Pham T - 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: pham t. Nat Genet. 1998 Sep;20(1):66-9. doi: 10.1038/1727. Nat Genet. 1998. PMID: 9731534

2

Concordance of genetic alterations in poorly differentiated colorectal neuroendocrine carcinomas and associated adenocarcinomas.

Vortmeyer AO, Lubensky IA, Merino MJ, Wang CY, Pham T, Furth EE, Zhuang Z. Vortmeyer AO, et al. Among authors: pham t. J Natl Cancer Inst. 1997 Oct 1;89(19):1448-53. doi: 10.1093/jnci/89.19.1448. J Natl Cancer Inst. 1997. PMID: 9326914

3

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: pham ta. Cancer Res. 1997 Nov 1;57(21):4682-6. Cancer Res. 1997. PMID: 9354421

4

LOH at 16p13 is a novel chromosomal alteration detected in benign and malignant microdissected papillary neoplasms of the breast.

Lininger RA, Park WS, Man YG, Pham T, MacGrogan G, Zhuang Z, Tavassoli FA. Lininger RA, et al. Among authors: pham t. Hum Pathol. 1998 Oct;29(10):1113-8. doi: 10.1016/s0046-8177(98)90422-1. Hum Pathol. 1998. PMID: 9781650

5

Loss of heterozygosity and microsatellite instability in non-neoplastic mucosa from patients with chronic ulcerative colitis.

Park WS, Pham T, Wang C, Pack S, Mueller E, Mueller J, Vortmeyer A, Zhuang Z, Fogt F. Park WS, et al. Among authors: pham t. Int J Mol Med. 1998 Aug;2(2):221-224. Int J Mol Med. 1998. PMID: 9855692

6

Detection of loss of heterozygosity on chromosome 9q22.3 in microdissected sporadic basal cell carcinoma.

Shen T, Park WS, Böni R, Saini N, Pham T, Lash AE, Vortmeyer AO, Zhuang Z. Shen T, et al. Among authors: pham t. Hum Pathol. 1999 Mar;30(3):284-7. doi: 10.1016/s0046-8177(99)90006-0. Hum Pathol. 1999. PMID: 10088546

7

Nuclear/cytoplasmic localization of the multiple endocrine neoplasia type 1 gene product, menin.

Huang SC, Zhuang Z, Weil RJ, Pack S, Wang C, Krutzsch HC, Pham TA, Lubensky IA. Huang SC, et al. Among authors: pham ta. Lab Invest. 1999 Mar;79(3):301-10. Lab Invest. 1999. PMID: 10092066

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: pham t. 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

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: pham t. Cancer Res. 1999 Nov 1;59(21):5560-4. Cancer Res. 1999. PMID: 10554035

10

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: pham t. Mod Pathol. 2000 Sep;13(9):973-7. doi: 10.1038/modpathol.3880177. Mod Pathol. 2000. PMID: 11007037

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