Bibliography
Gnarra, J. R., Tory, K., Weng, Y., Schmidt, L., Wei, M. H., Li, H., Latif, F., Liu, S., Chen, F., Duh, F.-M., Lubensky, I., Duan, D. R., Florence, C., Pozzatti, R., Walther, M. M., Bander, N. H., Grossman, H. B., Brauch, H., Pomer, S., ⦠Linehan, W. M. (1994). Mutations of the VHL tumour suppressor gene in renal carcinoma. Nature Genetics, 7(1), 85â90.
Authors
24
- J.R. Gnarra (first)
- K. Tory (additional)
- Y. Weng (additional)
- L. Schmidt (additional)
- M.H. Wei (additional)
- H. Li (additional)
- F. Latif (additional)
- S. Liu (additional)
- F. Chen (additional)
- F.-M. Duh (additional)
- I. Lubensky (additional)
- D.R. Duan (additional)
- C. Florence (additional)
- R. Pozzatti (additional)
- M. M. Walther (additional)
- N.H. Bander (additional)
- H.B. Grossman (additional)
- H. Brauch (additional)
- S. Pomer (additional)
- J.D. Brooks (additional)
- W.B. Isaacs (additional)
- M.I. Lerman (additional)
- B. Zbar (additional)
- W.M. Linehan (additional)
References
28
Referenced
1,360
- Knudson, A.G. Hereditary cancer, oncogenes, and antloncogenes. Cancer Res. 45, 1437–1443 (1985). / Cancer Res. by AG Knudson (1985)
-
Maher, E.R. et al. von Hippel-Lindau disease: a genetic study. J. med. Genet. 28, 443–447 (1991).
(
10.1136/jmg.28.7.443
) / J. med. Genet. by ER Maher (1991) - Linehan, W.M., Gnarra, J.R., Lerman, M.I., Latif, F. & Zbar, B. Genetic basis of renal cell cancer in Important Advances in Oncology (eds DeVita, V. T. et al) 47–70 (J.B. Lippincott Company, Philadelphia, 1993). / Important Advances in Oncology by WM Linehan (1993)
-
Lamiell, J.M., Salazar, F.G. & Hsia, Y.E. von Hippel-Lindau disease affecting 43 members of a single kindred. Medicine 68, 1–29 (1989).
(
10.1097/00005792-198901000-00001
) / Medicine by JM Lamiell (1989) - Glenn, G.M., Choyke, P.L., Zbar, B. & Linehan, W.M. von Hippel-Lindau disease: clinical review and molecular genetics. Problems Urol. 4, 312–330 (1990). / Problems Urol. by GM Glenn (1990)
-
Latif, F. et al. Identification of the von Hippel-Lindau disease tumour suppressor gene. Science 260, 1317–1320 (1993).
(
10.1126/science.8493574
) / Science by F Latif (1993) -
Cohen, A.J. et al. Hereditary renal cell carcinoma associated with a chromosomal translocation. New Engl. J. Med. 301, 592–595 (1979).
(
10.1056/NEJM197909133011107
) / New Engl. J. Med. by AJ Cohen (1979) -
Li, F.P. et al. Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Ann. int. Med. 118, 106–111 (1993).
(
10.7326/0003-4819-118-2-199301150-00005
) / Ann. int. Med. by FP Li (1993) - Farrow, G.M. Diseases of the kidney in Urological Pathology (ed Murphy, W. M.) 409–482 (W.B. Saunders Company, Philadelphia, 1989). / Urological Pathology by GM Farrow (1989)
- Kovacs, G. Papillary renal cell carcinoma: a morphologic and cytogenetic study of 11 cases. Am. J. Path. 134, 27–34 (1989). / Am. J. Path. by G Kovacs (1989)
-
Kovacs, G., Fuzesi, L., Emanuel, A. & Kung, H.-F. Cytogenetics of papillary renal cell tumors. Genes Chrom. Cancer 3, 249–255 (1991).
(
10.1002/gcc.2870030403
) / Genes Chrom. Cancer by G Kovacs (1991) -
Zbar, B. et al. Hereditary papillary renal cell carcinoma. J. Urol. 151, 561–566 (1994).
(
10.1016/S0022-5347(17)35015-2
) / J. Urol. by B Zbar (1994) - Anglard, P. et al. Molecular analysis of genetic changes in the origin and development of renal cell carcinoma. Cancer Res. 51, 1071–1077 (1991). / Cancer Res. by P Anglard (1991)
- Anglard, P. et al. Molecular and cellular characterization of human renal cell carcinoma cell lines. Cancer Res. 52, 348–356 (1992). / Cancer Res. by P Anglard (1992)
-
Brooks, J.D., Bova, G.S., Marshall, F.F. & Isaacs, W.B. Tumour suppressor gene allelic loss in human renal cancers. J. Urol. 150, 1278–1283 (1993).
(
10.1016/S0022-5347(17)35760-9
) / J. Urol. by JD Brooks (1993) - Makos, M. et al. Regional DNA hypermethylation at D17S5 precedes 17p structural changes in the progression of renal tumors. Cancer Res. 53, 2719–2722 (1993). / Cancer Res. by M Makos (1993)
- Reiter, R.E., Anglard, P., Liu, S., Gnarra, J.R. & Linehan, W.M. Chromosome 17p deletions and p53 mutations in renal cell carcinoma. Cancer Res. 53, 3092–3097 (1993). / Cancer Res. by RE Reiter (1993)
-
Mulligan, C.M. et al. Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. Nature Genet. 6, 70–74 (1994).
(
10.1038/ng0194-70
) / Nature Genet. by CM Mulligan (1994) -
Donis-Keller, H. et al. Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum. molec. Genetic. 2, 851–856 (1993).
(
10.1093/hmg/2.7.851
) / Hum. molec. Genetic. by H Donis-Keller (1993) -
Hofstra, R.M.W. et al. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medulary thyroid carcinoma. Nature 367, 375–376 (1994).
(
10.1038/367375a0
) / Nature by RMW Hofstra (1994) -
Romeo, G. et al. Point mutations affecting the tyroslne kinase domain of the RET proto-oncogene in Hirschsprung's disease. Nature 367, 377–378 (1994).
(
10.1038/367377a0
) / Nature by G Romeo (1994) -
Edery, P. et al. Mutations of the RET proto-oncogene in Hirschsprung's disease. Nature 367, 378–380 (1994).
(
10.1038/367378a0
) / Nature by P Edery (1994) -
Grossman, H.B., Wedemeyer, G. & Ren, L. Human renal carcinoma: characterization of five new cell lines. J. surg. Oncol. 28, 237–244 (1985).
(
10.1002/jso.2930280320
) / J. surg. Oncol. by HB Grossman (1985) - Ebert, T., Bander, N.H., Finstad, C.L., Ramsawak, R.D. & Old, L.J. Establishment and characterization of human renal cancer and normal kidney cell lines. Cancer Res. 50, 5531–5536 (1990). / Cancer Res. by T Ebert (1990)
-
Shrivastav, S., Sharief, Y., Day, J., Reich, C.F. & Bonar, R. Establishment and characterization of a cell line (SS78) from a human renal cell carcinoma. In Vitro 12, 1117–1124 (1981).
(
10.1007/BF02618614
) / In Vitro by S Shrivastav (1981) -
Robson, C.J., Churchill, B.M. & Anderson, W. The results of radical nephrectomy for renal cell carcinoma. J. Urol. 101, 297–301 (1969).
(
10.1016/S0022-5347(17)62331-0
) / J. Urol. by CJ Robson (1969) -
Zeiger, M.A., Gnarra, J.R., Zbar, B., Linehan, W.M. & Pass, H.I. Loss of heterozygosity on the short arm of chromosome 3 in mesothelioma cell lines and solid tumors. Genes Chrom. Can. (in the press).
(
10.1002/gcc.2870110104
) -
Herrmann, M.A. et al. Cytogenetic and moleculargenetic studies of follicular and papillary thyroid cancers. J. clin. Invest. 88, 1596–1604 (1991).
(
10.1172/JCI115472
) / J. clin. Invest. by MA Herrmann (1991)
Dates
Type | When |
---|---|
Created | 21 years ago (Aug. 18, 2004, 4:48 p.m.) |
Deposited | 2 years, 3 months ago (May 18, 2023, 4:35 p.m.) |
Indexed | 3 days, 19 hours ago (Aug. 21, 2025, 2:04 p.m.) |
Issued | 31 years, 3 months ago (May 1, 1994) |
Published | 31 years, 3 months ago (May 1, 1994) |
Published Print | 31 years, 3 months ago (May 1, 1994) |
@article{Gnarra_1994, title={Mutations of the VHL tumour suppressor gene in renal carcinoma}, volume={7}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/ng0594-85}, DOI={10.1038/ng0594-85}, number={1}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Gnarra, J.R. and Tory, K. and Weng, Y. and Schmidt, L. and Wei, M.H. and Li, H. and Latif, F. and Liu, S. and Chen, F. and Duh, F.-M. and Lubensky, I. and Duan, D.R. and Florence, C. and Pozzatti, R. and Walther, M. M. and Bander, N.H. and Grossman, H.B. and Brauch, H. and Pomer, S. and Brooks, J.D. and Isaacs, W.B. and Lerman, M.I. and Zbar, B. and Linehan, W.M.}, year={1994}, month=may, pages={85–90} }