169 related articles for article (PubMed ID: 2176283)
1. Variable mutations of the RB gene in small-cell lung carcinoma.
Mori N; Yokota J; Akiyama T; Sameshima Y; Okamoto A; Mizoguchi H; Toyoshima K; Sugimura T; Terada M
Oncogene; 1990 Nov; 5(11):1713-7. PubMed ID: 2176283
[TBL] [Abstract][Full Text] [Related]
2. Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer.
Hensel CH; Hsieh CL; Gazdar AF; Johnson BE; Sakaguchi AY; Naylor SL; Lee WH; Lee EY
Cancer Res; 1990 May; 50(10):3067-72. PubMed ID: 2159370
[TBL] [Abstract][Full Text] [Related]
3. Genomic organization and mutation analysis of Hel-N1 in lung cancers with chromosome 9p21 deletions.
Cairns P; Okami K; King P; Bonacum J; Ahrendt S; Wu L; Mao L; Jen J; Sidransky D
Cancer Res; 1997 Dec; 57(23):5356-9. PubMed ID: 9393760
[TBL] [Abstract][Full Text] [Related]
4. Inactivation of the retinoblastoma gene in a human lung carcinoma cell line detected by single-strand conformation polymorphism analysis of the polymerase chain reaction product of cDNA.
Murakami Y; Katahira M; Makino R; Hayashi K; Hirohashi S; Sekiya T
Oncogene; 1991 Jan; 6(1):37-42. PubMed ID: 1992444
[TBL] [Abstract][Full Text] [Related]
5. DNA aberrations at the retinoblastoma gene locus in human squamous cell carcinomas of the lung.
Sachse R; Murakami Y; Shiraishi M; Hayashi K; Sekiya T
Oncogene; 1994 Jan; 9(1):39-47. PubMed ID: 8302602
[TBL] [Abstract][Full Text] [Related]
6. Identification of a 428-kb homozygously deleted region disrupting the SEZ6L gene at 22q12.1 in a lung cancer cell line.
Nishioka M; Kohno T; Takahashi M; Niki T; Yamada T; Sone S; Yokota J
Oncogene; 2000 Dec; 19(54):6251-60. PubMed ID: 11175339
[TBL] [Abstract][Full Text] [Related]
7. Deletion of a splice donor site ablates expression of the following exon and produces an unphosphorylated RB protein unable to bind SV40 T antigen.
Shew JY; Chen PL; Bookstein R; Lee EY; Lee WH
Cell Growth Differ; 1990 Jan; 1(1):17-25. PubMed ID: 1964074
[TBL] [Abstract][Full Text] [Related]
8. Use of the single strand conformation polymorphism technique and PCR to detect p53 gene mutations in small cell lung cancer.
Hensel CH; Xiang RH; Sakaguchi AY; Naylor SL
Oncogene; 1991 Jun; 6(6):1067-71. PubMed ID: 1648702
[TBL] [Abstract][Full Text] [Related]
9. FHIT and FRA3B 3p14.2 allele loss are common in lung cancer and preneoplastic bronchial lesions and are associated with cancer-related FHIT cDNA splicing aberrations.
Fong KM; Biesterveld EJ; Virmani A; Wistuba I; Sekido Y; Bader SA; Ahmadian M; Ong ST; Rassool FV; Zimmerman PV; Giaccone G; Gazdar AF; Minna JD
Cancer Res; 1997 Jun; 57(11):2256-67. PubMed ID: 9187130
[TBL] [Abstract][Full Text] [Related]
10. Protein expression of the RB-related gene family and SV40 large T antigen in mesothelioma and lung cancer.
Modi S; Kubo A; Oie H; Coxon AB; Rehmatulla A; Kaye FJ
Oncogene; 2000 Sep; 19(40):4632-9. PubMed ID: 11030152
[TBL] [Abstract][Full Text] [Related]
11. Multiple genetic alterations in small-cell lung carcinoma.
Yokota J; Mori N; Akiyama T; Shimosato Y; Sugimura T; Terada M
Princess Takamatsu Symp; 1989; 20():43-8. PubMed ID: 2577337
[TBL] [Abstract][Full Text] [Related]
12. Deletions of chromosome 13q, mutations in Retinoblastoma 1, and retinoblastoma protein state in human hepatocellular carcinoma.
Zhang X; Xu HJ; Murakami Y; Sachse R; Yashima K; Hirohashi S; Hu SX; Benedict WF; Sekiya T
Cancer Res; 1994 Aug; 54(15):4177-82. PubMed ID: 8033150
[TBL] [Abstract][Full Text] [Related]
13. Homozygous deletion at chromosome 2q33 in human small-cell lung carcinoma identified by arbitrarily primed PCR genomic fingerprinting.
Kohno T; Morishita K; Takano H; Shapiro DN; Yokota J
Oncogene; 1994 Jan; 9(1):103-8. PubMed ID: 7905618
[TBL] [Abstract][Full Text] [Related]
14. Polymorphic sites within the MCC and APC loci reveal very frequent loss of heterozygosity in human small cell lung cancer.
D'Amico D; Carbone DP; Johnson BE; Meltzer SJ; Minna JD
Cancer Res; 1992 Apr; 52(7):1996-9. PubMed ID: 1348017
[TBL] [Abstract][Full Text] [Related]
15. High frequency of deletion mutations in p53 gene from squamous cell lung cancer patients in Taiwan.
Wang YC; Chen CY; Chen SK; Cherng SH; Ho WL; Lee H
Cancer Res; 1998 Jan; 58(2):328-33. PubMed ID: 9443413
[TBL] [Abstract][Full Text] [Related]
16. A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm.
Weir-Thompson E; Condie A; Leonard RC; Prosser J
Oncogene; 1991 Dec; 6(12):2353-6. PubMed ID: 1662795
[TBL] [Abstract][Full Text] [Related]
17. TSG101 is not mutated in lung cancer but a shortened transcript is frequently expressed in small cell lung cancer.
Oh Y; Proctor ML; Fan YH; Su LK; Hong WK; Fong KM; Sekido YS; Gazdar AF; Minna JD; Mao L
Oncogene; 1998 Sep; 17(9):1141-8. PubMed ID: 9764824
[TBL] [Abstract][Full Text] [Related]
18. Genetic alteration of the beta-catenin gene (CTNNB1) in human lung cancer and malignant mesothelioma and identification of a new 3p21.3 homozygous deletion.
Shigemitsu K; Sekido Y; Usami N; Mori S; Sato M; Horio Y; Hasegawa Y; Bader SA; Gazdar AF; Minna JD; Hida T; Yoshioka H; Imaizumi M; Ueda Y; Takahashi M; Shimokata K
Oncogene; 2001 Jul; 20(31):4249-57. PubMed ID: 11464291
[TBL] [Abstract][Full Text] [Related]
19. Lack of expression of aminoacylase-1 in small cell lung cancer. Evidence for inactivation of genes encoded by chromosome 3p.
Miller YE; Minna JD; Gazdar AF
J Clin Invest; 1989 Jun; 83(6):2120-4. PubMed ID: 2542383
[TBL] [Abstract][Full Text] [Related]
20. Inactivation of the retinoblastoma gene in human bladder and renal cell carcinomas.
Ishikawa J; Xu HJ; Hu SX; Yandell DW; Maeda S; Kamidono S; Benedict WF; Takahashi R
Cancer Res; 1991 Oct; 51(20):5736-43. PubMed ID: 1913692
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
