved in genesis of many tumor types. Science 264:436-440.
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
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
-
116
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis NA, Ding W, Hussey C, Tran T, Miki Y, et al. (1994b) Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nature Genet 8:22-26.
-
(1994)
Nature Genet
, vol.8
, pp. 22-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eeles, R.3
Liu, Q.4
Gruis, N.A.5
Ding, W.6
Hussey, C.7
Tran, T.8
Miki, Y.9
-
117
-
-
0025977735
-
Hereditary melanoma in Australia: Variable association with dysplastic nevi and absence of genetic linkage to chromosome 1p
-
Kefford RF, Salmon J, Shaw HM, Donald JA, McCarthy WH (1991) Hereditary melanoma in Australia: variable association with dysplastic nevi and absence of genetic linkage to chromosome 1p. Cancer Genet Cytogenet 51:45-55.
-
(1991)
Cancer Genet Cytogenet
, vol.51
, pp. 45-55
-
-
Kefford, R.F.1
Salmon, J.2
Shaw, H.M.3
Donald, J.A.4
McCarthy, W.H.5
-
118
-
-
0029115296
-
Chromosome 1p terminal deletion: Report of new findings and confirmation of two characteristic phenotypes
-
Keppler-Noreuil KM, Carroll AJ, Finley WH, Rutledge SL (1995) Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes. J Med Genet 32: 619-622.
-
(1995)
J Med Genet
, vol.32
, pp. 619-622
-
-
Keppler-Noreuil, K.M.1
Carroll, A.J.2
Finley, W.H.3
Rutledge, S.L.4
-
119
-
-
0025865768
-
Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas
-
Khosla S, Patel VM, Hay ID, Schaid DJ, Grant CS, van Heerden JA, Thibodeau SN (1991) Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas. J Clin Invest 87:1691-1699.
-
(1991)
J Clin Invest
, vol.87
, pp. 1691-1699
-
-
Khosla, S.1
Patel, V.M.2
Hay, I.D.3
Schaid, D.J.4
Grant, C.S.5
Van Heerden, J.A.6
Thibodeau, S.N.7
-
120
-
-
0025922875
-
Karyotype pecularities of human colorectal adenocarcinomas
-
Konstantinova LN, Fleischman EV, Knisch VI, Perevozchikov AG, Kopnin BP (1991) Karyotype pecularities of human colorectal adenocarcinomas. Hum Genet 86:491-496.
-
(1991)
Hum Genet
, vol.86
, pp. 491-496
-
-
Konstantinova, L.N.1
Fleischman, E.V.2
Knisch, V.I.3
Perevozchikov, A.G.4
Kopnin, B.P.5
-
121
-
-
0028799791
-
Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma
-
Kraus JA, Koopmann J, Kaskel P, Maintz D, Brandner S, Schramm J, Louis DN, Wiestler OD, von Deimling A (1995) Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma. J Neuropath Exp Neurol 54:91-95.
-
(1995)
J Neuropath Exp Neurol
, vol.54
, pp. 91-95
-
-
Kraus, J.A.1
Koopmann, J.2
Kaskel, P.3
Maintz, D.4
Brandner, S.5
Schramm, J.6
Louis, D.N.7
Wiestler, O.D.8
Von Deimling, A.9
-
122
-
-
0029001463
-
Isolation and mapping of 186 new DNA markers on human chromosome 1
-
Kugoh H, Nakagawa Y, Mitsuya K, Mita T, Suzuki M, Suzuki N, Uejima H, Yuasa Y, Oshimura M (1995) Isolation and mapping of 186 new DNA markers on human chromosome 1. Genomics 27: 207-210.
-
(1995)
Genomics
, vol.27
, pp. 207-210
-
-
Kugoh, H.1
Nakagawa, Y.2
Mitsuya, K.3
Mita, T.4
Suzuki, M.5
Suzuki, N.6
Uejima, H.7
Yuasa, Y.8
Oshimura, M.9
-
123
-
-
0028982642
-
Accumulation of genetic changes during development and progression of hepatocellular carcinoma: Loss of heterozygosity on chromosome arm 1 occurs at an early stage of hepatocarcinogenesis
-
Kuroki T, Fujiwara Y, Tsuchiya E, Nakamori S, Imaoka S, Kanematsu T, Nakamura Y (1995) Accumulation of genetic changes during development and progression of hepatocellular carcinoma: Loss of heterozygosity on chromosome arm 1 occurs at an early stage of hepatocarcinogenesis. Genes Chromosom Cancer 13: 163-167.
-
(1995)
Genes Chromosom Cancer
, vol.13
, pp. 163-167
-
-
Kuroki, T.1
Fujiwara, Y.2
Tsuchiya, E.3
Nakamori, S.4
Imaoka, S.5
Kanematsu, T.6
Nakamura, Y.7
-
124
-
-
0022610831
-
Familial neuroblastoma: Case reports, literature review, and etiologie considerations
-
Kushner BH, Gilbert F, Helson L (1986) Familial neuroblastoma: case reports, literature review, and etiologie considerations. Cancer 57:1887-1893.
-
(1986)
Cancer
, vol.57
, pp. 1887-1893
-
-
Kushner, B.H.1
Gilbert, F.2
Helson, L.3
-
125
-
-
0022615480
-
Cytogenetic study of a Merkel Cell Carcinoma
-
Kusyk CJ, Romsdahl MM (1986) Cytogenetic study of a Merkel Cell Carcinoma. Cancer Genet Cytogenet 20:311-316.
-
(1986)
Cancer Genet Cytogenet
, vol.20
, pp. 311-316
-
-
Kusyk, C.J.1
Romsdahl, M.M.2
-
126
-
-
0028227933
-
Alterations in the PITSLRE protein kinase gene complex on chromosome 1p36 in childhood neuroblastoma
-
Lahti JM, Valentine M, Xiang J, Jones B, Amann J, Grenet J, Richmond G, Look AT, Kidd VJ (1994) Alterations in the PITSLRE protein kinase gene complex on chromosome 1p36 in childhood neuroblastoma. Nature Genetics 7:370-375.
-
(1994)
Nature Genetics
, vol.7
, pp. 370-375
-
-
Lahti, J.M.1
Valentine, M.2
Xiang, J.3
Jones, B.4
Amann, J.5
Grenet, J.6
Richmond, G.7
Look, A.T.8
Kidd, V.J.9
-
127
-
-
0025049957
-
Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma
-
Laureys G, Speleman F, Opdenakker G, Benoit Y, Leroy J (1990) Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma. Genes Chromosom Cancer 2:252-254.
-
(1990)
Genes Chromosom Cancer
, vol.2
, pp. 252-254
-
-
Laureys, G.1
Speleman, F.2
Opdenakker, G.3
Benoit, Y.4
Leroy, J.5
-
128
-
-
0028923604
-
Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers
-
Laureys G, Speleman F, Versteeg R, van der Drift P, Chan A, Leroy J, Francke U, Opdenakker G, Van Roy N (1995) Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers. Oncogene 10:1087-1093.
-
(1995)
Oncogene
, vol.10
, pp. 1087-1093
-
-
Laureys, G.1
Speleman, F.2
Versteeg, R.3
Van Der Drift, P.4
Chan, A.5
Leroy, J.6
Francke, U.7
Opdenakker, G.8
Van Roy, N.9
-
129
-
-
0024543677
-
Current therapy for malignant melanoma
-
Legha SS (1989) Current therapy for malignant melanoma. Seminars in Oncology 16:34-44.
-
(1989)
Seminars in Oncology
, vol.16
, pp. 34-44
-
-
Legha, S.S.1
-
130
-
-
0025221248
-
Human colorectal cancer: High frequency of deletions at chromosome 1p35
-
Leister I, Weith A, Brüderlein S, Cziepluch C, Kangwanpong D, Schlag P, Schwab M (1990) Human colorectal cancer: High frequency of deletions at chromosome 1p35. Cancer Res 50:7232-7235.
-
(1990)
Cancer Res
, vol.50
, pp. 7232-7235
-
-
Leister, I.1
Weith, A.2
Brüderlein, S.3
Cziepluch, C.4
Kangwanpong, D.5
Schlag, P.6
Schwab, M.7
-
131
-
-
0028136578
-
AML1, AML2, and AML3, the human members of the runt domain gene-family: CDNA structure, expression, and chromosomal localization
-
Levanon D, Negreanu V, Bernstein Y, Bar-Am I, Avivi L, Groner Y (1994) AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization. Genomics 23:425-432.
-
(1994)
Genomics
, vol.23
, pp. 425-432
-
-
Levanon, D.1
Negreanu, V.2
Bernstein, Y.3
Bar-Am, I.4
Avivi, L.5
Groner, Y.6
-
132
-
-
0023935348
-
Chromosome changes in metastatic human melanoma
-
Limon J, Cin PD, Sait SNJ, Karakousis C, Sandberg AA (1988) Chromosome changes in metastatic human melanoma. Cancer Genet Cytogenet 30:201-211.
-
(1988)
Cancer Genet Cytogenet
, vol.30
, pp. 201-211
-
-
Limon, J.1
Cin, P.D.2
Sait, S.N.J.3
Karakousis, C.4
Sandberg, A.A.5
-
133
-
-
0028786695
-
Deletion of 1p loci and microsatellite instability in colorectal polyps
-
Lothe RA, Norheim Andersen S, Hofstad B, Meling GI, Peltomäki P, Heim S, Brøgger A, Vatn M, Rognum TO, Børresen A-L (1995) Deletion of 1p loci and microsatellite instability in colorectal polyps. Genes Chromosom Cancer 14:182-188.
-
(1995)
Genes Chromosom Cancer
, vol.14
, pp. 182-188
-
-
Lothe, R.A.1
Norheim Andersen, S.2
Hofstad, B.3
Meling, G.I.4
Peltomäki, P.5
Heim, S.6
Brøgger, A.7
Vatn, M.8
Rognum, T.O.9
Børresen, A.-L.10
-
134
-
-
0025178875
-
Cytogenetics of non-small cell lung cancer: Analysis of consistent non-random abnormalities
-
Lukeis R, Irving L, Garson M, Hasthorpe S (1990) Cytogenetics of non-small cell lung cancer: Analysis of consistent non-random abnormalities. Genes Chromosom Cancer 2:116-124.
-
(1990)
Genes Chromosom Cancer
, vol.2
, pp. 116-124
-
-
Lukeis, R.1
Irving, L.2
Garson, M.3
Hasthorpe, S.4
-
135
-
-
0027373023
-
Chromosome abnormalities in non-small cell lung cancer pleural effusions: Cytogenetic indicators of disease subgroups
-
Lukeis R, Ball D, Irving L, Garson OM, Hasthorpe S (1993) Chromosome abnormalities in non-small cell lung cancer pleural effusions: Cytogenetic indicators of disease subgroups. Genes Chromosom Cancer 8:262-269.
-
(1993)
Genes Chromosom Cancer
, vol.8
, pp. 262-269
-
-
Lukeis, R.1
Ball, D.2
Irving, L.3
Garson, O.M.4
Hasthorpe, S.5
-
136
-
-
0028151489
-
Expression of a RLF/L-MYC minigene inhibits differentiation of embryonic stem cells and embryoid body formation
-
MacLean-Hunter S, Mäkelä TP, Grzeschiczek A, Alitalo K, Möröy T (1994) Expression of a RLF/L-MYC minigene inhibits differentiation of embryonic stem cells and embryoid body formation. Oncogene 9:3509-3517.
-
(1994)
Oncogene
, vol.9
, pp. 3509-3517
-
-
MacLean-Hunter, S.1
Mäkelä, T.P.2
Grzeschiczek, A.3
Alitalo, K.4
Möröy, T.5
-
138
-
-
0025821561
-
A fusion protein formed by L-myc and a novel gene in SCLC
-
Mäkelä TP, Saksela K, Evan G, Alitalo K (1991) A fusion protein formed by L-myc and a novel gene in SCLC. EMBO J 10:1331-1335.
-
(1991)
EMBO J
, vol.10
, pp. 1331-1335
-
-
Mäkelä, T.P.1
Saksela, K.2
Evan, G.3
Alitalo, K.4
-
139
-
-
0028843729
-
Significance of chromosome 1p loss of heterozygosity in neuroblastoma
-
Maris JM, White PS, Beltinger CP, Sulman EP, Castleberry RP, Shuster JJ, Look AT, Brodeur GM (1995) Significance of chromosome 1p loss of heterozygosity in neuroblastoma. Cancer Res. 55:4664-4669.
-
(1995)
Cancer Res.
, vol.55
, pp. 4664-4669
-
-
Maris, J.M.1
White, P.S.2
Beltinger, C.P.3
Sulman, E.P.4
Castleberry, R.P.5
Shuster, J.J.6
Look, A.T.7
Brodeur, G.M.8
-
140
-
-
0025458633
-
Chromosomal abnormalities in human breast cancer
-
Mars WM, Saunders GF (1990) Chromosomal abnormalities in human breast cancer. Cancer Metastasis Rev 9:35-43.
-
(1990)
Cancer Metastasis Rev
, vol.9
, pp. 35-43
-
-
Mars, W.M.1
Saunders, G.F.2
-
141
-
-
0024952186
-
Chromosome 1 deletions in human neuroblastomas: Generation and fine mapping of microclones from the distal 1p region
-
Martinsson T, Weith A, Cziepluch C, Schwab M (1989) Chromosome 1 deletions in human neuroblastomas: Generation and fine mapping of microclones from the distal 1p region. Genes Chromosom Cancer 1:67-78.
-
(1989)
Genes Chromosom Cancer
, vol.1
, pp. 67-78
-
-
Martinsson, T.1
Weith, A.2
Cziepluch, C.3
Schwab, M.4
-
142
-
-
0028853718
-
Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms
-
Martinsson T, Sjöberg R-M, Hedborg F, Kogner P (1995) Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms. Cancer Res 55:5681-5686.
-
(1995)
Cancer Res
, vol.55
, pp. 5681-5686
-
-
Martinsson, T.1
Sjöberg, R.-M.2
Hedborg, F.3
Kogner, P.4
-
143
-
-
0023228919
-
Deletion of genes on chromosome 1 in endocrine neoplasia
-
Mathew CGP, Smith BA, Thorpe K, Wong Z, Royle NJ, Jeffreys AJ, Ponder BAJ (1987) Deletion of genes on chromosome 1 in endocrine neoplasia. Nature 328:524-526.
-
(1987)
Nature
, vol.328
, pp. 524-526
-
-
Mathew, C.G.P.1
Smith, B.A.2
Thorpe, K.3
Wong, Z.4
Royle, N.J.5
Jeffreys, A.J.6
Ponder, B.A.J.7
-
144
-
-
0028046406
-
Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors
-
Mathew S, Murty VWS, Bosl GJ, Chaganti RSK (1994) Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Res 54: 6265-6269.
-
(1994)
Cancer Res
, vol.54
, pp. 6265-6269
-
-
Mathew, S.1
Murty, V.W.S.2
Bosl, G.J.3
Chaganti, R.S.K.4
-
146
-
-
0029153013
-
Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma
-
Mead RS, Cowell JK (1995) Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma. Cancer Genet Cytogenet 81:151-157.
-
(1995)
Cancer Genet Cytogenet
, vol.81
, pp. 151-157
-
-
Mead, R.S.1
Cowell, J.K.2
-
147
-
-
0025643055
-
1p13 is the most frequent involved band in structural chromosomal rearrangements in human breast cancer
-
Mitchell ELD, Santibanez-Koref MF (1990) 1p13 is the most frequent involved band in structural chromosomal rearrangements in human breast cancer. Genes Chromosom Cancer 2:278-289.
-
(1990)
Genes Chromosom Cancer
, vol.2
, pp. 278-289
-
-
Mitchell, E.L.D.1
Santibanez-Koref, M.F.2
-
149
-
-
0021205863
-
A new translocation, t(1;3)(p36;q21), in myelodysplastic disorders
-
Moir DJ, Jones PAE, Pearson J, Duncan JR, Cook P, Buckle VJ (1984) A new translocation, t(1;3)(p36;q21), in myelodysplastic disorders. Blood 64:553-555.
-
(1984)
Blood
, vol.64
, pp. 553-555
-
-
Moir, D.J.1
Jones, P.A.E.2
Pearson, J.3
Duncan, J.R.4
Cook, P.5
Buckle, V.J.6
-
150
-
-
0026548844
-
Consistent association of 1p loss of heterozygosity with Pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes
-
Moley JF, Brother MB, Fong C-T, White PS, Baylin SB, Nelkin B, Wells SA, Brodeur GM (1992) Consistent association of 1p loss of heterozygosity with Pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes. Cancer Res 52:770-774.
-
(1992)
Cancer Res
, vol.52
, pp. 770-774
-
-
Moley, J.F.1
Brother, M.B.2
Fong, C.-T.3
White, P.S.4
Baylin, S.B.5
Nelkin, B.6
Wells, S.A.7
Brodeur, G.M.8
-
151
-
-
0025901088
-
Parameters of the human genome
-
Morton NE (1991) Parameters of the human genome. Proc Natl Acad Sci USA 88:7474-7476.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 7474-7476
-
-
Morton, N.E.1
-
153
-
-
0029061184
-
Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast
-
Munn KE, Walker RA, Varley JM (1995) Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast. Oncogene 10:1653-1657.
-
(1995)
Oncogene
, vol.10
, pp. 1653-1657
-
-
Munn, K.E.1
Walker, R.A.2
Varley, J.M.3
-
154
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density
-
Murray JC, Buetow KH, Weber JL, Ludwigsen S, Sherpbier-Heddema T, et al. (1994) A comprehensive human linkage map with centimorgan density. Science 265:2049-2054.
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Sherpbier-Heddema, T.5
-
155
-
-
0026305958
-
Comparative map for mice and humans
-
Nadeau JH, Davisson MT, Doolittle DP, Grant P, Hillyard AL, Kosowsky M, Roderick TH (1991) Comparative map for mice and humans. Mammalian Genome 1:461-515.
-
(1991)
Mammalian Genome
, vol.1
, pp. 461-515
-
-
Nadeau, J.H.1
Davisson, M.T.2
Doolittle, D.P.3
Grant, P.4
Hillyard, A.L.5
Kosowsky, M.6
Roderick, T.H.7
-
156
-
-
0028918250
-
Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer
-
Nagai H, Negrini M, Carter SL, Gillum DR, Rosenberg AL, Schwartz GF, Croce CM (1995) Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer. Cancer Res 55:1752-1757.
-
(1995)
Cancer Res
, vol.55
, pp. 1752-1757
-
-
Nagai, H.1
Negrini, M.2
Carter, S.L.3
Gillum, D.R.4
Rosenberg, A.L.5
Schwartz, G.F.6
Croce, C.M.7
-
157
-
-
0026580909
-
Exclusion of the familial melanoma locus (MLM) from the PND/D1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees
-
Nancarrow DJ, Palmer JM, Walters MK, Kerr BM, Hafner GJ, Garske L, McLeod GR, Hayward NK (1992) Exclusion of the familial melanoma locus (MLM) from the PND/D1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees. Genomics 12:18-25.
-
(1992)
Genomics
, vol.12
, pp. 18-25
-
-
Nancarrow, D.J.1
Palmer, J.M.2
Walters, M.K.3
Kerr, B.M.4
Hafner, G.J.5
Garske, L.6
McLeod, G.R.7
Hayward, N.K.8
-
158
-
-
0027507837
-
Confirmation of chromosome 9p linkage in familial melanoma
-
Nancarrow DJ, Mann GJ, Holland EA, Walker GJ, Beaton SC, Walters MK, Luxford C, et al. (1993) Confirmation of chromosome 9p linkage in familial melanoma. Am J Hum Genet 53:936-942.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 936-942
-
-
Nancarrow, D.J.1
Mann, G.J.2
Holland, E.A.3
Walker, G.J.4
Beaton, S.C.5
Walters, M.K.6
Luxford, C.7
-
159
-
-
0022392771
-
L-myc, a new myc-related gene amplified and expressed in human small cell lung cancer
-
Nau MM, Brooks BJ, Battney J, Sausville E, Gazdar AF, Kirsch IR, McBride OW, Bertness V, Hollis GF, Minna JD (1985) L-myc, a new myc-related gene amplified and expressed in human small cell lung cancer. Nature 318:69-73.
-
(1985)
Nature
, vol.318
, pp. 69-73
-
-
Nau, M.M.1
Brooks, B.J.2
Battney, J.3
Sausville, E.4
Gazdar, A.F.5
Kirsch, I.R.6
McBride, O.W.7
Bertness, V.8
Hollis, G.F.9
Minna, J.D.10
-
160
-
-
0027410910
-
Anchored reference loci for comparative genome mapping in mammals
-
O'Brien SJ, Womack JE, Lyons LA, Moore KJ, Jenkins NA, Copeland NG (1993) Anchored reference loci for comparative genome mapping in mammals. Nature Genetics 3:103-112.
-
(1993)
Nature Genetics
, vol.3
, pp. 103-112
-
-
O'Brien, S.J.1
Womack, J.E.2
Lyons, L.A.3
Moore, K.J.4
Jenkins, N.A.5
Copeland, N.G.6
-
161
-
-
0024801447
-
Abnormalities of chromosome 1 in relation to human malignant diseases
-
Oláh E, Balogh E, Kovács I, Kiss A (1989) Abnormalities of chromosome 1 in relation to human malignant diseases. Cancer Genet Cytogenet 43:179-194.
-
(1989)
Cancer Genet Cytogenet
, vol.43
, pp. 179-194
-
-
Oláh, E.1
Balogh, E.2
Kovács, I.3
Kiss, A.4
-
162
-
-
0027317609
-
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease Type 2 to chromosome 1p and evidence of genetic heterogeneity
-
Othmane KB, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA, Vance JM (1993) Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease Type 2 to chromosome 1p and evidence of genetic heterogeneity. Genomics 17: 370375.
-
(1993)
Genomics
, vol.17
, pp. 370375
-
-
Othmane, K.B.1
Middleton, L.T.2
Loprest, L.J.3
Wilkinson, K.M.4
Lennon, F.5
Rozear, M.P.6
Stajich, J.M.7
Gaskell, P.C.8
Roses, A.D.9
Pericak-Vance, M.A.10
Vance, J.M.11
-
163
-
-
0025227901
-
Preferential loss of maternal alleles in sporadic Wilms' tumour
-
Pal N, Wadey RB, Buckle B, Yeomans E, Pritchard J, Cowell JK (1990) Preferential loss of maternal alleles in sporadic Wilms' tumour. Oncogene 5:1665-1668.
-
(1990)
Oncogene
, vol.5
, pp. 1665-1668
-
-
Pal, N.1
Wadey, R.B.2
Buckle, B.3
Yeomans, E.4
Pritchard, J.5
Cowell, J.K.6
-
164
-
-
0028948713
-
Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups
-
Pandis N, Jin Y, Gorunova L, Petersson C, Bardi G, Idvall I, Johansson B, Ingvar C, Mandahl N, Mitelman F, Heim S (1995) Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups. Genes Chromosom Cancer 12:173-185.
-
(1995)
Genes Chromosom Cancer
, vol.12
, pp. 173-185
-
-
Pandis, N.1
Jin, Y.2
Gorunova, L.3
Petersson, C.4
Bardi, G.5
Idvall, I.6
Johansson, B.7
Ingvar, C.8
Mandahl, N.9
Mitelman, F.10
Heim, S.11
-
166
-
-
0026744941
-
PCR assay for chromosome 1p deletion in small neuroblastoma samples
-
Peter M, Michon J, Viehl P, Neuenschwander S, Nakamura Y, Sonsino E, Zucker JM, Vergnaud G, Thomas G, Delattre O (1992) PCR assay for chromosome 1p deletion in small neuroblastoma samples. Int J Cancer 52:544-548.
-
(1992)
Int J Cancer
, vol.52
, pp. 544-548
-
-
Peter, M.1
Michon, J.2
Viehl, P.3
Neuenschwander, S.4
Nakamura, Y.5
Sonsino, E.6
Zucker, J.M.7
Vergnaud, G.8
Thomas, G.9
Delattre, O.10
-
167
-
-
0028139010
-
Genetic basis of susceptibility to melanoma
-
Piepkorn MW (1994) Genetic basis of susceptibility to melanoma. J Am Acad Dermatol 31:1022-1039.
-
(1994)
J Am Acad Dermatol
, vol.31
, pp. 1022-1039
-
-
Piepkorn, M.W.1
-
168
-
-
0028788862
-
Deletion mapping defines different regions in 1p34.2-pter that may harbor genetic information related to human colorectal cancer
-
Praml C, Finke LH, Herfarth C, Schlag P, Schwab M, Amler L (1995a) Deletion mapping defines different regions in 1p34.2-pter that may harbor genetic information related to human colorectal cancer. Oncogene 11:1357-1362.
-
(1995)
Oncogene
, vol.11
, pp. 1357-1362
-
-
Praml, C.1
Finke, L.H.2
Herfarth, C.3
Schlag, P.4
Schwab, M.5
Amler, L.6
-
169
-
-
0028863895
-
The human homolog of a candidate for the Mom1 Locus, the Secretory Type II Phospholipase A2 (PLA2S-II), maps to 1p35-1p36. 1/D1S199
-
Praml C, Savelyeva L, Le Paslier D, Siracusa LD, Buchberg AM, Schwab M, Amler LC (1995b) The human homolog of a candidate for the Mom1 Locus, the Secretory Type II Phospholipase A2 (PLA2S-II), maps to 1p35-1p36. 1/D1S199. Cancer Res 55:5504-5506.
-
(1995)
Cancer Res
, vol.55
, pp. 5504-5506
-
-
Praml, C.1
Savelyeva, L.2
Le Paslier, D.3
Siracusa, L.D.4
Buchberg, A.M.5
Schwab, M.6
Amler, L.C.7
-
170
-
-
0025984266
-
Translocations, master genes, and differences between the origins of acute and chronic leukemias
-
Rabbitts TH (1991) Translocations, master genes, and differences between the origins of acute and chronic leukemias. Cell 67:641-644.
-
(1991)
Cell
, vol.67
, pp. 641-644
-
-
Rabbitts, T.H.1
-
171
-
-
0025914808
-
New recurring chromosomal translocations in childhood acute lymphoblastic leukemia
-
Raimondi SC, Privitera E, Williams DL, Look AT, Behm F, Rivera GK, Crist WM, PUI CH (1991) New recurring chromosomal translocations in childhood acute lymphoblastic leukemia. Blood 77:2016-2021.
-
(1991)
Blood
, vol.77
, pp. 2016-2021
-
-
Raimondi, S.C.1
Privitera, E.2
Williams, D.L.3
Look, A.T.4
Behm, F.5
Rivera, G.K.6
Crist, W.M.7
Pui, C.H.8
-
172
-
-
0028006633
-
Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p
-
Reifenberger J, Reifenberger G, Liu L, James CD, Wechsler W, Collins VP (1994) Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. Am J Path 145:1175-1190.
-
(1994)
Am J Path
, vol.145
, pp. 1175-1190
-
-
Reifenberger, J.1
Reifenberger, G.2
Liu, L.3
James, C.D.4
Wechsler, W.5
Collins, V.P.6
-
173
-
-
0028861983
-
Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome
-
Reish O, Berry S, Hirsch B (1995) Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome. Am J Med Genet 59:467-475.
-
(1995)
Am J Med Genet
, vol.59
, pp. 467-475
-
-
Reish, O.1
Berry, S.2
Hirsch, B.3
-
175
-
-
0024465781
-
Molecular analysis of chromosome 1 abnormalities in neuroblastoma
-
Ritke MK, Shah R, Valentine M, Douglass EC, Tereba A (1989) Molecular analysis of chromosome 1 abnormalities in neuroblastoma. Cytogenet Cell Genet 50:84-90.
-
(1989)
Cytogenet Cell Genet
, vol.50
, pp. 84-90
-
-
Ritke, M.K.1
Shah, R.2
Valentine, M.3
Douglass, E.C.4
Tereba, A.5
-
176
-
-
0028981328
-
Scl, a gene frequently activated in human T cell leukaemia, does not induce lymphomas in transgenic mice
-
Robb L, Rasko JEJ, Bath ML, Strasser A, Begley CG (1995) scl, a gene frequently activated in human T cell leukaemia, does not induce lymphomas in transgenic mice. Oncogene 10:205-209.
-
(1995)
Oncogene
, vol.10
, pp. 205-209
-
-
Robb, L.1
Rasko, J.E.J.2
Bath, M.L.3
Strasser, A.4
Begley, C.G.5
-
177
-
-
0017735005
-
Mapping of human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17
-
Rowley JD (1977) Mapping of human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17. Proc Natl Acad Sci USA 74:5729-5733.
-
(1977)
Proc Natl Acad Sci USA
, vol.74
, pp. 5729-5733
-
-
Rowley, J.D.1
-
178
-
-
0028023048
-
Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells
-
Savelyeva L, Corvi R, Schwab M (1994) Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells. Am J Hum Genet 55:334-340.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 334-340
-
-
Savelyeva, L.1
Corvi, R.2
Schwab, M.3
-
179
-
-
0021203960
-
Translocation 1;7 in dyshematopoiesis: Possibly induced with a non-random geographic distribution
-
Scheres JMJC, Hustinx TWJ, Holdrinet RSG, Geraedts JPM, Hagemeijer A, van der Blij-Philipsen M (1984) Translocation 1;7 in dyshematopoiesis: Possibly induced with a non-random geographic distribution. Cancer Genet Cytogenet 12:283-294.
-
(1984)
Cancer Genet Cytogenet
, vol.12
, pp. 283-294
-
-
Scheres, J.M.J.C.1
Hustinx, T.W.J.2
Holdrinet, R.S.G.3
Geraedts, J.P.M.4
Hagemeijer, A.5
Van Der Blij-Philipsen, M.6
-
180
-
-
0028067338
-
Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma
-
Schleiermacher G, Peter M, Michon J, Hugot J-P, Vielh P, Zucker J-M, Magdelénat H, Thomas G, Delattre O (1994) Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma. Genes Chromosom Cancer 10:275-281.
-
(1994)
Genes Chromosom Cancer
, vol.10
, pp. 275-281
-
-
Schleiermacher, G.1
Peter, M.2
Michon, J.3
Hugot, J.-P.4
Vielh, P.5
Zucker, J.-M.6
Magdelénat, H.7
Thomas, G.8
Delattre, O.9
-
181
-
-
9544241739
-
Clinical relevance of deletion of the short arm of chromosome 1 in neuroblastoma: A single institution study
-
in press
-
Schleiermacher G, Delattre O, Peter M, Mosseri V, Delonlay P, Thomas G, Zucker J-M, Magdelénat H, Michon J (1995) Clinical relevance of deletion of the short arm of chromosome 1 in neuroblastoma: A single institution study. Int J Oncol (in press).
-
(1995)
Int J Oncol
-
-
Schleiermacher, G.1
Delattre, O.2
Peter, M.3
Mosseri, V.4
Delonlay, P.5
Thomas, G.6
Zucker, J.-M.7
Magdelénat, H.8
Michon, J.9
-
182
-
-
0023256838
-
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors
-
Schroeder WT, Chao L-Y, Dao DD, Strong LC, Pathak S, Riccardi V, Lewis WH, Saunders GF (1987) Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors. Am J Hum Genet 40: 413-420.
-
(1987)
Am J Hum Genet
, vol.40
, pp. 413-420
-
-
Schroeder, W.T.1
Chao, L.-Y.2
Dao, D.D.3
Strong, L.C.4
Pathak, S.5
Riccardi, V.6
Lewis, W.H.7
Saunders, G.F.8
-
183
-
-
0025986106
-
Is there a neuroblastoma anti-oncogene? Advances in Neuroblastoma Research 3
-
Evans AE, D'Angio GJ, Knudson Jr AG, Seeger RC (eds): New York: Wiley-Liss
-
Schwab M (1991) Is there a neuroblastoma anti-oncogene? Advances in Neuroblastoma Research 3 in Evans AE, D'Angio GJ, Knudson Jr AG, Seeger RC (eds): Progress in clinical and biological research. Volume 366. New York: Wiley-Liss, pp. 1-9.
-
(1991)
Progress in Clinical and Biological Research
, vol.366
, pp. 1-9
-
-
Schwab, M.1
-
184
-
-
0024226877
-
Sustained expression of the human protooncogene MYCN rescues rat embryo cells from senescence
-
Schwab M, Bishop JM (1988) Sustained expression of the human protooncogene MYCN rescues rat embryo cells from senescence. Proc Natl Acad Sci USA 85:9585-9589.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 9585-9589
-
-
Schwab, M.1
Bishop, J.M.2
-
185
-
-
0029109403
-
Genetics, cellular biology and clinical management of human neuroblastoma
-
Oxford: Pergamon
-
Schwab M, Pearson A (1995) Special Issue: Europ J Cancer 31A: Genetics, cellular biology and clinical management of human neuroblastoma. Oxford: Pergamon.
-
(1995)
Europ J Cancer
, vol.31 A
, Issue.SPEC. ISSUE
-
-
Schwab, M.1
Pearson, A.2
-
186
-
-
0021063273
-
Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour
-
Schwab M, Alitalo K, Klempnauer K-H, Varmus HE, Bishop JM, Gilbert F, Brodeur G, Goldstein M, Trent J (1983) Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour. Nature 305:245-248.
-
(1983)
Nature
, vol.305
, pp. 245-248
-
-
Schwab, M.1
Alitalo, K.2
Klempnauer, K.-H.3
Varmus, H.E.4
Bishop, J.M.5
Gilbert, F.6
Brodeur, G.7
Goldstein, M.8
Trent, J.9
-
187
-
-
0013288537
-
Enhanced expression of the human N-myc gene consequent co amplification of DNA may contribute to malignant progression of neuroblastoma
-
Schwab M, Ellison JE, Busch M, Rosenau W, Varmus HE, Bishop JM (1984) Enhanced expression of the human N-myc gene consequent co amplification of DNA may contribute to malignant progression of neuroblastoma. Proc Natl Acad Sci USA 81:4940-4944.
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 4940-4944
-
-
Schwab, M.1
Ellison, J.E.2
Busch, M.3
Rosenau, W.4
Varmus, H.E.5
Bishop, J.M.6
-
188
-
-
0021800964
-
Human N-may gene contributes to neoplastic transformation of mammalian cells in-culture
-
Schwab M, Varmus HE, Bishop JM (1985) Human N-may gene contributes to neoplastic transformation of mammalian cells in-culture. Nature 316:160-162.
-
(1985)
Nature
, vol.316
, pp. 160-162
-
-
Schwab, M.1
Varmus, H.E.2
Bishop, J.M.3
-
189
-
-
84991167446
-
Genetic alterations in colorectal cancers in correlation to clinical parameters
-
Utsunomiya J, Lynch HT (eds) Tokyo, Springer-Verlag
-
Schwab M, Brüderlein S, van der Bosch K, Weith A, Leister I, Cziepluch C, Amler L, Schlag P (1990) Genetic alterations in colorectal cancers in correlation to clinical parameters. In: Utsunomiya J, Lynch HT (eds) Hereditary colorectal cancer. Tokyo, Springer-Verlag, pp 509-516.
-
(1990)
Hereditary Colorectal Cancer
, pp. 509-516
-
-
Schwab, M.1
Brüderlein, S.2
Van Der Bosch, K.3
Weith, A.4
Leister, I.5
Cziepluch, C.6
Amler, L.7
Schlag, P.8
-
190
-
-
84970417670
-
N-MYC oncogene amplification: A consequence of genomic instability in human neuroblastoma
-
Schwab M, Corvi R, Amler LC (1995) N-MYC oncogene amplification: A consequence of genomic instability in human neuroblastoma. The Neuroscientist 1:277-285.
-
(1995)
The Neuroscientist
, vol.1
, pp. 277-285
-
-
Schwab, M.1
Corvi, R.2
Amler, L.C.3
-
191
-
-
0024310196
-
Amplification of protooncogenes in surgical specimens of human lung carcinomas
-
Shirashi M, Noguchi M, Shimosato Y, Sekiya T (1989) Amplification of protooncogenes in surgical specimens of human lung carcinomas. Cancer Res 49:6474-6479.
-
(1989)
Cancer Res
, vol.49
, pp. 6474-6479
-
-
Shirashi, M.1
Noguchi, M.2
Shimosato, Y.3
Sekiya, T.4
-
194
-
-
0025801654
-
Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas
-
Simon D, Knowles BB, Weith A (1991) Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas. Oncogene 6:765-770.
-
(1991)
Oncogene
, vol.6
, pp. 765-770
-
-
Simon, D.1
Knowles, B.B.2
Weith, A.3
-
195
-
-
0023854206
-
Cytogenetic studies in primary and metastatic neuroendocrine Merkel cell carcinoma
-
Sozzi G, Bertoglio MG, Pilotti S, Rilke F, Pierotti MA, Della Porta G (1988) Cytogenetic studies in primary and metastatic neuroendocrine Merkel cell carcinoma. Cancer Genet Cytogenet 30:151-158.
-
(1988)
Cancer Genet Cytogenet
, vol.30
, pp. 151-158
-
-
Sozzi, G.1
Bertoglio, M.G.2
Pilotti, S.3
Rilke, F.4
Pierotti, M.A.5
Della Porta, G.6
-
196
-
-
0030064510
-
2 genes that map to human chromosome 1p35-36 are not mutated in individuals with attenuated adenomatous polyposis coli
-
2 genes that map to human chromosome 1p35-36 are not mutated in individuals with attenuated adenomatous polyposis coli. Cancer Res 56:955-958.
-
(1996)
Cancer Res
, vol.56
, pp. 955-958
-
-
Spirio, L.N.1
Kutchera, W.2
Winstead, M.V.3
-
197
-
-
0023810844
-
Chromosome 1 abnormalities in cervical carcinoma
-
Sreekantaiah C, Bhargava MK, Shetty NJ (1988) Chromosome 1 abnormalities in cervical carcinoma. Cancer 62:1317-1324.
-
(1988)
Cancer
, vol.62
, pp. 1317-1324
-
-
Sreekantaiah, C.1
Bhargava, M.K.2
Shetty, N.J.3
-
199
-
-
0025130536
-
Mapping the human genome: Current status
-
Stephens JC, Cavanaugh ML, Gradie MI, Mador ML, Kidd KK (1990) Mapping the human genome: Current status. Science 250: 237-244.
-
(1990)
Science
, vol.250
, pp. 237-244
-
-
Stephens, J.C.1
Cavanaugh, M.L.2
Gradie, M.I.3
Mador, M.L.4
Kidd, K.K.5
-
200
-
-
0021905415
-
Identification of a single chromosome in the normal human genome essential for suppression of hamster cell transformation
-
Stoler A, Bouck N (1985) Identification of a single chromosome in the normal human genome essential for suppression of hamster cell transformation. Proc Natl Acad Sci USA 82:570-574.
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 570-574
-
-
Stoler, A.1
Bouck, N.2
-
201
-
-
0025020081
-
Induction of cellular senescence in immortalized cells by human chromosome 1
-
Sugawara O, Oshimura M, Koi M, Annab LA, Barrett JC (1990) Induction of cellular senescence in immortalized cells by human chromosome 1. Science 247:707-710.
-
(1990)
Science
, vol.247
, pp. 707-710
-
-
Sugawara, O.1
Oshimura, M.2
Koi, M.3
Annab, L.A.4
Barrett, J.C.5
-
202
-
-
0026457950
-
Multistep carcinogenesis: A 1992 perspective
-
Sugimura T (1992) Multistep carcinogenesis: A 1992 perspective. Science 258:603-607.
-
(1992)
Science
, vol.258
, pp. 603-607
-
-
Sugimura, T.1
-
203
-
-
0024581779
-
Frequent loss of heterozygosity on chromosome 14q in neuroblastoma
-
Suzuki T, Yokota J, Mugishima H, Okabe I, Ookuni M, Sugimura T, Terada M (1989) Frequent loss of heterozygosity on chromosome 14q in neuroblastoma. Cancer Res 49:1095-1098.
-
(1989)
Cancer Res
, vol.49
, pp. 1095-1098
-
-
Suzuki, T.1
Yokota, J.2
Mugishima, H.3
Okabe, I.4
Ookuni, M.5
Sugimura, T.6
Terada, M.7
-
204
-
-
0025310254
-
Assignment of 12 loci to rat chromosome 5: Evidence that this chromosome is homologous to mouse chromosome 4 and to human chromosomes 9 and 1 (1p arm)
-
Szpirer C, Rivière M, Szpirer, Genet M, Drèze P, Islam MQ, Levan G (1990) Assignment of 12 loci to rat chromosome 5: Evidence that this chromosome is homologous to mouse chromosome 4 and to human chromosomes 9 and 1 (1p arm). Genomics 6:679-684.
-
(1990)
Genomics
, vol.6
, pp. 679-684
-
-
Szpirer, C.1
Rivière, M.2
Szpirer3
Genet, M.4
Drèze, P.5
Islam, M.Q.6
Levan, G.7
-
205
-
-
0027853058
-
Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q, and 9p in human malignant mesothelioma
-
Taguchi T, Jhanwar SC, Siegfried JM, Keller SM, Testa JR (1993) Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q, and 9p in human malignant mesothelioma. Cancer Res 53:4349-4355.
-
(1993)
Cancer Res
, vol.53
, pp. 4349-4355
-
-
Taguchi, T.1
Jhanwar, S.C.2
Siegfried, J.M.3
Keller, S.M.4
Testa, J.R.5
-
206
-
-
0026612493
-
Deletion mapping of chromosomes 14q and 1p in human neuroblastoma
-
Takayama H, Suzuki T, Mugishima H, Fujisawa T, Ookuni M, Schwab M, Gehring M, Nakamura Y, Sugimura T, Terada M, Yokota J (1992) Deletion mapping of chromosomes 14q and 1p in human neuroblastoma. Oncogene 7:1185-1189.
-
(1992)
Oncogene
, vol.7
, pp. 1185-1189
-
-
Takayama, H.1
Suzuki, T.2
Mugishima, H.3
Fujisawa, T.4
Ookuni, M.5
Schwab, M.6
Gehring, M.7
Nakamura, Y.8
Sugimura, T.9
Terada, M.10
Yokota, J.11
-
207
-
-
0028258815
-
There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma
-
Takeda O, Homma C, Maseki N, Sakurai M, Kanda N, Schwab M, Nakamura Y, Kaneko Y (1994) There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma. Genes Chromosom Cancer 10:30-39.
-
(1994)
Genes Chromosom Cancer
, vol.10
, pp. 30-39
-
-
Takeda, O.1
Homma, C.2
Maseki, N.3
Sakurai, M.4
Kanda, N.5
Schwab, M.6
Nakamura, Y.7
Kaneko, Y.8
-
208
-
-
0027171533
-
Suppression of tumourigenicity in human colon carcinoma cells by introduction of normal chromosome 1p36 region
-
Tanaka K, Yanoshita R, Konishi M, Oshimura M, Maeda Y, Mori T, Miyaki M (1993) Suppression of tumourigenicity in human colon carcinoma cells by introduction of normal chromosome 1p36 region. Oncogene 8:2253-2258.
-
(1993)
Oncogene
, vol.8
, pp. 2253-2258
-
-
Tanaka, K.1
Yanoshita, R.2
Konishi, M.3
Oshimura, M.4
Maeda, Y.5
Mori, T.6
Miyaki, M.7
-
209
-
-
0028267297
-
Rapid detection of prognostic genetic factors in neuroblastoma using fluorescene in situ hybridization on tumour imprints and bone marrow smears
-
Taylor CPF, McGuckin AG, Bown NP, Reid MM, Malcolm AJ, Pearson ADJ, Sheer D (1994) Rapid detection of prognostic genetic factors in neuroblastoma using fluorescene in situ hybridization on tumour imprints and bone marrow smears. Br J Cancer 69:445-451.
-
(1994)
Br J Cancer
, vol.69
, pp. 445-451
-
-
Taylor, C.P.F.1
McGuckin, A.G.2
Bown, N.P.3
Reid, M.M.4
Malcolm, A.J.5
Pearson, A.D.J.6
Sheer, D.7
-
210
-
-
0025134850
-
Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma
-
Tsuda H, Zhang W, Shimosato Y, Yokota J, Terada M, Sugimura T, Miyamura T, Hirohashi S (1990) Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma. Proc Natl Acad Sci USA 87:6791-6794.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6791-6794
-
-
Tsuda, H.1
Zhang, W.2
Shimosato, Y.3
Yokota, J.4
Terada, M.5
Sugimura, T.6
Miyamura, T.7
Hirohashi, S.8
-
211
-
-
0024561222
-
Loss of heterozygosity on chromosomes 1p and 11p in sporadic Pheochromocytoma
-
Tsutsumi M, Yokota J, Kakizoe T, Koiso K, Sugimura T, Terada M (1989) Loss of heterozygosity on chromosomes 1p and 11p in sporadic Pheochromocytoma. J Nat Cancer Inst 81:367-370.
-
(1989)
J Nat Cancer Inst
, vol.81
, pp. 367-370
-
-
Tsutsumi, M.1
Yokota, J.2
Kakizoe, T.3
Koiso, K.4
Sugimura, T.5
Terada, M.6
-
212
-
-
0025950015
-
Chromosomal translocations joining LCK and TCRB loci in human T cell leukemia
-
Tycko B, Smith SD, Sklar J (1991) Chromosomal translocations joining LCK and TCRB loci in human T cell leukemia. J Exp Med 174:867-873.
-
(1991)
J Exp Med
, vol.174
, pp. 867-873
-
-
Tycko, B.1
Smith, S.D.2
Sklar, J.3
-
213
-
-
0029166212
-
Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36
-
van der Drift P, Chan A, Laureys G, van Roy N, Sickmann G, den Dunnen J, Westerveld A, Speleman F, Versteeg R (1995) Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36. Genes Chromosom Cancer 14:35-42.
-
(1995)
Genes Chromosom Cancer
, vol.14
, pp. 35-42
-
-
Van Der Drift, P.1
Chan, A.2
Laureys, G.3
Van Roy, N.4
Sickmann, G.5
Den Dunnen, J.6
Westerveld, A.7
Speleman, F.8
Versteeg, R.9
-
214
-
-
0024693775
-
Exclusion of the dysplastic naevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families
-
van Haeringen A, Bergman W, Nelen MR, van der Kooij-Meijs E, Hendriksen I, Wijnen JT, Khan PM, Klasen EC, Frants RR (1989) Exclusion of the dysplastic naevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families. Genomics 5:61-64.
-
(1989)
Genomics
, vol.5
, pp. 61-64
-
-
Van Haeringen, A.1
Bergman, W.2
Nelen, M.R.3
Van Der Kooij-Meijs, E.4
Hendriksen, I.5
Wijnen, J.T.6
Khan, P.M.7
Klasen, E.C.8
Frants, R.R.9
-
215
-
-
0027484115
-
High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1
-
van Roy N, Laureys G, Versteeg R, Opdenakker G, Speleman F (1993) High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1. Genomics 18:71-78.
-
(1993)
Genomics
, vol.18
, pp. 71-78
-
-
Van Roy, N.1
Laureys, G.2
Versteeg, R.3
Opdenakker, G.4
Speleman, F.5
-
216
-
-
0029030524
-
1p36: Every subband a suppressor?
-
Versteeg R, Caron H, Cheng NC, van der Drift P, Slater R, Westerveld A, Voûte PA, Delattre O, Laureys G, Van Roy N, Speleman F (1995) 1p36: Every subband a suppressor? Europ J Cancer 31A:538-541.
-
(1995)
Europ J Cancer
, vol.31 A
, pp. 538-541
-
-
Versteeg, R.1
Caron, H.2
Cheng, N.C.3
Van Der Drift, P.4
Slater, R.5
Westerveld, A.6
Voûte, P.A.7
Delattre, O.8
Laureys, G.9
Van Roy, N.10
Speleman, F.11
-
217
-
-
0024514647
-
Allelotype of colorectal carcinomas
-
Vogelstein B, Fearon ER, Kern SE, Hamilton SR, Preisinger AC, Nakamura Y, White R (1989) Allelotype of colorectal carcinomas. Science 244:207-211.
-
(1989)
Science
, vol.244
, pp. 207-211
-
-
Vogelstein, B.1
Fearon, E.R.2
Kern, S.E.3
Hamilton, S.R.4
Preisinger, A.C.5
Nakamura, Y.6
White, R.7
-
219
-
-
0018844895
-
Nonrandom abnormalities in chromosome 1 in human testicular cancers
-
Wang N, Trend B, Bronson D, Fraley EE (1980) Nonrandom abnormalities in chromosome 1 in human testicular cancers. Cancer Res 40:796-802.
-
(1980)
Cancer Res
, vol.40
, pp. 796-802
-
-
Wang, N.1
Trend, B.2
Bronson, D.3
Fraley, E.E.4
-
220
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M (1992) A second-generation linkage map of the human genome. Nature 359:794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
221
-
-
0024887501
-
Neuroblastoma consensus deletion maps to 1p36.1-2
-
Weith A, Martinsson T, Cziepluch C, Brüderlein S, Amler LC, Berthold F, Schwab M (1989) Neuroblastoma consensus deletion maps to 1p36.1-2. Genes Chromosom Cancer 1:159-166.
-
(1989)
Genes Chromosom Cancer
, vol.1
, pp. 159-166
-
-
Weith, A.1
Martinsson, T.2
Cziepluch, C.3
Brüderlein, S.4
Amler, L.C.5
Berthold, F.6
Schwab, M.7
-
222
-
-
0023513865
-
Diagnostic and prognostic significance of t(1;3)(p36;p21) in the disorders of hematopoiesis
-
Welborn JL, Lewis JP, Jenks H, Walling P (1987) Diagnostic and prognostic significance of t(1;3)(p36;p21) in the disorders of hematopoiesis. Cancer Genet Cytogenet 28:277-285.
-
(1987)
Cancer Genet Cytogenet
, vol.28
, pp. 277-285
-
-
Welborn, J.L.1
Lewis, J.P.2
Jenks, H.3
Walling, P.4
-
223
-
-
0027151846
-
Use of the single-strand conformation polymorphism technique to detect loss of heterozygosity in neuroblastoma
-
White PS, Kaufman BA, Marshall HN, Brodeur GM (1993) Use of the single-strand conformation polymorphism technique to detect loss of heterozygosity in neuroblastoma. Genes Chromosom Cancer 7:102-108.
-
(1993)
Genes Chromosom Cancer
, vol.7
, pp. 102-108
-
-
White, P.S.1
Kaufman, B.A.2
Marshall, H.N.3
Brodeur, G.M.4
-
224
-
-
0029049717
-
A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3
-
White PS, Maris JM, Beltinger C, Sulman E, Marshall HN, Fujimori M, Kaufman BA, Biegel JA, Allen C, Hilliard C, Valentine MB, Look AT, Enomoto H, Sakiyama S, Brodeur GM (1995) A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3. Proc Natl Acad Sci USA 92:5520-5524.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 5520-5524
-
-
White, P.S.1
Maris, J.M.2
Beltinger, C.3
Sulman, E.4
Marshall, H.N.5
Fujimori, M.6
Kaufman, B.A.7
Biegel, J.A.8
Allen, C.9
Hilliard, C.10
Valentine, M.B.11
Look, A.T.12
Enomoto, H.13
Sakiyama, S.14
Brodeur, G.M.15
-
225
-
-
0027501967
-
Molecular events including p53 and k-ras alterations in the in vitro progression of a human colorectal adenoma cell line to an adenocarcinoma
-
Williams AC, Browne SJ, Yeudal WA, Paterson IC, Marshall CJ, Lane DP, Paraskeva C (1993) Molecular events including p53 and k-ras alterations in the in vitro progression of a human colorectal adenoma cell line to an adenocarcinoma. Oncogene 8:3063-3072.
-
(1993)
Oncogene
, vol.8
, pp. 3063-3072
-
-
Williams, A.C.1
Browne, S.J.2
Yeudal, W.A.3
Paterson, I.C.4
Marshall, C.J.5
Lane, D.P.6
Paraskeva, C.7
-
226
-
-
0028372205
-
A rat genetic linkage map and comparative maps for mouse or human homologous rat genes
-
Yamada J, Kuramoto T, Serikawa S (1994) A rat genetic linkage map and comparative maps for mouse or human homologous rat genes. Mammalian Genome 5:63-83.
-
(1994)
Mammalian Genome
, vol.5
, pp. 63-83
-
-
Yamada, J.1
Kuramoto, T.2
Serikawa, S.3
-
227
-
-
0025284307
-
Deletion mapping on the distal third region of chromosome 1p in multiple endocrine neoplasia type IIa
-
Yang K-P, Nguyen CV, Castillo SG, Samaan NA (1990) Deletion mapping on the distal third region of chromosome 1p in multiple endocrine neoplasia type IIa. Anticancer Res 10:527-534.
-
(1990)
Anticancer Res
, vol.10
, pp. 527-534
-
-
Yang, K.-P.1
Nguyen, C.V.2
Castillo, S.G.3
Samaan, N.A.4
-
228
-
-
0028111570
-
Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas
-
Yeh S-H, Chen P-J, Chen H-L, Lai M-Y, Wang C-C, Chen D-S (1994) Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res 54: 4188-4192.
-
(1994)
Cancer Res
, vol.54
, pp. 4188-4192
-
-
Yeh, S.-H.1
Chen, P.-J.2
Chen, H.-L.3
Lai, M.-Y.4
Wang, C.-C.5
Chen, D.-S.6
-
229
-
-
0026544198
-
Loss of heterozygosity at the human RAP1A/Krev-1 locus is a rare event in colorectal tumors
-
Young J, Searle J, Stitz R, Cowen A, Ward M, Chenevix-Trench G (1992) Loss of heterozygosity at the human RAP1A/Krev-1 locus is a rare event in colorectal tumors. Cancer Res 52:285-289.
-
(1992)
Cancer Res
, vol.52
, pp. 285-289
-
-
Young, J.1
Searle, J.2
Stitz, R.3
Cowen, A.4
Ward, M.5
Chenevix-Trench, G.6
-
230
-
-
0028215339
-
Association of the SS genotype of the L-myc gene and loss of 18q sequences with a worse clinical prognosis in colorectal cancers
-
Young J, Buttenshaw R, Butterworth L, Ward M, Searle J, Leggett B, Chenevix-Trench G (1994) Association of the SS genotype of the L-myc gene and loss of 18q sequences with a worse clinical prognosis in colorectal cancers. Oncogene 9:1053-1056.
-
(1994)
Oncogene
, vol.9
, pp. 1053-1056
-
-
Young, J.1
Buttenshaw, R.2
Butterworth, L.3
Ward, M.4
Searle, J.5
Leggett, B.6
Chenevix-Trench, G.7
-
231
-
-
0021690129
-
Constitutive fragile sites and cancer
-
Yunis JJ, Soreng AL (1984) Constitutive fragile sites and cancer. Science 226:1199-1204.
-
(1984)
Science
, vol.226
, pp. 1199-1204
-
-
Yunis, J.J.1
Soreng, A.L.2
|