Parsons RE - Search Results

1

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

2

Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability.

Liu B, Nicolaides NC, Markowitz S, Willson JK, Parsons RE, Jen J, Papadopolous N, Peltomäki P, de la Chapelle A, Hamilton SR, et al. Liu B, et al. Among authors: parsons re. Nat Genet. 1995 Jan;9(1):48-55. doi: 10.1038/ng0195-48. Nat Genet. 1995. PMID: 7704024

3

Genetic instability occurs in the majority of young patients with colorectal cancer.

Liu B, Farrington SM, Petersen GM, Hamilton SR, Parsons R, Papadopoulos N, Fujiwara T, Jen J, Kinzler KW, Wyllie AH, Vogelstein B, Dunlop MG, et al. Liu B, et al. Nat Med. 1995 Apr;1(4):348-52. doi: 10.1038/nm0495-348. Nat Med. 1995. PMID: 7585065

4

Microsatellite instability and mutations of the transforming growth factor beta type II receptor gene in colorectal cancer.

Parsons R, Myeroff LL, Liu B, Willson JK, Markowitz SD, Kinzler KW, Vogelstein B. Parsons R, et al. Cancer Res. 1995 Dec 1;55(23):5548-50. Cancer Res. 1995. PMID: 7585632

5

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. Science. 1995 Jun 30;268(5219):1915-7. doi: 10.1126/science.7604266. Science. 1995. PMID: 7604266

6

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. Nat Med. 1996 Feb;2(2):169-74. doi: 10.1038/nm0296-169. Nat Med. 1996. PMID: 8574961

7

The molecular basis of Turcot's syndrome.

Hamilton SR, Liu B, Parsons RE, Papadopoulos N, Jen J, Powell SM, Krush AJ, Berk T, Cohen Z, Tetu B, et al. Hamilton SR, et al. Among authors: parsons re. N Engl J Med. 1995 Mar 30;332(13):839-47. doi: 10.1056/NEJM199503303321302. N Engl J Med. 1995. PMID: 7661930 Free article.

8

Mismatch repair deficiency in phenotypically normal human cells.

Parsons R, Li GM, Longley M, Modrich P, Liu B, Berk T, Hamilton SR, Kinzler KW, Vogelstein B. Parsons R, et al. Science. 1995 May 5;268(5211):738-40. doi: 10.1126/science.7632227. Science. 1995. PMID: 7632227

9

Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.

Nyström-Lahti M, Parsons R, Sistonen P, Pylkkänen L, Aaltonen LA, Leach FS, Hamilton SR, Watson P, Bronson E, Fusaro R, et al. Nyström-Lahti M, et al. Am J Hum Genet. 1994 Oct;55(4):659-65. Am J Hum Genet. 1994. PMID: 7942843 Free PMC article.

10

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. Cell. 1993 Dec 17;75(6):1215-25. doi: 10.1016/0092-8674(93)90330-s. Cell. 1993. PMID: 8261515 Free article.

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