Park WS - Search Results

1

Use of microdissection and molecular genetics in the pathologic diagnosis of retinoblastoma.

Whitcup SM, Park WS, Gasch AT, Eagle RC, Filie AC, Nussenblatt RB, Zhuang Z, Chan CC. Whitcup SM, et al. Among authors: park ws. Retina. 1999;19(4):318-24. doi: 10.1097/00006982-199907000-00009. Retina. 1999. PMID: 10458298

2

Fine-needle aspiration of metastatic clear cell carcinoma of the kidney: employment of microdissection and the polymerase chain reaction as a potential diagnostic tool.

Beaty MW, Zhuang Z, Park WS, Emmert-Buck MR, Linehan WM, Lubensky IA, Abati A. Beaty MW, et al. Among authors: park ws. Cancer. 1997 Jun 25;81(3):180-6. Cancer. 1997. PMID: 9196017

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

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

5

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

6

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

7

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

8

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

9

Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas.

Zhuang Z, Vortmeyer AO, Pack S, Huang S, Pham TA, Wang C, Park WS, Agarwal SK, Debelenko LV, Kester M, Guru SC, Manickam P, Olufemi SE, Yu F, Heppner C, Crabtree JS, Skarulis MC, Venzon DJ, Emmert-Buck MR, Spiegel AM, Chandrasekharappa SC, Collins FS, Burns AL, Marx SJ, Lubensky IA, et al. Zhuang Z, et al. Among authors: park ws. Cancer Res. 1997 Nov 1;57(21):4682-6. Cancer Res. 1997. PMID: 9354421

10

Loss of heterozygosity is detected at chromosomes 1p35-36 (NB), 3p25 (VHL), 16p13 (TSC2/PKD1), and 17p13 (TP53) in microdissected apocrine carcinomas of the breast.

Lininger RA, Zhuang Z, Man Y, Park WS, Emmert-Buck M, Tavassoli FA. Lininger RA, et al. Among authors: park ws. Mod Pathol. 1999 Dec;12(12):1083-9. Mod Pathol. 1999. PMID: 10619258

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