Gnarra J - Search Results

1

Loss of heterozygosity of the human cytosolic glutathione peroxidase I gene in lung cancer.

Moscow JA, Schmidt L, Ingram DT, Gnarra J, Johnson B, Cowan KH. Moscow JA, et al. Among authors: gnarra j. Carcinogenesis. 1994 Dec;15(12):2769-73. doi: 10.1093/carcin/15.12.2769. Carcinogenesis. 1994. PMID: 8001233

2

Examination of human tumors for rhoA mutations.

Moscow JA, He R, Gnarra JR, Knutsen T, Weng Y, Zhao WP, Whang-Peng J, Linehan WM, Cowan KH. Moscow JA, et al. Among authors: gnarra jr. Oncogene. 1994 Jan;9(1):189-94. Oncogene. 1994. PMID: 8302578

3

Mutations of the VHL tumour suppressor gene in renal carcinoma.

Gnarra JR, Tory K, Weng Y, Schmidt L, Wei MH, Li H, Latif F, Liu S, Chen F, Duh FM, et al. Gnarra JR, et al. Nat Genet. 1994 May;7(1):85-90. doi: 10.1038/ng0594-85. Nat Genet. 1994. PMID: 7915601

4

Molecular cloning of the von Hippel-Lindau tumor suppressor gene and its role in renal carcinoma.

Gnarra JR, Duan DR, Weng Y, Humphrey JS, Chen DY, Lee S, Pause A, Dudley CF, Latif F, Kuzmin I, Schmidt L, Duh FM, Stackhouse T, Chen F, Kishida T, Wei MH, Lerman MI, Zbar B, Klausner RD, Linehan WM. Gnarra JR, et al. Biochim Biophys Acta. 1996 Mar 18;1242(3):201-10. doi: 10.1016/0304-419x(95)00012-5. Biochim Biophys Acta. 1996. PMID: 8603073 Review. No abstract available.

5

Loss of heterozygosity on the short arm of chromosome 3 in mesothelioma cell lines and solid tumors.

Zeiger MA, Gnarra JR, Zbar B, Linehan WM, Pass HI. Zeiger MA, et al. Among authors: gnarra jr. Genes Chromosomes Cancer. 1994 Sep;11(1):15-20. doi: 10.1002/gcc.2870110104. Genes Chromosomes Cancer. 1994. PMID: 7529042

6

von Hippel-Lindau syndrome: cloning and identification of the plasma membrane Ca(++)-transporting ATPase isoform 2 gene that resides in the von Hippel-Lindau gene region.

Latif F, Duh FM, Gnarra J, Tory K, Kuzmin I, Yao M, Stackhouse T, Modi W, Geil L, Schmidt L, et al. Latif F, et al. Among authors: gnarra j. Cancer Res. 1993 Feb 15;53(4):861-7. Cancer Res. 1993. PMID: 8428366

7

Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma.

Zeiger MA, Zbar B, Keiser H, Linehan WM, Gnarra JR. Zeiger MA, et al. Among authors: gnarra jr. Genes Chromosomes Cancer. 1995 Jul;13(3):151-6. doi: 10.1002/gcc.2870130303. Genes Chromosomes Cancer. 1995. PMID: 7669733

8

von Hippel-Lindau disease gene deletion detected in microdissected sporadic human colon carcinoma specimens.

Zhuang Z, Emmert-Buck MR, Roth MJ, Gnarra J, Linehan WM, Liotta LA, Lubensky IA. Zhuang Z, et al. Among authors: gnarra j. Hum Pathol. 1996 Feb;27(2):152-6. doi: 10.1016/s0046-8177(96)90368-8. Hum Pathol. 1996. PMID: 8617456

9

Loss of heterozygosity occurs centromeric to RB without associated abnormalities in the retinoblastoma gene in tumors from patients with metastatic renal cell carcinoma.

Walther MM, Gnarra JR, Elwood L, Xu HJ, Florence C, Anglard P, Hu SX, King C, Trahan E, Hurley K, et al. Walther MM, et al. Among authors: gnarra jr. J Urol. 1995 Jun;153(6):2050-4. J Urol. 1995. PMID: 7752392

10

Molecular analysis of the von Hippel-Lindau disease tumor suppressor gene in human lung cancer cell lines.

Sekido Y, Bader S, Latif F, Gnarra JR, Gazdar AF, Linehan WM, Zbar B, Lerman MI, Minna JD. Sekido Y, et al. Among authors: gnarra jr. Oncogene. 1994 Jun;9(6):1599-604. Oncogene. 1994. PMID: 8183553

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