Nilbert M - Search Results

1

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. Eur J Cancer. 1999 Jun;35(6):942-5. doi: 10.1016/s0959-8049(99)00045-3. Eur J Cancer. 1999. PMID: 10533476

2

A somatic BRCA2 mutation in RER+ endometrial carcinomas that specifically deletes the amino-terminal transactivation domain.

Koul A, Nilbert M, Borg A. Koul A, et al. Among authors: nilbert m. Genes Chromosomes Cancer. 1999 Mar;24(3):207-12. doi: 10.1002/(sici)1098-2264(199903)24:3<207::aid-gcc5>3.0.co;2-3. Genes Chromosomes Cancer. 1999. PMID: 10451700

3

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. Among authors: nilbert m. 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

4

Involvement of adenomatous polyposis coli (APC)/beta-catenin signalling in human breast cancer.

Jönsson M, Borg A, Nilbert M, Andersson T. Jönsson M, et al. Among authors: nilbert m. Eur J Cancer. 2000 Jan;36(2):242-8. doi: 10.1016/s0959-8049(99)00276-2. Eur J Cancer. 2000. PMID: 10741284

5

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. Among authors: nilbert m. 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

6

Lack of activating c-SRC mutations at codon 531 in rectal cancer.

Nilbert M, Fernebro E. Nilbert M, et al. Cancer Genet Cytogenet. 2000 Aug;121(1):94-5. doi: 10.1016/s0165-4608(00)00226-0. Cancer Genet Cytogenet. 2000. PMID: 10958949

7

Prognostic importance of the soluble plasminogen activator receptor, suPAR, in plasma from rectal cancer patients.

Fernebro E, Madsen RR, Fernö M, Brünner N, Bendahl P, Christensen IJ, Johnson A, Nilbert M. Fernebro E, et al. Among authors: nilbert m. Eur J Cancer. 2001 Mar;37(4):486-91. doi: 10.1016/s0959-8049(00)00422-6. Eur J Cancer. 2001. PMID: 11267858

8

Beta-catenin activation through mutation is rare in rectal cancer.

Nilbert M, Rambech E. Nilbert M, et al. Cancer Genet Cytogenet. 2001 Jul 1;128(1):43-5. doi: 10.1016/s0165-4608(01)00397-1. Cancer Genet Cytogenet. 2001. PMID: 11454429

9

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. Among authors: nilbert m. Cancer Genet Cytogenet. 2002 Apr 1;134(1):46-54. doi: 10.1016/s0165-4608(01)00587-8. Cancer Genet Cytogenet. 2002. PMID: 11996796

10

Distinct sets of gene alterations in endometrial carcinoma implicate alternate modes of tumorigenesis.

Koul A, Willén R, Bendahl PO, Nilbert M, Borg A. Koul A, et al. Among authors: nilbert m. Cancer. 2002 May 1;94(9):2369-79. doi: 10.1002/cncr.10498. Cancer. 2002. PMID: 12015762 Free article.

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