Salovaara R - Search Results

1

Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer.

Hemminki A, Peltomäki P, Mecklin JP, Järvinen H, Salovaara R, Nyström-Lahti M, de la Chapelle A, Aaltonen LA. Hemminki A, et al. Among authors: salovaara r. Nat Genet. 1994 Dec;8(4):405-10. doi: 10.1038/ng1294-405. Nat Genet. 1994. PMID: 7894494

2

Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability.

Kuismanen SA, Moisio AL, Schweizer P, Truninger K, Salovaara R, Arola J, Butzow R, Jiricny J, Nyström-Lahti M, Peltomäki P. Kuismanen SA, et al. Among authors: salovaara r. Am J Pathol. 2002 Jun;160(6):1953-8. doi: 10.1016/S0002-9440(10)61144-3. Am J Pathol. 2002. PMID: 12057899 Free PMC article.

3

Little evidence for involvement of MLH3 in colorectal cancer predisposition.

Hienonen T, Laiho P, Salovaara R, Mecklin JP, Järvinen H, Sistonen P, Peltomäki P, Lehtonen R, Nupponen NN, Launonen V, Karhu A, Aaltonen LA. Hienonen T, et al. Among authors: salovaara r. Int J Cancer. 2003 Aug 20;106(2):292-6. doi: 10.1002/ijc.11218. Int J Cancer. 2003. PMID: 12800209 Free article.

4

Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancer.

Renkonen E, Zhang Y, Lohi H, Salovaara R, Abdel-Rahman WM, Nilbert M, Aittomaki K, Jarvinen HJ, Mecklin JP, Lindblom A, Peltomaki P. Renkonen E, et al. Among authors: salovaara r. J Clin Oncol. 2003 Oct 1;21(19):3629-37. doi: 10.1200/JCO.2003.03.181. J Clin Oncol. 2003. PMID: 14512394

5

Semiautomated assessment of loss of heterozygosity and replication error in tumors.

Canzian F, Salovaara R, Hemminki A, Kristo P, Chadwick RB, Aaltonen LA, de la Chapelle A. Canzian F, et al. Among authors: salovaara r. Cancer Res. 1996 Jul 15;56(14):3331-7. Cancer Res. 1996. PMID: 8764130

6

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis.

Hemminki A, Tomlinson I, Markie D, Järvinen H, Sistonen P, Björkqvist AM, Knuutila S, Salovaara R, Bodmer W, Shibata D, de la Chapelle A, Aaltonen LA. Hemminki A, et al. Among authors: salovaara r. Nat Genet. 1997 Jan;15(1):87-90. doi: 10.1038/ng0197-87. Nat Genet. 1997. PMID: 8988175

7

Features of gastric cancer in hereditary non-polyposis colorectal cancer syndrome.

Aarnio M, Salovaara R, Aaltonen LA, Mecklin JP, Järvinen HJ. Aarnio M, et al. Among authors: salovaara r. Int J Cancer. 1997 Oct 21;74(5):551-5. doi: 10.1002/(sici)1097-0215(19971021)74:5<551::aid-ijc13>3.0.co;2-9. Int J Cancer. 1997. PMID: 9355980 Free article.

8

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.

Hemminki A, Markie D, Tomlinson I, Avizienyte E, Roth S, Loukola A, Bignell G, Warren W, Aminoff M, Höglund P, Järvinen H, Kristo P, Pelin K, Ridanpää M, Salovaara R, Toro T, Bodmer W, Olschwang S, Olsen AS, Stratton MR, de la Chapelle A, Aaltonen LA. Hemminki A, et al. Among authors: salovaara r. Nature. 1998 Jan 8;391(6663):184-7. doi: 10.1038/34432. Nature. 1998. PMID: 9428765

9

Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease.

Aaltonen LA, Salovaara R, Kristo P, Canzian F, Hemminki A, Peltomäki P, Chadwick RB, Kääriäinen H, Eskelinen M, Järvinen H, Mecklin JP, de la Chapelle A. Aaltonen LA, et al. Among authors: salovaara r. N Engl J Med. 1998 May 21;338(21):1481-7. doi: 10.1056/NEJM199805213382101. N Engl J Med. 1998. PMID: 9593786 Free article.

10

Cancer risk in mutation carriers of DNA-mismatch-repair genes.

Aarnio M, Sankila R, Pukkala E, Salovaara R, Aaltonen LA, de la Chapelle A, Peltomäki P, Mecklin JP, Järvinen HJ. Aarnio M, et al. Among authors: salovaara r. Int J Cancer. 1999 Apr 12;81(2):214-8. doi: 10.1002/(sici)1097-0215(19990412)81:2<214::aid-ijc8>3.0.co;2-l. Int J Cancer. 1999. PMID: 10188721 Free article.

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