Lindblom A - Search Results

1

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.

Clendenning M, Senter L, Hampel H, Robinson KL, Sun S, Buchanan D, Walsh MD, Nilbert M, Green J, Potter J, Lindblom A, de la Chapelle A. Clendenning M, et al. Among authors: lindblom a. J Med Genet. 2008 Jun;45(6):340-5. doi: 10.1136/jmg.2007.056150. Epub 2008 Jan 4. J Med Genet. 2008. PMID: 18178629 Free PMC article.

2

MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer.

Huang J, Kuismanen SA, Liu T, Chadwick RB, Johnson CK, Stevens MW, Richards SK, Meek JE, Gao X, Wright FA, Mecklin JP, Järvinen HJ, Grönberg H, Bisgaard ML, Lindblom A, Peltomäki P. Huang J, et al. Among authors: lindblom a. Cancer Res. 2001 Feb 15;61(4):1619-23. Cancer Res. 2001. PMID: 11245474

3

[Essential to discover hereditary colorectal and endometrial cancer. Mutations in "HNPCC individuals" can cause several different tumors].

Nilbert M, Grönberg H, Lindblom A. Nilbert M, et al. Among authors: lindblom a. Lakartidningen. 2002 Aug 22;99(34):3296-300. Lakartidningen. 2002. PMID: 12362848 Review. Swedish.

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: lindblom a. J Clin Oncol. 2003 Oct 1;21(19):3629-37. doi: 10.1200/JCO.2003.03.181. J Clin Oncol. 2003. PMID: 14512394

5

Microsatellite instability analysis and/or immunostaining for the diagnosis of hereditary nonpolyposis colorectal cancer?

Halvarsson B, Lindblom A, Rambech E, Lagerstedt K, Nilbert M. Halvarsson B, et al. Among authors: lindblom a. Virchows Arch. 2004 Feb;444(2):135-41. doi: 10.1007/s00428-003-0922-z. Epub 2003 Dec 2. Virchows Arch. 2004. PMID: 14652751

6

Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC.

Di Fiore F, Charbonnier F, Martin C, Frerot S, Olschwang S, Wang Q, Boisson C, Buisine MP, Nilbert M, Lindblom A, Frebourg T. Di Fiore F, et al. Among authors: lindblom a. J Med Genet. 2004 Jan;41(1):18-20. doi: 10.1136/jmg.2003.012062. J Med Genet. 2004. PMID: 14729822 Free PMC article. Review. No abstract available.

7

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.

Umar A, Boland CR, Terdiman JP, Syngal S, de la Chapelle A, Rüschoff J, Fishel R, Lindor NM, Burgart LJ, Hamelin R, Hamilton SR, Hiatt RA, Jass J, Lindblom A, Lynch HT, Peltomaki P, Ramsey SD, Rodriguez-Bigas MA, Vasen HF, Hawk ET, Barrett JC, Freedman AN, Srivastava S. Umar A, et al. Among authors: lindblom a. J Natl Cancer Inst. 2004 Feb 18;96(4):261-8. doi: 10.1093/jnci/djh034. J Natl Cancer Inst. 2004. PMID: 14970275 Free PMC article.

8

BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing.

Domingo E, Laiho P, Ollikainen M, Pinto M, Wang L, French AJ, Westra J, Frebourg T, Espín E, Armengol M, Hamelin R, Yamamoto H, Hofstra RM, Seruca R, Lindblom A, Peltomäki P, Thibodeau SN, Aaltonen LA, Schwartz S Jr. Domingo E, et al. Among authors: lindblom a. J Med Genet. 2004 Sep;41(9):664-8. doi: 10.1136/jmg.2004.020651. J Med Genet. 2004. PMID: 15342696 Free PMC article.

9

Loss of mismatch repair protein immunostaining in colorectal adenomas from patients with hereditary nonpolyposis colorectal cancer.

Halvarsson B, Lindblom A, Johansson L, Lagerstedt K, Nilbert M. Halvarsson B, et al. Among authors: lindblom a. Mod Pathol. 2005 Aug;18(8):1095-101. doi: 10.1038/modpathol.3800392. Mod Pathol. 2005. PMID: 15731775 Free article.

10

Long-range PCR facilitates the identification of PMS2-specific mutations.

Clendenning M, Hampel H, LaJeunesse J, Lindblom A, Lockman J, Nilbert M, Senter L, Sotamaa K, de la Chapelle A. Clendenning M, et al. Among authors: lindblom a. Hum Mutat. 2006 May;27(5):490-5. doi: 10.1002/humu.20318. Hum Mutat. 2006. PMID: 16619239

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