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Amanda B Spurdle

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Gynecologic Oncology|June 25, 2003
The prohibitin 3' untranslated region polymorphism is not associated with risk of ovarian cancerAmanda B Spurdle, David M Purdie, Xiaoqing Chen, et al.
HGG Advances|March 13, 2023
Splicing annotation of endometrial cancer GWAS risk loci reveals potentially causal variants and supports a role for <i>NF1</i> and <i>SKAP1</i> as susceptibility genesDaffodil M Canson, Tracy A O'Mara, Amanda B Spurdle, et al.
Cancer Letters|December 22, 2006
Ovarian cancer survival and polymorphisms in hormone and DNA repair pathway genesChristina M Nagle, Georgia Chenevix-Trench, Penelope M Webb, et al.
Cancer Causes & Control : CCC|January 17, 2012
Use of talcum powder and endometrial cancer riskAnnette S Neill, Christina M Nagle, Amanda B Spurdle, et al.
European Journal of Cancer (Oxford, England : 1990)|November 7, 2006
The role of glutathione-S-transferase polymorphisms in ovarian cancer survivalChristina M Nagle, Georgia Chenevix-Trench, Amanda B Spurdle, et al.
Gynecologic Oncology|September 20, 2011
Gynecological conditions and the risk of endometrial cancerIngrid J Rowlands, Christina M Nagle, Amanda B Spurdle, et al.
American Journal of Human Genetics|May 30, 2024
Regional-specific calibration enables application of computational evidence for clinical classification of 5' cis-regulatory variants in Mendelian diseaseRehan M Villani, Maddison E McKenzie, Aimee L Davidson, et al.
Cancer Causes & Control : CCC|October 19, 2010
Polycystic ovary syndrome increases the risk of endometrial cancer in women aged less than 50 years: an Australian case-control studyEmily J Fearnley, Louise Marquart, Amanda B Spurdle, et al.
Cancer Letters|January 27, 2005
RAD52 Y415X truncation polymorphism and epithelial ovarian cancer risk in Australian womenLivia Kelemen, Amanda B Spurdle, David M Purdie, et al.
Breast Cancer Research and Treatment|December 21, 2007
Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriersLogan C Walker, Nic Waddell, Anette Ten Haaf, et al.
Pageof 40

Showing results (21-30 of 397) with videos related to

Sort By:
Pageof 40
Gynecologic Oncology|June 25, 2003
The prohibitin 3' untranslated region polymorphism is not associated with risk of ovarian cancerAmanda B Spurdle, David M Purdie, Xiaoqing Chen, et al.
HGG Advances|March 13, 2023
Splicing annotation of endometrial cancer GWAS risk loci reveals potentially causal variants and supports a role for <i>NF1</i> and <i>SKAP1</i> as susceptibility genesDaffodil M Canson, Tracy A O'Mara, Amanda B Spurdle, et al.
Cancer Letters|December 22, 2006
Ovarian cancer survival and polymorphisms in hormone and DNA repair pathway genesChristina M Nagle, Georgia Chenevix-Trench, Penelope M Webb, et al.
Cancer Causes & Control : CCC|January 17, 2012
Use of talcum powder and endometrial cancer riskAnnette S Neill, Christina M Nagle, Amanda B Spurdle, et al.
European Journal of Cancer (Oxford, England : 1990)|November 7, 2006
The role of glutathione-S-transferase polymorphisms in ovarian cancer survivalChristina M Nagle, Georgia Chenevix-Trench, Amanda B Spurdle, et al.
Gynecologic Oncology|September 20, 2011
Gynecological conditions and the risk of endometrial cancerIngrid J Rowlands, Christina M Nagle, Amanda B Spurdle, et al.
American Journal of Human Genetics|May 30, 2024
Regional-specific calibration enables application of computational evidence for clinical classification of 5' cis-regulatory variants in Mendelian diseaseRehan M Villani, Maddison E McKenzie, Aimee L Davidson, et al.
Cancer Causes & Control : CCC|October 19, 2010
Polycystic ovary syndrome increases the risk of endometrial cancer in women aged less than 50 years: an Australian case-control studyEmily J Fearnley, Louise Marquart, Amanda B Spurdle, et al.
Cancer Letters|January 27, 2005
RAD52 Y415X truncation polymorphism and epithelial ovarian cancer risk in Australian womenLivia Kelemen, Amanda B Spurdle, David M Purdie, et al.
Breast Cancer Research and Treatment|December 21, 2007
Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriersLogan C Walker, Nic Waddell, Anette Ten Haaf, et al.
Pageof 40