Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

1,094 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
WAF1, a potential mediator of p53 tumor suppression.
el-Deiry WS, Tokino T, Velculescu VE, Levy DB, Parsons R, Trent JM, Lin D, Mercer WE, Kinzler KW, Vogelstein B. el-Deiry WS, et al. Among authors: parsons r. Cell. 1993 Nov 19;75(4):817-25. doi: 10.1016/0092-8674(93)90500-p. Cell. 1993. PMID: 8242752
Hypermutability and mismatch repair deficiency in RER+ tumor cells.
Parsons R, Li GM, Longley MJ, Fang WH, Papadopoulos N, Jen J, de la Chapelle A, Kinzler KW, Vogelstein B, Modrich P. Parsons R, et al. Cell. 1993 Dec 17;75(6):1227-36. doi: 10.1016/0092-8674(93)90331-j. Cell. 1993. PMID: 8261516
Mutations of GTBP in genetically unstable cells.
Papadopoulos N, Nicolaides NC, Liu B, Parsons R, Lengauer C, Palombo F, D'Arrigo A, Markowitz S, Willson JK, Kinzler KW, et al. Papadopoulos N, et al. Among authors: parsons r. Science. 1995 Jun 30;268(5219):1915-7. doi: 10.1126/science.7604266. Science. 1995. PMID: 7604266
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.
Liu B, Parsons R, Papadopoulos N, Nicolaides NC, Lynch HT, Watson P, Jass JR, Dunlop M, Wyllie A, Peltomäki P, de la Chapelle A, Hamilton SR, Vogelstein B, Kinzler KW. Liu B, et al. Among authors: parsons r. Nat Med. 1996 Feb;2(2):169-74. doi: 10.1038/nm0296-169. Nat Med. 1996. PMID: 8574961
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
Leach FS, Nicolaides NC, Papadopoulos N, Liu B, Jen J, Parsons R, Peltomäki P, Sistonen P, Aaltonen LA, Nyström-Lahti M, et al. Leach FS, et al. Among authors: parsons r. Cell. 1993 Dec 17;75(6):1215-25. doi: 10.1016/0092-8674(93)90330-s. Cell. 1993. PMID: 8261515
PTEN: life as a tumor suppressor.
Simpson L, Parsons R. Simpson L, et al. Among authors: parsons r. Exp Cell Res. 2001 Mar 10;264(1):29-41. doi: 10.1006/excr.2000.5130. Exp Cell Res. 2001. PMID: 11237521 Review.
Point mutation and homozygous deletion of PTEN/MMAC1 in primary bladder cancers.
Cairns P, Evron E, Okami K, Halachmi N, Esteller M, Herman JG, Bose S, Wang SI, Parsons R, Sidransky D. Cairns P, et al. Among authors: parsons r. Oncogene. 1998 Jun 18;16(24):3215-8. doi: 10.1038/sj.onc.1201855. Oncogene. 1998. PMID: 9671402
Mutations in PTEN are frequent in endometrial carcinoma but rare in other common gynecological malignancies.
Tashiro H, Blazes MS, Wu R, Cho KR, Bose S, Wang SI, Li J, Parsons R, Ellenson LH. Tashiro H, et al. Among authors: parsons r. Cancer Res. 1997 Sep 15;57(18):3935-40. Cancer Res. 1997. PMID: 9307275
Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease.
Arch EM, Goodman BK, Van Wesep RA, Liaw D, Clarke K, Parsons R, McKusick VA, Geraghty MT. Arch EM, et al. Among authors: parsons r. Am J Med Genet. 1997 Sep 5;71(4):489-93. Am J Med Genet. 1997. PMID: 9286463
hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
Liu B, Parsons RE, Hamilton SR, Petersen GM, Lynch HT, Watson P, Markowitz S, Willson JK, Green J, de la Chapelle A, et al. Liu B, et al. Among authors: parsons re. Cancer Res. 1994 Sep 1;54(17):4590-4. Cancer Res. 1994. PMID: 8062247
1,094 results
Jump to page
Feedback