-
1
-
-
0030043446
-
Cancer statistics, 1996
-
Parker S L, Tong T, Bolden S, Wingo P A. Cancer statistics, 1996. CA Cancer J Clin. 65:1995;5-27.
-
(1995)
CA Cancer J Clin
, vol.65
, pp. 5-27
-
-
Parker, S.L.1
Tong, T.2
Bolden, S.3
Wingo, P.A.4
-
3
-
-
0029029912
-
Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112
-
Yong W H, Chou D, Ueki K, Harsh G R, vonDeimling A, Gusella J F, Mohrenweiser H W, Lewis D N. Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112. J Neuropathol Exp Neurol. 54:1995;622-626.
-
(1995)
J Neuropathol Exp Neurol
, vol.54
, pp. 622-626
-
-
Yong, W.H.1
Chou, D.2
Ueki, K.3
Harsh, G.R.4
VonDeimling, A.5
Gusella, J.F.6
Mohrenweiser, H.W.7
Lewis, D.N.8
-
4
-
-
0027269573
-
Human epithelial ovarian cancer allelotype
-
Cliby W, Ritland S, Hartmann L, Dodson M, Halling K C, Keeney G, Podratz K C, Jenkins R B. Human epithelial ovarian cancer allelotype. Cancer Res. 53:1993;2393-2398.
-
(1993)
Cancer Res
, vol.53
, pp. 2393-2398
-
-
Cliby, W.1
Ritland, S.2
Hartmann, L.3
Dodson, M.4
Halling, K.C.5
Keeney, G.6
Podratz, K.C.7
Jenkins, R.B.8
-
6
-
-
0028207637
-
Polymerase chain reaction allelotyping of human ovarian cancer
-
Osborne R J, Leech V. Polymerase chain reaction allelotyping of human ovarian cancer. Br J Cancer. 69:1994;429-439.
-
(1994)
Br J Cancer
, vol.69
, pp. 429-439
-
-
Osborne, R.J.1
Leech, V.2
-
7
-
-
0027772394
-
Cytogenetic studies of epithelial ovarian carcinoma
-
Jenkins R B, Bartelt D Jr, Stalboerger P, Persons D, Dahl R J, Podartz K, Keeney G, Hartmann L. Cytogenetic studies of epithelial ovarian carcinoma. Cancer Genet Cytogenet. 71:1993;76-86.
-
(1993)
Cancer Genet Cytogenet
, vol.71
, pp. 76-86
-
-
Jenkins, R.B.1
Bartelt D., Jr.2
Stalboerger, P.3
Persons, D.4
Dahl, R.J.5
Podartz, K.6
Keeney, G.7
Hartmann, L.8
-
8
-
-
0026727299
-
Molecular genetic changes in human epithelial ovarian malignancies
-
Gallion H H, Powell D E, Morrow J K, Pieretti M, Case E, Turker M S, DePriest P D, Hunter J E, van Nagell J R Jr. Molecular genetic changes in human epithelial ovarian malignancies. Gynecol Oncol. 47:1992;137-142.
-
(1992)
Gynecol Oncol
, vol.47
, pp. 137-142
-
-
Gallion, H.H.1
Powell, D.E.2
Morrow, J.K.3
Pieretti, M.4
Case, E.5
Turker, M.S.6
DePriest, P.D.7
Hunter, J.E.8
Van Nagell J.R., Jr.9
-
10
-
-
0028946062
-
Malignant and nonmalignant brain tissues differ in their messenger RNA expression patterns for ERCC1 and ERCC2
-
Dabholkar M D, Berger M S, Vionnet J A, Egwuagu C, Silber J R, Yu J J, Reed E. Malignant and nonmalignant brain tissues differ in their messenger RNA expression patterns for ERCC1 and ERCC2. Cancer Res. 55:1995;1-6.
-
(1995)
Cancer Res
, vol.55
, pp. 1-6
-
-
Dabholkar, M.D.1
Berger, M.S.2
Vionnet, J.A.3
Egwuagu, C.4
Silber, J.R.5
Yu, J.J.6
Reed, E.7
-
11
-
-
0028863261
-
Genomic copy number changes of DNA repair genes ERCC1 and ERCC2 in human gliomas
-
Liang B C, Ross D A, Reed E. Genomic copy number changes of DNA repair genes ERCC1 and ERCC2 in human gliomas. J Neuro-Oncol. 26:1995;17-23.
-
(1995)
J Neuro-Oncol
, vol.26
, pp. 17-23
-
-
Liang, B.C.1
Ross, D.A.2
Reed, E.3
-
12
-
-
17444437679
-
Amplification of 19q13.1-q13.2 sequences in ovarian cancer
-
Thompson F H, Nelson M A, Trent J M, Guan X, Liu Y, Yang J, Emerson J, Adair L, Wymer J, Balfour C, Massey K, Weinstein R, Alberts D S, Teatle R. Amplification of 19q13.1-q13.2 sequences in ovarian cancer. Cancer Genet Cytogenet. 87:1996;55-62.
-
(1996)
Cancer Genet Cytogenet
, vol.87
, pp. 55-62
-
-
Thompson, F.H.1
Nelson, M.A.2
Trent, J.M.3
Guan, X.4
Liu, Y.5
Yang, J.6
Emerson, J.7
Adair, L.8
Wymer, J.9
Balfour, C.10
Massey, K.11
Weinstein, R.12
Alberts, D.S.13
Teatle, R.14
-
13
-
-
0028006633
-
Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p
-
Reifenberger J, Reifenberger G, Liu L, James C D, Wechsler W, Collins V P. Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. Am J Pathol. 145:1994;1175-1190.
-
(1994)
Am J Pathol
, 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
-
14
-
-
0028942314
-
Molecular abnormalities of chromosome 19 in malignant gliomas: Preferntial involvement of the 19q13.2-19q13.4 region
-
Bello M J, Leone P E, Nebreda P, Kusak M E, DeCampos J M, Vaquero J, Sarasa J L, Pestana A, Rey J A. Molecular abnormalities of chromosome 19 in malignant gliomas: preferntial involvement of the 19q13.2-19q13.4 region. Int J Oncol. 6:1995;655-658.
-
(1995)
Int J Oncol
, vol.6
, pp. 655-658
-
-
Bello, M.J.1
Leone, P.E.2
Nebreda, P.3
Kusak, M.E.4
DeCampos, J.M.5
Vaquero, J.6
Sarasa, J.L.7
Pestana, A.8
Rey, J.A.9
-
15
-
-
0029059911
-
Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors
-
Bello M J, Leone P E, Vaquero J, De Campos J M, Kusak M E, Sarasa J L, Pestana A, Rey J A. Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors. Int J Cancer. 64:1995;207-210.
-
(1995)
Int J Cancer
, vol.64
, pp. 207-210
-
-
Bello, M.J.1
Leone, P.E.2
Vaquero, J.3
De Campos, J.M.4
Kusak, M.E.5
Sarasa, J.L.6
Pestana, A.7
Rey, J.A.8
-
16
-
-
0028954148
-
Region-specific loss of heterozygosity on chromosome 19 is related to the morphologic type of human glioma
-
Ritland S R, Ganju V, Jenkins R B. Region-specific loss of heterozygosity on chromosome 19 is related to the morphologic type of human glioma. Genes Chromosom Cancer. 12:1995;277-282.
-
(1995)
Genes Chromosom Cancer
, vol.12
, pp. 277-282
-
-
Ritland, S.R.1
Ganju, V.2
Jenkins, R.B.3
-
17
-
-
0028335222
-
Deletion mapping of chromosome 19 in human gliomas
-
vonDeimling A, Nagel J, Bender B, Lenartz D, Schramm J, Louis D N, Wiestler O D. Deletion mapping of chromosome 19 in human gliomas. Int J Cancer. 57:1994;676-680.
-
(1994)
Int J Cancer
, vol.57
, pp. 676-680
-
-
VonDeimling, A.1
Nagel, J.2
Bender, B.3
Lenartz, D.4
Schramm, J.5
Louis, D.N.6
Wiestler, O.D.7
-
18
-
-
0027980906
-
The putative glioma tumor suppressor gene on chromosome 19q maps between APOC2 and HRC
-
Rubio M P, Correa D M, Ueki K, Mohrenweiser H W, Gusella J F, von Deimling A, Louis D N. The putative glioma tumor suppressor gene on chromosome 19q maps between APOC2 and HRC. Cancer Res. 54:1994;4760-4763.
-
(1994)
Cancer Res
, vol.54
, pp. 4760-4763
-
-
Rubio, M.P.1
Correa, D.M.2
Ueki, K.3
Mohrenweiser, H.W.4
Gusella, J.F.5
Von Deimling, A.6
Louis, D.N.7
-
19
-
-
0028365909
-
Integrated human genome-wide maps constructed using the CEPH reference panel
-
Buetow K H, Weber J L, Ludwigsen S, Scherpbier-Heddema T, Duyk G M, Sheffield V C, Wang Z, Murray J C. Integrated human genome-wide maps constructed using the CEPH reference panel. Nature Genet. 6:1994;391-393.
-
(1994)
Nature Genet
, vol.6
, pp. 391-393
-
-
Buetow, K.H.1
Weber, J.L.2
Ludwigsen, S.3
Scherpbier-Heddema, T.4
Duyk, G.M.5
Sheffield, V.C.6
Wang, Z.7
Murray, J.C.8
-
20
-
-
0027365391
-
Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19
-
Weber J L, Wang Z, Hansen K, Stephenson M, Kappel C, Salzman S, Wilkie P J, Keats B, Dracopoli N C, Brandriff B F, Olsen A S. Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19. Am J Hum Genet. 53:1993;1079-1095.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1079-1095
-
-
Weber, J.L.1
Wang, Z.2
Hansen, K.3
Stephenson, M.4
Kappel, C.5
Salzman, S.6
Wilkie, P.J.7
Keats, B.8
Dracopoli, N.C.9
Brandriff, B.F.10
Olsen, A.S.11
-
21
-
-
0028887026
-
A 30-MB metric flourescence in situ hybridization map of human chromosome 19q
-
Gordon L A, Bergmann A, Christensen M, Danganan L, Lee D A, Ashworth L K, Nelson D O, Olsen A S, Mohrenwieser H W, Carrano A V, Brandriff B F. A 30-MB metric flourescence in situ hybridization map of human chromosome 19q. Genomics. 30:1995;187-192.
-
(1995)
Genomics
, vol.30
, pp. 187-192
-
-
Gordon, L.A.1
Bergmann, A.2
Christensen, M.3
Danganan, L.4
Lee, D.A.5
Ashworth, L.K.6
Nelson, D.O.7
Olsen, A.S.8
Mohrenwieser, H.W.9
Carrano, A.V.10
Brandriff, B.F.11
-
22
-
-
0028866218
-
An integrated metric physical map of human chromosome 19
-
Ashworth L K, Batzer M A, Brandriff B, Branscomb E, deJong P, Garcia E, Garnes J A, Gordon L A, Lamerdin J E, Lennon G, Mohrenweiser H, Olsen A S, Slezak T, Carrano A V. An integrated metric physical map of human chromosome 19. Nature Genet. 1:1995;422-427.
-
(1995)
Nature Genet
, vol.1
, pp. 422-427
-
-
Ashworth, L.K.1
Batzer, M.A.2
Brandriff, B.3
Branscomb, E.4
DeJong, P.5
Garcia, E.6
Garnes, J.A.7
Gordon, L.A.8
Lamerdin, J.E.9
Lennon, G.10
Mohrenweiser, H.11
Olsen, A.S.12
Slezak, T.13
Carrano, A.V.14
-
24
-
-
0029091012
-
Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer
-
Amfo K, Neyns B, Teugels E, Lissens W, Bourgain C, De Sutter P, Vandamme B, Vamos E, De Greve J. Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer. Oncogene. 11:1995;351-358.
-
(1995)
Oncogene
, vol.11
, pp. 351-358
-
-
Amfo, K.1
Neyns, B.2
Teugels, E.3
Lissens, W.4
Bourgain, C.5
De Sutter, P.6
Vandamme, B.7
Vamos, E.8
De Greve, J.9
-
25
-
-
0028052254
-
Recurrent cytogenetic aberration and loss of constitutional heterozygosity in ovarian carcinomas
-
Kiechle-Schwarz M, Bauknecht T, Karck U, Kommoss F, DuBois A, Pfleiderer A. Recurrent cytogenetic aberration and loss of constitutional heterozygosity in ovarian carcinomas. Gynecol Oncol. 55:1994;198-205.
-
(1994)
Gynecol Oncol
, vol.55
, pp. 198-205
-
-
Kiechle-Schwarz, M.1
Bauknecht, T.2
Karck, U.3
Kommoss, F.4
DuBois, A.5
Pfleiderer, A.6
|