Golovleva I - Search Results

1

The Genetic Architecture of Gliomagenesis-Genetic Risk Variants Linked to Specific Molecular Subtypes.

Wu WY, Johansson G, Wibom C, Brännström T, Malmström A, Henriksson R, Golovleva I, Bondy ML, Andersson U, Dahlin AM, Melin B. Wu WY, et al. Among authors: golovleva i. Cancers (Basel). 2019 Dec 12;11(12):2001. doi: 10.3390/cancers11122001. Cancers (Basel). 2019. PMID: 31842352 Free PMC article. Review.

2

Cloning, characterization, and expression of human LIG1.

Nilsson J, Vallbo C, Guo D, Golovleva I, Hallberg B, Henriksson R, Hedman H. Nilsson J, et al. Among authors: golovleva i. Biochem Biophys Res Commun. 2001 Jun 29;284(5):1155-61. doi: 10.1006/bbrc.2001.5092. Biochem Biophys Res Commun. 2001. PMID: 11414704

3

Characterization and tissue-specific expression of human LRIG2.

Holmlund C, Nilsson J, Guo D, Starefeldt A, Golovleva I, Henriksson R, Hedman H. Holmlund C, et al. Among authors: golovleva i. Gene. 2004 May 12;332:35-43. doi: 10.1016/j.gene.2004.02.002. Gene. 2004. PMID: 15145052

4

Increased copy number at 3p14 in breast cancer.

Ljuslinder I, Malmer B, Golovleva I, Thomasson M, Grankvist K, Höckenström T, Emdin S, Jonsson Y, Hedman H, Henriksson R. Ljuslinder I, et al. Among authors: golovleva i. Breast Cancer Res. 2005;7(5):R719-27. doi: 10.1186/bcr1279. Epub 2005 Jul 6. Breast Cancer Res. 2005. PMID: 16168117 Free PMC article.

5

LRIG1 expression in colorectal cancer.

Ljuslinder I, Golovleva I, Palmqvist R, Oberg A, Stenling R, Jonsson Y, Hedman H, Henriksson R, Malmer B. Ljuslinder I, et al. Among authors: golovleva i. Acta Oncol. 2007;46(8):1118-22. doi: 10.1080/02841860701426823. Acta Oncol. 2007. PMID: 17851870

6

Co-incidental increase in gene copy number of ERBB2 and LRIG1 in breast cancer.

Ljuslinder I, Golovleva I, Henriksson R, Grankvist K, Malmer B, Hedman H. Ljuslinder I, et al. Among authors: golovleva i. Breast Cancer Res. 2009;11(3):403. doi: 10.1186/bcr2248. Epub 2009 May 12. Breast Cancer Res. 2009. PMID: 19490591 Free PMC article. No abstract available.

7

Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma.

Ghasimi S, Wibom C, Dahlin AM, Brännström T, Golovleva I, Andersson U, Melin B. Ghasimi S, et al. Among authors: golovleva i. J Neurooncol. 2016 May;127(3):483-92. doi: 10.1007/s11060-016-2066-4. Epub 2016 Feb 2. J Neurooncol. 2016. PMID: 26839018 Free PMC article.

8

A population based cohort study of patients with multiple colon and endometrial cancer: correlation of microsatellite instability (MSI) status, age at diagnosis and cancer risk.

Cederquist K, Golovleva I, Emanuelsson M, Stenling R, Grönberg H. Cederquist K, et al. Among authors: golovleva i. Int J Cancer. 2001 Feb 15;91(4):486-91. doi: 10.1002/1097-0215(200002)9999:9999<::aid-ijc1093>3.0.co;2-p. Int J Cancer. 2001. PMID: 11251970 Free article.

9

hTERT gene copy number is not associated with hTERT RNA expression or telomerase activity in colorectal cancer.

Palmqvist R, Zhang A, Xu D, Golovleva I, Norrback KF, Gruber A, Oberg A, Stenling R, Roos G. Palmqvist R, et al. Among authors: golovleva i. Int J Cancer. 2005 Sep 1;116(3):395-400. doi: 10.1002/ijc.21020. Int J Cancer. 2005. PMID: 15818616 Free article.

10

Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.

Cederquist K, Emanuelsson M, Wiklund F, Golovleva I, Palmqvist R, Grönberg H. Cederquist K, et al. Among authors: golovleva i. Clin Genet. 2005 Dec;68(6):533-41. doi: 10.1111/j.1399-0004.2005.00537.x. Clin Genet. 2005. PMID: 16283884

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