Allinen M - Search Results

1

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer.

Pylkäs K, Tommiska J, Syrjäkoski K, Kere J, Gatei M, Waddell N, Allinen M, Karppinen SM, Rapakko K, Kääriäinen H, Aittomäki K, Blomqvist C, Mustonen A, Holli K, Khanna KK, Kallioniemi OP, Nevanlinna H, Winqvist R. Pylkäs K, et al. Among authors: allinen m. Carcinogenesis. 2007 May;28(5):1040-5. doi: 10.1093/carcin/bgl237. Epub 2006 Dec 13. Carcinogenesis. 2007. PMID: 17166884

2

Germline TP53 alterations in Finnish breast cancer families are rare and occur at conserved mutation-prone sites.

Rapakko K, Allinen M, Syrjäkoski K, Vahteristo P, Huusko P, Vähäkangas K, Eerola H, Kainu T, Kallioniemi OP, Nevanlinna H, Winqvist R. Rapakko K, et al. Among authors: allinen m. Br J Cancer. 2001 Jan 5;84(1):116-9. doi: 10.1054/bjoc.2000.1530. Br J Cancer. 2001. PMID: 11139324 Free PMC article.

3

Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: indications of TSLC1 promoter hypermethylation.

Allinen M, Peri L, Kujala S, Lahti-Domenici J, Outila K, Karppinen SM, Launonen V, Winqvist R. Allinen M, et al. Genes Chromosomes Cancer. 2002 Aug;34(4):384-9. doi: 10.1002/gcc.10079. Genes Chromosomes Cancer. 2002. PMID: 12112527

4

Genome-wide scanning for linkage in Finnish breast cancer families.

Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, Leisti J, Blanco G, Puistola U, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi OP. Huusko P, et al. Among authors: allinen m. Eur J Hum Genet. 2004 Feb;12(2):98-104. doi: 10.1038/sj.ejhg.5201091. Eur J Hum Genet. 2004. PMID: 14560309

5

Mutation analysis of the CHK2 gene in families with hereditary breast cancer.

Allinen M, Huusko P, Mäntyniemi S, Launonen V, Winqvist R. Allinen M, et al. Br J Cancer. 2001 Jul 20;85(2):209-12. doi: 10.1054/bjoc.2001.1858. Br J Cancer. 2001. PMID: 11461078 Free PMC article.

6

Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families.

Lahti-Domenici J, Rapakko K, Pääkkönen K, Allinen M, Nevanlinna H, Kujala M, Huusko P, Winqvist R. Lahti-Domenici J, et al. Among authors: allinen m. Cancer Genet Cytogenet. 2001 Sep;129(2):120-3. doi: 10.1016/s0165-4608(01)00437-x. Cancer Genet Cytogenet. 2001. PMID: 11566341

7

No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families.

Karppinen SM, Vuosku J, Heikkinen K, Allinen M, Winqvist R. Karppinen SM, et al. Among authors: allinen m. Eur J Cancer. 2003 Feb;39(3):366-71. doi: 10.1016/s0959-8049(02)00498-7. Eur J Cancer. 2003. PMID: 12565990

8

Characterization and expression of the human WNT4; lack of associated germline mutations in high--to moderate--risk breast and ovarian cancer.

Peltoketo H, Allinen M, Vuosku J, Kujala S, Lundan T, Salminen A, Winqvist R, Vainio S. Peltoketo H, et al. Among authors: allinen m. Cancer Lett. 2004 Sep 15;213(1):83-90. doi: 10.1016/j.canlet.2004.02.024. Cancer Lett. 2004. PMID: 15312687

9

ATM mutations in Finnish breast cancer patients.

Allinen M, Launonen V, Laake K, Jansen L, Huusko P, Kääriäinen H, Børresen-Dale AL, Winqvist R. Allinen M, et al. J Med Genet. 2002 Mar;39(3):192-6. doi: 10.1136/jmg.39.3.192. J Med Genet. 2002. PMID: 11897822 Free PMC article. No abstract available.

10

Connexin 26 mutations and nonsyndromic hearing impairment in northern Finland.

Löppönen T, Väisänen ML, Luotonen M, Allinen M, Uusimaa J, Lindholm P, Mäki-Torkko E, Väyrynen M, Löppönen H, Leisti J. Löppönen T, et al. Among authors: allinen m. Laryngoscope. 2003 Oct;113(10):1758-63. doi: 10.1097/00005537-200310000-00018. Laryngoscope. 2003. PMID: 14520102

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