448 related articles for article (PubMed ID: 12561436)
1. [Mutations of fragile histidine triad gene in Peutz-Jeghers syndrome and canceration].
Zhao XR; Kang LC; Zhou YS; Jia YX; Chen Z; Kang SH; Li WM; Zhao M; Cui JT; Sun AL; Lu YY
Ai Zheng; 2003 Jan; 22(1):50-4. PubMed ID: 12561436
[TBL] [Abstract][Full Text] [Related]
2. Homozygous deletion but not mutation of exons 5 and 8 of the fragile histidine triad (FHIT) gene is associated with features of differentiated thyroid carcinoma.
Yin DT; Wang L; Sun J; Yin F; Yan Q; Shen RL; Gao JX; He G
Ann Clin Lab Sci; 2010; 40(3):267-72. PubMed ID: 20689140
[TBL] [Abstract][Full Text] [Related]
3. Two novel STK11 mutations in three Chinese families with Peutz-Jeghers syndrome.
Zuo YG; Xu KJ; Su B; Ho MG; Liu YH
Chin Med J (Engl); 2007 Jul; 120(13):1183-6. PubMed ID: 17637250
[TBL] [Abstract][Full Text] [Related]
4. Analysis of the FHIT gene and FRA3B region in sporadic breast cancer, preneoplastic lesions, and familial breast cancer probands.
Ahmadian M; Wistuba II; Fong KM; Behrens C; Kodagoda DR; Saboorian MH; Shay J; Tomlinson GE; Blum J; Minna JD; Gazdar AF
Cancer Res; 1997 Sep; 57(17):3664-8. PubMed ID: 9288768
[TBL] [Abstract][Full Text] [Related]
5. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
[TBL] [Abstract][Full Text] [Related]
6. [Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome].
Mao X; Zhang Y; Wang H; Mao G; Ning S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):186-90. PubMed ID: 27060312
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. FHIT mutations in human primary gastric cancer.
Gemma A; Hagiwara K; Ke Y; Burke LM; Khan MA; Nagashima M; Bennett WP; Harris CC
Cancer Res; 1997 Apr; 57(8):1435-7. PubMed ID: 9108441
[TBL] [Abstract][Full Text] [Related]
9. Alterations of the fragile histidine triad gene in hepatitis C virus-associated hepatocellular carcinoma.
Zekri AR; Bahnassy AA; Hafez M; El-Shehaby AM; Sherif GM; Khaled HM; Zakhary N
J Gastroenterol Hepatol; 2005 Jan; 20(1):87-94. PubMed ID: 15610452
[TBL] [Abstract][Full Text] [Related]
10. Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4).
Abed AA; Günther K; Kraus C; Hohenberger W; Ballhausen WG
Hum Mutat; 2001 Nov; 18(5):397-410. PubMed ID: 11668633
[TBL] [Abstract][Full Text] [Related]
11. [Analysis of instability and deletion on chromosome 3p14 in Peutz-Jeghers syndrome].
Kang L; Zhao M; Zhang J
Zhonghua Yi Xue Za Zhi; 1999 Oct; 79(10):735-8. PubMed ID: 11715518
[TBL] [Abstract][Full Text] [Related]
12. Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients.
Yoon KA; Ku JL; Choi HS; Heo SC; Jeong SY; Park YJ; Kim NK; Kim JC; Jung PM; Park JG
Br J Cancer; 2000 Apr; 82(8):1403-6. PubMed ID: 10780518
[TBL] [Abstract][Full Text] [Related]
13. Chromosome 3p14 alterations in lung cancer: evidence that FHIT exon deletion is a target of tobacco carcinogens and asbestos.
Nelson HH; Wiencke JK; Gunn L; Wain JC; Christiani DC; Kelsey KT
Cancer Res; 1998 May; 58(9):1804-7. PubMed ID: 9581816
[TBL] [Abstract][Full Text] [Related]
14. [Mutation characteristic of STK].
Li Y; Lu X; Xia J; Tang X; Xia K; He Y; Zhang G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):4-7. PubMed ID: 11172631
[TBL] [Abstract][Full Text] [Related]
15. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
16. Gene mutations in esophageal mucosa of chagas disease patients.
DA Silva Manoel-Caetano F; Silveira AF; Silva AE
Anticancer Res; 2009 Apr; 29(4):1243-7. PubMed ID: 19414370
[TBL] [Abstract][Full Text] [Related]
17. Promoter methylation and loss of coding exons of the fragile histidine triad (FHIT) gene in intrahepatic cholangiocarcinomas.
Foja S; Goldberg M; Schagdarsurengin U; Dammann R; Tannapfel A; Ballhausen WG
Liver Int; 2005 Dec; 25(6):1202-8. PubMed ID: 16343073
[TBL] [Abstract][Full Text] [Related]
18. Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11.
Trojan J; Brieger A; Raedle J; Roth WK; Zeuzem S
Am J Gastroenterol; 1999 Jan; 94(1):257-61. PubMed ID: 9934767
[TBL] [Abstract][Full Text] [Related]
19. [Association of fragile histidine triad gene (FHIT) with susceptibility to esophageal cancer. A preliminary study].
Li W; Wang X; Cheng G
Zhonghua Zhong Liu Za Zhi; 1998 Jul; 20(4):258-60. PubMed ID: 10920977
[TBL] [Abstract][Full Text] [Related]
20. An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
Chow E; Meldrum CJ; Crooks R; Macrae F; Spigelman AD; Scott RJ
Clin Genet; 2006 Nov; 70(5):409-14. PubMed ID: 17026623
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]