Planck M - Search Results

1

Defective mismatch-repair in patients with multiple primary tumours including colorectal cancer.

Ericson K, Halvarsson B, Nagel J, Rambech E, Planck M, Piotrowska Z, Olsson H, Nilbert M. Ericson K, et al. Among authors: planck m. Eur J Cancer. 2003 Jan;39(2):240-8. doi: 10.1016/s0959-8049(02)00584-1. Eur J Cancer. 2003. PMID: 12509957

2

hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden.

Planck M, Koul A, Fernebro E, Borg A, Kristoffersson U, Olsson H, Wenngren E, Mangell P, Nilbert M. Planck M, et al. Int J Cancer. 1999 Oct 8;83(2):197-202. doi: 10.1002/(sici)1097-0215(19991008)83:2<197::aid-ijc9>3.0.co;2-x. Int J Cancer. 1999. PMID: 10471527

3

Microsatellite instability is rare in rectal carcinomas and signifies hereditary cancer.

Nilbert M, Planck M, Fernebro E, Borg A, Johnson A. Nilbert M, et al. Among authors: planck m. Eur J Cancer. 1999 Jun;35(6):942-5. doi: 10.1016/s0959-8049(99)00045-3. Eur J Cancer. 1999. PMID: 10533476

4

Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation.

Planck M, Wenngren E, Borg A, Olsson H, Nilbert M. Planck M, et al. Genes Chromosomes Cancer. 2000 Sep;29(1):33-9. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1004>3.0.co;2-r. Genes Chromosomes Cancer. 2000. PMID: 10918391

5

Increased cancer risk in offspring of women with colorectal carcinoma: a Swedish register-based cohort study.

Planck M, Anderson H, Bladström A, Möller T, Wenngren E, Olsson H. Planck M, et al. Cancer. 2000 Aug 15;89(4):741-9. Cancer. 2000. PMID: 10951335

6

Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer.

Planck M, Halvarsson B, Pålsson E, Hallén M, Ekelund M, Pålsson B, Baldetorp B, Nilbert M. Planck M, et al. Cancer Genet Cytogenet. 2002 Apr 1;134(1):46-54. doi: 10.1016/s0165-4608(01)00587-8. Cancer Genet Cytogenet. 2002. PMID: 11996796

7

High frequency of microsatellite instability and loss of mismatch-repair protein expression in patients with double primary tumors of the endometrium and colorectum.

Planck M, Rambech E, Möslein G, Müller W, Olsson H, Nilbert M. Planck M, et al. Cancer. 2002 May 1;94(9):2502-10. doi: 10.1002/cncr.10501. Cancer. 2002. PMID: 12015776 Free article.

8

Microsatellite instability and expression of MLH1 and MSH2 in carcinomas of the small intestine.

Planck M, Ericson K, Piotrowska Z, Halvarsson B, Rambech E, Nilbert M. Planck M, et al. Cancer. 2003 Mar 15;97(6):1551-7. doi: 10.1002/cncr.11197. Cancer. 2003. PMID: 12627520 Free article.

9

Familial risk of tumors associated with hereditary non-polyposis colorectal cancer: a Swedish population-based study.

Ericson K, Nilbert M, Bladström A, Anderson H, Olsson H, Planck M. Ericson K, et al. Among authors: planck m. Scand J Gastroenterol. 2004 Dec;39(12):1259-65. doi: 10.1080/00365520410003506. Scand J Gastroenterol. 2004. PMID: 15743004

10

Phenotypic heterogeneity in hereditary non-polyposis colorectal cancer: identical germline mutations associated with variable tumour morphology and immunohistochemical expression.

Halvarsson B, Müller W, Planck M, Benoni AC, Mangell P, Ottosson J, Hallén M, Isinger A, Nilbert M. Halvarsson B, et al. Among authors: planck m. J Clin Pathol. 2007 Jul;60(7):781-6. doi: 10.1136/jcp.2006.040402. Epub 2006 Aug 10. J Clin Pathol. 2007. PMID: 16901974 Free PMC article.

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