Park WS - Search Results

1

Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas.

Zhuang Z, Park WS, Pack S, Schmidt L, Vortmeyer AO, Pak E, Pham T, Weil RJ, Candidus S, Lubensky IA, Linehan WM, Zbar B, Weirich G. Zhuang Z, et al. Among authors: park ws. Nat Genet. 1998 Sep;20(1):66-9. doi: 10.1038/1727. Nat Genet. 1998. PMID: 9731534

2

Missense mutation of the MET gene detected in human glioma.

Moon YW, Weil RJ, Pack SD, Park WS, Pak E, Pham T, Karkera JD, Kim HK, Vortmeyer AO, Fuller BG, Zhuang Z. Moon YW, et al. Among authors: park ws. Mod Pathol. 2000 Sep;13(9):973-7. doi: 10.1038/modpathol.3880177. Mod Pathol. 2000. PMID: 11007037

3

Allelic deletion at chromosome 9p21(p16) and 17p13(p53) in microdissected sporadic dysplastic nevus.

Park WS, Vortmeyer AO, Pack S, Duray PH, Böni R, Guerami AA, Emmert-Buck MR, Liotta LA, Zhuang Z. Park WS, et al. Hum Pathol. 1998 Feb;29(2):127-30. doi: 10.1016/s0046-8177(98)90221-0. Hum Pathol. 1998. PMID: 9490270

4

Mutations of the STK11 gene in sporadic gastric carcinoma.

Park WS, Moon YW, Yang YM, Kim YS, Kim YD, Fuller BG, Vortmeyer AO, Fogt F, Lubensky IA, Zhuang Z. Park WS, et al. Int J Oncol. 1998 Sep;13(3):601-4. Int J Oncol. 1998. PMID: 9683800

5

Mutation of the uracil DNA glycosylase gene detected in glioblastoma.

Moon YW, Park WS, Vortmeyer AO, Weil RJ, Lee YS, Winters TA, Zhuang Z, Fuller BG. Moon YW, et al. Among authors: park ws. Mutat Res. 1998 Nov 3;421(2):191-6. doi: 10.1016/s0027-5107(98)00165-1. Mutat Res. 1998. PMID: 9852992

6

Somatic mutations in the kinase domain of the Met/hepatocyte growth factor receptor gene in childhood hepatocellular carcinomas.

Park WS, Dong SM, Kim SY, Na EY, Shin MS, Pi JH, Kim BJ, Bae JH, Hong YK, Lee KS, Lee SH, Yoo NJ, Jang JJ, Pack S, Zhuang Z, Schmidt L, Zbar B, Lee JY. Park WS, et al. Cancer Res. 1999 Jan 15;59(2):307-10. Cancer Res. 1999. PMID: 9927037

7

Molecular cytogenetic fingerprinting of esophageal squamous cell carcinoma by comparative genomic hybridization reveals a consistent pattern of chromosomal alterations.

Pack SD, Karkera JD, Zhuang Z, Pak ED, Balan KV, Hwu P, Park WS, Pham T, Ault DO, Glaser M, Liotta L, Detera-Wadleigh SD, Wadleigh RG. Pack SD, et al. Among authors: park ws. Genes Chromosomes Cancer. 1999 Jun;25(2):160-8. doi: 10.1002/(sici)1098-2264(199906)25:2<160::aid-gcc12>3.0.co;2-u. Genes Chromosomes Cancer. 1999. PMID: 10338000

8

Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.

Vortmeyer AO, Stavrou T, Selby D, Li G, Weil RJ, Park WS, Moon YW, Chandra R, Goldstein AM, Zhuang Z. Vortmeyer AO, et al. Among authors: park ws. Cancer. 1999 Jun 15;85(12):2662-7. Cancer. 1999. PMID: 10375116

9

Multiple endocrine neoplasia type 1: atypical presentation, clinical course, and genetic analysis of multiple tumors.

Vortmeyer AO, Lubensky IA, Skarulis M, Li G, Moon YW, Park WS, Weil R, Barlow C, Spiegel AM, Marx SJ, Zhuang Z. Vortmeyer AO, et al. Among authors: park ws. Mod Pathol. 1999 Sep;12(9):919-24. Mod Pathol. 1999. PMID: 10496602

10

Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization.

Pack SD, Zbar B, Pak E, Ault DO, Humphrey JS, Pham T, Hurley K, Weil RJ, Park WS, Kuzmin I, Stolle C, Glenn G, Liotta LA, Lerman MI, Klausner RD, Linehan WM, Zhuang Z. Pack SD, et al. Among authors: park ws. Cancer Res. 1999 Nov 1;59(21):5560-4. Cancer Res. 1999. PMID: 10554035

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