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Items: 1 to 20 of 74

1.

Absence of GNAS and EGFL6 mutations in common human cancers.

Lee SH, Jeong EG, Soung YH, Lee JW, Yoo NJ, Lee SH.

Pathology. 2008 Jan;40(1):95-7. No abstract available.

PMID:
18038328
2.

Analysis of the frequency of GNAS codon 201 mutations in advanced colorectal cancer.

Idziaszczyk S, Wilson CH, Smith CG, Adams DJ, Cheadle JP.

Cancer Genet Cytogenet. 2010 Oct 1;202(1):67-9. doi: 10.1016/j.cancergencyto.2010.04.023. No abstract available.

PMID:
20804925
3.

GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation.

Nault JC, Fabre M, Couchy G, Pilati C, Jeannot E, Tran Van Nhieu J, Saint-Paul MC, De Muret A, Redon MJ, Buffet C, Salenave S, Balabaud C, Prevot S, Labrune P, Bioulac-Sage P, Scoazec JY, Chanson P, Zucman-Rossi J.

J Hepatol. 2012 Jan;56(1):184-91. doi: 10.1016/j.jhep.2011.07.018. Epub 2011 Aug 9.

PMID:
21835143
4.

Absence of GNAS mutation in colorectal carcinogenesis.

Lee H, La BM, Hwang I, Kang YN, Choi IJ, Lee JH.

Tumori. 2017 Mar 24;103(2):209-211. doi: 10.5301/tj.5000400. Epub 2015 Aug 26.

PMID:
26350188
5.

Mutational analysis of UBR5 gene encoding an E3 ubiquitin ligase in common human cancers.

Kim MS, Oh JE, Eom HS, Yoo NJ, Lee SH.

Pathology. 2010 Jan;42(1):93-4. doi: 10.3109/00313020903434322. No abstract available.

PMID:
20025491
6.

Mutational analysis of oncogenic AKT E17K mutation in common solid cancers and acute leukaemias.

Kim MS, Jeong EG, Yoo NJ, Lee SH.

Br J Cancer. 2008 May 6;98(9):1533-5. doi: 10.1038/sj.bjc.6604212. Epub 2008 Apr 8.

7.

Mutational analysis of caspase-14 gene in common carcinomas.

Yoo NJ, Soung YH, Lee SH, Jeong EG, Lee SH.

Pathology. 2007 Jun;39(3):330-3.

PMID:
17558860
8.

Frequent lack of GNAS mutations in colorectal adenocarcinoma associated with GNAS-mutated villous adenoma.

Sekine S, Ogawa R, Oshiro T, Kanemitsu Y, Taniguchi H, Kushima R, Kanai Y.

Genes Chromosomes Cancer. 2014 Apr;53(4):366-72. doi: 10.1002/gcc.22147. Epub 2014 Jan 28.

PMID:
24470207
9.

Absence of E17K mutation in the pleckstrin homology domain of AKT1 in gastrointestinal and liver cancers in the Korean population.

Cao Z, Song JH, Kim CJ, Cho YG, Kim SY, Nam SW, Lee JY, Park WS.

APMIS. 2008 Jun;116(6):530-3. No abstract available.

PMID:
18754328
10.

Mutational and expressional analyses of MYD88 gene in common solid cancers.

Je EM, Kim SS, Yoo NJ, Lee SH.

Tumori. 2012 Sep-Oct;98(5):663-9. doi: 10.1700/1190.13209.

PMID:
23235763
11.

GNAS mutation affecting codon 201 is rare in most human tumors.

Je EM, An CH, Chung YJ, Yoo NJ, Lee SH.

Pathol Oncol Res. 2015 Jul;21(3):859-60. doi: 10.1007/s12253-015-9919-6. Epub 2015 Mar 5. No abstract available.

PMID:
25740075
12.

Mutational analysis of tumour suppressor gene NF2 in common solid cancers and acute leukaemias.

Yoo NJ, Park SW, Lee SH.

Pathology. 2012 Jan;44(1):29-32. doi: 10.1097/PAT.0b013e32834c3599.

PMID:
22081132
13.

Somatic mutation of pro-cell death Bif-1 gene is rare in common human cancers.

Kim MS, Yoo NJ, Lee SH.

APMIS. 2008 Oct;116(10):939-40. doi: 10.1111/j.1600-0463.2008.01091.x. No abstract available.

PMID:
19132989
14.

High frequency of mutations of the PIK3CA gene in human cancers.

Samuels Y, Wang Z, Bardelli A, Silliman N, Ptak J, Szabo S, Yan H, Gazdar A, Powell SM, Riggins GJ, Willson JK, Markowitz S, Kinzler KW, Vogelstein B, Velculescu VE.

Science. 2004 Apr 23;304(5670):554. Epub 2004 Mar 11. No abstract available.

15.
16.

Absence of paxillin gene mutation in lung cancer and other common solid cancers.

Kim MS, Yoo NJ, Lee SH.

Tumori. 2011 Mar-Apr;97(2):211-3. doi: 10.1700/667.7785.

17.

Somatic mutations of BECN1, an autophagy-related gene, in human cancers.

Lee JW, Jeong EG, Lee SH, Yoo NJ, Lee SH.

APMIS. 2007 Jun;115(6):750-6.

PMID:
17550384
18.

Mutational analysis of proapoptotic ARTS P-loop domain in common human cancers.

Lee JW, Soung YH, Young Kim S, Woo Nam S, Sang Park W, Young Lee J, Jin Yoo N, Lee SH.

Pathol Res Pract. 2006;202(2):67-70. Epub 2005 Dec 22.

PMID:
16376484
19.
20.

Mutations in the ST7/RAY1/HELG locus rarely occur in primary colorectal, gastric, and hepatocellular carcinomas.

Yoshimura S, Yamada T, Ohwada S, Koyama T, Hamada K, Tago K, Sakamoto I, Takeyoshi I, Ikeya T, Makita F, Iino Y, Morishita Y.

Br J Cancer. 2003 Jun 16;88(12):1909-13.

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