Lindblom A - Search Results

1

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

2

Familial breast cancer and genes involved in breast carcinogenesis.

Lindblom A. Lindblom A. Breast Cancer Res Treat. 1995 May;34(2):171-83. doi: 10.1007/BF00665789. Breast Cancer Res Treat. 1995. PMID: 7647334 Review.

3

High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium.

Cornelis RS, Neuhausen SL, Johansson O, Arason A, Kelsell D, Ponder BA, Tonin P, Hamann U, Lindblom A, Lalle P, et al. Cornelis RS, et al. Among authors: lindblom a. Genes Chromosomes Cancer. 1995 Jul;13(3):203-10. doi: 10.1002/gcc.2870130310. Genes Chromosomes Cancer. 1995. PMID: 7669740

4

Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families.

Tannergård P, Lipford JR, Kolodner R, Frödin JE, Nordenskjöld M, Lindblom A. Tannergård P, et al. Among authors: lindblom a. Cancer Res. 1995 Dec 15;55(24):6092-6. Cancer Res. 1995. PMID: 8521398

5

Low frequency of hMSH2 mutations in Swedish HNPCC families.

Wahlberg SS, Nyström-Lahti M, Kane MF, Kolodner RD, Peltomäki P, Lindblom A. Wahlberg SS, et al. Among authors: lindblom a. Int J Cancer. 1997 Feb 20;74(1):134-7. doi: 10.1002/(sici)1097-0215(19970220)74:1<134::aid-ijc22>3.0.co;2-e. Int J Cancer. 1997. PMID: 9036882 No abstract available.

6

A screening for BRCA1 mutations in breast and breast-ovarian cancer families from the Stockholm region.

Zelada-Hedman M, Wasteson Arver B, Claro A, Chen J, Werelius B, Kok H, Sandelin K, Håkansson S, Andersen TI, Borg A, Børresen Dale AL, Lindblom A. Zelada-Hedman M, et al. Among authors: lindblom a. Cancer Res. 1997 Jun 15;57(12):2474-7. Cancer Res. 1997. PMID: 9192828

7

Tumorigenesis in colorectal tumors from patients with hereditary non-polyposis colorectal cancer.

Tannergård P, Liu T, Weger A, Nordenskjöld M, Lindblom A. Tannergård P, et al. Among authors: lindblom a. Hum Genet. 1997 Nov;101(1):51-5. doi: 10.1007/s004390050585. Hum Genet. 1997. PMID: 9385369

8

DGGE screening of mutations in mismatch repair genes (hMSH2 and hMLH1) in 34 Swedish families with colorectal cancer.

Liu T, Wahlberg S, Rubio C, Holmberg E, Grönberg H, Lindblom A. Liu T, et al. Among authors: lindblom a. Clin Genet. 1998 Feb;53(2):131-5. doi: 10.1111/j.1399-0004.1998.tb02660.x. Clin Genet. 1998. PMID: 9611074

9

The APC gene I1307K variant is rare in Norwegian patients with familial and sporadic colorectal or breast cancer.

Lothe RA, Hektoen M, Johnsen H, Meling GI, Andersen TI, Rognum TO, Lindblom A, Børresen-Dale AL. Lothe RA, et al. Among authors: lindblom a. Cancer Res. 1998 Jul 15;58(14):2923-4. Cancer Res. 1998. PMID: 9679946

10

MSH2 codon 322 Gly to Asp seems not to confer an increased risk for colorectal cancer susceptibility.

Liu T, Stathopoulos P, Lindblom P, Rubio C, Wasteson Arver B, Iselius L, Holmberg E, Grönberg H, Lindblom A. Liu T, et al. Among authors: lindblom a, lindblom p. Eur J Cancer. 1998 Nov;34(12):1981. doi: 10.1016/s0959-8049(98)00217-2. Eur J Cancer. 1998. PMID: 10023327 No abstract available.

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