-
2
-
-
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 and Collins VP: Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. Am J Pathol 145: 1175-1190, 1994. (Pubitemid 24345665)
-
(1994)
American Journal of Pathology
, vol.145
, Issue.5
, pp. 1175-1190
-
-
Reifenberger, J.1
Reifenberger, G.2
Liu, L.3
James, C.D.4
Wechsler, W.5
Collins, V.P.6
-
3
-
-
0029059911
-
Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors
-
Bello MJ, Leone PE, Vaquero J, de Campos JM, Kusak ME, Sarasa JL, Pestaña A and Rey JA: Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors. Int J Cancer 64: 207-210, 1995.
-
(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
Pestaña, A.7
Rey, J.A.8
-
4
-
-
0031929020
-
Screening for loss of heterozygosity and microsatellite instability in oligodendrogliomas
-
DOI 10.1002/(SICI)1098-2264(199803)21:3<207::AID
-
Zhu JJ, Santarius T, Wu X, Tsong J, Guha A, Wu JK, Hudson TJ and Black PM: Screening for loss of heterozygosity and microsatellite instability in oligodendrogliomas. Genes Chromosomes Cancer 21: 207-216, 1998. (Pubitemid 28136437)
-
(1998)
Genes Chromosomes and Cancer
, vol.21
, Issue.3
, pp. 207-216
-
-
Zhu, J.J.1
Santarius, T.2
Wu, X.3
Tsong, J.4
Guha, A.5
Wu, J.K.6
Hudson, T.J.7
Black, P.McL.8
-
5
-
-
0032858569
-
Identification of two distinct deleted regions on the short arm of chromosome 1 and rare mutation of the CDKN2C gene from 1p32 in oligodendroglial tumors
-
Husemann K, Wolter M, Buschges R, Bostrom J, Sabel M and Reifenberger G: Identification of two distinct deleted regions on the short arm of chromosome 1 and rare mutation of the CDKN2C gene from 1p32 in oligodendroglial tumors. J Neuropathol Exp Neurol 58: 1041-1050, 1999. (Pubitemid 29468265)
-
(1999)
Journal of Neuropathology and Experimental Neurology
, vol.58
, Issue.10
, pp. 1041-1050
-
-
Husemann, K.1
Wolter, M.2
Buschges, R.3
Bostrom, J.4
Sabel, M.5
Reifenberger, G.6
-
6
-
-
0033566061
-
Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype
-
DOI 10.1038/sj.onc.1202759
-
Smith JS, Alderete B, Minn Y, Borell TJ, Perry A, Mohapatra G, et al: Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype. Oncogene 18: 4144-4152, 1999. (Pubitemid 29363922)
-
(1999)
Oncogene
, vol.18
, Issue.28
, pp. 4144-4152
-
-
Smith, J.S.1
Alderete, B.2
Minn, Y.3
Borell, T.J.4
Perry, A.5
Mohapatra, G.6
Hosek, S.M.7
Kimmel, D.8
O'Fallon, J.9
Yates, A.10
Feuerstein, B.G.11
Burger, P.C.12
Scheithauer, B.W.13
Jenkins, R.B.14
-
7
-
-
1342339254
-
Oligodendroglial tumors: Refinement of candidate regions on chromosome arm 1p and correlation of 1p/19q status with survival
-
Felsberg J, Erkwoh A, Sabel MC, et al: Oligodendroglial tumors: Refinement of candidate regions on chromosome arm 1p and correlation of 1p/19q status with survival. Brain Pathol 14: 121-130, 2004. (Pubitemid 38656383)
-
(2004)
Brain Pathology
, vol.14
, Issue.2
, pp. 121-130
-
-
Felsberg, J.1
Erkwoh, A.2
Sabel, M.C.3
Kirsch, L.4
Fimmers, R.5
Blaschke, B.6
Schlegel, U.7
Schramm, J.8
Wiestler, O.D.9
Reifenberger, G.10
-
8
-
-
0032887584
-
ink4cgene on the short arm of chromosome 1 in anaplastic oligodendrogliomas
-
ink4cgene on the short arm of chromosome 1 in anaplastic oligodendrogliomas. Brain Pathol 9: 639-643, 1999.
-
(1999)
Brain Pathol
, vol.9
, pp. 639-643
-
-
Pohl, U.1
Cairncross, J.G.2
Louis, D.N.3
-
9
-
-
0034718533
-
P18 tumor suppressor gene and progression of oligodendrogliomas to anaplasia
-
He J, Hoang-Xuan K, Marie Y, Leuraud P, Mokhtari K, Kujas M, Delattre JY and Sanson M: P18 tumor suppressor gene and progression of oligodendrogliomas to anaplasia. Neurology 55: 867-869, 2000.
-
(2000)
Neurology
, vol.55
, pp. 867-869
-
-
He, J.1
Hoang-Xuan, K.2
Marie, Y.3
Leuraud, P.4
Mokhtari, K.5
Kujas, M.6
Delattre, J.Y.7
Sanson, M.8
-
10
-
-
0032143910
-
Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions
-
DOI 10.1006/geno.1998.5387
-
Mai M, Huang H, Reed C, Qian C, Smith JS, Alderete B, Jenkins R, Smith DI and Liu W: Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions. Genomics 51: 359-363, 1998. (Pubitemid 28413202)
-
(1998)
Genomics
, vol.51
, Issue.3
, pp. 359-363
-
-
Mai, M.1
Huang, H.2
Reed, C.3
Qian, C.4
Smith, J.S.5
Alderete, B.6
Jenkins, R.7
Smith, D.I.8
Liu, W.9
-
11
-
-
0033992082
-
hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas
-
Bello MJ, de Campos JM, Vaquero J, Ruiz-Barnes P, Kusak ME, Sarasa JL and Rey JA: hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas. Cancer Genet Cytogenet 116: 142-147, 2000.
-
(2000)
Cancer Genet Cytogenet
, vol.116
, pp. 142-147
-
-
Bello, M.J.1
De Campos, J.M.2
Vaquero, J.3
Ruiz-Barnes, P.4
Kusak, M.E.5
Sarasa, J.L.6
Rey, J.A.7
-
12
-
-
17844407158
-
Mutation analysis of the p73 gene in nonastrocytic brain tumours
-
DOI 10.1054/bjoc.2001.1855
-
Alonso ME, Bello MJ, Gonzalez-Gomez P, Lomas J, Arjona D, de Campos JM, Kusak ME, Sarasa JL, Isla A and Rey JA: Mutation analysis of the p73 gene in non-astrocytic brain tumours. Br J Cancer 85: 204-208, 2001. (Pubitemid 32695740)
-
(2001)
British Journal of Cancer
, vol.85
, Issue.2
, pp. 204-208
-
-
Alonso, M.E.1
Bello, M.J.2
Gonzalez-Gomez, P.3
Lomas, J.4
Arjona, D.5
Campos, J.M.D.6
Kusak, M.E.7
Sarasa, J.L.8
Isla, A.9
Rey, J.A.10
-
13
-
-
0031989439
-
Ptch2, a second mouse Patched gene is co-expressed with Sonic hedgehos
-
Motoyama J, Takabatake T, Takeshima K and Hui C: Ptch2, a second mouse Patched gene is co-expressed with Sonic hedgehos. Nat Genet 18: 104-106, 1998.
-
(1998)
Nat Genet
, vol.18
, pp. 104-106
-
-
Motoyama, J.1
Takabatake, T.2
Takeshima, K.3
Hui, C.4
-
14
-
-
0032506115
-
Characterization of two patched receptors for the vertebrate hedgehog protein family
-
DOI 10.1073/pnas.95.23.13630
-
Carpenter D, Stone DM, Brush J, Ryan A, Armanini M, Frantz G, Rosenthal A and de Sauvage FJ: Characterization of two patched receptors for the vertebrate hedgehog protein family. Proc Natl Acad Sci USA 95: 13630-13634, 1998. (Pubitemid 28523023)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.23
, pp. 13630-13634
-
-
Carpenter, D.1
Stone, D.M.2
Brush, J.3
Ryan, A.4
Armanini, M.5
Frantz, G.6
Rosenthal, A.7
De Sauvage, F.J.8
-
15
-
-
0035991441
-
Nucleotide alteration of retinoblastoma protein-interacting zinc finger gene, RIZ, in human leukemia
-
DOI 10.1620/tjem.196.193
-
Sasaki O, Meguro K, Tohmiya Y, Funato T, Shibahara S and Sasaki T: Nucleotide alteration of retinoblastoma protein-interacting zinc finger gene, RIZ, in human leukemia. Tohoku J Exp Med 196: 193-201, 2002. (Pubitemid 34727555)
-
(2002)
Tohoku Journal of Experimental Medicine
, vol.196
, Issue.3
, pp. 193-201
-
-
Sasaki, O.1
Meguro, K.2
Tohmiya, Y.3
Funato, T.4
Shibahara, S.5
Sasaki, T.6
-
16
-
-
0032188763
-
2-M cell cycle arrest and/or apoptosis
-
He L, Yu JX, Liu L, Buyse IM, Wang MS, Yang QC, et al: RIZ1, but not the alternative RIZ2 product of the same gene, is underexpressed in breast cancer, and forced RIZ1 expression causes G2-M cell cycle arrest and/or apoptosis. Cancer Res 58: 4238-4244, 1998. (Pubitemid 28450017)
-
(1998)
Cancer Research
, vol.58
, Issue.19
, pp. 4238-4244
-
-
He, L.1
Yu, J.X.2
Liu, L.3
Buyse, I.M.4
Wang, M.-S.5
Yang, Q.-C.6
Nakagawara, A.7
Brodeur, G.M.8
Shi, Y.E.9
Huang, S.10
-
17
-
-
0032880408
-
Decreased RIZ1 expression but not RIZ2 in hepatoma and suppression of hepatoma tumorigenicity by RIZ1
-
DOI 10.1002/(SICI)1097-0215(19991112)83:4<541::AID
-
Jiang G, Liu L, Buyse IM, Simon D and Huang S: Decreased RIZ1 expression, but not RIZ2 in hepatoma and suppression of hepatoma tumorigenicity by RIZ1. Int J Cancer 83: 541-546, 1999. (Pubitemid 29489871)
-
(1999)
International Journal of Cancer
, vol.83
, Issue.4
, pp. 541-546
-
-
Jiang, G.-L.1
Liu, L.2
Buyse, I.M.3
Simon, D.4
Huang, S.5
-
18
-
-
0034283031
-
Frequent frameshift mutations of RIZ in sporadic gastrointestinal and endometrial carcinomas with microsatellite instability
-
Piao Z, Fang W, Malkhosyan S, Kim H, Horii A, Perucho M and Huang S: Frequent frameshift mutations of RIZ in sporadic gastrointestinal and endometrial carcinomas with microsatellite instability. Cancer Res 60: 4701-4704, 2000.
-
(2000)
Cancer Res
, vol.60
, pp. 4701-4704
-
-
Piao, Z.1
Fang, W.2
Malkhosyan, S.3
Kim, H.4
Horii, A.5
Perucho, M.6
Huang, S.7
-
19
-
-
0035369084
-
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
-
DOI 10.1016/S0092-8674(01)00363-4
-
Zhao C, Takita J, Tanaka Y, Setou M, Nakagawa T, et al: Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1B beta. Cell 105: 587-597, 2001. (Pubitemid 32524112)
-
(2001)
Cell
, vol.105
, Issue.5
, pp. 587-597
-
-
Zhao, C.1
Takita, J.2
Tanaka, Y.3
Setou, M.4
Nakagawa, T.5
Takeda, S.6
Yang, H.W.7
Terada, S.8
Nakata, T.9
Takei, Y.10
Saito, M.11
Tsuji, S.12
Hayashi, Y.13
Hirokawa, N.14
-
20
-
-
2342624703
-
Genomic structure and mutational analysis of the human KIF1B alpha gene located at 1p36.2 in neuroblastoma
-
Chen YY, Takita J, Chen YZ, Yang HW, Hanada R, Yamamoto K and Hayashi Y: Genomic structure and mutational analysis of the human KIF1B alpha gene located at 1p36.2 in neuroblastoma. Int J Oncol 23: 737-744, 2003.
-
(2003)
Int J Oncol
, vol.23
, pp. 737-744
-
-
Chen, Y.Y.1
Takita, J.2
Chen, Y.Z.3
Yang, H.W.4
Hanada, R.5
Yamamoto, K.6
Hayashi, Y.7
-
21
-
-
0035899352
-
Genomic structure and mutational analysis of the human KIF1B gene which is homozygously deleted in neuroblastoma at chromosome 1p36.2
-
DOI 10.1038/sj.onc.1204456
-
Yang HW, Chen YZ, Takita J, Soeda E, Piao HY and Hayashi Y: Genomic structure and mutational analysis of the human KIF1B gene which is homozygously deleted in neuroblastoma at chromosome 1p36.2. Oncogene 20: 5075-5083, 2000. (Pubitemid 32769799)
-
(2001)
Oncogene
, vol.20
, Issue.36
, pp. 5075-5083
-
-
Yang, H.W.1
Chen, Y.Z.2
Takita, J.3
Soeda, E.4
Piao, H.Y.5
Hayashi, Y.6
-
22
-
-
0037678573
-
Aberrant promoter methylation of multiple genes in oligodendrogliomas and ependymomas
-
DOI 10.1016/S0165-4608(02)00928-7
-
Alonso ME, Bello MJ, Gonzalez-Gomez P, Arjona D, Lomas J, de Campos JM, Isla A, Sarasa JL and Rey JA: Aberrant promoter methylation of multiple genes in oligodendrogliomas and ependymomas. Cancer Genet Cytogenet 144: 134-142, 2003. (Pubitemid 36808960)
-
(2003)
Cancer Genetics and Cytogenetics
, vol.144
, Issue.2
, pp. 134-142
-
-
Alonso, M.E.1
Bello, M.J.2
Gonzalez-Gomez, P.3
Arjona, D.4
Lomas, J.5
De Campos, J.M.6
Isla, A.7
Sarasa, J.L.8
Rey, J.A.9
-
23
-
-
0026627772
-
Loss of herterozygosity for distal markers on 22q in human gliomas
-
Rey JA, Bello MJ, Jimenez-Lara A, Vaquero J, Kusak ME, de Campos JM, Sarasa JL and Pestaña A: Loss of herterozygosity for distal markers on 22q in human gliomas. Int J Cancer 51: 703-706, 1992.
-
(1992)
Int J Cancer
, vol.51
, pp. 703-706
-
-
Rey, J.A.1
Bello, M.J.2
Jimenez-Lara, A.3
Vaquero, J.4
Kusak, M.E.5
De Campos, J.M.6
Sarasa, J.L.7
Pestaña, A.8
-
24
-
-
0032898184
-
Isolation and characterization of human Patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32
-
DOI 10.1093/hmg/8.2.291
-
Smyth I, Narang MA, Evans T, Heimann C, Nakamura Y, Chenevix-Trench G, Pietsch T, Wicking C and Wainwright BJ: Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32. Hum Mol Genet 8: 291-297, 1999. (Pubitemid 29054270)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.2
, pp. 291-297
-
-
Smyth, I.1
Narang, M.A.2
Evans, T.3
Heimann, C.4
Nakamura, Y.5
Chenevix-Trench, G.6
Pietsch, T.7
Wicking, C.8
Wainwright, B.J.9
-
25
-
-
0034083469
-
Mapping of a minimal deleted region in human hepatocellular carcinoma to 1p36.13-p36.23 and mutational analysis of the RIZ (PRDM2) gene localized to the region
-
DOI 10.1002/1098-2264(200007)28:3<269::AID
-
Fang W, Piao Z, Simon D, Sheu JC and Huang S: Mapping of a minimal deleted region in human hepatocellular carcinoma to 1p36.13-p36.23 and mutational analysis of the RIZ (PRDM2) gene localized to the region. Genes Chromosomes Cancer 28: 269-275, 2000. (Pubitemid 30399556)
-
(2000)
Genes Chromosomes and Cancer
, vol.28
, Issue.3
, pp. 269-275
-
-
Fang, W.1
Piao, Z.2
Simon, D.3
Sheu, J.-C.4
Huang, S.5
-
26
-
-
0030999555
-
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
-
Mitelman F, Mertens F and Johansson B: A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet 15: 417-474, 1997.
-
(1997)
Nat Genet
, vol.15
, pp. 417-474
-
-
Mitelman, F.1
Mertens, F.2
Johansson, B.3
-
27
-
-
0029092061
-
Allelic status of chromosome 1 in neoplasms of the nervous system
-
Bello MJ, Leone PE, Nebreda P, de Campos JM, Kusak ME, et al: Allelic status of chromosome 1 in neoplasms of the nervous system. Cancer Genet Cytogenet 83: 160-164, 1995.
-
(1995)
Cancer Genet Cytogenet
, vol.83
, pp. 160-164
-
-
Bello, M.J.1
Leone, P.E.2
Nebreda, P.3
De Campos, J.M.4
Kusak, M.E.5
-
28
-
-
0028582034
-
INK4B/MTS2-related CDK6 inhibitor, correlates with wild-type pRb function
-
INK4B/MTS2-related CDK6 inhibitor, correlates with wild-type pRb function. Genes Dev 8: 2939-2952, 1994.
-
(1994)
Genes Dev
, vol.8
, pp. 2939-2952
-
-
Guan, K.L.1
Jenkins, C.W.2
Li, Y.3
Nichols, M.A.4
Wu, X.5
O'Keefe, C.L.6
Matera, A.G.7
Xiong, Y.8
-
29
-
-
0032494479
-
Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas
-
Cairncross JG, Ueki K, Zlatescu MC, Lisle DK, Finkelstein DM, Hammond RR, Silver JS, Stark PC, Macdonald DR, Ino Y, Ramsay DA and Louis DN: Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas. J Natl Cancer Inst 90: 1473-1479, 1998. (Pubitemid 28482012)
-
(1998)
Journal of the National Cancer Institute
, vol.90
, Issue.19
, pp. 1473-1479
-
-
Cairncross, J.G.1
Ueki, K.2
Zlatescu, M.C.3
Lisle, D.K.4
Finkelstein, D.M.5
Hammond, R.R.6
Silver, J.S.7
Stark, P.C.8
Macdonald, D.R.9
Ino, Y.10
Ramsay, D.A.11
Louis, D.N.12
-
30
-
-
0030738693
-
Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system
-
Wolter M, Reifenberger J, Sommer C, Ruzicka T and Reifenberger G: Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system. Cancer Res 57: 2581-2585, 1997. (Pubitemid 27283761)
-
(1997)
Cancer Research
, vol.57
, Issue.13
, pp. 2581-2585
-
-
Wolter, M.1
Reifenberger, J.2
Sommer, C.3
Ruzicka, T.4
Reifenberger, G.5
-
31
-
-
16044363842
-
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas
-
DOI 10.1038/ng0996-78
-
Gailani MR, Stahle-Backdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C, Unden AB, Dean M, Brash DE, Bale AE and Toftgard R: The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas. Nat Genet 14: 78-81, 1996. (Pubitemid 26301550)
-
(1996)
Nature Genetics
, vol.14
, Issue.1
, pp. 78-81
-
-
Gailani, M.R.1
Stahle-Backdahl, M.2
Leffell, D.J.3
Glynn, M.4
Zaphiropoulos, P.G.5
Pressman, C.6
Unden, A.B.7
Dean, M.8
Brash, D.E.9
Bale, A.E.10
Toftgard, R.11
-
32
-
-
12844276949
-
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the patched protein, and no genotype- phenotype correlations are evident
-
Wicking C, Shanley S, Smyth I, Gillies S, Negus K, Graham S, Suthers G, Haites N, Edwards M, Chenevix-Trench G and Wainwright B: Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. Am J Hum Genet 60: 21-26, 1997. (Pubitemid 26427774)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.1
, pp. 21-26
-
-
Wicking, C.1
Shanley, S.2
Smyth, I.3
Gillies, S.4
Negus, K.5
Graham, S.6
Suthers, G.7
Haites, N.8
Edwards, M.9
Wainwright, B.10
Chenevix-Trench, G.11
-
33
-
-
0034183777
-
Patched 2, located in 1p32-34, is not mutated in high stage neuroblastoma tumors
-
Jogi A, Abel F, Sjoberg RM, Toftgard R, Zaphiropoulos PG, Pahlman S, Martinsson T and Axelson H: Patched 2, located in 1p32-34, is not mutated in high stage neuroblastoma tumors. Int J Oncol 16: 943-949,2000.
-
(2000)
Int J Oncol
, vol.16
, pp. 943-949
-
-
Jogi, A.1
Abel, F.2
Sjoberg, R.M.3
Toftgard, R.4
Zaphiropoulos, P.G.5
Pahlman, S.6
Martinsson, T.7
Axelson, H.8
-
34
-
-
0347517693
-
Intragenic allelic loss and promoter hypermethylation of the RIZ1 tumor suppressor gene in parathyroid tumors and pheochromocytomas
-
Carling T, Du Y, Fang W, Correa P and Huang S: Intragenic allelic loss and promoter hypermethylation of the RIZ1 tumor suppressor gene in parathyroid tumors and pheochromocytomas. Surgery 134: 932-939, 2003.
-
(2003)
Surgery
, vol.134
, pp. 932-939
-
-
Carling, T.1
Du, Y.2
Fang, W.3
Correa, P.4
Huang, S.5
-
35
-
-
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 and Kefford RF: 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. (Pubitemid 19164600)
-
(1989)
Proceedings of the National Academy of Sciences of the United States of America
, vol.86
, Issue.12
, 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
-
36
-
-
0037007440
-
Frameshift mutations of RIZ, but no point mutations in RIZ1 exons in malignant melanomas with deletions in 1p36
-
DOI 10.1038/sj/onc/1205457
-
Poetsch M, Dittberner T, Woenckhaus C: Frameshift mutations of RIZ, but no point mutations in RIZ1 exons in malignant melanomas with deletions in lp36. Oncogene 21: 3038-3042, 2002. (Pubitemid 34522903)
-
(2002)
Oncogene
, vol.21
, Issue.19
, pp. 3038-3042
-
-
Poetsch, M.1
Dittberner, T.2
Woenckhaus, C.3
-
37
-
-
12944281108
-
Candidate tumor suppressor RIZ is frequently involved in colorectal carcinogenesis
-
DOI 10.1073/pnas.040579497
-
Chadwick RB, Jiang GL, Bennington GA, Yuan B, Johnson CK, Stevens MW, Niemann TH, Peltomaki P, de la Chapelle A and Huang S: Candidate tumor suppressor RIZ is frequently involved in colorectal carcinogenesis. Proc Natl Acad Sci USA 97: 2662-2667, 2000. (Pubitemid 30159228)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.6
, pp. 2662-2667
-
-
Chadwick, R.B.1
Jiang, G.-L.2
Bennington, G.A.3
Yuan, B.4
Johnson, C.K.5
Stevens, M.W.6
Niemann, T.H.7
Peltomaki, P.8
Huang, S.9
De La, C.A.10
-
38
-
-
0029774136
-
Genomic instability in 1p and human malignancies
-
DOI 10.1002/(SICI)1098-2264(199608)16:4<211::AID
-
Schwab M, Praml C and Amler LC: Genomic instability in 1p and human malignancies. Genes Chromosomes Cancer 16: 211-229, 1996. (Pubitemid 26299976)
-
(1996)
Genes Chromosomes and Cancer
, vol.16
, Issue.4
, pp. 211-229
-
-
Schwab, M.1
Praml, C.2
Amler, L.C.3
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